Prevalence of early onset
neonatal septicemia in babies born to mother with pre-eclampsia
Madavi
D.1, Tirpude B.2, Daberao S.3
1Dr. Dipak Madavi, Associate Professor, 2Dr. Bhagyashree Tirpude, Assistant
Professor, Department of Pediatrics, Indira Gandhi Government Medical College,
Nagpur, 3Dr. Santosh Daberao, Junior Resident;
all authors are affiliatd with Department of Pediatrics, Indira Gandhi
Government Medical College, Nagpur, India.
Corresponding Author: Dr. Bhagyashree Tirpude, Assistant Professor,
Department of Pediatrics, Indira Gandhi Government Medical College, Nagpur,
India. E-mail: bhagyashree.tirpude2@gmail.com, drdipakm@gmail.com
Abstract
Context: Pregnancy induced hypertension (PIH) is one of the important
risk factor for preterm delivery. Neutropenia
and thrombocytopenia are well recognized neonatal sequelae to
maternal hypertension
in pregnancy. Preeclampsia-associated neutropenia is
a risk factor for an increased incidence of infection in preterm neonates. Methods
& material: 87 neonates born to
mother with preeclampsia were included with aim to find prevalence of EOS and
their haematological profile. Diagnostic work up includes complete blood count,
CRP, blood culture and sensitivity (C/S) and other relevant investigations
according to cases. Result: Out of 87 neonates, 7 neonates had EOS (8%)
with blood culture proven bacterial sepsis, Klebsiella pneumonia (57.14%) was
commonest organism isolated followed by E. Coli (28.57%) and Enterococci (14.28%).
About 32 (36.76%) mothers had severe hypertension and 55(68.22%) mothers had mild to moderate
preeclampsia. About 60(68.79%) neonates were born preterm. 40 (45%) neonates had
neutropenia. 38 (43.65%) babies had thrombo-cytopenia. All 7 septic babies had
neutropenia and thrombocytopenia. Conclusion: Early onset septicemia is
more common in babies born to mother with preeclampsia due to associated Prematurity,
Neutropenia and Thrombocytopenia. Hence preventive measures should focus on
recognition of these high risk neonates with prompt laboratory screening for
sepsis and early institution of empirical antibiotics based on local data.
Keywords: Preeclampsia, Prematurity, Neutropenia, Early onset
sepsis
Author Corrected: 24th March 2019 Accepted for Publication: 28th March 2019
Introduction
Pregnancy induced hypertension (PIH) is one of the most
common cause of both maternal and neonatal morbidity,
affecting about 5-8% of pregnant women [1]. Pre-eclampsia is a
multi-system disorder of the mother that affects the fetus because of
utero-placental insufficiency. In consequence these children are at risk for
intra-uterine growth restriction and may be delivered prematurely[2].
Preterm birth is a
common complication of hypertensive disease, either due to the spontaneous
labour or to the obstetric conduct of interrupting the pregnancy due to the
compromised maternal-fetal health. Prematurity increases perinatal morbidity
and mortality rates with possible immediate or late sequels[3].
Neutropenia
and thrombocytopenia are well recognized neonatal sequel to maternal
hypertension in pregnancy. Neutropenia
hasbeen reported to occur in
50% of infants born
to mothers with
hypertension compared to 4% in babies born
after a normal
pregnancy [4]. Neutropenia is a common
hematologic disorder in the newborn intensive care unit, particularly in
preterm neonates. Although its cause varies, a significant proportion of the
episodes are associated with pregnancy complicated by preeclampsia [5].
Pre-eclampsia-associated
neutropenia is a risk factor for an increased incidence of infection in neonates
born to mothers with pre-eclampsia. Preeclampsia associated neutrophil function
disorders also contribute to the high incidence of infection in neutropenic
infants [6].
The risk of early onset septicemia is more in neutropenic
babies than in non-neutropenic babies of pre-eclamptic mothers [4,6]. Considering
pre-eclampsia as a risk factor for early onset neonatal septicemia in babies
born to mother with pre-eclampsia early detection and timely intervention can
decline death rate because of sepsis. Sowith the aim to find prevalence of
early onset septicaemia and to know haematological profile in newborns born to
mothers with pre-eclampsia this study was planned.
