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Risk Factors Associated With Neonatal Jaundice: A Cross-Sectional Study From Iran

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ID Design Press, Skopje, Republic of Macedonia

Open Access Macedonian Journal of Medical Sciences. 2018 Aug 20; 6(8):1387-1393.
https://doi.org/10.3889/oamjms.2018.319
eISSN: 1857-9655
Clinical Science

Risk Factors Associated with Neonatal Jaundice: A Cross-


Sectional Study from Iran

1 2 3 4,5 6*
Sayed Yousef Mojtahedi , Anahita Izadi , Golnar Seirafi , Leila Khedmat , Reza Tavakolizadeh

1 2
Department of Pediatrics, Ziyaeian Hospital, Tehran University of Medical Sciences, Tehran, Iran; Department of Pediatric
3
Infection Disease, Tehran University of Medical Science, Tehran, Iran; School of Medicine, Ziyaeian Hospital, Tehran
4
University of Medical Sciences, Tehran, Iran; Department of Community Medicine, School of Medicine,Tehran University of
5
Medical Science, Tehran, Iran; Health Management Research Center and Department of Community Medicine, Faculty of
6
Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran; Department of Pediatrics, Tehran University of Medical
Sciences, Tehran, Iran

Abstract
Citation: Mojtahedi SY, Izadi A, Seirafi G, Khedmat L, BACKGROUND: Neonatal jaundice is one of the main causes of the patient's admission in the neonatal period
Tavakolizadeh R. Risk Factors Associated With Neonatal
Jaundice; a Cross-Sectional Study from Iran. Open
and is potentially linked to morbidity.
Access Maced J Med Sci. 2018 Aug 20; 6(8):1387-1393.
https://doi.org/10.3889/oamjms.2018.319 AIM: This study aimed to determine the possible risk factors for neonatal jaundice.
Keywords: Neonatal Jaundice; Predisposing factors;
Jaundice METHODS: We investigated the case of infants who were admitted to the neonatal department of Ziyaeian
*Correspondence: Reza Tavakolizadeh. Department of hospital and Imam Khomeini Hospital for jaundice. Simple random sampling was used to evaluate variables
Pediatrics, Tehran University of Medical Sciences, related to maternal and neonatal predisposing factors based on the medical records and clinical profiles. All
Tehran, Iran. E-mail: rezatavakolizadeh@yahoo.com
variables in this study were analysed using SPSS software.
Received: 06-Jul-2018; Revised: 23-Jul-2018;
Accepted: 07-Jul-2018; Online first: 11-Aug-2018 RESULTS: In this study, about 200 mothers and neonates were examined. Our findings depicted that mother's
Copyright: © 2018 Sayed Yousef Mojtahedi, Anahita WBC, Hb, PLT, and gestational age were associated with jaundice (P < 0.05). Furthermore, there were significant
Izadi, Golnar Seirafi, Leila khedmat, Reza Tavakolizadeh.
This is an open-access article distributed under the terms relationships between different degrees of bilirubin with TSH, T4 levels and G6PD (P < 0.05). In fact, TSH, T4
of the Creative Commons Attribution-NonCommercial 4.0 levels and G6PD were found to be linked to neonatal hyperbilirubinemia. The risk factors for jaundice in our study
International License (CC BY-NC 4.0)
population comprise some predisposing factors such as WBC, Hb, PLT, gestational age, TSH, and T4 levels, as
Funding: This research did not receive any financial well as G6PD. Neonates at risk of jaundice are linked to some maternal and neonatal factors that can provide
support
necessary interventions to reduce the burden of the disease. Therefore, identification of associated factors can
Competing Interests: The authors have declared that no
competing interests exist facilitate early diagnosis, and reduce subsequent complications.

CONCLUSION: Neonatal jaundice should be considered as the main policy in all health care settings of the
country. Therefore, identification of factors affecting the incidence of jaundice can be effective in preventing
susceptible predisposing factors in newborns and high-risk mothers.

Introduction day of birth and is not usually harmful, and a self-


limiting condition, where disease usually improves
without treatment after reaching the normal amount of
Neonatal jaundice is a common event that bilirubin [6] [7], but very high levels of bilirubin may
occurs especially in the first week of birth [1] [2] [3] lead to kernicterus as permanent brain damage.
and is one of the most common causes of Nevertheless, diagnosis of newborn jaundice and its
hospitalisation of the term and preterm neonates in management will play an important role in the health
neonatal wards [1]. Based on the present evidence, of newborns [8]. If jaundice lasts more than 14 days, it
80% of premature infants have clinical symptoms, is called to be prolonged neonatal jaundice [6].
including yellowish skin and sclera, caused by serum An imbalance between bilirubin production
bilirubin levels [4] [5]. Hyperbilirubinemia is a common and conjugation is the main mechanism of jaundice,
disease that occurs especially in the first week of birth which leads to an increase in bilirubin levels. This
[1] [2] [3] and is one of the most common causes of imbalance often occurs due to the immature liver and
hospitalisation of the term and preterm infants in the rapid breakdown of red blood cells, which may be
neonatal hospitals [1]. It usually occurs on the second involved with several factors [9] [10] [11] [12].
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Open Access Maced J Med Sci. 2018 Aug 20; 6(8):1387-1393. 1387
Clinical Science
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The indirect bilirubin value in the physiologic Material and Methods


