Severe Acut Malnutrition
Severe Acut Malnutrition
Severe Acut Malnutrition
https://www.ncbi.nlm.nih.gov/books/NBK15
4454/
Publication Details
Children who are <-3SD weight-for-age may be stunted (short stature) but not severely
wasted. Stunted children who are not severely wasted do not require hospital admission
unless they have a serious illness.
Diagnosis
Children with severe acute malnutrition should first be assessed with a full clinical
examination to confirm whether they have any general danger sign, medical complications
and an appetite.
Children with severe acute malnutrition with loss of appetite or any medical complication
have complicated severe acute malnutrition and should be admitted for inpatient care.
Children who have a good appetite and no medical complications can be managed as
outpatients.
Child with marasmus
• shock: lethargic or unconscious; with cold hands, slow capillary refill (> 3 s), or weak
(low volume), rapid pulse and low blood pressure
• signs of dehydration
• severe palmar pallor
• bilateral pitting oedema
• eye signs of vitamin A deficiency:
corneal ulceration
–
keratomalacia
When pressure is applied for a few seconds, a pit remains after the finger is removed.
Children with vitamin A deficiency are likely to be photophobic and will keep their eyes
closed. It is important to examine the eyes very gently to prevent corneal rupture.
• localizing signs of infection, including ear and throat infections, skin infection or
pneumonia
• signs of HIV infection (see Chapter 8)
• fever (temperature ≥ 37.5 °C or ≥ 99.5 °F) or hypothermia (rectal temperature < 35.5
°C or < 95.9 °F)
• mouth ulcers
• skin changes of kwashiorkor:
hypo- or hyperpigmentation
desquamation
ulceration (spreading over limbs, thighs, genitalia, groin and behind the ears)
exudative lesions (resembling severe burns) often with secondary infection (including
Candida).
• Conduct an appetite test:
Facilities and sufficient staff should be available to ensure correct preparation of appropriate
therapeutic foods and to feed the child regularly, day and night. Accurate weighing machines
or MUAC tapes are needed, and records of the feeds given and the child's weight or
anthropometric measurements should be kept so that progress can be monitored.
For triage assessment of children with severe acute malnutrition and management of shock,
see Chapter 1. When there is corneal ulceration, give vitamin A, instil chloramphenicol or
tetracycline and atropine drops into the eye, cover with a saline-soaked eye pad, and bandage
(see section 7.5.1). Severe anaemia, if present, will require urgent treatment (see section
7.5.2).
General treatment involves 10 steps in two phases: initial stabilization and rehabilitation (see
Table 21).
Table 21
Time frame for the management of a child with complicated severe acute malnutrition.
7.4.1. Hypoglycaemia
Diagnosis
If there is any suspicion of hypoglycaemia and when blood glucose can be measured quickly
(e.g. with Dextrostix®), this should be done immediately. Hypoglycaemia is present when
the blood glucose is < 3 mmol/litre (< 54 mg/dl). If blood glucose cannot be measured, it
should be assumed that all children with severe acute malnutrition are hypoglycaemic and
given treatment.
Treatment
Give the first feed of F-75 therapeutic milk, if it is quickly available, and then
continue with feeds every 2 h for 24 h; then continue feeds every 2 or 3 h, day and
night.
If the child is unconscious, treat with IV 10% glucose at 5 ml/kg or, if IV access
cannot be quickly established, then give 10% glucose or sucrose solution by
nasogastric tube. If IV glucose is not available, give one teaspoon of sugar moistened
with one or two drops of water sublingually, and repeat every 20 min to prevent
relapse. Children should be monitored for early swallowing, which leads to delayed
absorption; in this case another dose of sugar should be given. Continue with 2 h oral
or nasogastric feeds to prevent recurrence.
Monitoring
If the initial blood glucose was low, repeat the measurement (using finger or heel prick blood
and measure with the Dextrostix®, when available) after 30 min.
• If blood glucose falls to < 3 mmol/litre (< 54 mg/dl), repeat the 10% glucose or oral
sugar solution.
• If the rectal temperature falls to < 35.5 °C, or if the level of consciousness
deteriorates, repeat the Dextrostix® measurement and treat accordingly.
Prevention
Feed every 2 h, starting immediately (see initial refeeding) or, when dehydrated,
rehydrate first. Continue feeding throughout the night.