Material and Methods
Study
design and setting: This was aprospective observational study carried
out in neonatal unit in Indira Gandhi Government Medical College and Hospital
in central India.
Sample
calculation: 87 Neonates born to mother with history of pre-eclampsia between
October 2016 to October 2017 and admitted in NICU were taken in to study after
informed written parent consent. Considering the prevalence of 6% of EOS in
neonates born to mothers with preeclampsia from previous studies (R), absolute
allowable error of 8% and normal deviate of 5% the minimum required sample size
(n) was 87.
Inclusion
criteria:
All neonates born to pre-eclamptic mothers in our hospital and admitted in our NICU
for various complaintswere included.
Exclusion
criteria: Neonates
with Congenital malformation, Severe birth asphyxia, any illness to mother
likely to cause changes in haematological profile like severe anemia,
connective tissue disorders, diabetes and chronic hypertension and mothers with
chorioamnitis, genital tract infections and prolonged rupture of membranes were
excluded.
Ethical
approval:
This study was approved by institutional ethics committee.
Method
of data collection: At the time of enrolment details regarding
antenatal history including mother age, parity, blood pressure records,
antihypertensive drugs taken and hospitalization during antenatal period were
noted. Gestational age, mode of delivery, birth weight, perinatal complications
and details of NICU admission, physical examination were done for each neonate.
Their haematological profile was estimated through CBC. Other investigations
includes-Sepsis screen, Blood culture and sensitivity. Chest X-ray, Urine
culture, cerebrospinal fluid (CSF) analysis and fungal culture were done
wherever necessary. Neonates with blood culture positive sepsis were only
considered as having septicemia.
Statistical
analysis: The data was analyzed using SPSS version 20.0.
Pre-eclampsia:
Pre-eclamptic mothers will be identified by finding hypertension (systolic
BP >140 mm of Hg or diastolic BP>90 mm of Hg on two occasions) plus
proteinuria and edema after 20th week in a previously normotensive
and nonproteinuric woman [7].Severe hypertension: Blood pressure
≥ 160/110 mm of hg [8].Mild to moderate hypertension (Nonsevere hypertension): Blood pressure 140/90 to <160/110 mm of hg[8].Neutropenia
means Absolute neutrophil count <1800/mm3 as per Manroe chart for term and Mouzinhos
chart for preterm neonates [9,10].Thrombocytopenia considered as platelet count
<1.5 lac/mm3. Early onset sepsis (EOS): Defined as neonatal sepsis which
occurred within 3 days (72 hours) of birth [7].
Results
Over
the study period 87 neonates born to mothers with pre-eclampsia were included
in the study. In this study, 32 mothers (36.78%)
were having severe hypertension (BP >160/110 mm of hg) and remaining 55 (63.22%) had mild to
moderate hypertension (BP between 140/90 to 160/110 mm of hg).
Out of 87 neonates,
27(31.03%) neonates were
born full term and 60(68.9%) neonates were born preterm. The
rate of lower segment caesarean section was high (69%) as compared to normal
vaginal delivery (31%). Out of 87 neonates, 7 neonates of total
cases fulfilled the criteria for early onset septicaemia hence prevalence rate
of EOS was 8%. Out of 87 neonates,
40(45.97%) neonates had neutropenia. Of total mothers with severe hypertension, 18 (56.25%)
neonates born to them had neutropenia and out of total mothers with mild to
moderate hypertension22 (40%) neonates born to them had neutropenia. (Table 1)
Amongst 40 neutropenic neonates, 7(17.5%) neonates had developed culture positive sepsis (Table 2)
Association of early onset septicemia and neutropenia with
gestational age shown in Table no. 3, 33
(37.93% ) neonates were born <32 wks gestation, 23(26.43%)
neonates were between 32- <34 wks gestation and 21(24.13%) neonates were
born between 34-<36 wksgestation, 10(11.49 %) neonates born > 36 wks. Of
the total 40 neutropenic neonates, 19(47.5%) neonates were born <32 wks
gestation, 12(26.43%) neonates were born between 32-<34 wks, 6(15%) neonates
born between 34-36 wks and 3(7.5%) neonates were >36 wks gestation.