jaundice of the term neonates does not exceed 12
mg/dL on the third day, and, this maximum increase
reaches 15 mg/dL in preterm infants on the fifth day This cross-sectional study was conducted on
[13]. 207 neonates (<15 days) with hyperbilirubinemia (>
In physiologic jaundice, the maximum indirect 15 mg/dL) admitted to Ziaeean and Imam Khomeini
bilirubin of infants who fed breast milk may be higher hospitals in Tehran from April 2010 to May 2016.
than those fed with skimmed milk (15-17 mg/dL All neonates were examined for neonatal
versus 12 mg/dL); this higher level is probably due to jaundice risk factors. Neonates born with jaundice
the lower consumption of fluid by infants who are were selected based on the clinical outcomes of the
breastfeeding [14]. neonates. Furthermore, data from medical records
Jaundice on the first day of life is always and interviews with mothers were collected by survey
pathologic, and urgent attention is needed to find its staff. A checklist including demographic information
cause. Early jaundice is often due to hemolysis and and other information was also provided.
internal haemorrhage (cephalohematoma, liver or Maternal variables including blood group, RH,
spleen hematoma) or infection. Furthermore, jaundice Gestational diabetes mellitus (GDM), familial history of
is considered to be pathologic after two weeks and diabetes, history of anemia and thalassemia minor,
suggests direct hyperbilirubinemia [13] history of thyroid disease during and before
Jaundice is usually seen in newborns when the pregnancy, history of birth of a newborn with jaundice,
concentration of bilirubin reaches 5-10 mg/dl; history of smoking during pregnancy, use of herbal
however, it is seen as 2-3 mg/dl in adults. If the medicines during pregnancy, history of perinatal
jaundice is observed, the total bilirubin should be infections (TORCH: syphilis, rubella, toxoplasmosis),
measured to determine its severity. On the other CMV, CBC were evaluated in the current study.
hand, If the concentration in the newborn is more than Neonatal variables included gender, the age of birth,
5 in the first day of life or higher than 13 mg/dl in the birth season, birth weight, blood group and Rh.
following days, further studies are needed to
determine the direct and indirect bilirubin value, blood Hyperbilirubinemia was the criteria for
group, Coombs test, CBC, Peripheral blood smear entering this study. Also, exclusion criteria included
and reticulocytes count [13]. incomplete medical records. However, 20% of the
sample size was considered as additional samples in
Identification of predisposing factors in the the current study.
management of the disease is important [15] [16],
there are a number of predisposing factors in the Finally, data were collected from medical
occurrence of this disease, including maternal records and questionnaires. All data were then
diabetes, race, prematurity, height, polycythemia, analysed by using SPSS software version 19. In this
male sex, cephalohematoma, medications, Trisomy study, all principles of the Helsinki Statement were
21, weight loss, breastfeeding, delayed meconium considered as a statement of ethical principles for
passage and family history of jaundice [17] [18] [19] medical studies. It is worth noting that parents were
[20] [21]. The most common cause of jaundice can be informed about the study.
ABO incompatibility. Rh incompatibility and type of 20% of the extra sample size was added to
delivery can be among the controversial factors. prevent loss and withdrawal (N = 200). P is
Furthermore, some factors may contribute to jaundice, considered to be the first pregnancy in the formula, as
such as congenital infections (Syphilis, CMV, rubella, reported previously (24 and 25). Thus, the sample
toxoplasmosis), and age more than 25 years [22]. To size was calculated as 200 individuals: alfa = 0.05, Z1-
the best of our knowledge, there were not many a/2= 1.961150776, d= 0.03, p= 0.96, n= 165.
studies on the epidemiology of jaundice in Iran.
Data were collected by a questionnaire that
On the other hand, there has also been no was asked by the researcher from the patient.
program for the prevention and management of Moreover, a set of data was collected from medical
jaundice. Regarding the importance of irreversible records. Then, the data were analysed by SPSS
complications of hyperbilirubinemia and the software. Frequency was calculated for qualitative
prevention of these complications, the present study variables, while the mean, range and standard
was aimed to investigate the predisposing factors deviation were calculated for quantitative variables.
(maternal and neonatal risk factors) in the incidence of The chi-square test was used to examine qualitative
jaundice in newborn infants admitted to Ziaeean data, and t-test for non-dependent samples was used
medical centre. Identifying predisposing factors in to study quantitative data. It should be noted that the
predicting the occurrence and prevention of such risks P-value of < 0.05 was considered significant.
in neonates is important to reduce the morbidity and
mortality of hyperbilirubinemia.

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Mojtahedi et al. Risk Factors Associated With Neonatal Jaundice
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Results Also, there was no significant difference in the