Encourage mothers to watch for any deterioration, help feed and keep the child warm.
7.4.2. Hypothermia
Diagnosis
• If the axillary temperature is < 35 °C (< 95°F) or does not register on a normal
thermometer, assume hypothermia. When a low-reading thermometer is available,
take the rectal temperature (< 35.5 °C or < 95.9 °F) to confirm hypothermia.
Treatment
All children with hypothermia should be treated routinely for hypoglycaemia and infection.
Feed the child immediately and then every 2 h unless they have abdominal distension;
if dehydrated, rehydrate first.
Re-warm the child: Make sure the child is clothed (especially the head); cover with a
warmed blanket and place a heater (not pointing directly at the child) or lamp nearby,
or put the child on the mother's bare chest or abdomen (skin-to-skin) and cover them
with a warmed blanket and/or warm clothing.
Monitoring
• Take the child's rectal temperature every 2 h until it rises to > 36.5 °C. Take it every
30 min if a heater is being used.
• Ensure that the child is covered at all times, especially at night. Keep the head
covered, preferably with a warm bonnet, to reduce heat loss.
• Check for hypoglycaemia whenever hypothermia is found.
Prevention
Place the bed in a warm, draught-free part of the ward, and keep the child covered.
Use the Kangaroo technique for infants, cover with a blanket and let the mother sleep
with child to keep the child warm.
Avoid exposing the child to cold (e.g. after bathing or during medical examinations).
Change wet nappies, clothes and bedding to keep the child and the bed dry. Dry
carefully after bathing, but do not bathe if very ill.
7.4.3. Dehydration
Diagnosis
Dehydration tends to be overdiagnosed and its severity overestimated in children with severe
acute malnutrition because it is difficult to determine dehydration accurately from clinical
signs alone. Assume that all children with watery diarrhoea or reduced urine output have
some dehydration. It is important to note that poor circulatory volume or perfusion can co-
exist with oedema.
Treatment
Do not use the IV route for rehydration, except in cases of shock. Rehydrate slowly, either
orally or by nasogastric tube, using oral rehydration solution for malnourished children (5–
10ml/kg per h up to a maximum of 12 hours). The standard WHO ORS solution for general
use has a high sodium and low potassium content, which is not suitable for severely
malnourished children. Instead, give special rehydration solution for malnutrition, ReSoMal.
Give the ReSoMal rehydration fluid orally or by nasogastric tube, more slowly than
you would when rehydrating a well-nourished child:
Then give 5–10 ml/kg per h for the next 4–10 h on alternate hours, with F-75 formula.
The exact amount depends on how much the child wants, the volume of stool loss and
whether the child is vomiting.
If not available then give half strength standard WHO oral rehydration solution with
added potassium and glucose as per the ReSoMal recipe below, unless the child has
cholera or profuse watery diarrhoea.
Monitoring
During rehydration, respiration and pulse rate should fall and urine start to be passed. The
return of tears, a moist mouth, less sunken eyes and fontanelle, and improved skin turgor are
also signs that rehydration is proceeding, but many severely malnourished children will not
show these changes even when fully rehydrated. Monitor weight gain.
Monitor the progress of rehydration every 30 min for 2 h, then every hour for the next 4–10
h. Be alert for signs of overhydration, which is very dangerous and may lead to heart failure.
Check for:
Table
This solution is used in the preparation of starter and catch-up feeding formulas and
ReSoMal. Electrolyte and mineral powders are produced by some manufacturers. If these are
not available or affordable, prepare the solution (2500 ml) using the following ingredients:
Table
If available, also add selenium (0.028 g sodium selenate, NaSeO4.10H2O) and iodine (0.012 g
potassium iodide, KI) per 2500 ml.
For the oral rehydration solution ReSoMal, use 45 ml of the stock potassium chloride
solution instead of 40 ml electrolyte/mineral solution
For milk feeds F-75 and F-100, add 22.5 ml of the stock potassium chloride solution instead
of 20 ml of the electrolyte/mineral solution to 1000 ml of feed. Give the 1.5% zinc acetate
solution by mouth at 1 ml/kg per day. Give 0.3 ml/kg of 50% magnesium sulfate
intramuscularly once to a maximum of 2 ml.