Neonates
with septicaemia, 4 (57.14%) neonates were <32 wks gestation, 2(28.57%)
neonates were between 32-<34 wks and 1(14.28%) neonate was between 34-36
wks. Approximately one third neonates (36.78%) had a low birth weight (1.5-2.5kg),
another one third (31.03%) neonates had very low birth weight (1-<1.5kg) and
20(22.9%) neonates were extremely low birth weight(<1kg). Out of total
neutropenic neonates, 18(45%) neonates had very low birth weight and 13(32.5%)
were having birth weight <1kg. Also the rate of septicaemia was high in very
low birth weight neonates (Table 4). Common
indication for admission was respiratory
distress (63.21%).
Amongst the 7 septicemic neonates,commonest organism isolated
was Klebsiella pneumoniae in blood culture of 4 (57.14%) neonates followed by E-coli (28.57%) and Enterococci (14.28%).
Out of 87 neonates, 38 (43.67%) neonates had neutropenia as
well as thrombocytopenia. All septic neonates were thrombocytopenic (Table 5). Mortality
rate in this study was 1.14% due to
severe septicemia.
Table-1: Neutropenic babies born to mother according to severity
of hypertension
Pre-Eclamptic Mothers |
Total Number of Pre Eclamptic Mothers |
Neutropenic Babies |
Non Neutropenic
Babies |
With severe hypertension |
32
(100%) |
18
(56.25%) |
14
(43.75%) |
With mild to moderate
hypertension |
55
(100%) |
22 (40
%) |
33
(60%) |
Total |
87 |
40 |
47 |
In above table it is seen that, 32 mothers has severe hypertension and 18
(56.25%) neonates born to them were having neutropenia, similarly 55 mothers with mild to moderate
hypertension and 22 (40%) neonates born
to them had neutropenia.
Table-2: Association between neutropenia and sepsis
|
Culture
positive sepsis |
Total |
P
value |
|
|
Present |
Absent |
|
|
Neutropenic neonates |
7 |
33 |
40 |
0.0027 |
Non neutropenic neonates |
0 |
47 |
47 |
Chi-square : 8.945 |
Total |
7 |
80 |
87 |
|
Above table shows that out of total 40 neutropenic neonates, 7
(17.5%) neonates developed sepsis and none of the non neutropenic neonates found to have
sepsis. P value 0.0027 was sugnificant, it means neutropenia
is associated factor for sepsis.
Table-3: Early
onset septisemia and neutropenia as per gestational age
Gestational Age |
Total Number |
Neonatal Neutropenia |
Early Onset Neonatal Septicemia |
P value |
< 32 WKS |
33(37.93%) |
19(47.5%) |
4(57.14) |
= 0.004 |
32 WKS –< 34 WKS |
23(26.43%) |
12(30%) |
2(28.57%) |
Chi-square=13.06 |
34 -36 WKS |
21(24.13%) |
6(15) |
1(14.28%) |
|
> 36 WKS |
10(11.49%) |
3(7.5%) |
0(0%) |
|
Total |
87(100%) |
40(100% |
7(100%) |
|
In above table we can see neonates of following gestational
age, 33(37.93%) neonates of < 32 weeks, 23(26.43%) neonates between 32-< 34 weeks, 21(24.13%) neonates
between 34-<36 weeks and 10 (11.49%0 neonates were > 36 weeks gestation.The
percentage of neutropenia and septicemia
was less as gestational age advances in
neonates. It was statistically significant with p value 0.004 which is
statasticaly significant with chi-squre 13.06. It is also seen that as the
gestational age decreases more is chance of having neutropenia and septicemia
in babies.
Table-4: Neutropenic
and septicemic neonates according WT
WT IN KGS |
Number of Neonates 87(100%) |
Neonates with neutropenia 40(100%) |
Early Onset Neonatal Septicemia 7(100%) |
< 1 KG |
20(22.98%) |
13(32.5%) |
2(28.57%) |
1 TO< 1.5 KG |
27(31.03%) |
18(45%) |
4(57.14%) |
1.5 TO 2.5KG |
32(36.78%) |
9(22.5%) |
1(14.28%) |
>2.5 KG |
8(9.19%) |
0(0%) |
0(0%) |
TOTAL |
87(100%) |
40(100%) |
7(100%) |
Table No. 4 shows that
32 (36.78%) neonates were between 1.5- 2.5kg birth weight, 27(31.03%) neonates
were between 1-<1.5kg birth weight, 20(22.9%) neonates had birth weight <1kg.
