Evaluation of acid base status
and outcome of neonatal respiratory distress
Chaudhary GS1, KumarV2,
Chaurasiya O S3, Singh M4
1Dr Ghanshyam Chaudhary, Associate Professor, Department of
Paediatrics, MLB Medical College Jhansi, UP, India, 2Dr Vipin,Kumar, JR
III, Department of Pediatrics, MLB Medical College Jhansi, Uttar
Pradesh, India, 3Dr Om Shankar Chaurasiya, MD (Paediatrics), Assistant
Professor, Department of Paediatrics, MLB Medical College Jhansi, Uttar
Pradesh, India, 4Dr Mayank Singh, MD (Pathology), Assistant professor,
Department of Pathology, MLB Medical College Jhansi, Uttar Pradesh,
India.
Address for
correspondence: Dr Ghanshyam Chaudhary, MD (Paediatrics),
Associate Professor, Department of Paediatrics, MLB Medical College
Jhansi, UP, India. Email: drgschaudhary@rediffmail.com
Abstract
Objective:
Both pulmonary and extra pulmonary causes could present as tachypnea
and respiratory distress. We have planned a study to evaluate acid base
status and outcome of neonatal respiratory distress. Methods: A
prospective study carried on neonates admitted in intensive care unit
from 1st November 2014 to 31st October 2015 in Department of
Paediatrics of a tertiary care centre of UP. Ethical Clearance was
taken by Ethics Committee of the college. Newborns brought to our NICU
with respiratory distress were included in study randomly. After
detailed clinical history, examination, arterial blood was taken in all
the babies for ABG analysis with necessary precautions along with other
routine investigation and stabilization of the baby. Results: A total of
115 neonates with respiratory distress were selected for study, out of
these about 24.34% had normal pH, 45.21% had metabolic acidosis, 21.73%
neonates had respiratory acidosis and 8.69% had mixed pH disorder.
Neonates having respiratory distress with normal pH 85.71% were
discharged from the hospital, 7.14% went LAMA and 7.14% expired during
the treatment. Neonates having respiratory distress with abnormal pH
77.01% were discharged from the hospital, 2.29% went LAMA and 20.68%
expired during the treatment. Conclusion:
The expiry rate was significantly higher in neonates having abnormal pH
with respiratory distress than in neonates with normal pH with
respiratory distress (p<0.05).
Keywords:
Neonatal respiratory distress, Acid base abnormality, Meconium
aspiration syndrome, Transient tachypnea of newborn
Manuscript received: 12th
Dec 2015, Reviewed:
25th Dec 2015
Author Corrected;
04th Jan 2016, Accepted
for Publication: 13th Jan 2016
Introduction
Neonatal respiratory distress is a heterogeneous group of illness with
varying incidence, underlying etiology, clinical course and outcome. It
is one of the commonest disorders encountered within the first 48-72
hours of life. It occurs in approximately 0.96%-6% of live births, and
is responsible for about 20% of neonatal mortality [1]. Respiratory
distress is a common reason for a neonate seeking medical attention.
The clinical features of tachypnea, intercostal retractions, grunting
or cyanosis could be the manifestations of a variety of etiological
causes. Both pulmonary and extra pulmonary causes could present as
tachypnea and respiratory distress [2]. Respiratory distress due to
either medical or surgical causes occurs commonly in neonates. It is
the most common cause of admission to a neonatal surgical intensive
care facility in a tertiary care hospital [3]. Blood gas measurements
and complementary, noninvasive monitoring techniques provide the
clinician with information essential to patient assessment, therapeutic
decision making, and prognostication. Blood gas measurements are as
important for ill newborns as for other critically ill patients, but
rapidly changing physiology, difficult access to arterial and mixed
venous sampling sites, and small blood volumes present unique
challenges [4].
Considering above facts the present study was planned with aims and
objective of
1. To see incidence of various causes of respiratory distress
in newborns
2. To see acid base status of neonates with respiratory
distress
3. To see the outcome of abnormal acid base neonates with
distress
Material
& Methods
The present study carried out on neonates admitted in intensive care
unit from 1st November 2014 to 31st October 2015 in Department of
Paediatrics, M.L.B. Medical College, Jhansi UP. Ethical Clearance was
taken by Ethics Committee of the college. Newborns brought to our NICU
with one or more of following for more than two hours would be
considered to have respiratory distress and included in study-
• Respiratory rate > 60/min
• Respiratory grunting
• Intercostal / subcostal retraction
• Xiphoid retraction
• Sub sternalin drawing
• Flaring of alae nasi
• Cyanosis in room air
Exclusion
criteria
• Babies more than 28 days.
• Babies weight less than 1000gm
• Babies less than 28 weeks of age.
After detailed clinical history, examination, arterial blood was taken
in all the babies for ABG analysis with necessary precautions along
with other routine investigation and stabilization of the baby.
Informed consent was taken in the cases. The sealed syringe taken to
blood gas analyzer immediately or otherwise within 30 minutes it should
be always analyzed.
