Pediatric Clerkship Manual Website 021420
Pediatric Clerkship Manual Website 021420
Pediatric Clerkship Manual Website 021420
Sites
V.02/20 (Web)
Core Pediatric Clerkship Manual Directory (Website)
Overview Tab
Educational Objectives 3
Pediatric Clinical Skills 4
Minimal Competency Outline for Pediatric Clinical Skills 5-13
Assignments Tab
Checklist of Assignments (Use page based on location or program)
WWAMI Regional Sites and LIC Program 18
Seattle Children's Hospital (6-week) 19
WRITE Program 20
1
OVERVIEW
2
Educational Objectives
The practice of Pediatrics involves addressing the health needs of children. Every child should have
the opportunity to grow and develop to achieve his or her maximum potential; the job of the
Pediatrician is to assist in that process by treating and preventing illness, guiding children and their
families toward good health choices, and offering information and interventions that support the
overall well-being of the child.
Goals of the core pediatric clerkship: Provide foundational skills and knowledge about the
fundamental issues of childhood health and illness in order to prepare UW SOM medical students to
provide safe and compassionate care to children.
Learning Objectives:
1. Collect both focused and comprehensive, developmentally appropriate patient histories using
triadic interviewing skills.
2. Perform an age appropriate physical examination on newborns, infants and older children.
3. Construct an appropriate approach to common pediatric clinical problems by:
a. Identifying essential clinical features.
b. Outlining natural history of disease processes.
c. Creating a stratified differential diagnosis.
d. Formulating evidence-based diagnostic and therapeutic approaches.
e. Discussing how age and development influence our thinking.
4. Conduct healthcare maintenance visits that include the following components: childhood
immunizations, assessment of child development and nutrition, and the principles of
anticipatory guidance.
5. Discuss the effects of growth and maturation on pharmacokinetics and use this knowledge to
select the appropriate treatment regimens of commonly used fluids and medications in
patients of different ages.
6. Analyze common professional and ethical dilemmas in pediatrics.
7. Deliver well-organized, appropriately focused, and accurate oral patient presentations.
8. Write well-organized, appropriately focused, and accurate patient notes, including admission,
progress and outpatient visit notes.
9. Demonstrate relationship building skills in each clinical encounter and interprofessional
exchange.
10. Work effectively as a member of the healthcare team.
11. Elicit and recognize the perspectives and needs of families and provide care for patients
within their social and cultural context.
12. Set personal and professional goals for learning.
3
Pediatric Clinical Skills:
After completing your Pediatrics clerkship, we expect that you will have gained knowledge and
developed skills in the following areas related to the care of children:
For each area, we will describe the skills you are expected to learn and methods to demonstrate your
capabilities.
4
Minimal Competency Outline for Pediatric Clinical Skills
5
Growth
Normal growth is a marker of child health and well-being. Abnormal growth can be an indicator of chronic
illness, genetic disorders, malnutrition, psychosocial problems, or other issues which require intervention. You
should be able to address growth issues for children as follows:
6
Development and Behavior (includes issues of normal development and also concerns about behavior)
Although there is variation for each individual, childhood development and behavior should follow a generally
recognized pattern. Abnormalities of development or behavior may suggest organic or psychosocial problems
that require intervention; many problems can be avoided with appropriate guidance. You should be able to
recognize and address development and behavior issues in children as follows:
7
Nutrition for Children
Appropriate nutrition is of paramount importance so that children can achieve their goals of growth and
development. Nutritional problems can interfere with growth and development and lead to health issues.
During illness or in special chronic medical conditions, nutritional needs will differ from the norm. You should
be able to address the following basic issues related to nutrition for children:
8
Issues Unique to Adolescents
The changes of adolescence present unique health issues and new challenges for the patient, family, and
pediatrician. You should be able to recognize and address these issues when caring for adolescents:
9
Newborn Care (includes newborn anticipatory guidance and the newborn physical exam)
Pediatric care begins at birth, with careful evaluation of the newborn and support to the parents; this holds
true for the normal infant and for those with health challenges. You should be able to assess and provide
guidance for a newborn as follows:
10
Fluid/Electrolyte Management and Pediatric Therapeutics
Maintaining effective circulating volume is necessary to assure organ perfusion. Children may be at increased
risk for volume depletion due to their smaller size and higher propensity to develop volume-depleting
ailments. Assessment of volume status and correction of fluid/electrolyte abnormalities are core pediatric
skills. Since children come in many sizes, understanding how to address fluid or medication management that
is appropriately scaled to the individual patient is of paramount importance. You should understand and be
able to address the issues listed below:
11
Assessment of the Acutely Ill Child
You may be called upon to provide emergency care to a patient at any time. One must be able to recognize
and rapidly assess a sick child and understand how the presentation of illness may differ from that seen in an
adult. Basic topics in pediatric acute assessment and emergency care, with which you should be familiar,
include the following:
13
Grading and Evaluation
14
Pediatric Clerkship Grading Rubric
To pass the Pediatric Clerkship you must:
• Complete all assignments
• Meet professionalism standards
• Perform at a passing level or higher on your clinical performance (Clinical Grade)
• Receive a passing grade of 60% or higher on the final examination (Exam Grade)
Your Final Grade is determined from a combination of your Clinical Grade and your Exam Grade.
CLINICAL GRADE
Your Clinical Grade is determined by the Site Director, who reviews the information provided by each evaluator
with whom you worked during the clerkship. The Site Director assigns a numerical Clinical Grade based on the
submitted values for Recommended Level of Evaluation for Time Spent, weighted appropriately for the level of
time spent by each evaluator who observed your work and interacted with you.
Evaluators indicate Time Spent with Student and provide a Recommended Level of Evaluation for Time Spent:
TIME SPENT WITH STUDENT RECOMMENDED LEVEL OF EVALUATION FOR TIME SPENT
Little or no contact Exceptional Performance (Honors) 5
Sporadic and superficial contact Exceeds Expectations (High Pass) 4
Infrequent but in-depth contact Meets Expectations (Pass) 3
Frequent and in-depth contact Below Expected Performance for Level (Marginal) 2
Unacceptable Performance (Fail) 1
Please note that the Recommended Level of Evaluation from each evaluator, and thus the numerical Clinical Grade
assigned by the Site Director, is not a simple average of values reported in the 12-item evaluation form. Rather,
since each domain in the 12-item evaluation form may be considered differently depending on the types of
patients you see and the environments where you work, the Recommended Level of Evaluation and the resultant
numerical Clinical Grade represent overall assessments of your performance as a doctor-in-training.
All evaluations are reviewed regardless of the level of contact for comments that may be included in your final
evaluation to provide specific feedback on your performance, to highlight areas of strength or to identify areas of
concern. Significant areas of concern may constitute special circumstances which require individualized review.
EXAM GRADE
Your Exam Grade is the final percent correct score as reported on the standardized exam used in the clerkship. For
the Pediatric Clerkship, the standardized exam is the Aquifer Pediatrics exam. Please note that you must score
75% or higher on your Exam Grade to be eligible for a Final Grade of Honors.
FINAL GRADE
Your Exam Grade adjusts your Clinical Grade giving an Adjusted Total Grade. The Final Grade is based on the
Adjusted Total Grade with consideration also of your Exam Grade for Honors eligibility. Note that to receive
Honors, you must achieve the appropriate Adjusted Total Grade and also score 75% or higher on your Exam Grade;
if your Adjusted Total Grade is Honors eligible but your Exam Grade is <75%, your Final Grade is High Pass.
EXAM GRADE and ADJUSTMENT ADJUSTED TOTAL GRADE, RANGE, and FINAL GRADE
90% and above + 0.15 Adjusted Total Grade Greater than 4.5 and Exam >75% Honors
70%-89% No Adjustment is the Sum of Clinical 3.75 – 4.5 or >4.5 but Exam <75% High Pass
60%-69% - 0.10 Grade and Adjustment 3.0 – 3.74 Pass
Less than 60% Fail from Exam Grade Less than 3.0 or Exam Fail Fail
15
GRADING PHILOSOPHY
There is no curve and no forced normal distribution of grades for the Pediatric Clerkship. Each student is evaluated
individually on the merits of clinical performance, knowledge of pediatric medicine, assignment completion and
professionalism. Therefore, any student is eligible for any grade based on demonstrated performance.
We believe that every student who participates in the Pediatric Clerkship will be able to demonstrate the
knowledge, skills and attitudes necessary to achieve a passing grade. Given our faith in you we assume that every
student starts the Pediatric Clerkship at the level of Pass. If you participate fully, complete all assignments, act in
the appropriately professional manner, and demonstrate the expected clinical skills, you will have met
expectations and will achieve a Clinical Grade with a numerical value in the range of Pass. If you exceed the
expected level of performance in multiple areas you will be eligible for a Clinical Grade with a numerical value in
the range of High Pass. If you do not meet the minimum expectations for knowledge, skills, attitudes or
professionalism you may receive a Clinical Grade of Fail; students who appear to be at risk for a failing grade will
meet with the Site Director promptly to review performance and develop a plan for improvement.
A Clinical Grade in the numerical range of Honors is awarded to students who consistently perform at an
exceptionally high level throughout the Pediatric Clerkship. To be eligible for a Clinical Grade in the numerical
range of Honors we would expect you to demonstrate the following attributes, consistently over time, in multiple
settings:
To receive a Final Grade of Honors, we believe that a student must demonstrate a high level of clinical skill and
engagement as noted above along with showing mastery of the knowledge base related to Pediatric medicine.
This is why a minimum performance level on the standardized exam is also required to receive the Final Grade of
Honors. Please note that to receive a Final Grade of Honors, you must achieve the appropriate Adjusted Total
Grade and also score 75% or higher on your Exam Grade; if your Adjusted Total Grade is Honors eligible but your
Exam Grade is <75%, your Final Grade is High Pass (see above).
Questions regarding the grading rubric, grading philosophy or your final grade should be directed to the clerkship
director, Dr. Jordan Symons (jordan.symons@seattlechildrens.org).