Out of 40 neutropenic neonates, 18 (45%) neonates had birth weight between
1-<1.5kg, 13(32.5%) neonates were < 1kg birth weight and 9(22.5%)
neonates had birth between 1.5-2.5kg. Similarly out of total septicaemic
neonates 4(57.14%) neonates had birth weight between 1-<1.5 kg, 2(28.57%)
neonates were <1kg birth weight and 1(14.28%) neonate between 1.5-2.5kg
birth weight.
Table-5: Association between thrombocytopenia and neutropaenia
|
Thrombocytopenic Neonates |
Non
Thrombocytopenic Neonates |
Total |
P
value |
Neutropenic
neonates |
38 |
2 |
40 |
0.0000001 |
Non
neutropenic neonates |
0 |
47 |
47 |
Chi
Square -79.28 |
Total(87) |
38 |
49 |
87 |
|
In above table it is seen that out of 40 neutropenic babies
38 babies (95%) found thrombocytopenia and both these factor thrombocytopenia
and neutropenia related to sepsis .
Discussion
Hypertensive
disorders of pregnancy have been identified as a major worldwide health
problem, associated with increased perinatal morbidity and mortality [11]. Studies
have shown that hypertensive disorders of pregnancy predisposes women to acute
or chronic uteroplacental insufficiency, there by having an effect on perinatal
and neonatal outcome that may result in ante or intrapartum anoxia that may
lead to fetal death, intrauterine growth retardation and/or preterm delivery
[11].
In present study the prevalence of early onset
septicemia in neonates born to pre-eclamptic mother was 8%. S. Bhaumik et al found risk of early onset neonatal septicaemia in
babies born to mother with preeclampsia is6.7%
[7]. Doron MW et alin his study found sepsis in 6% neonates [6]. Procianoy RS et al [12] in his study
of sepsis and neutropenia in very low birth weight babies found similar
incidence of early onset sepsis in neonates born to mothers in preeclampsia
group 4.6% and in non preeclampsia group 4.2%.
In present study the rate of lower segment
caesarean section and preterm delivery rate were high (68.96%). Similar results were found in study done by Sikha Maria Siromani et al[13](63.01%), Nadkarni
etal[11](44.3%) and Sibai et al[14]S. Shivkumar et al in his study stated that there was higher
number of preterm, intrauterine growth restriction(IUGR) and small for
gestational age (SGA) babies among the infants of hypertensive mothers [2].
Inpresentstudy 45.97% neonates born to mother with
pre-eclampsia had neutropenia. Ziba Mosayebi
et al in 2013 evaluated laboratory disorders in admitted neonates in NICU who
were born to pre-eclamptic mothers found 37% cases with neutropenia [15].
Carl H. Bakers et al found incidence of neutropenia in 50% neonates born to
pre-eclamptic mothers [16]. Similar results found by Doron MW et al [6]. It is
a transient haematological alteration, lasting days to weeks, related to the
severity of pregnancy induced hypertension. Neutropenia mainly affects the
smaller and younger neonates and may be associated with an increased risk of
nosocomial infections [15].
In
this study, out of total mothers with severe hypertension, 56.25% neonates
developed neutropenia and 40% neonates developed neutropenia which were born to
mothers with mild to moderate hypertension. Similar result was found in study
done by Bhaumik S et althat Neonatal
neutropenia was about three-fold more when maternal hypertension was
Severe (diastolic >110 mm of Hg)
compared to moderate <110 mm of Hg) [7].Carl H Bakers et al states that
infants with neutropenia had mothers with more severe pre-eclampsia, were born
more premature, weigh less and more likely small for gestational age [16].
In present study amongst
40 neutropenic neonates 7 developed septicemia that was 17.5% (P <0.002).
Doron MW et al found 6% neonates amongst neutropenic babies had developed
sepsis [6]. Cadnapaphornchai M et al in his study shows increased nosocomial
infection in neutropenic low birth weight (2000 grams or less) infants of
hypertensive mothers [17]. However David A Paul et al in their study states
that neonatal neutropenia associated with preeclampsia does not increase the
risk for culture proven sepsis [18].