maternal blood group in the neonates with different
levels of bilirubin (P = 0.1; Table 2).
The mean age of the pregnancy (weekly) Our findings have revealed that there was no
based on the level of bilirubin was shown in Table 1. significant difference in maternal hematologic Rh
The result of statistical analysis indicated that the among neonates with different levels of bilirubin (P =
gestational age was significantly related to jaundice (P 0.8; Table 3).
= 0.003).
Table 3: Evaluation of RH Blood Groups in Maternal Different
Table 1: Evaluation of Blood Factors and Other Neonatal Ages of Bilirubin (Rh/m)
Factors in Different Levels of Bilirubin
Total Bilirubin P = 0.8
t4/n tsh/n hct/n plt/n mcv/n hb/n wbc/n Retic bili/d bili/ b/w g/age Bilirubin 20-24.9 15-19.9 10-14.9
total
0.105 0.003 0.704 0.192 0.107 0.389 0.370 0.079 0.740 0.000 0.105 0.003 p-value 154 4 24 126 Number Positive Rh/m
8.98 4.96 40.22 290.59 98.44 15.14 11.82 0.03 0.50 9.75 2727.84 36.01 Average 10- 77.0% 66.7% 77.4% 77.3% Percent
2.72 3.52 9.27 95.97 7.92 3.23 4.03 0.02 0.38 2.55 715.43 3.29 Deviation 14.9
standard 46 2 7 37 Number Negative
8.74 3.88 40.85 299.48 99.61 15.67 10.70 0.03 0.50 16.24 2896.29 37.94 Average 15- 23.0% 33.3% 22.6% 22.7% Percent
3.08 1.62 8.38 64.59 8.58 2.45 3.02 0.02 0.21 0.82 572.05 1.59 Deviation 19.9
standard 200 6 31 163 Number Total
10.45 1.80 48.24 341.33 102.58 16.83 8.90 0.03 0.38 19.25 3250.00 38.00 Average 20- 100.0% 100.0% 100.0% 100.0% Percent
1.34 0.71 8.59 115.11 4.30 3.43 2.51 0.01 0.16 1.29 388.59 1.10 Deviation 24.9
standard
8.97 4.75 40.56 293.49 98.75 15.28 11.56 0.03 0.49 11.04 2769.62 36.37 Average Total
2.75 3.31 9.18 92.42 7.96 3.13 3.89 0.02 0.35 3.61 693.32 3.13 Deviation
standard

Based on Table 4, out of 163 patients, 41


neonates (25.2%), who their mothers suffered from
Moreover, as shown in Table, the findings of GDM, exhibited a serum bilirubin level of 10-14.9,
the statistical analysis revealed that the birth weight of followed by a bilirubin level of 20-24.9 (16.7%) and a
the infant was not significantly associated with the bilirubin level of 15-19.9 (16.1%). Neonates with
incidence of jaundice based on the bilirubin levels (P = different levels of bilirubin exhibited no significant
0.105). difference regarding gestational diabetes mellitus (P =
Assessment of neonatal bilirubin based on the 0.5).
different bilirubin level revealed that total bilirubin had
Table 4: Evaluation of Gestational Diabetes Mellitus in Different
a significant relationship with jaundice (P = 0.000). Ages of Bilirubin
Furthermore, there was no significant correlation
Bilirubin
between direct bilirubin with jaundice (P = 0.740). Total
20-24.9 15-19.9 10-14.9
P = 0.5
47 1 5 41 Number Gestational
Yes
The average reticulocyte count of the infant 23.5% 16.7% 16.1% 25.2% Percent diabetes
153 5 26 122 Number mellitus
indicated that the reticulocyte was not significantly 76.5% 83.3% 83.9% 74.8% Percent
No
(GDM)
200 6 31 163 Number
associated with the incidence of jaundice at the 100.0% 100.0% 100.0% 100.0% Percent
Total

different levels of bilirubin (P = 0.079). The mean of


Hb regarding bilirubin level exhibited that Hb of
neonate was strongly associated with jaundice (P = In the present study, out of 163 neonates, 72
0.389). Evaluation of the mean of mcv by the level of patients (44.2%) with a history of familial diabetes
bilirubin depicted that there was no significant revealed bilirubin levels of 10 to 14.9, following a
difference in infant mcv in different levels of bilirubin bilirubin level of 15-19.9 (54.8%) and a bilirubin level
(P = 0.107). of 20-24.9 (16.7%), (Table 5). No significant difference
The mean of PLT and WBC were markedly was found in the familiar history of diabetes among
associated with jaundice (P = 0.192; (P = 0.370). The neonates with different levels of bilirubin (P = 0.2). As
results of our study showed that the mean of Hct a matter of fact, familial history of diabetes was not
neonates had a significant correlation with found to be correlated with hyperbilirubinemia.
hyperbilirubinemia (P = 0.704).
Table 5: Evaluation of Familiar Diabetes Mellitus in Different
Based on the findings, it was revealed that the Ages of Bilirubin
TSH and T4 were significantly associated with Total
Bilirubin
P=0.2
jaundice (P = 0.003; P = 0.105). 20-24.9 15-19.9 10-14.9
90 1 17 72 Number
Yes
45.0% 16.7% 54.8% 44.2% Percent
Familiar/dm
110 5 14 91 Number
Table 2: Evaluation of Maternal Blood Groups in Different Ages 55.0% 83.3% 45.2% 55.8% Percent
No
of Bilirubin (bg/m) 200 6
31 163 Number Total
Total Bilirubin P = 0.1
20-24.9 15-19.9 10-14.9
54 1 9 44 Number A Bg/m
27.0% 16.7% 29.0% 27.0% Percent Table 6 indicated that out of 163 neonates 35
20 0 7 13 Number Ab
10.0% 0% 22.6% 8.0% Percent newborns (21.5%) with a maternal history of anaemia
45 1 8 36 Number B
22.5% 16.7% 25.8% 22.1% Percent
showed the bilirubin level of 10-14.9, following a
81 4 7 70 Number O bilirubin level of 15-19.9 (32.3%) and a bilirubin level
40.5% 66.7% 22.6% 42.9% Percent
200 6 31 163 Number Total of 20-24.9 (33.3%). There was no significant
100.0% 100.0% 100.0% 100.0% Percent
difference in the maternal history of anaemia between
neonates with different levels of bilirubin (P = 0.3).
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Clinical Science
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Table 6: Evaluation of Maternal Anemia in Different Ages of associated with hyperbilirubinemia.