SPECIAL CIRCUMSTANCES
Final Grade of Fail or other special circumstances will be referred to the Associate Dean for Student Affairs and/or
Student Progress Committee in accordance with UWSOM policy.
16
ASSIGNMENTS
17
Checklist for Core Pediatric Clerkship (WWAMI Region Sites and LIC Program)
The following list is an outline of the assignments you will need to complete to pass your clerkship. You will be using
The Pediatric Tracker to upload and log all of your completed assignments throughout the course of your clerkship.
PDFs all of all required forms can be found linked on the Tracker. Your site coordinator/director will provide
information about completion of assignments at your WWAMI site.
Access to the Pediatric Tracker is assigned to each user by their UW net ID.
Link: https://courses.washington.edu/fmclerk/wordpress/pedsclerk/tracker
Required Assignments:
Pediatric Assignment Tracker (https://courses.washington.edu/fmclerk/wordpress/pedsclerk/tracker)
o UW Net ID required
o PDFs of all required forms can be found linked on the Tracker
o Upload and log all of your completed assignments throughout the course of your clerkship
Aquifer Pediatrics cases (https://aquifer.org/)
E-Value Clinical Encounters Program (https://sites.uw.edu/medevalu/clinical-encounters/) UW Net ID
o Log the patients you see using the 8 required domains. (required one of each domain)
Mid-Clerkship Feedback form: 1st half of clerkship as directed by your site.
History and physical examination write-up: Submit 2 complete ups for evaluation and feedback
o Note: Upload these into the tracker with required feedback comments included.
Observed physical examinations (Mini-CEX):
o Infant-Toddler
o Pediatric
Required Problem Set Exercises:
Volume Depletion Problem Set
Maintenance Fluids Problem Set
Medication Ordering Problem Set
Aquifer Pediatric Active Learning Module: Fever
Growth Chart Problem Set
Perform full H&Ps on inpatients, new to the service or “new to you”, 2-3/week while on inpatient service
(adjusted as per your site)
Ethics in Pediatrics (as directed by your site director)
Work as an integral part of the care team during your rotation
If applicable: All electronic notes signed and sent to your direct supervisor BEFORE you leave on your last day.
Pass the final examination for the course (taken at your site, unless directed otherwise)
18
Checklist for Core Pediatric Clerkship (Seattle Children’s Hospital / 6-week rotation)
The following list is an outline of the assignments you will need to complete to pass your clerkship. You will be using
The Pediatric Tracker to upload and log all of your completed assignments throughout the course of your clerkship.
PDFs all of all required forms can be found linked on the Tracker.
Access to the Pediatric Tracker is assigned to each user by their UW net ID.
Link: https://courses.washington.edu/fmclerk/wordpress/pedsclerk/tracker
Required Assignments:
19
Checklist for Core Pediatric Clerkship (WRITE Program)
The following list is an outline of the assignments you will need to complete to pass your clerkship. You will be using
The Pediatric Tracker to upload and log all of your completed assignments throughout the course of your clerkship.
Access to the Pediatric Tracker is assigned to each user by their UW net ID.
Link: https://courses.washington.edu/fmclerk/wordpress/pedsclerk/tracker
Required assignments
Items to be completed during inpatient or at the WRITE outpatient experience
Aquifer Pediatrics cases (https://aquifer.org/)
The final examination for the course
At the end of your clerkship, please turn in your ID badge and return borrowed books and/or pagers.
20
Pediatric Core Medical Knowledge: Online Cases and Problem Sets
Aquifer Pediatrics Online Cases: During the course of the clerkship, you will learn about common pediatric
illnesses/problems in all age groups as well as approach to healthcare maintenance for children. This
material is covered in the Aquifer Pediatrics cases:
Go to https://aquifer.org/
Sign in/Register: Follow the instructions to sign in or register. You must use your UW email account to sign
up (the program won’t recognize domains like @gmail or @hotmail). If you have used the Aquifer cases in
the past (SIMPLE and fmCASES), you will use your previous login information.
Cases: Under “Courses”, open “Aquifer Pediatrics”. You do not have to do the cases all at once. When you
quit the program, the website will save the place where you stopped. You can return to the case at that
progress point. You are expected to complete all the Aquifer Pediatrics cases during the course of the
clerkship.
Please contact the Medical Student Office if you need additional login assistance.
Required Problem Sets: There are 5 problem sets for you to complete:
To facilitate learning, we have developed a series of assignments and corresponding didactic sessions. To
help you prepare for didactics, we created the materials on the website here:
http://depts.washington.edu/uwpeds/medstudents/?p=401
Collectively, this content will provide you with a solid foundation for caring for common pediatric problems
and prepare you for your final examination.
To further prepare for the USMLE Step II CK, we recommend thorough review of the content presented in
the clerkship, completion of additional practice questions, use of review books as appropriate, adequate
study time and following the guidance of the learning specialists at UW School of Medicine.
21
Inpatient Experience - Pediatric H&Ps
Performing H&Ps in the inpatient setting helps you both improve and demonstrate your skills of
gathering, organizing and synthesizing information about pediatric patients, developing assessments of
the patient’s status and then building a plan. Depending on your site, there will be different
opportunities for patients with varied complaints and complexity. Challenge yourself to do full
evaluations on the patients newly admitted or transferred to your service, or a patient who has been
there for a while but is “new to you”. The more you do the more practice you get, and the more your
preceptors can observe your skills and provide feedback.
We expect you to complete 2-3 full H&Ps for every week that you participate on the inpatient service.
Since the number of weeks on inpatient service, inpatient census, or the nature of the experience, may
differ at the various sites (inpatient-only at some sites vs. blended inpatient/outpatient at others), the
exact number of full H&Ps by the end of the rotation may vary. Please remember that the more you
engage in this activity, the more you learn and improve, and the more your preceptors can observe your
skills.
You should write up and submit to your site director/preceptor at least two of your H&Ps for formal
review and feedback. Your local site will clarify the method.
22
Required Problem Set Exercises
Clinical Problems
1. A normally healthy 18-month-old girl who weighed 11kg two weeks ago comes to the ER with
the complaint of “the flu”. She had emesis four times this morning and now has had two loose
stools. She weighs 10.8kg on admission to the ER; her physical exam is significant for a weepy,
unhappy appearing child.
What would you do to assess and treat this child’s fluid and electrolyte abnormality?
2. A normally healthy 18-month-old girl who weighed 11kg two weeks ago comes to the ER with
the complaint of “the flu”. She has only been taking water and juice; now she refuses all fluids.
She weighs 10.2kg on admission to the ER; her physical exam is significant for tachycardia and
dry mucous membranes.
What would you do to assess and treat this child’s fluid and electrolyte abnormality?
3. A normally healthy 18-month-old girl who weighed 11kg two weeks ago comes to the ER with
the complaint of “the flu”. She has only been taking water and juice for several days; now she
refuses all fluids and her parents say she is lethargic. Her parents do not remember the last
time she made any urine. She weighs 9.2kg on admission to the ER; her physical exam is
significant for tachycardia, dry mucous membranes, cool extremities and tenting skin. She is
afebrile. She arouses to noxious stimuli.
What would you do to assess and treat this child’s fluid and electrolyte abnormality?
23
Required Problem Set Exercises
Things to remember:
The volume of fluid required to keep a patient in normal balance is often called “maintenance”
Maintenance needs may differ from person to person or from day to day
Based on assumptions of normal physiology, it is possible to calculate maintenance needs
The assumptions about maintenance needs do not always hold in the setting of illness
Clinical Problems
Write the intravenous maintenance fluid order for the following patients. Remember to include the type of
intravenous fluid (i.e., amount of dextrose, sodium chloride, potassium, etc.) and the hourly rate.
1. A previously healthy 8-year-old girl is seen in the pediatric emergency department with abdominal
pain. An ultrasound shows concerns for appendicitis. The patient must remain NPO (nothing by
mouth) until after her surgery. Weight is 25kg.
2. An 18-month-old boy is seen in the emergency department with gastroenteritis. Family tried to give
oral fluids at home but over the last 24 hours his oral intake has been reduced. In the emergency
department he appeared volume deplete with tachycardia and delayed capillary refill; he received
normal saline bolus 20ml/kg intravenously. He looks better after bolus but he will only take small sips
of clear liquids; it is felt he would “bounce back” to the emergency department were he to be
discharged home. Weight is 12kg.
3. A 17-year-old girl with a kidney transplant comes in for a routine surveillance kidney biopsy. The
biopsy goes well but she feels nauseous from her anesthetic and is uninterested in drinking fluids. The
nurse contacts you for maintenance IV fluid orders until the patient is feeling better and will take fluids
by mouth. The patient weighs 65kg. Kidney transplant function is normal with serum creatinine of 0.8
mg/dL. She took all of her appropriate medications this morning and is not due for her medications
again until 8pm (5 hours from now). The renal transplant team has instructed her to take 2.5 liters of
fluid every day to “keep her transplant healthy” – normally she has no problem taking this volume of
daily fluid.
4. A newborn term infant male, birth weight 3400 grams, is admitted to the neonatal ICU for observation
due to tachypnea. He has good oxygenation and does not require mechanical ventilation but the
neonatology team wishes to observe; they will keep the baby NPO for the first 12-24 hours.
24
Required Problem Set Exercises
Using a pediatric formulary reference, determine the appropriate dose of medications for the following clinical
situations. Write the dose, route, frequency, and if necessary the duration, formulation (tablets, liquid, etc.)
and/or the “as needed” (PRN) indication.