In
this study average gestational age was 33 wks (32-34 weeks) and average birth
weight was 1839 grams. Solange Regina et al in their study of pregnancy induced
hypertension and neonatal outcome found DBP >110 mm of hg was associated with
low birth weight and prematurity [3]. Less gestational age and low birth weight
neonates were at more risk to developed neutropenia and septicemia. Patricia et
alfound that infants <1200g and <32 weeks gestation and born to mothers
with gestational hypertension, preeclampsia, or eclampsia syndrome were
associated with leukopenia, absolute neutropenia and thrombocytopenia [19]. Similar results found in various studies [13,15,20,24].
Common
manifestation at the time admission was respiratory distress found in this
study. Respiratory distress stays one of the majorproblem among these neonates.
Mother’s illnesses, especially hypertension are
very strong risk factor for RD in preterm babies [21].
In present study, 7 neonates had early onset septicaemia.Organism
isolated were K. Pneumonia, E.coli and Enterococcus.
In
present study it was seen that 43.67% of neonates had thrombocytopenia and 95% of
neutropenic babies had associated thrombocytopenia. All septicemic babies found
with thrombocytopenia (100%). So there is strong association between early
onset septicemia and thrombocytopenia in babies born to mother with pre-eclampsia
and it can be indirect indicator of sepsis to be used for accessing diagnosis
and prognosis. Similar resultsfound in
study done by Y.R. Bhatt and Carol S. Cherian, thrombocytopenia occurred in 36%
of neonates born to mothers with pregnancy induced hypertension and was severe
in 20% [22]. Similar results were also found in studies by SH Fraser et al and Prekshya L Prakash et althat
babies of hypertensive mothers are more prone for development of leucopenia,
neutropenia and thrombocytopenia during the early neonatal period, these babies
should be closely monitored and managed in order to decrease the perinatal
morbidity and mortality [4,23].
Conclusion
Pregnancy
induced hypertension is one of the most common causes of both maternal and neonatal
morbidity. The risk for delivering prematurely is high in babies born to
mothers with pre-eclampsia. Pre-eclampsia is one of the causative factors for
preterm and low birth weight babies. There is higher no. of interventional
surgical deliveries amongst preeclamptic mothers.
Abnormal
hematological finding like neutropenia and thrombocytopenia occurs in newborns
born to mother with pre-eclampsia. Babies of pre-eclamptic mothers have
relatively more risk of developing early onset septicemia than those of normal
mothers. In neonates of pre-eclamptic mothers, neutropenia tends to increase
with decreasing gestational age.
The
risk of early onset sepsis is more in babies born to mothers with pre-eclampsia
due to prematurity, low birth weight and associated neutropenia.
Therefore
the management strategy for high risk neonates born to mother with
pre-eclampsia should focus on identification of early signs of clinical sepsis
with prompt laboratory screening for sepsis and early institution of empirical
antibiotic treatmentcan avoid morbidity and mortality in babies of pre-eclamptic
mother.
What this study adds to existing knowledge: The
effect of maternal pre-eclampsia on fetal outcome has been a subject of concern
for a long time. Two decades back an association between pre-eclampsia and
neonatal neutropenia was recognized. In the recent past the main focus of
workers is to study the risk of sepsis amongst the neonates of pre-eclamptic
mothers particularly among those with neutropenia. So considering preeclampsia
as a risk factor for early onset septicaemia in babies born to mother with
preeclampsia early detection and timely intervention can decline death rate
because of sepsis. So we need to find indigenous data in our institute to know
about incidence and prevalence of EOS and their causative organisms also to
know other risk factors for development of EOS. So we can make policy in our
institute for management of these high risk neonates so that moratality and
morbidity can decrease in our institute.
Contributions by
Authors: Data collection done by Dr Santosh Daberao and Dr
Bhagyashree Tirpude. Analysis and manuscript preparation done by Dr Bhagy shree
Tirpude. All research work had been done under the guidance of Dr Dipak Madavi.
Abbreviations: EOS (Early onset sepsis)
Funding:
None
Conflict of interest:
None
References