Results
A total of 115 neonates admitted in SNCU with respiratory distress were
taken in to this study. A total of 115 neonates with respiratory
distress were selected for study randomly who met the inclusion
criteria. Out of above 85(73.91%) babies were male and 30(26.08%) were
female. The mode of delivery was normal for 48(41.73%) babies and
Caesarian for 67(58.26%) babies.
Table I: Distribution of
neonates with causes of respiratory distress in relation to gestational
age
Gestational Age
|
Total
|
RDS
|
MAS
|
TTN
|
PNM
|
HIE
|
Others
|
28-30Weeks
|
8
|
7
|
0
|
0
|
1
|
0
|
0
|
30-32Weeks
|
4
|
3
|
0
|
0
|
1
|
0
|
0
|
32-34Weeks
|
20
|
11
|
3
|
3
|
2
|
1
|
0
|
34-36Weeks
|
30
|
7
|
6
|
5
|
6
|
5
|
1
|
36-38Weeks
|
40
|
5
|
8
|
8
|
10
|
5
|
4
|
38-40Weeks
|
11
|
0
|
3
|
4
|
4
|
0
|
0
|
>40Weeks
|
2
|
0
|
1
|
1
|
0
|
0
|
0
|
(RDS- Respiratory distress syndrome, MAS- Meconium
Aspiration Syndrome, TTN- Transient Tachypnea of Newborn, PNM-
Pneumonia, HIE- Hypoxic Ischemic Encephalopathy)
We observed as shown in Table I that Respiratory distress syndrome is
the most common cause of respiratory distress in early gestational age
group. In gestational age 28-30wks Respiratory distress syndrome 87.5%
is the most common cause followed by pneumonia 12.5%. In gestational
age 30-32wks Respiratory distress syndrome 75% is the most common cause
followed by pneumonia 25%. In gestational age 32-34wks Respiratory
distress syndrome 55% is the most common cause followed by TTN 15%, MAS
15%, pneumonia 10%, and HIE 5%. In gestational age 34-36wks Respiratory
distress syndrome 21.21% is the most common cause followed by PNM
18.18%, MAS 18.18%, TTN 16.66%, HIE 16.66%, and others 3.33%. In
gestational age 36-38wks PNM 25% is the most common cause followed by
TTN 20%, MAS 20%, RDS 12.5%, HIE 5% and others 10%.. In gestational age
38-40 weeks PNM and TTN 36.36% each is the most common cause followed
by MAS 27.27%. In gestational age >40wks we observed that MAS
and TTN are the more predominant causes. We have observed that as the
gestational age advances TTN and Pneumonia were the common causes while
RDS was most commonly seen in lesser gestational age.
Table II: Incidence of
acid base disturbance in neonates with respiratory distress
Total
|
Normal
|
Metabolic acidosis
|
Respiratory acidosis
|
Mixed
|
n=
115
|
28 (24.34%)
|
52(45.21%)
|
25(21.73%)
|
10(8.69%)
|
Partially compensated
|
Uncompensated
|
Partially compensated
|
Uncompensated
|
29(25.21%)
|
23(20%)
|
11(9.56%)
|
14(12.17%)
|
Out of 115 neonates included in the study about 24.34% had
normal pH, 45.21% had metabolic acidosis, 21.73% neonates had
respiratory acidosis and 8.69% had mixed pH disorder. None of them had
metabolic and respiratory alkalosis. Neonates with metabolic acidosis
again divided into partially compensated and uncompensated. 25.21% had
partially compensated and 20% uncompensated metabolic acidosis.
Neonates with Respiratory acidosis again divided into partially
compensated and uncompensated. 9.56% had partially compensated, 12.17%
uncompensated metabolic acidosis. About 8.69% had mixed type of pH
disorder. We observed that metabolic acidosis was the most common pH
disorder in newborns with respiratory distress.
Table III: Comparison
outcomes of neonates with acid base abnormality and without acid base
abnormality with symptoms & signs of respiratory distress
|
Total
|
Discharge
|
LAMA
|
Expiry
|
Normal pH
|
n=28 (24.34%)
|
24(85.71%)
|
2(7.14%)
|
2(7.14%)
|
Abnormal pH
|
n=87 (75.65%)
|
67(77.01%)
|
2(2.29%)
|
18(20.68%)
|
By ABG analysis in the neonates with respiratory distress
observed that about 24.34% had normal pH and 75.65% had abnormal pH.
Neonates having respiratory distress with normal pH 85.71% discharged
from the hospital, 7.14% went LAMA and 7.14% expired during the
treatment. Neonates having respiratory distress with abnormal pH 77.01%
discharged from the hospital, 2.29% went LAMA and 20.68% expired during
the treatment. The discharge and expiry of neonates with and without
normal pH was statistically significant (p value 0.0124) by Fisher's
exact test.