Clinical Situation Medication
18-month-old boy admitted Rx: ACETAMINOPHEN
for fever and respiratory
distress
Weight: 12kg
Height: 82cm
4-year-old girl admitted for Rx: CEFTRIAXONE
pyelonephritis
Weight: 16kg
Height: 100cm
16-year-old girl seen in the Rx: TRIMETHOPRIM-SULFAMETHOXAZOLE
clinic with probable UTI
Weight: 72kg
Height: 155cm
7-year-old boy treated in the Rx: ALBUTEROL
ER for acute asthma
exacerbation
Weight: 21 kg
Height: 122 cm
3-year-old girl with new- Rx: PREDNISONE
onset nephrotic syndrome
Weight: 14 kg
Height: 95 cm
25
Required Problem Set Exercises
Fever is a common presenting problem in pediatrics and can be related to many potential etiologies.
Understanding how to evaluate and manage a child with a fever is an important skill which requires you to
employ multiple concepts of assessment and medical decision-making.
To prepare for this exercise, please be sure to complete Aquifer cases 10, 17, 23 prior to the session. These
cases provide a clinical background related to the evaluation and management of children with fever.
At the session, you will begin with a short quiz that will help you to assess your understanding of the core
knowledge presented in the Aquifer cases noted above. After this you will work together as a group to
evaluate a case of a child with a fever.
26
Required Problem Set Exercises
2. Interpret the following growth charts (scenarios A-D) and create a differential diagnosis (if
needed) for the growth pattern and explain your rationale for each choice. Finally, for each
scenario, outline a strategy for assessment and management of the patient. Remember,
some scenarios may represent normal growth!
27
28
29
30
31
32
Case 3 / Scenario C
33
34
35
Tools, References and
Resources
36
Communication Skills Learning Tools for the Pediatric Clerkship
One important goal of your pediatric training is to learn to gather histories from parents and patients in
a variety of settings. The resource presented here will help you to learn and improve on these skills,
building on experiences you have had working with adult patients.
Practicing with real patients is the core part of learning and developing these skills. Depending on your
experiences prior to your clerkship, you may find it useful to use some or all of the resource presented
here.
1. Observe your preceptor doing different types of pediatric interviews and note their approach.
Directed observation and then discussion afterwards will help you notice specific skills we want
you to practice during the clerkship. Communication skills may differ for well child exams or for
new/acute visits. We have developed a Communication Checklist that identifies areas for
review when speaking to patients and families in these settings. You can find the checklist on
the clerkship website:
http://www.washington.edu/medicine/pediatrics/students/current/third-year
While observing your preceptor performing a well child exam and an acute care visit, fill out the
appropriate checklist (“Medical Interviewing Rating Tool Established Well Child Care” or
“Medical Interviewing Rating Tool Acute care/sick visit”). Afterwards, discuss with your
preceptor how to approach different aspects of communication and any elements about which
you have questions. As you know, the clinical encounter is complex, and there is no “right way”
to conduct patient histories.
3. Ask your preceptor to observe part/all of a well-child and/or acute care visit. They can use the
SAME checklist you did when you observed them. Review your technique with your preceptor,
using the checklist as a guide for your discussion.
4. Get feedback on your skills – this should be continuous throughout the clerkship – from
patients, faculty and your own self-feedback. The checklist on the observed patient interactions
is there to guide you on our expectations for minimal competency and to make sure feedback
happens.
37
Approach to the Pediatric Patient in the Medical Setting
Taking a history & physical exam from toddlers, children, or adolescents & their caregivers
Toddlers/Preschoolers
• Are afraid of being away from their parents
• Have difficulty sitting still
• May conceptualize illness as a punishment
• Engage in concrete and “magical” thinking (e.g., “I am in the hospital because I didn’t listen to mommy last night.”)
• Often rely on imitation and look to others, especially parents, for how they should respond
Childhood/School Age
• Begin to understand their bodies and how they work
• Will likely have many questions
• May be afraid that their bodies won’t work or they will look different
38
Adolescents
• Are very worried about privacy and how they look
• Want to feel competent and have their opinions validated
• Can cognitively understand most things about their care, but behaviorally they continue to require monitoring.
Adherence difficulties are common, often due to poor education/transfer of skills and desire to fit-in.
• Can fail to see long-term consequences (e.g., explaining that poor diabetes control can lead to dialysis is not often
a convincing way to improve adherence in teenagers with diabetes)
• Will often not be forthcoming with sensitive topics unless asked directly
***
Involving and Interacting with Parents/Caregivers
• Always introduce yourself in full, including role on team. Again, don’t be shy showing your name on your badge.
• With younger children, try to meet with one or both parents alone first (although this can be challenging in the in-
patient setting).
• With adolescents, it is often better – when possible -to meet with them first. Better yet: give adolescents the
choice!
• Remember that caregivers have a unique understanding of their child’s medical experiences and therefore provide
key details of the medical history including:
o Patient’s experience of and expression of pain or discomfort
o Patient’s knowledge of or understanding of diagnosis
o Treatment regimen
Medication dosage and tolerance
Previous hospitalizations & frequency of outpatient care
Previous degree of cooperation with each aspect of the regimen
Patient’s previous level of involvement in care
Developmental history, school history, and cognitive functioning
***
Tips on Entering the Room & Doing the Physical Exam
• If you need to gown/glove, introduce yourself first with face visible then dress and enter.
• Seat yourself to include patient and caregiver at patient’s eye-level.
• With toddler/school-age patients, demonstrate use of the stethoscope or other instruments on yourself, a
caregiver, a toy or a non-threatening body part (e.g. hand) first.
• If the child appears intimidated by you, try providing distance from the child and visibly engage with the
caregiver(s) first before turning to the child. It allows the child to see a positive interaction between you and
caregiver making the child more amenable to approaching you.
• Leave the most invasive or painful parts of the physical examination to the end.
• Use distraction as much as possible.
39
Explanation of Pediatric H&Ps/Pediatric Database
History:
HPI:
The information is the same for any medical problem. A careful and complete description of the
presenting problem, with appropriate chronology is key. Always include pertinent
positives/negatives and relevant family history or social history items. An important distinction is
that much of the history will be observations from a third party (parent/caregiver). Important
questions include: mood, activity level, eating pattern, urine output (specific as possible), sleep
pattern and a description in the parent’s words what the problem is, how it has changed, what
they have tried to alleviate the symptoms and what they think is causing the child’s illness.
Birth/Pregnancy History:
For infants, this component is particularly important. Often birth/pregnancy history is either
relevant to the chief complaint or represents the majority of the PMH. Make sure to include
these questions on all infants and any child with a problem that might be related to
perinatal/neonatal issues.
Maternal: Mother’s age, gravida, para, health problems and medications
Pregnancy: Complications, prenatal care/labs/tests
Labor: Duration of membrane rupture and complications
Delivery: Gestational age (at a minimum whether term or premature), Mode (vaginal/C-
section/forceps/vacuum), Apgars.
Neonatal: Duration of hospitalization and any events that occurred shortly after birth.
Medical history:
Any medical problems or hospitalizations with a brief summary and dates.
Specifically ask about the last health supervision visit.
Surgical history:
Any surgeries and dates
Allergies:
Allergies and reactions
Medications:
Any prescription medications, over the counter medications or herbs/supplements.
Include doses when known.
Diet:
Description of diet. Particularly important in the first year of life or if growth is abnormal. In
infants comment whether breast feeding (frequency, duration and volume if known) or formula
feeding (type of formula, volume and frequency) in infants. In older children ask about typical
diet or about concerns the parents may have.
40
Growth and Development:
This should be part of every history.
The way you ask the questions will change over time. Start with an open ended question to
parents like “tell me what types of things your child is doing now”. Childhood development is
often categorized into 4 domains (social, fine motor, gross motor and language) and screening
questions in each domain should be explored. In older children, make sure to ask about their
hobbies, activities, school and friends. Assess academic achievement from parents/patient.
Immunizations:
In every patient ask about receipt of immunizations; there are standard immunizations given at
specific ages. Parents sometimes have the immunization record. If the child has not received
immunizations, explore the reasons why. Saying “up to date” without checking actual
documents or registries is an insufficient response. Try to document what immunizations were
given and when.
Social history:
Ask who lives in the home and whether there are other siblings and the state of the siblings’
health. Explore childcare arrangements—whether it is the family, an in-home setting or center-
based (larger classrooms). Inquire about what languages are spoken at home. If the child is
verbal, directly ask them about school/daycare, friends, and favorite pastimes/toys, pets and
siblings/family members. Identify sources of stress for the parents.
Environmental History:
Ask about smokers in the house, firearms, seatbelts, hot water heaters and car seats.
Also ask about travel history, pets and exposures to ill people.
Review of Systems:
This section is similar to that for adult patients. Remember that preverbal children cannot report
many of the symptoms, so parental observation is the main source of information. A sample
review of systems:
General: fever, weight loss, activity GU: frequency, dysuria ,urine output, hematuria
Endocrine: change in habitus, weight gain Skin: rashes
Eyes: crossing, pain, redness, drainage Neuro: seizures, loss of consciousness
HEENT: ear pain, drainage, hearing loss GI: feeding/appetite, vomiting, diarrhea,
Nose: drainage, discharge, sinusitis constipation, blood in the stool, abdominal pain
Throat: tooth pain, sore throat, hoarseness
Resp: cough, wheezing, apnea, cyanosis, Musculoskeletal: joint swelling, tenderness,
difficulty breathing weakness
CV: murmurs, chest pain Psych: mood changes, sleep problems
Heme/lymph: bleeding, anemia, jaundice, swollen glands
Physical Examination:
41
The approach to the physical examination will vary with the age of the child. There are special
maneuvers that are done at each age. There are specific benchmarks and appendices available in the
clerkship manual and on the pediatric student website.
General: Describe the state of alertness, mood, and willingness to cooperate with the exam and whether
the child is in distress
Head: For infants and children feel for the fontanelle. Comment on the shape of the head
Eyes: Note presence of the red reflex in all children. Check pupillary reaction, lids/conjunctiva
NB: Fundoscopic exam is difficulty to perform on infants but can usually be done in children over 5-6
years of age. (The examination in this age group provides an excellent opportunity to see the optic disc
and vessels.)
Ears: Check for tenderness of pinna, discharge and gross assessment of hearing. Check tympanic
membranes bilaterally with insufflation.