If you find signs of overhydration (early signs are respiratory rate increasing by 5/min and
pulse rate by 25/min), stop ReSoMal immediately and reassess after 1 h.
Prevention
Measures to prevent dehydration due to continuing watery diarrhoea are similar to those for
well-nourished children (see treatment plan A), except that ReSoMal fluid is used instead of
standard ORS.
Give ReSoMal between feeds to replace stool losses. As a guide, give 50–100 ml after
each watery stool.
All severely malnourished children have deficiencies of potassium and magnesium, which
may take about 2 weeks to correct. Oedema is partly a result of potassium deficiency and
sodium retention. Do not treat oedema with a diuretic. Excess body sodium exists even
though the plasma sodium may be low. Giving high sodium loads could kill the child.
Treatment
►
Give extra magnesium (0.4–0.6 mmol/kg per day).
The extra potassium and magnesium should be added to the feed during its preparation if not
pre-mixed. See recipefor a combined electrolyte/mineral solution. Add 20 ml of this solution
to 1 litre of feed to supply the extra potassium and magnesium required. Alternatively, use
commercially available pre-mixed sachets (specially formulated for malnourished children).
When rehydrating, give low sodium rehydration fluid (ReSoMal) (see recipe).
7.4.5. Infection
In severe acute malnutrition, the usual signs of bacterial infection, such as fever, are often
absent, yet multiple infections are common. Therefore, assume that all children with severe
acute malnutrition have an infection on their arrival in hospital, and treat with antibiotics
immediately. Hypoglycaemia and hypothermia are often signs of severe infection.
Treatment
a broad-spectrum antibiotic
measles vaccine if the child is ≥ 6 months and not vaccinated or was vaccinated
before 9 months age. Delay vaccination if the child is in shock.
If the child has uncomplicated severe acute malnutrition, give oral amoxicillin (for
dosage, see annex 2) for 5 days.
Note: Metronidazole 7.5 mg/kg every 8 h for 7 days may be given in addition to broad-
spectrum antibiotics; however, the efficacy of this treatment has not been established in
clinical trials.
If you identify other specific infections (such as pneumonia, dysentery, skin or soft-
tissue infections), give antibiotics as appropriate.
Add antimalarial treatment if the child has a positive blood film for malaria parasites
or a positive malaria rapid diagnostic test.
If there is evidence of worm infestation, treatment should be delayed until the rehabilitation
phase. Give albendazole as a single dose or mebendazole 100 mg orally twice a day for 3
days. In countries where infestation is prevalent, also give mebendazole to children with no
evidence of infestation 7 days after admission.
HIV infection
Where HIV infection is common, children with severe acute malnutrition should be tested for
HIV to determine their need for antiretroviral therapy (ART). If the child is infected with
HIV, start ART as soon as possible after stabilization of metabolic complications and sepsis.
They should be monitored closely (inpatient and outpatient) in the first 6–8 weeks following
initiation of ART to identify early metabolic complications and opportunistic infections (see
Chapter 8).
Monitoring
If the child is still anorexic after 7 days of antibiotic treatment, continue for a full 10-day
course. If anorexia persists, reassess the child fully.
All severely malnourished children have vitamin and mineral deficiencies. Although anaemia
is common, do not give iron initially, but wait until the child has a good appetite and starts
gaining weight (usually in the second week), because iron can make infections worse.
Multvitamins including vitamin A and folic acid, zinc and copper are already present in F-75,
F-100 and ready-to-use therapeutic food packets. When premixed packets are used, there is
no need for additional doses.
In addition, if there are no eye signs or history of measles, then do not give a high dose of
vitamin A because the amounts already present in therapeutic foods are enough.
Treatment
Give vitamin A on day 1 and repeat on days 2 and 14 only if child has any signs of
vitamin A deficiency like corneal ulceration or a history of measles (see section
7.5.1).
►
Start iron at 3 mg/kg per day after 2 days on F-100 catch-up formula. Do not give iron
in the stabilization phase, and do not give iron if the child is receiving ready-to-use
therapeutic food (RUTF).