Bilirubin

Total
Bilirubin
P = 0.3
Table 10: Evaluation of Asphyxia in Neonatal Different Ages of
20-24.9 15-19.9 10-14.9 Bilirubin
47 2 10 35 Number
Yes
23.5% 33.3% 32.3% 21.5% Percent Bilirubin
Anaemia Total P=0.002
153 4 21 128 Number 20-24.9 15-19.9 10-14.9
No
76.5% 66.7% 67.7% 78.5% Percent 51 0 1 50 Number
200 6 31 163 Number Yes
Total 25.5% 0% 3.2% 30.7% Percent
100.0% 100.0% 100.0% 100.0% Percent Asphyxia
149 6 30 113 Number
No
74.5% 100.0% 96.8% 69.3% Percent
200 6 31 163 Number
Total
100.0% 100.0% 100.0% 100.0% Percent
Bilirubin levels of 10-14.9% were seen in
9.2% of neonates with maternal thalassemia, followed
by a bilirubin level of 15-19.9 (22.6%) and a bilirubin According to Table 11, 15.5% of neonates
level of 20-24.9 (0%), (Table 7). The maternal showed cephalohematoma, while 84.5% of them did
thalassemia was not associated with different levels of not show this complication. Of the total number of 163
bilirubin (P = 0.06). neonates, 13.5% of neonates with hematoma showed
a bilirubin level of 10-14.9, while bilirubin levels of 19-
Table 7: Evaluation of Maternal Thalcemia in Different Ages of 15 and 20-24.9 were found in 25.8% and 16.7% of
Bilirubin
neonates, respectively. Findings demonstrated that
Total
Bilirubin
P = 0.06 there was no significant relationship between
20-24.9 15-19.9 10-14.9
22 0 7 15 Number cephalohematoma and disease (P = 0.2, Table 10). In
Yes
11.0% 0% 22.6% 9.2% Percent
178 6 24 148 Number
Thalassemia the present study, G6PD was also related to the
No
89.0% 100.0% 77.4% 90.8% Percent disease (P = 0.02).
200 6 31 163 Number
Total
100.0% 100.0% 100.0% 100.0% Percent
Table 11: Evaluation of Cephalohematoma in Neonatal
Different Ages of Bilirubin
Bilirubin
We also found that the baby's blood group Total
20-24.9 15-19.9 10-14.9
P = 0.2
was not significantly related to Hyperbilirubinemia 31 1 8 22 Number
Yes
15.5% 16.7% 25.8% 13.5% Percent
(P=0.3l Table 8), followed by a bilirubin level of 15- 169 5 23 141 Number
Cephalohematoma
+ No
19.9 in 80.6% of RH infants and bilirubin levels of 20- 84.5% 83.3% 74.2% 86.5% Percent
+ 200 6 31 163 Number
Total
24.9 in 66.7% of Rh infants. 100.0% 100.0% 100.0% 100.0% Percent

Table 8: Evaluation of Neonatal Blood Groups in Different


Ages of Bilirubin
Bilirubin
Total P = 0.3
20-24.9 15-19.9 10-14.9
66 1 7 58 Number
A
33.0% 16.7% 22.6% 35.6% Percent
27 0 7 20 Number
AB
Discussion
13.5% 0% 22.6% 12.3% Percent
49 2 6 41 Number
B
24.5% 33.3% 19.4% 25.2% Percent
58 3 11 44 Number
O
29.0% 50.0% 35.5% 27.0% Percent Recent studies have demonstrated neonatal
200 6 31 163 Number
100.0% 100.0% 100.0% 100.0% Percent
Total jaundice occurrence in more than 60% of term and
80% of premature neonates in the first week, where
bilirubin is non-conjugate, lipid-soluble, and non-polar
Based on the data presented in Table 9, it pigment. Bilirubin is one of the final products of
was found that the RH blood group was not related to haemoglobin catabolism and its clinical significance in
hyperbilirubinemia (P = 0.7). the neonates is due to sedimentation in the skin and
mucous membrane and the formation of jaundice.
Table 9: Evaluation of RH Blood Groups in Neonatal Different
Ages of Bilirubin (Rh/m)
This complication is also the most common
cause of hospitalisation of the neonates in the first
Bilirubin
Total
20-24.9 15-19.9 10-14.9
P = 0.7 month after birth (about 19%). In most cases, jaundice
157 4 25 128 Number
Positive can be transient, usually resolved by the end of the
78.5% 66.7% 80.6% 78.5% Percent
43 2 6 35 Number
Negative
Rh/n first week after birth, when the total serum bilirubin
21.5% 33.3% 19.4% 21.5% Percent
200 6 31 163 Number
concentration is not considered to be a harmful
Total
100.0% 100.0% 100.0% 100.0% Percent condition. Severe hyperbilirubinemia has been
described to develop with a potential risk for acute
As shown in Table 10, out of 163 patients, 50 bilirubin encephalopathy and kernicterus [23] [24] [25]
neonates (30.7%) with asphyxia showed a bilirubin [26] [27] [28] [32] [33] [34] [35] [36] [37]. Neonatal
level of 10-14.9, following a bilirubin level of 15-19.9 jaundice usually starts from the face and progresses
(3.2%). There was no significant difference in with the increase in the serum level to the abdomen
asphyxia among newborns with different levels of and legs. Based data described before, Jaundice is
bilirubin (P = 0.002). In other words, asphyxia was not one of the most common neonatal problems [23] [24]
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Mojtahedi et al. Risk Factors Associated With Neonatal Jaundice
_______________________________________________________________________________________________________________________________