Mouth/Throat: Check for teeth/caries. Inspect the tongue, buccal mucosal and the posterior pharynx for
erythema, enlarged tonsils. Feel for submucousal cleft palate.
Neck: Gently palpate neck for masses and assess range of motion (often by observation).
Chest: Observe for signs of respiratory distress (nasal flaring, retractions and grunting). Normal
respiratory rate varies with age. Palpate for tactile fremitus then auscultate anterior and posterior lung
fields. Note the inspiratory:expiratory ratio (I:E ratio).
Cardiovascular: Observe for cyanosis, respiratory distress and hyperdynamic precordium. Palpate the
precordium (for thrills). Auscultate as in adults---pediatric heart rates are faster than adults thus
distinguishing systole and diastole is more difficult. An S3 may be found in normal children (represents
rapid ventricular filling). Many children will have benign murmurs (of no medical importance) ---train
your ears to hear them! Palpate the peripheral pulses as in adults. (Femoral pulses are particularly
important to check in neonates when screening for coarctation of the aorta).
Abdomen: observe, auscultate and palpate as in adults. Children often have a palpable liver
edge…always palpate from the pelvic brim up.
GU: See Sexual Maturity Rating (SMR) information in the Aquifer Pediatric cases and physical exam
benchmarks in the clerkship manual and on the medical student website.
42
Musculoskeletal: Much of this portion of the examination is observation for tone and strength. In
neonates, observe for increased or decreased tone…both are pathological. When children are older and
can follow directions, the approach is similar to an adult exam. There are also special maneuvers to
screen for congenital hip dysplasia (Barlow/Ortolani maneuvers).
Neurological: Much of this exam is by observation (especially the cranial nerves). Children have deep
tendon reflexes just like adults that should be tested. Neonates have primitive reflexes that are
considered normal (like an upgoing toe with a Babinski test).
43
Example H&P (Older Patient)
CC: AB is a 16-year-old female presenting to the Emergency Department with 4 days of bloody diarrhea,
abdominal pain and fever.
HPI: AB was in her usual state of health until 7 days prior to admission when she started experiencing
nasal congestion, clear rhinorrhea and low-grade fever (maximum temperature 99-100). She went to
her primary care provider, had a CT scan of her sinuses done, was diagnosed with a sinus infection and
was treated with a nasal spray (patient not sure what type). Five days prior to admission, she began
having intermittent fevers to 101.9, which have continued until the time of admission. Four days prior to
admission, AB started having severe (7/10) generalized abdominal pain, worse in her subgastrium. She
describes the pain as constant, dull, non-migratory, not relieved by anything, including acetaminophen,
and exacerbated by eating. During the three days prior to admission, she has also had 3-4 episodes of
bloody red diarrhea with the abdominal pain. She says that having a bowel movement makes her
abdominal pain worse. AB has also had 2 episodes of nonbloody, nonbilious emesis in the past two days.
She has noticed increased fatigue and has lost 2 lbs in the last week, though she still has a good
appetite.
Notably, AB was seen approximately 5 months ago in the Emergency Department in Everett with
abdominal pain. She had no diarrhea or emesis at that time. Her stool guaiac was negative, but was
diagnosed with iron deficient anemia with a hemoglobin of 12.2 g/dL. She was sent home on iron
supplements and no clear diagnosis for her abdominal pain. Since that episode she has noticed
intermittent abdominal pain, fatigue and has lost 10 lbs.
She denies any rashes, arthralgias or myalgias, eye discharge or inflammation, oral lesions,
cough, jaundice, petechiae or easy bruising. She has normal urine output. Her past medical history is
also remarkable for cholecystitis requiring cholecystectomy at the age of 10. Her travel history is
significant for being in N. Europe on a cruise 3 months before the onset of symptoms. She has two dogs
and one cat. Her LMP was last week and was normal in volume and duration. AB does not have a family
history of inflammatory bowel disease or rheumatological diseases.
Family History: No history of inflammatory bowel disease (Crohn’s or ulcerative colitis); No history of
childhood rheumatological diseases or systemic lupus erythematosus. Paternal grandmother has
psoriasis. Maternal grandmother with osteoarthritis. Paternal grandfather with heart disease
and diabetes. No sick contacts.
44
Is in the 11th grade, same school as last year; good grades (A’s and B’s).
Plays soccer and tennis; sings in the school choir
Denies EtOH, nicotine, and other drug use.
Is not and has not been sexually active. No current partner (boyfriend or girlfriend).
Review of systems:
General: See HPI
Endocrine: Weight loss as in HPI. No polyuria/polydipsia
Eyes: see HPI; no redness, no blurred vision or double vision.
Ears, Nose, Throat:
Ears: ear pain or drainage, no hearing loss.
Nose: see HPI
Throat: no tooth pain, sore throat or hoarseness
Cardiovascular: no chest pain or murmurs
Genitourinary: normal urine output, no frequency, dysuria, hematuria
Gastrointestinal: see HPI
Musculoskeletal: See HPI
Hematology/Lymphatic: see HPI; no jaundice or swollen glands
Psychiatric: no mood changes or sleep problems
Admitting PE:
Vitals: T 37.8 HR 110 RR 18 SaO2 97% on RA BP 113/82 Pain 5/10
Weight 42.5 Kg (< 3%) Height: 158 cm (25%)
General: well developed but thin young female, looks fatigued w/o significant distress
Skin: pale skin, no rashes or erythema, no petechiae or bruising
HEENT:
Eyes: PERRLA, full EOM, conjunctiva without exudates; sclera anicteric without injection, no
periorbital edema
Ears: pinna and canals normal; TMs gray w/o erythema
Nose: nasal turbinates are slightly swollen and mildly pale with some clear rhinorrhea
Oropharynx: dry lips, mildly dry oral MM, 2+ tonsils w/o exudates or crypts, no pharyngeal
erythema.
Neck: Supple with full range of motion; non tender to palpation. Thyroid soft and without nodules.
Lymphatic: no cervical, supraclavicular, axillary, inguinal adenopathy.
Chest: Symmetric inspiration, clear to auscultation bilaterally with no wheezes, crackles or rhonchi.
Breasts: SMR stage V
CV: Tachycardic, regular rhythm, prominent PMI over 5th intercostal space ~ MCL, normal S1 and S2, I-
II/VI systolic ejection murmur over L sternal border, < 5cm CVP; 1+ radial and pedal and inguinal pulses
which are symmetric, capillary refill 2-3 seconds.
GI: several small well healed scars from previous lap cholecystectomy, active bowel sounds,
tenderness on light palpation in all 4 quadrants and worse in LLQ and RLQ, + guarding in LLQ, +
peritoneal signs by moving the patient and rebound tenderness in LLQ, negative obturator and psoas
signs, liver edge and spleen not felt. Liver span estimated to be 7 cm. No masses palpated.
Rectal examination: normal tone, no masses; no fissures; guaiac positive.
GU: 3 skin tags in the peri-anal region, no abscesses, erythema or fistulas in perineal region, SMR stage
V genitalia and pubic hair.
MS: full ROM w/o pain, no erythema or increased warmth over joints, no effusions. No clubbing
45
Neuro: CN II-XII intact, Muscle strength 4-5+ throughout, 1+ and symmetric patellar reflexes, sensation
to light touch intact in all extremities
Laboratory:
CBC: 8.1 WBC (28%pmns, 33%lymphs, 12%mono, 23%bands); Hemoglobin 9.1, Hct 27.4; MCV 89;
RDW 13; RBC morphology is normal; Platelets 622K
U/A: pH 6.5; 1.025 sp gravity; tr protein; 0-5 WBC; 0-5 RBC; LE neg; Nitrite neg
Chemistry: Na 143, K 3.8, Cl 103, HCO3 29, BUN 11, Cr 0.7, Glu 97
CRP 4.3
ESR 114
Assessment:
AB is a 16 y.o. female with several month history of intermittent diffuse abdominal pain, fatigue, ten
pound weight loss, with an acute course of profuse bloody diarrhea with low-grade fever. Her physical
examination is remarkable for signs of peritonitis and volume depletion without signs of shock. Notable
laboratory data include elevated inflammatory markers, anemia, normal platelet count and a left shift
on her CBC.
AB’s bloody diarrhea with fever and abdominal pain can be from infectious enterocolitis (parasite and
bacteria), inflammatory bowel disease (IBD), malabsorptive (celiac), vasculitis (HSP, PAN), carcinoma of
ileum or colon, carcinoid tumor, intestinal lymphoma as well as other less likely diseases. Given AB’s
long standing illness course with weight loss and anemia it is likely that she has a chronic illness thus
making inflammatory bowel disease (IBD) the most likely diagnosis. Other chronic illnesses such as
carcinoma, lymphoma or carcinoid tumors are unlikely in this age group. There are no specific
signs/symptoms that differentiate ulcerative colitis (UC) and Crohn’s disease (CD). Weight loss, bloody
diarrhea, abdominal pain, fever and anemia can occur in both CD or UC. Given her skin tags, and past
cholecystitis, it is more likely that she has CD than UC. In addition, she has significant elevation of CRP
and ESR, and a left shift on her CBC indicating severe acute inflammation, which is all consistent with
inflammatory bowel disease.
An infectious agent is less likely because of the chronic course, no significant travel risks, lack of
suspicious foods eaten and no sick contacts. While she did travel before the onset of the symptoms, the
travel was not temporally related to her symptoms. Possible agents could include E. coli O157:H7, E. coli
(other pathogenic strains), Shigella, Salmonella, Yersinia enterocolitica, C. jejuni, C. difficile, amebiasis,
giardiasis and cryptosporidium. Stool culture and O&P exams are necessary to diagnose an infection.
Celiac disease rarely presents with bloody stools, but could explain her weight loss and abdominal pain.
She has no other features of vasculitis, such as rash, swollen joints or kidney dysfunction to suggest
these possibilities as the cause of her symptoms. However, if no unifying diagnosis is determined,
further consideration and testing of these causes of her symptoms should be pursued.