If child is not on any of the pre-mixed therapeutic foods, give the following micronutrients
daily for at least 2 weeks:
multivitamin syrup at 5 ml
Treatment
• frequent (every 2–3 h) oral small feeds of low osmolality and low lactose
• nasogastric feeding if the child is eating ≤ 80% of the amount offered at two
consecutive feeds
• calories at 100 kcal/kg per day
• protein at 1–1.5 g/kg per day
• liquid at 130 ml/kg per day or 100 ml/kg per day if the child has severe oedema
• in addition, if the child is breastfed, encourage continued breastfeeding, but make sure
the prescribed amounts of starter formula are given:
Table
The suggested starter formula and feeding schedules given below are designed to meet these
targets. Milk-based formulas, such as starter F-75 (with 75 kcal and 0.9 g protein/100 ml),
will be satisfactory for most children (see recipes). As cereal-based F-75 partially replaces
sugar with cereal flour, it has the advantage of lower osmolarity, which may benefit some
children with persistent diarrhoea, but it has to be cooked.
Feed from a cup or a bowl. Use a spoon, dropper or syringe to feed very weak children.
A recommended schedule, with a gradual increase in the feed volume and a gradual decrease
in feeding frequency, see Table 22. For children with a good appetite and no oedema, this
schedule can be completed in 2–3 days.
Table 22
Volumes of F-75 per feed for malnourished children (approximately 130 ml/kg per day).
Note: If staff resources are limited, give priority to 2-hourly feeds for only the most seriously
ill children, and aim for at least 3-hourly feeds initially. Ask mothers and other carers to help
with feeding. Show them what to do, and supervise them. Night feeds are essential, and staff
rosters may have to be adjusted. If, despite all efforts, not all the night feeds can be given, the
feeds should be spaced equally through the night to avoid long periods without a feed (with
the risk of increased hypoglycaemia and mortality).
If the child's intake (after allowing for any vomiting) does not reach 80 kcal/kg per day,
despite frequent feeds, coaxing and re-offering, give the remaining feed by nasogastric tube.
Do not exceed 100 kcal/kg per day in this initial phase.
In very hot climates, children might need extra water, as these foods may not contain enough
water if the children are sweating.
Monitoring
Children in the catch-up phase should in most cases be managed as outpatients. Signs that a
child has reached rehabilitation phase for catch-up growth are:
• return of appetite
• no episodes of hypoglycaemia (metabolically stable)
• reduced or disappearance of all oedema
Table
Treatment
Make a gradual transition from starter F-75 to catch-up formula F-100 or ready-to-use
therapeutic food over 2–3 days, as tolerated.
Replace starter F-75 with an equal amount of catch-up F-100 for 2 days. Give a milk-
based formula, such as catch-up F-100 containing 100 kcal/100 ml and 2.9 g of
protein per 100 ml (see recipes) or ready-to-use therapeutic food (see below).
►
On the third day if on F-100, increase each successive feed by 10 ml until some feed
remains uneaten. The point at which some feed remains unconsumed is likely to be
when intake reaches about 200 ml/kg per day.
Start with small but regular meals of RUTF and encourage the child to eat often (first
8 meals per day, and later 5–6 meals per day). If the child cannot eat the whole
amount of RUTF per meal in the transition phase, top up with F-75 to complete the
feed, until is able to eat a full RUTF meal.
If the child cannot take at least half of recommended amount of RUTF in 12 h, stop
RUTF and give F-75. Try introducing RUTF again in 1–2 days until the child is able
to take adequate amounts.
If still breastfeeding, offer breast milk first before every RUTF feed.
After the transition phase, refer the child for rehabilitation in outpatient care or to a
community feeding programme.
–
Sit with the child on the lap and gently offer the feeds.
Offer plenty of clean water in a cup, when the child is eating RUTF.
Table
Recommended amounts per day of ready-to-use therapeutic food containing 500 kcal.
Monitoring
Avoid causing heart failure. Monitor for early signs of congestive heart failure (rapid pulse,
fast breathing, basal lung crepitations, enlarging liver, gallop heart rhythm, raised jugular
venous pressure). If both pulse and breathing rates increase (breathing by 5 breaths/min and
pulse by 25 beats/min), and the increase is sustained for two successive 4-hourly readings,
then:
Assess progress. After the transition, monitor progress by the rate of weight gain:
• Weigh the child every morning before feeding, and plot the weight.
• Calculate and record the weight gain every 3 days as g/kg per day (see box below).
Step 1.
Step 2.
Step 3.