[25] [26] [27] [28] [29]. study. However, our findings have revealed that
maternal and neonatal blood group and RH were not
This complication may lead to death in the first
significantly associated with hyperbilirubinemia
months, and infants who are still alive often suffer from
mental retardation, movement and balance disorders, A previous study indicated that blood type and
seizures, hearing loss at high frequencies, and speech Rh incompatibilities had been the important causes of
impairment. Therefore, the timely diagnosis and kernicterus [45]. It has been depicted that ABO
treatment of neonatal jaundice are very important in incompatibility, idiopathic jaundice, G6PD deficiency
preventing its complications. Identifying the and Rh incompatibility be the most important
predisposing factors of neonatal jaundice is still a predisposing factors for acute kernicterus [45].
serious discussion and can be effective in controlling
Based on the data presented in the current
jaundice and controlling the primary problem. In the
study, G6PD was also related to the disease. While
natural state, since liver enzymes have not evolved
the exact mechanism for linking G6PD deficiency to
enough, some icterus appears on the second to third
hyperbilirubinemia is still not fully understood, early
day, reaching its maximum on the second to fourth day
diagnosis of G6PD deficiency in infants can
and decreasing on the fifth to seventh days. This type
adequately reduce the risk of hyperbilirubinemia in
of jaundice is called physiologic jaundice. Factors such
affected neonates [40] [46], indicating the importance
as maternal diabetes, race, premature infant,
of prevention and timely treatment due to the
medication use of mother, male gender,
incompatibility of ABO and Rh. According to the
cephalohaematoma, breastfeeding, weight loss,
recommendations of the WHO Working Group,
delayed stools in the baby may be correlated with
screening for all neonates should be performed in
physiologic jaundice [23] [24] [25] [26] [27] [28] [29]
areas with a prevalence of 3-5% for G6PD deficiency
[30]. We also evaluated neonates for jaundice -specific
[47]. It is worth noting that the incompatibility of the
risk association such as gestational age, birth weight
blood group can be managed through daily care and
gestational diabetes, familial history of diabetes, low
the diagnosis of mothers whose neonates are at risk
birth weight, maternal history of anemia, maternal
for these disorders [40][48].
thalassemia, asphyxia, cephalohematoma, TSH and T4
and related blood factors including, blood count (Hb, A study indicated that the main causes of the
Hct. MCV. WBC and PLT) maternal-fetal blood group high prevalence of Jaundice complications in icteric
and their Rh for potential risks. newborns include incomplete follow-up in acrylic
babies due to ABO incompatibility, physician
The result of our study indicated that the
insensitivity, lack of routine examination of neonatal
gestational age was significantly linked to jaundice.
babies born to mothers with type O (Rh+) and
Consist of our study; It has been described that the
parental insensitivity [49].
risk of hyperbilirubinemia significantly increases with
decreasing gestational age [31] [32] [33] [34] [35]. Our data demonstrated that gestational
Furthermore, weight loss in the neonatal period is diabetes mellitus was not linked to hyperbilirubinemia.
considered as another risk factor for jaundice [35] Also family history of diabetes was not observed to be
[36]. Low-calorie intake has been indicated to be associated with hyperbilirubinemia.
associated with increased hepatic circulation of
A study has reported that gestational diabetes
bilirubin and often occurs within the first few days
has various and dangerous side effects on the baby,
before milk comes in [35] [36] [37]; however, we didn’t
the most common being neonatal jaundice (3.7%),
find a significant association of birth weight with the
incidence of jaundice. Based on the evidence present [50]. It is also described that the incidence of neonatal
in literature, neonates with low gestational age (less jaundice in diabetic mothers is three times higher than
that in the control group. Perhaps the reason for the
than 37 weeks) and increased level of bilirubin in the
difference in the prevalence of maternal diabetes
first hours of life should be evaluated to confirm and
associated- jaundice in different studies could be due
monitor them adequately. Also, rapid diagnosis of low
birth weight infants with or without visual evidence of to differences in study type and sample size [51]. In
weight loss at admission is needed to be included into the current study, the maternal thalassemia and
anaemia were not found to be associated with
clinical guideline for the control of neonatal
neonatal jaundice. However, further studies are
hyperbilirubinemia [38]. Another known risk factors
needed to clarify the role of maternal thalassemia and
identified in different investigations for the
anaemia in the development of hyperbilirubinemia. It
development of jaundice in neonates such as Asian
race, birth weight, exclusive breastfeeding, difficulty is worth noting that anaemia may range from
feeding, male sex, labour with oxytocin, primiparity, asymptomatic to life-threatening and reported to
potentially be linked to severe hyperbilirubinemia [52].
etc., [39] [40] [41] [42] [43] [44].
Patients with haemoglobin H has been indicated to
Risk factors identified in different usually born with hypochromic anaemia, where may
investigations for the development of jaundice in be at high risk for neonatal hyperbilirubinemia [53]
neonates among blood count variables, the mean of [54]. Also, Based on our findings, cephalohematoma
Hb, Hct, PLT and WBC were found to be markedly and asphyxia were not observed to be significantly
associated with hyperbilirubinemia in the present linked to hyperbilirubinemia.
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Neonatal asphyxia can inhibit the activity of hyperbilirubinemia: emerging clinical insights. Pediatr Clin North
uridine diphosphate glucuronyltransferase (UDPGT) in Am. 2009; 56(3):671–87. https://doi.org/10.1016/j.pcl.2009.04.005
PMid:19501698
the liver, consequently increasing the level of