AB’s anemia is normocytic with an MCV of 89 and a Hct of 27.4. Typically iron deficiency anemia is
microcytic making this diagnosis less likely. Her RBC morphology is normal, making intravascular
hemolysis less likely. The anemia is most likely due to acute blood loss, and/or anemia due to chronic
inflammatory state and poor iron utilization. Her anemia can also be complicated by B12 or folate
deficiencies due to poor absorption. Her RDW is within normal range. If needed, a ZPPH, iron studies,
B12 and folate levels, and reticulocyte count can be ordered to work up a continued anemia. Since she is
likely volume depleted as suggested by her tachycardia, she may be more anemic that she appears to be
at the time of admission.
46
Plan:
Bloody Diarrhea:
1. Abdominal x-ray for focal abdominal pain. Monitor abdominal exam for increased pain, nausea,
continued bloody diarrhea and signs of obstruction (bilious emesis, severe abdominal pain,
leukocytosis, SIRS, sepsis).
2. Consider H2 or PPI for gastritis.
3. Consult gastroenterology for consideration of diagnostic endoscopy.
4. Obtain Stool Cx, stool O&P, C. difficile toxin screen. No empirical antibiotics but monitor closely
for clinical deterioration or signs of sepsis. If C. difficile toxin positive, initiate treatment.
Anemia:
1. Recheck CBC x 2 if she continues to have bloody diarrhea
2. Consider transfusion if Hbg < 8.5 gm/dL. It is very possible that she will need a transfusion
because she is volume depleted and has on going hematochezia which will make her hematocrit
lower.
Fluids/Electrolytes/Nutrition:
1. FEN: D5 + NS + KCl 20meq/L @ 100cc/hr. Monitor urine output to determine if additional
normal saline boluses will be needed to correct volume depletion. Continue IV fluids until she is
taking adequate PO and vitals are stable. Monitor vitals for orthostasis. Optimize fluids to
maintain normal heart rate for age.
2. Clear diet, ad lib.
47
Example H&P (infant)
ID/CC: 7 mo old ex-40 week AGA healthy infant male presents w/ a 3 month history of faltering
growth and a 1 mo history of recurrent upper respiratory symptoms
HPI
TS’s mother believed her infant to be in good health until earlier today when during a routine primary
care visit his pediatrician was alarmed by his thin appearance and fall in his weight for age from the 30th
percentile to the 2nd over the past 3 months. His length and head circumference for age also dropped
across percentiles during this period but have remained on the normal curve. The mother denies any
recent changes in TS’s appetite and explains that he eagerly breastfeeds every 2-3 hours for 5-10
minutes at a time during the day (without nighttime feedings from 10 pm to 7 am) plus soft baby foods
1-2 times per day. She believes that this “is approximately the same amount that her two older
daughters ate at that age”. She also believes that her milk supply is “good” because she is easily able to
express milk by squeezing her breast. She is also currently 16 weeks pregnant.
She denies TS having symptoms of fatigue, diaphoresis or rapid breathing during feeding as well as post-
feeding fussiness, emesis or diarrhea. He has 2-3 wet or mixed diapers per day and his stools are brown
in color without melena, clay color or bright red blood, and they are not particularly foul smelling. TS’s
development thus far has been appropriate for age and growth was following a normal curve at least
until 4 months of age. Neither parent has a known history of HIV or other sexually transmitted
infections nor any high risk behaviors. There is no history of recent travel or exposure to persons
infected with TB. He has had one newborn metabolic screen at 1 day old which was normal; the second
screen was not obtained.
Of note, TS has also experienced approximately 1 month of recurring fever, cough and rhinorrhea that
lasts for 3-4 days at a time. He is having some of these symptoms today with a transient fever to 101.2
earlier today but no wheezing, stridor or increased work of breathing. He has had all of his childhood
immunizations up to the age of 4 months with the exception of rotavirus and influenza. Several family
members have also had these symptoms all of which have self-resolved. The mother describes no
changes in TS’s appetite or feeding frequency/duration while ill.
ED Course
On arrival to SCH ED, TS was afebrile and all vital signs were within normal limits. He was given a 300 ml
NS bolus via peripheral IV. CBC, electrolytes, CRP and a viral panel were obtained. He arrived to the
floor shortly thereafter.
Birth Hx
Born at 40 +3/7 AGA to G3P2 mother via uncomplicated vaginal delivery. APGARs at birth were 7 at one
minute, 8 at five minutes. The mother’s screening was remarkable only for lack of Rubella immunity.
Neonatal course remarkable for mild jaundice (Tbili max = 6.8) which required no intervention and initial
difficulty latching. Both resolved prior to discharge.
PMH
Stable/Resolved Problems
1. Neonatal jaundice: see Birth Hx
2. Difficulty breastfeeding: see Birth Hx
PSH
None
Allergies
None known
48
Medications
No medications or supplements
Diet
See HPI.
TS is able to sit up on his own with good head control, starting to crawl, reaching for objects, stacking
blocks and babbling. His mother reports that he is developing similarly to his sisters, even during the
time he has lost weight.
Immunizations
Routine vaccinations up to age 4 months with the exception of Rotavirus and Influenza
Family Hx
Hyperthyroidism: paternal grandfather and cousins
Type II DM: maternal grandmother
Both parents and 2 older siblings with no significant PMH
Social/Environmental Hx
Lives in home in Everett, WA with mother, father and two sisters (ages 2 and 4). Mother stays at home
while father works outside of the home as an engineer during the day. No additional care providers. TS
does not attend day care. Mother does not have any concerns for safety in the home.
Exposures: both parents are non-smokers, cleaning supplies and toxins out of reach, pets include 2
Guinea pigs.
ROS
Gen: +transient fevers over past month (see HPI), no chills or sweats, activity at baseline,
Endo: no change in habitus, + weight loss (see HPI)
HEENT: no head trauma, + stork bites over bilateral eyelids, no eye crossing, no rhinorrhea, +moderate
clear nasal drainage, no ear pain, drainage, or hearing loss, + thick white coating on tongue and lips, no
hoarseness.
Resp: + intermittent wet cough (see HPI), no snoring, apnea, increased work of breathing, cyanosis or
wheezing
CV: no murmurs, no fatigue, sweating or tachypnea with feeding, no cool extremities
Heme/Lymph: no easy bruising or bleeding, anemia, jaundice or lymphadenopathy
GI: no signs of abdominal pain, normal appetite, no dysphagia or choking, no hematemesis, diarrhea,
melena or hematochezia, no constipation
GU: no change in frequency, urine output or urine color, no hematuria
Neuro: no seizures or LOC
MSK: no joint swelling or erythema, no asymmetry or weakness
Skin: erythematous papules in diaper region
Psych: no changes in sleep pattern or appetite
Physical Examination:
Vital Signs (on admission)
Weight: 6.322 kg (2%); Height 65cm ( 15% ); Head Circumference 42.5 cm (40% )
49
Gen: pale and thin appearing, alert and interactive, consolable when fussy
HEENT
Head: NC/AT, anterior fontanelle 1 cm and flat, sutures normal with no overriding.
Eyes: normal position, normal red reflex, PERRLA, EOMI, conjunctiva somewhat pale, no scleral icterus
Ears: pinna normally positioned; no drainage, external canal without erythema or exudate, TMs slightly
red bilaterally but no bulging or pus.
Nose: non-purulent drainage, nares patent, no nasal flaring
Throat: 2 erupting bottom teeth, palate intact, posterior pharynx without erythema or exudate,
normal appearing tonsils without pus, tongue, buccal mucosa and soft palate with thick white plaque
Chest: normal inspiratory: expiratory ratio, symmetrical chest expansion, no wheezing, rales, ronchi or
stridor, no increased WOB
CV: RRR, no murmurs, rubs or gallops, brachial, femoral and dorsalis pedis pulses full and symmetrical,
no cyanosis
GU: SMR stage 1, normal genitalia, testes descended bilaterally, anus patent, erythematous patch with
satellite lesions along inguinal folds and beneath scrotum
Labs/Studies
CBC w/diff
WBC: 8.6
Hb: 10
Hct: 30 (L) MCV 72 (L)
Plts: 167K
50
Assessment/Plan
7 month old previously healthy and developmentally normal breastfed male presents with poor
growth since last assessed by PCP at age 5 months. He has a normal appetite without vomiting or
diarrhea, no loss of developmental milestones but 1 month of recurring URI symptoms of fever, cough
and rhinorrhea. Physical examination is remarkable for white plaques on his tongue/buccal mucosa,
rhinorrhea, and erythematous diaper rash. Viral PCR positive for RSV.
The most likely cause of faltering growth in this previously healthy and developmentally normal
7 mo male is inadequate nutrition both because it is epidemiologically most likely and because there are
no obvious signs/symptoms of organic causes. There is also some suggestion from his mother’s
lactation history and current 16 week pregnancy that her breast milk may be inadequate to support this
infant. In addition, TS is being offered only once daily table foods which is likely too little to make up for
deficiencies in breast milk. Poor latching and inadequate frequency of feeding are unlikely given the
mother’s ability to provide detailed history of his feeding schedule. UTI and prolonged URI are also
possible given the recent fevers and accompanying symptoms, however these would be unlikely to
cause such a dramatic change in growth over a 1 month period in the setting of normal PO intake.
The report of recurrent URI symptoms, mouth plaques c/w thrush, and yeast infection also
raises suspicion for possible congenital immune deficiencies such as severe combined immune
deficiency (SCID), selective IgA deficiency or x-linked agammaglobulinemia. SCID commonly presents
with faltering growth and thrush but usually also includes chronic diarrhea which TS has not had. I
would also not expect normal growth for the first 4 months of life with this etiology.
Agammaglobulinemia fits TS’s age (decreased maternal IgG by 6 months) but he has not experienced
recurrent bacterial infections and tonsils are present. Selective IgA deficiency is possible in the setting
of recent recurrent URI symptoms but usually doesn’t present as faltering growth as the first symptom; I
would expect more sinopulmonary symptoms. HIV and TB are much less likely given no maternal or
paternal h/o HIV infection or risky sexual behavior and lack of travel or exposure to contacts with TB.