Divide by child's average weight in kg: 100 g/day ÷ 6.15 kg = 16.3 g/kg per day
• poor (< 5 g/kg per day), the child requires a full re-assessment
• moderate (5–10 g/kg per day), check whether the intake targets are being met or if
infection has been overlooked
• good (> 10 g/kg per day).
Provide:
Severe acute malnutrition is less common in infants < 6 months than in older children. An
organic cause for the malnutrition or failure to thrive should be considered, and, when
appropriate, treated. Infants less than 6 months of age with severe acute malnutrition with any
of the following complicating factors should be admitted for inpatient care:
• general danger signs or serious clinical condition as outlined for infants 6 months or
older.
• recent weight loss or failure to gain weight.
• ineffective breastfeeding (attachment, positioning or suckling) directly observed for
15–20 min, ideally in a supervised separated area.
• any pitting bilateral oedema of the feet.
• any medical problem needing more detailed assessment
• any social issue requiring detailed assessment or intensive support (e.g. disability or
depression of caretaker or other adverse social circumstances).
Treatment
Give parenteral antibiotics to treat possible sepsis, and appropriate treatment for other
medical complications.
For infants with severe acute malnutrition and oedema, give infant formula or F-75 or
diluted F-100 (add water to formula in recipes up to 1.5 litres instead of 1 litre) to
supplement breastfeeding.
For infants with severe acute malnutrition with no oedema, give expressed breast
milk; and when not possible, commercial infant formula or F-75 or diluted F-100, in
this order of preference.
During nutritional rehabilitation, the basic principles for older children apply; however,
young infants are less able to excrete salt and urea in their urine, especially in hot climates.
Therefore, the preferred diets in the stabilization phase are (in order of preference):
Assessment of the physical and mental health of mothers or caretakers should be promoted
and relevant treatment or support provided.
Discharge
Infants less than 6 months of age admitted to inpatient care can be transferred to outpatient
care if:
• all clinical conditions or medical complications including oedema are resolved or the
child is clinically well and alert,
• the child is breastfeeding effectively or feeding well,
• weight gain is satisfactory e.g. above the median of the WHO growth velocity
standards or more than 5gm/kg per day for at least 3 successive days.
Before discharge, the infant's vaccination status and other routine interventions should be
checked and provided as appropriate. Mothers or caregivers should then be linked with any
necessary community follow-up and support. A child should only be discharged from all
nutritional care only when he or she:
Give vitamin A orally on days 1, 2 and 14 (age < 6 months, 50 000 IU; age 6–12
months, 100 000 IU; older children, 200 000 IU). If the first dose was given in the
referring centre, treat on days 1 and 14 only.
If the eyes show signs of corneal clouding or ulceration, give the following additional care to
prevent corneal rupture and extrusion of the lens:
Instil chloramphenicol or tetracycline eye drops four times a day, as required, for 7–
10 days.
Instil atropine eye drops, one drop three times a day, for 3–5 days.
• Hb is < 4 g/dl
• Hb is 4–6 g/dl and the child has respiratory distress.
In severe acute malnutrition, the transfusion must be slower and of smaller volume than for a
well-nourished child. Give:
If the child has signs of heart failure, give 10 ml/kg of packed cells, because whole blood is
likely to worsen this condition. Children with severe acute malnutrition with oedema may
have redistribution of fluid leading to apparent low Hb, which does not require transfusion.
Monitoring
Monitor the pulse and breathing rates, listen to the lung fields, examine the abdomen for liver
size and check the jugular venous pressure every 15 min during the transfusion.
If there are basal lung crepitations or an enlarging liver, stop the transfusion and give
furosemide at 1 mg/kg IV.
Note: Do not repeat transfusion even if the Hb is still low or within 4 days of the last
transfusion.
Zinc deficiency is usual in children with kwashiorkor, and their skin quickly improves with
zinc supplementation. In addition:
Bathe or soak the affected areas for 10 min/day in 0.01% potassium permanganate
solution.
Apply barrier cream (zinc and castor oil ointment, petroleum jelly or tulle gras) to the
raw areas, and gentian violet or nystatin cream to skin sores.
►
Treatment
Giardiasis
If cysts or trophozoites of Giardia lamblia are found, give metronidazole (7.5 mg/kg
every 8 h for 7 days). Treat with metronidazole if stool microscopy cannot be
undertaken or if there is only clinical suspicion of giardiasis.