unconjugated bilirubin. Cephalohematoma or 6. Stoll BJ, Kliegman RM. Jaundice and hyperbilirubinemiain the
newborn, Nelson textbook of pediatrics. 18th ed.Philadelphia:
ecchymosis can lead to extravascular hemolysis, Saunders, 2007: 592-598.
consequently increasing the level of bilirubin.
7. Fanaroff AA, Martin RJ. Neonatal-perinatal medicine: diseases
A study believed that infants' asphyxia could of the fetus and infant. 1987.
inhibit the activity of uridine diphosphate 8. National Institute for Health and Care Excellence. Neonatal
glucuronyltransferase (UDPGT) in the liver, leading to jaundice [homepage on the Internet]. Clinical guideline 98. London:
Royal College of Obstetricians and Gynaecologists, 2010 [cited
an increase in unconjugated bilirubin. 2016 Jun 15]. Available from:
Cephalohematoma may be associated with vascular https://www.nice.org.uk/guidance/cg98/evidence/full-guideline-pdf-
hemolysis, resulting in elevated levels of bilirubin [55]. 245411821
A study found no relationship between thyroid 9. Adhikari M, Mackenjee H. Care of the newborn. In: Wittenberg
hormones (iodine deficiency) and jaundice [56]. DF, editor. Coovadia's paediatrics and child health. 6th ed. Cape
However, more detailed studies are needed to Town, South Africa: Oxford University Press, 2010:129–130
evaluate the role of thyroid hormones on jaundice. 10. Porter ML, Dennis BL. Hyperbilirubinemia in the term newborn.
Am Fam Physician. 2002; 65(4):599–606. PMid:11871676
In the present study, it was revealed that the 11. Kramer LI. Advancement of dermal icterus in the jaundiced
TSH and T4 were significantly correlated with the newborn. Am J Dis Child. 1969; 118(3):454–458.
occurrence of jaundice. Our study has shown that https://doi.org/10.1001/archpedi.1969.02100040456007
high TSH increases the likelihood of jaundice (global 12. Moyer VA, Ahn C, Sneed S. Accuracy of clinical judgment in
statistics also indicate this); therefore, paediatricians neonatal jaundice. Arch Pediatr Adolesc Med. 2000; 154(4):391–
are more interested in conducting TSH tests on the 394. https://doi.org/10.1001/archpedi.154.4.391 PMid:10768679
fifth day of birth and comparing with the level of 13. Kleigman R, Bonita S, Richard E,Joseph St. Nelson text book
bilirubin. The risk factors for jaundice in our study of pediatrics.Translation by Nurozi E, Mohammadpor M. and Fallah
R. 3rd ed. Tehran: Andisheh Rafi, 2007.
population comprise some predisposing Factors such
as WBC, Hb, PLT, gestational age, TSH, and T4 14. Bradley JS. Nelson's Pediatric Antimicrobial Therapy 22nd Ed.
Am Acad Pediatrics, 2016.
levels, as well as G6PD. Our study may be helpful in
explaining the relationship between some of the 15. Mercier CE, Barry SE, Paul K, Delaney TV, Horbar JD,
Wasserman RC, Berry P, Shaw JS. Improving newborn preventive
predisposing factors with newborn jaundice to provide services at the birth hospitalization: a collaborative, hospital-based
more evidence for managing disease in hospitals. quality-improvement project. Pediatrics. 2007; 120(3):481-8.
Evaluation of risk factors for neonatal https://doi.org/10.1542/peds.2007-0233 PMid:17766519
hyperbilirubinemia is important because high risk 16. Sezik M. Does marriage between first cousins have any
factors play an important role in neonatal jaundice in a predictive value for maternal and perinatal outcomes in pre-
Hospital. Large-scale studies are also needed for eclampsia? J Obstet Gynaecol. 2006; 32:481–475.
https://doi.org/10.1111/j.1447-0756.2006.00432.x
further and also by the control group. Since the
promotion of neonatal health as a vulnerable group in 17. Javadi T, Mohsen Zadeh A. Examine the causes of jaundice in
newborns admitted in Hospital of shahidmadani khoramabad in
the health care services has a special place, so the 2000. J Lorestan Univ Med Sci. 2005; 4:73-8.
evaluation of neonatal jaundice in all levels of health
18. Linn S, Schoenbaum SC, Monson RR, Rosner B, Stubblefield
services should be considered as a fundamental PG, Ryan KJ. Epidemiology of neonatal hyperbilirubinemia.
policy. Pediatrics. 1985; 75(4):770-4. PMid:3982909
19. Maisels MJ, Gifford K, Antle CE, Leib GR. Jaundice in the
healthy newborn infant: a new approach to an old problem.
Pediatrics. 1988; 81(4):505-11. PMid:3353184
20. Boskabadi H, Maamouri G, Ebrahimi M, Ghayour-Mobarhan M,
References Esmaeily H, Sahebkar A. Neonatal hypernatremia and dehydration
in infants receiving inadequate breastfeeding. Asia Pac J Clin Nutr.
2003; 19:301-307.
21. Engle W A, Tomashek K M, Wallman C. "Late-preterm"infants:
1. Jardine LA, Woodgate P. Neonatal jaundice. American Family
A population at risk. Pediatrics. 2007; 120:1390-1401.
Physician. 2012; 85:824-825
https://doi.org/10.1542/peds.2007-2952 PMid:18055691
2. Paul IM, Lehman EB, Hollenbeak CS, Maisels MJ. Preventable
22. Zarrinkoub F, Beigi A. Epidemiology of hyperbilirubinemia in
newborn readmissions since passage of the Newborns' and
the first 24 hours after birth. Tehran University Medical Journal.
Mothers' Health Protection Act. Pediatrics. 2006; 118(6):2349-
2007; 65(6):54-9.
2358. https://doi.org/10.1542/peds.2006-2043 PMid:17142518
23. Stoll BJ, Kliegman RM. Jaundice and hyperbilirubinemia in the
3. Hall RT, Simon S, Smith MT.Readmission of breastfed infants in
newborn. Nelson textbook of pediatrics. 19th ed. Philadelphia: WB
the first 2 weeks of life. J Perinatol. 2000; 20(7):432-437.
Saunders, 2011:562-96.
https://doi.org/10.1038/sj.jp.7200418 PMid:11076327
24. Halamek LP. Neonatal jaundice and liver disease. Neonatal-
4. Newman TB, Xiong B, Gonzales VM, Escobar GJ. Prediction
perinatal medicine: diseases of the fetus and infant, 1997:1345-89.
and prevention of extreme neonatal hyperbilirubinemia in a mature
health maintenance organization. Arch Pediatr Adolesc Med. 2000; 25. Facchini FP, Mezzacappa MA, Rosa IR, Mezzacappa Filho F,
154(11):1140–1147. https://doi.org/10.1001/archpedi.154.11.1140 Aranha Netto A, Marba ST. Follow-up of neonatal jaundice in term
PMid:11074857 and late premature newborns. Jornal de pediatria. 2007; 83(4):313-
8. https://doi.org/10.2223/JPED.1676
5. Watchko JF. Identification of neonates at risk for hazardous
_______________________________________________________________________________________________________________________________