Malignancy should also be considered given his recent pattern of fevers and weight loss; however this is
also less likely than inadequate feeding. Neglect and/or abuse should be considered although there are
no overly concerning findings on social history or physical exam to raise significant suspicion.
Other possibilities including CHD, CF, milk protein intolerance, IBD, GERD, pyloric stenosis,
diabetes, inborn errors of metabolism, and RTA are least likely given the lack of suggestive history and
physical exam findings. CHD would likely present as fatigue, diaphoresis, tachypnea during feeding. CF
would present with greasy, foul smelling stools and possibly rickets. He has no h/o high blood glucoses
or polyuria to suggest diabetes. Milk protein intolerance and IBD would be suggested by bloody stools
of which there is no history. GERD and pyloric stenosis would present with significant post-feeding
symptoms (projective vomiting, fussiness, tachypnea). Inborn errors of metabolism would have likely
been discovered on his newborn screen (although he did not have a 2nd screen) and presented earlier in
infancy. I would also expect developmental delays with this etiology. RTA or chronic renal insufficiency
would be considered if urinalysis and/or electrolyte abnormalities were present (elevated BUN,
creatinine), but there is no e/o this currently.
-Pre- and post-feeding weights to determine adequacy of breast feeding
-Calorie counts
-Strict I&O’s
51
-Nutrition and lactation consults
-Social work consult to evaluate for psychosocial contributors
-UA to r/o UTI and renal causes
-Stool elastase to r/o malabsorption
-Q6 vital signs
-No maintenance fluids at this time, reassess if become tachycardic or hypotensive
-Nutrition and lactation consults as above
-Consider re-feeding labs
Problem 2: Anemia
TS’s anemia is most likely secondary to combined iron and possibly folate deficiencies given current
state of malnutrition. Will want to reassess as outpatient if does not resolve with improved nutrition.
-Multivitamin supplementation
-Consider infant formula if breastfeeding determined to be inadequate
-F/u CBC as outpatient
Disposition
-home, pending ability to gain weight in hospital and parental education regarding adequate
intake or determination of organic cause.
52
Pediatric Physical Examination
Students often feel intimidated about performing the pediatric physical examination.
We have provided some tools to make learning this skill easier and hopefully fun for you!
• You may have to do the physical examination out of order in many children. Be flexible.
• You can’t stop and write down your findings as you go. You have to remember what you
saw/heard/felt. Write it down afterwards.
• Save the most invasive parts for last (ears and mouth).
• Children over 5 can usually follow directions, so their examination is similar to adults.
• Enlist the caregiver’s help as needed!
• Have fun and think of how to make this a game (for yourself and your patient).
Review the following video that provides additional tips for performing physical examinations in
children. The video is found on the COMSEP website (Council of Medical Student Education in
Pediatrics—the national pediatric clerkship organization).
https://www.comsep.org/multimedia-teaching-resources/
After you have watched the video, look through the Physical Examination Benchmarks and Appendices.
Remember, the more you practice, the better you will become. Ask the people you work with to show
you how to do the physical examination. Be honest if you don’t hear or see a physical exam finding. And
remember, the more you practice….
53
Benchmarks for the Pediatric Physical Examination
General Approach
One should be flexible when examining children. You must establish rapport with the child and the parent
before starting the exam. In general, children between the ages of 8 months and 4 years require the most
flexible approach. For younger children you should perform the most “invasive” part of the examination (e.g.
the head and neck examination) last.
Do
Use an age appropriate approach to the examination
•Newborn: Place the newborn on the examination table. Conduct a general assessment by
observing the child and then listen to the heart and lungs. Once those are accomplished
proceed with the remainder of the exam.
•Infant/Toddler: You may examine the child in the caregivers lap. Begin slowly with a non-
threatening part of the examination, perhaps the hands. Then move to the heart and lung
exam. End with the head and neck examination, focusing on the ears and throat last.
•Older child/adolescent: The sequence of the examination is the same as that of the adult. Pay
particular attention to modesty and whether parents will remain in the room.
54
Premature infants: the growth of premature infants is typically “corrected” for
their premature birth. Although special growth charts are available, many
pediatricians plot the current weight at the “chronological” age and then subtract
the months/weeks of prematurity (e.g. if the child was born at 30 weeks they
subtract 10 weeks) and plot the growth parameters at the “corrected” age.
Plotting the corrected age usually continues until age 2 years.
Other populations: there are special growth charts available to plot the growth for
children with Down syndrome, Turner syndrome and achondroplasia.
Know
• Be alert to the possibility of a problem when the head circumference is at one extreme or
the other.
• Sequential measurements of growth are sensitive measures of overall health.
• Alteration in the rate of growth “crossing percentiles” should alert you to possible
underlying problems.
• Typical weight gain in the newborn period: 20-30 grams/day.
• Typical height velocity:
In children 5years –puberty, normal growth velocity is ≥ 5 cm/year;
< 5 cm/year should be investigated; <4 cm/year is pathologic.
• Patterns of growth:
Growth hormone deficiency: high weight-to-height ratio.
Chronic disease (e.g. inflammatory bowel disease):(low weight-to-height ratio).
Constitutional growth delay: normal weight-to-height ratio.
The maneuvers you use in the adult physical examination are also used when examining children with
appropriate adjustment for age and size. It is expected that you will be able to correctly execute the
basic physical examination maneuvers commonly used for all patients.
55
Newborn Examination
You should be able to conduct a complete examination of all organ systems in a newborn using an age
appropriate approach. These examination techniques are the same as for adults with adjustments for age and
size. Specific maneuvers that are a part of the neonatal examination that you should be able to demonstrate
include:
Fontanel assessment:
Do
• Palpate the anterior fontanel, assessing size and firmness
Place the infant in an upright position (and hopefully she/he will remain calm!)
Gently place your fingers over the anterior fontanel, located midline on the
superior tempero-frontal portion of the skull.
Gently palpate for the edges of the fontanel.
• Palpate the posterior fontanel (closes earlier than anterior)
Repeat the same procedure outlined above, feeling for the posterior fontanel,
located in the midline occipital region.
Know
• The posterior fontanel usually closes by 6 weeks of age. The anterior fontanel closes by 18
months in most infants.
• Changes in intracranial pressure or hydration status are reflected in changes of the
palpable tension of the fontanel (increased with increased intracranial pressure, decreased
with dehydration).
• Fontanel size varies tremendously; persistent delays in closure or unusually large size of
fontanels (particularly the posterior fontanel) may indicate pathologic bone growth delay.
• Craniosynostosis: premature closure of cranial sutures. It may result from a primary defect
of ossification (primary craniosynostosis) or, more commonly, from a failure of brain
growth (secondary craniosynostosis).
• Conditions associated with a large anterior fontanel (greater than 3 cm) include
hydrocephaly, achondroplasia, hypothyroidism, osteogenesis imperfecta, and vitamin D
deficient rickets.
Eye Exam:
Do
• Assess whether the red reflex is present
Set the ophthalmoscope lens power to “0”. Turn on the lamp and look through the
ophthalmoscope into both eyes of the child simultaneously from approximately 18
inches away.
The newborn infant spontaneously opens his/her eyes if the head is gently tipped
forward/backward. This is easier than trying to force open tightly shut eyelids!
• Test corneal light reflex
Shine your ophthalmoscope or penlight in the newborn’s eyes; you are assessing
whether the light symmetrically reflects from the corneas bilaterally.
Know
• A normal red reflex emanates from both eyes and is symmetric.
56
• Leukocoria (white pupillary reflex) suggests cataracts, chorioretinitis, retinopathy of
prematurity, persistent hyperplastic vitreous or retinoblastoma. Leukocoria mandates an
urgent ophthalmologic evaluation.
• Many newborns appear to be “cross eyed” because of prominent epicanthal folds. A
normal (symmetric) corneal light reflex suggests normal alignment (no strabismus).
• Asymmetric corneal light reflex is a sign of strabismus, an imbalance of ocular muscle tone.
Uncorrected strabismus can lead to blindness. Proper coordination of eye movements
should be achieved by 3-6 months. Persistent eye deviation requires evaluation.
• Visual acuity of a newborn is approximately 20/400; this rapidly normalizes and by 2-3
years of age is 20/30-20/20.
Hip Exam:
Do
• Assess the neonate for developmental dysplasia of the hip by performing the
Barlow maneuver and Ortolani test:
Place the baby on a firm surface in the supine position.
Flex the thighs to a right angle to the abdomen and the knees at right angles to the
thighs.
(Barlow maneuver)
Grasp each thigh with your forefinger along the outside shaft of the femur, with
your middle finger on the greater trochanter and thumb medially.
Adduct the femora fully and push down toward the bed.
(Ortolani test)
Gently abduct each leg from the position of full adduction so that the knees
come to lie laterally on the table.
During abduction, push the greater trochanters medially and forward with your
fingers.
Know
• The infant may have a congenitally dislocated or subluxable hip if:
You feel or hear a click during either adduction or abduction.
There is spasm or discomfort of the adductor muscles of the femur.
• Developmental dysplasia of the hip:
1/100 infants have clinically unstable hips; 1/800-1000 experience true dislocation.
There is a positive family history in 20% of patients and associated generalized
ligamentous laxity. 9:1 female-to-male ratio.
Developmental dysplasia typically presents after birth in most infants. If it is
present at birth, you should look for an underlying neuromuscular disorder. This
type of developmental dysplasia of the hip is called teratologic DDH.
Newborn reflexes:
Do
• As part of your newborn exam, elicit the following primitive reflexes:
Asymmetric tonic neck reflex (Fencer’s position).
o Place the infant on his/her back.
o Turn the newborn’s head to one side.
o Observe the gradual extension of the arm on the side to which the head is
turned.
o Observe the flexion of the other arm.