Lactose intolerance
Diarrhoea is only rarely due to lactose intolerance. Intolerance should be diagnosed only if
copious watery diarrhoea occurs promptly after milk-based feeds are begun and if the
diarrhoea clearly improves when milk intake is reduced or stopped. Starter F-75 is a low-
lactose feed. In exceptional cases:
Osmotic diarrhoea
Use cereal-based starter F-75 (see recipes) or, if necessary, a commercially available
isotonic starter F-75.
7.5.5. Tuberculosis
If TB is strongly suspected:
Children admitted to hospital with complicated severe acute malnutrition can be transferred
to outpatient care during the rehabilitation phase. Social factors, such as loss of earnings for
the mother and care for other children, should also be taken into account, as should the fact
that those without complications can be managed as outpatients or in the community.
Carefully assess the child and the available community support. The child will require
continuing care as an outpatient to complete rehabilitation and prevent relapse.
The decision to transfer children to outpatient care should not be based on achievement of
specific anthropometric or weight-for-height/length outcomes. Children should be discharged
from hospital to outpatient or a nutritional programme when:
• they have completed parenteral antibiotic treatment, and are clinically well and alert
• medical complications are resolved
• their appetite has fully recovered and they are eating well
• oedema has reduced or resolved.
Children with severe acute malnutrition should be discharged from the nutritional treatment
programme only when their:
The decision should be based on the same anthropometric indicator that was used on
admission. Thus, if mid-upper arm circumference was used, then it should be used to assess
and confirm nutritional recovery, and similarly for weight for length/height. Children
admitted with only bilateral pitting oedema, should be discharged on the basis of either mid-
upper arm circumference or weight-for-height/length depending on the indicator used
routinely in the national nutrition programme. Percentage weight gain should not be used as a
discharge criterion.
The child should be fed at least five times a day with foods that contain approximately 100
kcal and 2–3 g protein per 100 g of food. It is essential to give frequent meals with a high
energy and protein content. The mother should be counselled on appropriate feeding to:
give appropriate meals (and the correct quantity of food) at least five times daily.
give high-energy snacks between meals (e.g. milk, banana, bread, biscuits).
give food separately to the child so that the child's intake can be checked.
7.6.3. Follow-up
When a child is discharged to outpatient, make a plan for following up of the child until full
recovery, and contact the outpatient department, nutrition rehabilitation centre, local health
clinic or health worker who will take responsibility for continuing supervision of the child. In
general, the child should be weighed weekly after discharge.
If he or she fails to gain weight over a 2-week period or loses weight between two
measurements or develops loss of appetite or oedema, the child should be referred back to
hospital for further assessment. Once discharged from the nutritional treatment, he or she
should be periodically monitored to avoid relapse.
A register of admissions, discharges and deaths should be kept. This should contain
information about the children (such as weight, age and sex), day of admission, date of
discharge or date and time of death.
To identify factors that can be changed to improve care, determine whether most of the
deaths occurred:
Standardize weighing on the hospital ward. Calibrate the scales every day. Weigh children at
the same time each day (e.g. morning) after removing clothes (but avoid hypothermia).
If the weight gain is < 5 g/kg per day, determine whether this occurred:
in all children being treated (if so, a major review of case management is required)
Inadequate feeding
Check:
Untreated infection
• re-examine carefully
• repeat urine microscopy for white blood cells
• examine the stools
• if possible, take a chest X-ray.
HIV/AIDS
Children with HIV and AIDS can recover from malnutrition, but it may take longer, and
treatment failures are commoner. Initial nutritional treatment of severe acute malnutrition in
children with HIV/AIDS should be the same as for HIV-negative children.
Psychological problems
Check for abnormal behaviour, such as stereotyped movements (rocking), rumination (i.e.
self-stimulation through regurgitation) and attention-seeking. Treat by giving the child
special love and attention. For children who ruminate, firmness with affection can assist.
Encourage the mother to spend time playing with her child.
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Publisher
NLM Citation
Pocket Book of Hospital Care for Children: Guidelines for the Management of Common
Childhood Illnesses. 2nd edition. Geneva: World Health Organization; 2013. 7, Severe acute
malnutrition.