1392 https://www.id-press.eu/mjms/index
Mojtahedi et al. Risk Factors Associated With Neonatal Jaundice
_______________________________________________________________________________________________________________________________

26. Boskabadi H, Maamouri GH. Mafinejad Sh. The relationship 2001; 15(4):352–358. https://doi.org/10.1046/j.1365-
between traditional supplements' intake (camelthorn, flix weld and 3016.2001.00374.x PMid:11703683
glucose water) and idiopathic neonatal jaundice. Iranian Journal of
42. AAP Subcommittee on Neonatal Hyperbilirubinemia. Neonatal
pediatrics, 2011. PMid:23056809 PMCid:PMC3446180
jaundice and kernicterus. Pediatrics. 2001; 108(3):763–765.
27. Boskabad H, Maamouri GA, Mafi nejad SH, Rezagholizadeh F. https://doi.org/10.1542/peds.108.3.763 PMid:11533348
Clinical Course and Prognosis of Hemolytic Jaundice in Neonates
43. Watchko JF. Hyperbilirubinemia and bilirubin toxicity in the late
in North East of Iran. Macedonian Journal of Medical Sciences.
preterm infant. Clin Perinatol. 2006; 33(4):839–852.
2011; 4(4):403-407. https://doi.org/10.3889/MJMS.1857-
https://doi.org/10.1016/j.clp.2006.09.002 PMid:17148008
5773.2011.0177
44. Differential risk for early breastfeeding jaundice in a multi-ethnic
28. Segel GB. Glucose-6-phosphate dehydrogenase (G-6-PD) and
Asian cohort. Ann Acad Med Singapore. 2009; 38(3):217–224.
related deficiencies. Nelson textbook of pediatrics. Philadelphia,
PMid:19347075
PA: WB Saunders, 2004:1636-8.
45. Boskabad H, Maamouri GA, Mafinejad S, Rezagholizadeh F.
29. Wood B, Culley PH, Roginski CL, Powell JE, Waterhouse JO.
Clinical course and prognosis of hemolytic jaundice in neonates in
Factors affecting neonatal jaundice. Archives of disease in
north east of Iran. Maced J Med Sci. 2011; 4(4):403-7.
childhood. 1979; 54(2):111-5. https://doi.org/10.1136/adc.54.2.111
https://doi.org/10.3889/MJMS.1857-5773.2011.0177
PMid:434885 PMCid:PMC1545363
46. Kaplan M, Hammerman C. The need for neonatal glucose-6-
30. Diwan VK1, Vaughan TL, Yang CY, Maternal smoking in
phosphate dehydrogenase screening: a global perspective. Journal
relation to the incidence of early neonatal jaundice, Gynecol Obstet
of Perinatology. 2009; 29(S1):S46.
Invest. 1989; 27(1):22-25. https://doi.org/10.1159/000293609
https://doi.org/10.1038/jp.2008.216 PMid:19177059
PMid:2920968
47. WHO Working Group. WHO, glucose-6-phosphate
31. Sarici SU, Serdar MA, Korkmaz A, Erdem G, Oran O, Tekinalp
dehydrogenase deficiency. Bull World Health Organ. 1981; 67:61–
G, et al. Incidence, course, and prediction of hyperbilirubinemia in
67.
near-term and term newborns. Pediatrics. 2004; 113(4):775–780.
https://doi.org/10.1542/peds.113.4.775 PMid:15060227 48. Bhutani VK, Zipursky A, Blencowe H, Khanna R, Sgro M,
Ebbesen F, Bell J, Mori R, Slusher TM, Fahmy N, Paul VK.
32. Newman TB, Xiong B, Gonzales VM, Escobar GJ. Prediction
Neonatal hyperbilirubinemia and Rhesus disease of the newborn:
and prevention of extreme neonatal hyperbilirubinemia in a mature
incidence and impairment estimates for 2010 at regional and global
health maintenance organization. Arch Pediatr Adolesc Med. 2000;
levels. Pediatric research. 2013; 74(S1):86.
154(11):1140–1147. https://doi.org/10.1001/archpedi.154.11.1140
https://doi.org/10.1038/pr.2013.208 PMid:24366465
PMid:11074857
PMCid:PMC3873706
33. Darcy AE. Complications of the late preterm infant. J Perinat