57
Moro reflex (startle response)
o Hold the infant supine and support the infant’s head with one hand.
o Gently move the infant’s head (while supporting it) below the level of the rest
of the body.
o Observe the infant extend both arms suddenly and rapidly with open hands.
o Observe the infant bring both hands back to midline in an “embrace”
movement.
Palmar grasp
o Place your index finders in each of the infant’s open hands.
o Observe the infant’s fingers close around your fingers in a firm grasp.
Plantar grasp
o Place your thumb on the sole of the infant’s foot under the toes.
o Observe the toes curl around your thumb.
Know
• Reflexes should be symmetric. Asymmetry suggests weakness in a particular muscle group.
• Primitive reflexes disappear as the infant matures; persistence of these reflexes is a signal
of underlying neurological dysfunction.
Asymmetric tonic neck reflex (Fencer’s position)
o Appears by 35 wks gestation, is fully developed at 1 month & lasts 6-7 months.
Moro reflex (startle response)
o Appears by 28-30 wks gestation; is fully developed at term & lasts 5-6 months.
Palmar grasp
o Appears by 28 wks, is fully developed by 32 wks gestation & lasts 2-3 months.
Skin exam
Do
• Inspect all of the infant’s skin (including diaper area).
• Describe (size, shape, color, distribution) any rashes.
• Note any areas lacking skin.
Know
• Benign lesions that parents may have questions about include:
Small angiomata present on the eye lids, nape of the neck, forehead.
Milia: small white spots on the skin, particularly on the nose and cheeks.
Erythema toxicum: yellowish/white pustules on an erythematous base that occur
singly or in groups.
Hyperpigmented macules or slate gray macules (previously called Mongolian
spots): blueish-green to black in color, more common in people of color, can be
mistaken for bruises.
• Concerning changes include large angiomatous lesions, vesicles, pustules or areas lacking
skin.
• Midline abnormalities (dimple, hair tuff, moles) on the back may indicate an underlying
abnormality in the bones/nervous system.
58
Infant/Toddler Examination
You should be able to conduct a complete examination of all organ systems in all infants/toddlers using an age
appropriate approach. These examination techniques are the same as for adults with adjustments for age and
size. Specific maneuvers that are a part of the infant/toddler examination include:
Ear examination
Do
• Ask about hearing concerns
Inquire about infant’s response to noises, voice
Observe an older infant’s/toddler’s speech pattern
• Inspect the ears
Assess the shape of the ears
o Determine if both ears are well formed
Assess the position
o Examine the child from the front, with the child’s head held erect and the eyes
facing forward.
o Draw an imaginary line between the inner canthi and extend it around the
head.
o This line should be below the top of the pinnae
• Palpate the tragus and posterior auricular area
• Otoscopic exam including insufflation
Position the child for an ear examination
o This part of the exam can be performed either on the examination table or in
the caregiver’s lap. The head should be stabilized to prevent movement during
otoscopy.
o A parent or assistant can help with the examination by folding the child’s wrists
and arms over the child’s abdomen with one hand and then holding the child’s
head against the parent’s/assistant’s chest with the other.
Visualize the external canal
o Gently hold the tragus and insert the otoscope while visualizing the canal. In
contrast to adults, gentle posterior traction may help you visualize the canal
and eventually the tympanic membrane.
Visualize the tympanic membrane
o Identify the landmarks starting with the long handle of the malleus then
moving to the “cone of light” in the pars tensa.
o Carefully visualize the pars flaccida.
59
Courtesy of M. Whipple, MD
Perform pneumatic otoscopy
o Hold the otoscope and bulb with one hand and retract the pinna with the
other.
o Gently apply a small “puff” of air to the tympanic membrane.
o Normal movement: medially (away from you) with the application of air and
laterally (toward you) when the bulb is released.
Know
• Hearing:
Any delay in language acquisition or loss of language milestones should prompt a
referral for formal hearing testing.
Hearing impairment is estimated to occur in 1-2/1000 live births.
Some etiologies of hearing loss in childhood:
o Sensorineural: cochlear malformation, damage to hair cells (due to noise,
disease, ototoxic agents) or 8th nerve damage.
o Conductive (most common): ear canal atresia, cerumen impaction, otitis
media with effusion.
• Position/Shape of the ears
Malformed external and middle ears may be associated with serious renal or other
craniofacial malformations.
• Palpation:
Tenderness to palpation of the tragus is indicative of otitis externa.
o You will also typically see white cheesy material in the external auditory canal.
o Treatment is aural toilet and topical antibiotics.
Tenderness to palpation and/or redness in the posterior auricular area may
suggest mastoiditis.
• Otoscopy:
Areas of retraction in the pars flaccida may represent a cholesteatoma and should
be further evaluated. A cholesteatoma acts as a benign tumor causing local bone
destruction and is a nidus for bacteria to grow and cause chronic infections.
The most common reason for an immobile tympanic membrane (TM) with
pneumatic otoscopy is a poor seal between the otoscope and ear canal.
You must assess the movement of the TM to determine if a patient has otitis
media. In addition to pneumatic otoscopy, acoustic tympanometry can be used.
60
Changes in the appearance of the TM that are highly suggestive of acute infection
include bulging or purulent material visualized behind the tympanic membrane.
Guidelines for the diagnosis and treatment of otitis media: www.aap.org
Removal of cerumen is difficult but sometimes necessary to adequately see the
TMs. The external auditory canal bleeds easily with minor trauma so ask for help if
you need to clear out cerumen. It can be done by gentle irrigation with warm
water, H 2 O 2 or with direct visualization and use of a wire/plastic loop.
Mouth examination
Do
• The approach
In young children save the mouth exam for the very last.
Ask child to open the mouth and show you their teeth (appropriate for an older
toddler/child). If this doesn’t work, be prepared to be fast with your tongue blade.
An alternative is to be flexible and look in the mouth when the child is crying for
some other reason!!!
• Inspect the teeth
Count the number of teeth and note position.
Note any defects or discolorations.
• Inspect gums, mucosal surfaces and posterior pharynx
Inspect the buccal mucosal and gums looking for ulcers, candida or trauma.
To see the posterior pharynx, you may have to use the tongue blade and gag the
child. Alternative tricks you can use include asking the child to “roar like a lion”,
“pant like a dog”, have their parents model what you would like to child to do or
have the child look in your mouth.
Know
• The numbering system for primary teeth is different than the system used in adults.
There are 20 primary teeth
o Time for first tooth eruption is variable. Delayed eruption may be familial or
associated with other syndromes/conditions (like hypothyroidism)
o There may be developmental anomalies associated with tooth development.
• Dental caries is the most common chronic illness in the United States. More than half of
children within the U.S. have dental caries. Steptococcus mutans is associated with the
development of dental caries.
Early childhood caries may occur on the smooth surfaces of upper/lower incisors
because of prolonged exposure to sugar containing substances.
Sites for caries in older children (> 3 years) include pits/fissures of biting (occlusal)
surfaces.
• Using a tongue blade in this population is challenging. Inserting it along the side of the
mouth and then gagging the child will allow for an unobstructed view of the posterior
pharynx in most children.
• The size of tonsils are described in the following way:
Grade Appearance
0 Absent
1 Visible between the tonsillar pillars
2 Easily visible outside of the tonsillar fossae
3 Enlarged and occupying >75% of posterior pharynx
61
Touching in the midline occupying all of the posterior
4
pharynx
• The diagnosis of streptococcal pharyngitis is a laboratory, not clinical diagnosis. Other
infections that can cause tonsillar exudates include EBV infections, CMV infections, S.
aureus infections, adenoviral infections.
Heart Examination
The approach to the pediatric heart examination is the same as in an adult. Included here is a brief discussion
of murmurs in children.
• Newborn period
As the pulmonary vascular resistance decreases, flow through the ductus ateriosus
or foramen ovale stops as these structures close. Some murmurs heard shortly
after birth will disappear.
However, as the pulmonary vascular resistance decreases, this may allow left to
right shunting and new murmurs may appear (such as seen with a VSD).
Presence of central cyanosis is an important clue for congenital heart disease.
Those lesions associated with cyanotic heart disease are the “Ts”: tetralogy of
Fallot, tricuspid atresia, transposition of the great arteries, total anomalous venous
return and truncus arteriosus (there are others but these are easy to remember).
• Beyond the newborn period
50% of children have innocent murmurs.
Non-pathologic murmurs include:
o Peripheral pulmonary flow murmur:
• Soft (1-2/6) systolic ejection murmur heard at L upper sternal border with
radiation to the axilla and back.
o Venous hum:
• Soft (1-2/6) continuous murmur heard in 1st or 2nd intercostal space.
o Innocent murmur:
• Soft (<3/6) early systolic murmur heard along the L sternal border
between the 2nd/3rd or 4th/5th ribs. Intensity varies with position & might
be heard with the bell. “Vibratory/blowing/musical” in quality.
o Hemic murmur (flow murmur):
• Heard in states with increased physiologic need (fever, anemia). Heard
at base of the heart, soft (<3/6) and often associated with tachycardia.
Musculoskeletal Examination
Do
• Observe the child closely, noting in particular range of motion and limb use
An excellent time to get this information is before the examination while the child
is playing or interacting with their parents.
• Inspect the joints for redness or swelling
Start with the hands or some non-threatening part of the examination; examine
the affected joint last.
• Palpate methodically and in a systematic manner the involved area and all other areas that
influence the involved area.
62
Note muscles, bony prominences, other important landmarks, and joints of the
involved body part.
Be observant for pain or warmth.
• Assess active and passive range of motion for each major joint.
Young children may not cooperate with this part of the examination; you may
have to range their joints and gauge how much they resist you to judge function.
63
Older child/Adolescent Examination
You should be able to conduct a complete examination of all organ systems in all adolescents using an age
appropriate approach. The physical examination in an older child/adolescent is very similar to that done in
adults. Pay particular attention to patient modesty. Specific maneuvers that are a part of the older
child/adolescent examination include:
Know
Pubertal changes typically occur between the ages of 8 and 14 in girls and 9 and 16 in boys.
Occurrence of pubertal changes outside these ranges should be evaluated.
• Precocious puberty:
Benign precocious adrenarche: may occur in boys before age 9 and girls before age
8. Absence of penile enlargement in boys or of clitoral enlargement in girls
distinguishes this from pathologic virilization.
Precocious thelarche: isolated premature breast development in girls.
Other causes include: CNS tumors, ovarian cysts, gonadal tumors, congenital
adrenal hyperplasia, exogenous sources.
• Delayed puberty:
Constitutional (physiologic): most common, occurs in boys more often and is
associated with delayed growth and bone age; ask about family history.
Other causes: Malnutrition (including anorexia nervosa), chronic disease, central
causes (hypothalamic/pituitary abnormality, tumors, drugs, other endocrine
problems like hypothyroidism), gonadal causes (chromosomal—XXY, XO, anatomic
abnormalities, immunologic).
64
Musculoskeletal exam
An excellent demonstration of the 2 minute orthopedic examination in an older child can be
found in Aquifer Pediatrics case # 6 (Mike pre-sports physical); also Chapter 17 in Goldbloom’s
Pediatric Clinical Skills (p 311).
Do
• Be able to perform a basic musculoskeletal examination (see Foundations-level
resources).
• Additional techniques:
Assess the strength of the upper and lower extremities’ major muscle groups.
o Be able to test pelvic girdle strength: Ask the patient to sit on the floor and
then stand up.
o Lower extremity strength/joint function: Ask the child to squat and walk like a
duck across the room.
Back examination
o Inspect the back for spinal dimples & midline abnormalities such as a tuft of
hair, midline nevi or central dimple. This should be done beginning in infancy.
o Assess whether the spinal dimples are level
• Inspect the patient back from behind when they stand. If the spinal
dimples are at the same level there is not significant leg length
discrepancy.
o Assess symmetry/screening for scoliosis:
• Shoulders should be at the same level, as should posterior superior
iliac crest.
• Inspect the patient’s back when they are facing away from you.
• Have the child bend forward at the waist keeping knees straight and
allowing arms to hang freely; ribs/thorax should be symmetric.
Know
• Gowers’ sign occurs when a child is unable to rise from a sitting to standing position
without assistance. This sign indicates proximal muscle weakness.
• Midline abnormalities may indicate an underlying spinal cord or vertebral abnormality.
• Scoliosis is common in children and screening is a part of the adolescent examination.
• Excessive thoracic kyphosis that persists when the child lies down is pathologic.
65
Ethics Cases and Additional Resources in Pediatric Bioethics
Introduction:
At times during the practice of Pediatrics, clinicians must make difficult ethical and moral decisions to
serve the best interest of their patients. The scenarios described below are real cases, address ethical
issues unique to pediatric patients and give you the chance to develop practical approaches to these
problems. We have also included a list of online resources to introduce you to broader materials
available in pediatric bioethics.
Find the Ethic Cases and resources here:
http://www.washington.edu/medicine/pediatrics/students/current/third-year
Group Discussion:
Your bioethical learning objective can be met by a group discussion of the cases. Be prepared to discuss
the following for BOTH case 1 and 2, as everyone is expected to participate:
• The ethical issues raised by each case;
• How you would weigh the various sides of the conflicts/view the different arguments;
• How you would develop a plan to resolve the problem and the ethical conflicts;
• Basic ethical principles that would guide your plans.
Ethics Cases
Case 1
You are a primary care physician who is assuming the care of a family. Upon review of the past medical
history of the 1-year-old daughter, you find that she has had no immunizations although she received
several well child examinations with their homeopathic caregiver. Her current medications include
Chinese herbal supplements and the family follows a vegan diet. You ask the parents why your patient
hasn’t received immunizations and they state, "We don’t believe in immunizations".
Case 2
A 14 year-old boy is admitted to the Hematology-Oncology ward with acute lymphoblastic leukemia. He
presented to the Emergency Department with pallor and dizziness and was found to have a hematocrit
of 14.9%. The oncologist would like to start best available chemotherapy immediately, but the patient
and his legal guardians (aunt and uncle) have made it clear both verbally and in writing that, as
Jehovah’s Witnesses, they will refuse all blood products. His chemotherapy is myeloablative and will
cause a further decline in his hematocrit. There is virtually a 100% chance of death with this leukemia if
it is not treated and an approximately 75% chance of survival with best available chemotherapy.
Case 3 (Optional):
A 7-week old previously healthy full term Hmong female infant presents to your clinic with 24 hours of
fever, mild cough, nasal congestion and irritability. Mom measured an axillary temperature of 104.5
degrees Fahrenheit this morning. On physical exam, you find the infant sleeping comfortably in no acute
distress in her mother’s arms but who begins to whimper when you try to move her. Overall, her exam is
non-focal with a full but soft anterior fontanelle. Initial labs show a normal white blood cell count but
with a left shift, a negative urinalysis, and an elevated C-reactive protein. Mom declines any further
work-up—including a lumbar puncture—saying she is “against any more invasive tests”.
66
Resources in Pediatric Bioethics
(4) American Medical Association’s Journal of Ethics is a terrific resource sponsored by the AMA. It
offers case scenarios, brief discussions and helpful presentations. Enter: “child” as the search
word to bring up additional discussions in pediatric ethics.
Immunization Information
67
Ethics and Professionalism Benchmarks for Pediatrics
Many of the ethical principles that apply to caring for adults also apply to caring for children. These
benchmarks outline several topics unique to pediatric patients that are highlighted in your clerkship.
This is not an all-inclusive list. Useful links to additional cases are also included in the final section of the
document.
ETHICS:
68
Care of adolescent patients
Know
General approach:
Adolescent patients are capable of participating and guiding their medical therapy. The extent of
each patient’s ability will depend on the developmental maturation of the patient. In general,
parents retain the responsibility to direct care for patients less than 18 years of age unless there
is disagreement about the course of therapy.
Special considerations:
As a caregiver for pediatric patients you should be able to define the following special categories
of patients:
1. Emancipated minor:
There are specific categories of adolescents who are legally capable of directing
their medical care. The categories include: 1) married, 2) pregnant/parent, 3) in
the military, 4) self-supporting.
2. Mature minor:
Courts can grant decision-making capacity to minors; this may be limited to
specific categories of care (see below) or in some cases of chronic illness when
the PHYSICIAN has determined that the patients is capable of informed consent.
3. Specific categories of care:
Decision-making capacity is given to minors for the treatment/care of
pregnancy, drug or alcohol abuse and sexually transmitted infection. Laws vary
by state.
As a caregiver for pediatric patients you should be able to define the difference between:
1. Informed consent: requires that the patient be competent to make health care
decisions, physician disclosure of relevant information, patient understanding of the
information and a voluntary, un-coerced patient decision.
2. Parental permission: parents give permission for therapy provided to their children.
The same standards and procedures for giving informed consent to a competent
patient apply.
3. Child Assent: helps patients acquire a developmentally appropriate understanding
of patients’ condition, telling the patient what patient can expect for the treatment,
assessing the patient’s understanding of the situation, including determining
whether the patient felt pressured to accept/reject the treatment. It also includes
soliciting the patient’s willingness to undergo the procedure (you can see how this is
probably a team effort with the parents!). This approach is not limited to adolescent
patients but is appropriate for ALL pediatric patients.
Do
Use appropriate language for the patient’s developmental level when explaining medical care
options.
Respect the patient’s privacy.
Discuss sensitive issues when you are alone with older patients (e.g. drug or alcohol use,
sexual practices/preferences, suicide risk etc.).
Obtain parental permission about therapeutic interventions.
Obtain child assent from patients about therapeutic interventions.
69
PROFESSIONALISM:
Admitting Mistakes
Know
A medical error or mistake is a preventable or unexpected outcome of a medical treatment.
An adverse event is a side effect that may occur in a certain percentage of cases that are
treated.
Medical mistakes are usually not due to negligence. They arise from incomplete knowledge
base, an error of judgment, lapse in attention or a “systems” error. You have a professional
responsibility as a health care provider to disclose errors to your patients. Although it is difficult
and uncomfortable disclosing errors, most patient appreciate honesty (wouldn’t you?). Loss of
trust usually arises from nondisclosure of errors.
Do
When you identify a medical error:
Determine the effect (actual or potential) on the patient.
Investigate/identify possible causes.
Explain in a calm, unhurried, truthful and apologetic manner that an error has occurred.
Answer all questions the patient has and be open for additional questions in the future
Provide information about follow up of the incident.
Accept responsibility and apologize as (or if) necessary.
70
DEPARTMENT CONTACTS
AND
CAREER ADVISORS
71
University of Washington School of Medicine
Department of Pediatrics Medical Student Program
Director
Jordan Symons, MD
jordan.symons@seattlechildrens.org
72
Pediatrics Career Advisors
Our career advisors are happy to provide individualized help with your decision making. These advisors
are excellent resources and are happy to meet with you at various points throughout the long
application process. With your initiative, your advisor will become acquainted with you and your record,
and will be able to provide you with individual feedback to help you with these important decisions.
The current Department of Pediatrics faculty members who serve as advisors for aspiring pediatricians:
Pediatrics:
Dr. Jimmy Beck: jimmy.beck@seattlechildrens.org
Dr. Rebekah Burns: rebekah.burns@seattlechildrens.org
Dr. Mollie Grow: mollie.grow@seattlechildrens.org
Dr. Abena Knight: abena.knight@seattlechildrens.org
Dr. Caitlin McGrath: caitlin.mcgrath@seattlechildrens.org
Dr. Emily Myers: emily.myers@seattlechildrens.org
Dr. Jordan Symons: jordan.symons@seattlechildrens.org
Dr. Glen Tamura: glen.tamura@seattlechildrens.org
Med/Peds:
Dr. Susan Hunt: susan.hunt@seattlechildrens.org
73