49. Boskabadi H, Ashrafzadeh F, Azarkish F, Khakshour A.
Neonatal Nurs. 2009; 23(1):78–86.
Complications of Neonatal Jaundice and the Predisposing Factors
https://doi.org/10.1097/JPN.0b013e31819685b6 PMid:19209064
in Newborns. J Babol Univ Med Sci. 2015; 17:7-13.
34. American Academy of Pediatrics Subcommittee on
50. Keren R, Bhutani V, Luan X, Nihtianova S, Cnaan A, Schwartz
Hyperbilirubinemia. Management of hyperbilirubinemia in the
J. Identifying newborns at risk of significant hyperbilirubinaemia: a
newborn infant 35 or more weeks of gestation. Pediatrics. 2004;
comparison of two recommended approaches. Arch Dis Child.
114(1):297–316. https://doi.org/10.1542/peds.114.1.297
2005; 90(4):415-421. https://doi.org/10.1136/adc.2004.060079
PMid:15231951
PMid:15781937 PMCid:PMC1720335
35. Scrafford CG, Mullany LC, Katz J. Incidence and Risk Factors
51. Mohammad Beigi AAF, Tabatabaee SHR, Yazdani M,
for Neonatal Jaundice among Newborns in Southern Nepal.
Mohammad Salehi N. Gestational diabetes related unpleasant
Tropical medicine & international health : TM & IH. 2013;
outcomes of pregnancy. Feyz. 2007; 11(1):33-38.
18(11):1317-1328. https://doi.org/10.1111/tmi.12189
PMid:24112359 PMCid:PMC5055829 52. Steiner LA, Gallagher PG. Erythrocyte Disorders in the
Perinatal Period in Adverse Pregnancy Outcome and the
36. Huang A, Tai BC, Wong LY, Lee J, Yong EL. Differential risk
Fetus/Neonate. Seminars in perinatology. 2007; 31(4):254-261.
for early breastfeeding jaundice in a multi-ethnic Asian cohort. Ann
https://doi.org/10.1053/j.semperi.2007.05.003 PMid:17825683
Acad Med Singapore. 2009; 38(3):217–224. PMid:19347075
PMCid:PMC2098040
37. Maisels MJ. Neonatal jaundice. Pediatr Rev. 2006; 27(12):443–
53. Chan V, Chan TK, Liang ST, Ghosh A, Kan YW, Todd D.
454. https://doi.org/10.1542/pir.27-12-443 PMid:17142466
Hydrops fetalis due to an unusual form of Hb H disease. Blood.
38. Olusanya BO, Osibanjo FB, Slusher TM. Risk Factors for 1985; 66:224–228. PMid:2988669
Severe Neonatal Hyperbilirubinemia in Low and Middle-Income
54. Chan V, Chan VW, Tang M, Lau K, Todd D, Chang TK.
Countries: A Systematic Review and Meta-Analysis. Carlo WA, ed.
Molecular defects in Hb H hydrops fetalis. Br J Haematol. 1997;
PLoS ONE. 2015; 10(2):e0117229.
96:224–228. https://doi.org/10.1046/j.1365-2141.1997.d01-2017.x
https://doi.org/10.1371/journal.pone.0117229
PMid:9029003
39. Porter ML, Dennis BL. Hyperbilirubinemia in the term newborn.
55. Han J, Liu X, Zhang F. Effect of the early intervention on
Am Fam Physician. 2002; 65(4):599–606. PMid:11871676
neonate with hyperbilirubinemia and perinatal factors. Biomedical
40. Olusanya BO, Osibanjo FB, Slusher TM. Risk factors for Research. 2017; 28:231-236.
severe neonatal hyperbilirubinemia in low and middle-income
56. Singh B, Ezhilarasan R, Kumar P, Narang A. Neonatal
countries: A systematic review and meta-analysis. PLoS One.
hyperbilirubinemia and its association with thyroid hormone levels
2015; 10(2):e0117229.
and urinary iodine excretion. Indian J Pediatr. 2003; 70(4):311-315.
https://doi.org/10.1371/journal.pone.0117229 PMid:25675342
https://doi.org/10.1007/BF02723587 PMid:12793308
PMCid:PMC4326461
41. Geiger AM, Petitti DB, Yao JF. Rehospitalisation for neonatal
jaundice: risk factors and outcomes. Paediatr Perinat Epidemiol.

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