Discussion
Respiratory distress in a newborn is a challenging problem. It accounts
for significant morbidity and mortality. Respiratory distress in
newborn is one of the commonest conditions contributing to 30-40% of
admissions in NICU. Respiratory distress occurs in 2.2% of all newborns
and in almost 60% of the infants below 1000gms (ELBW
infants).Maintaining acid base balance presents a considerable
challenge to the neonate[5]
Out of 115 patient included in the study 73.91 %( 85) are male and
26.09% (30) females. From this study we observed that there is a male
predominance. Male to female ratio is 2.83:1.Lekhvani S et al [6] also
did a study in in 2010 and found the male-to-female ratio was 4.56:1
(41 males to 9 females).Male ratio is greater than female ratio because
female fetal lung produces surfactant earlier in gestation than the
male fetal lung. Seaborn T et al in 2010[7], Bresson E. et al in
2010[8] also reported similar reason for male and female lung
maturation. Santosh S et al in 2013[9] studied that respiratory
distress accounts most common cause of all NICU admissions and preterm
babies were more in number with male predominance.
In our study 41.73% (48) are born by normal vaginal delivery and 58.26%
(67) are born by LSCS. We observed that predominant mode of delivery is
LSCS. Jing Liu et al [10] in 2014 conducted a study and stated that
cesarean section and male sex are at risk for respiratory distress. We
found most common cause for respiratory distress was Respiratory
Distress Syndrome about 28.69%, followed by pneumonia 20.86%.Lekhvani S
et al [6] found that acid–base status ismajor pathological
disorders in birth asphyxia, bronchopneumonia, sepsis, and diarrhea,
but they have included infants also not only neonates as in present
study.
Anitha B, Sethi et al [11] in2015 studied the acid base disturbances in
sick neonates admitted in NICU and they also found metabolic acidosis
was the most common acid base disorder. In our study, we also observed
similar findings.
In our study the neonates having respiratory distress with normal pH
85.71% discharged from the hospital and 7.14% expired during the
treatment as compared to abnormal pH 77.01% discharged from the
hospital and 20.68% expired during the treatment. This is statistically
significant with p value 0.0124 by Fisher's exact test. Lekhvani S et
al also found increased mortality in babies with abnormal acid base
status.
Conclusions
We concluded that neonatal respiratory distress is more common in male
babies and babies born by caesarian delivery. Most common cause for
respiratory distress was Respiratory Distress Syndrome about 28.69%
followed by Pneumonia in 20.86 %.As the gestational age advances most
common cause for respiratory distress in a neonates was TTN. Near term
neonates most common cause was pneumonia. While in lower gestational
ages Respiratory Distress Syndrome was the most common cause. Neonates
with respiratory distress had 24.34% normal pH and 75.64% abnormal pH.
The expiry rate was significantly higher in neonates having abnormal pH
with respiratory distress than in neonates with normal pH with
respiratory distress (p<0.05).
Funding:
Nil, Conflict of
interest: Nil
Permission from IRB:
Yes
References
1. Neonatal morbidity and mortality: report of the National
Neonatal-Perinatal Database. Indian Pediatr. 1997 Nov;34(11):1039-42.
2. Diwakar KK. Clinical approach to Respiratory Distress in Newborn.
Indian J Pediatr (Supplement- optimum pulmonary care of neonates)
2003;70: S53 – S59. [PubMed]
3. Kumar A, Bhatnagar V. Respiratory distress in neonates. Indian J
Pediatr. 2005 May;72(5):425-8. [PubMed]
4. Brouillette RT, Waxman DH. Evaluation of the newborn's blood gas
status. National Academy of Clinical Biochemistry. Clin Chem. 1997
Jan;43(1):215-21. [PubMed]
5. Quigley R, Baum M. Neonatal acid base balance and disturbances.
Semin Perinatol. 2004 Apr;28(2):97-102. [PubMed]
6. Lekhwani S, Shanker V, Gathwala G, Vaswani ND. Acid-base disorders
in critically ill neonates. Indian J Crit Care Med. 2010
Apr;14(2):65-9. doi: 10.4103/0972-5229.68217. [PubMed]
7. Seaborn T, Simard M, Provost PR, Piedboeuf B, Tremblay Y. Sex
hormone metabolism in lung development and maturation. Trends
Endocrinol Metab. 2010 Dec;21(12):729-38. doi:
10.1016/j.tem.2010.09.001. [PubMed]
8. Bresson E, Seaborn T,
Côté M, Cormier G, Provost PR, Piedboeuf B,
Tremblay Y. Gene expression profile of androgen modulated genes in the
murine fetal developing lung. Reprod Biol Endocrinol. 2010 Jan 8;8:2.
doi: 10.1186/1477-7827-8-2. [PubMed]
9. Santosh S, Kushal Kumar K, Adarsha E. A
clinical study of respiratory distress in newborn and its outcome.
Indian Journal of Neonatal Medicine and Research 2013; 2(1):2-4.
10. Jing Liu. Respiratory Distress Syndrome in
Term Neonates: Published online 2014 Mar 1. doi:
10.5152/balkanmedj.2014.8733.
11. Anitha B. Sethi et al., IOSR Journal of
Dental and Medical Sciences 2015;14(12): 35-38.
How to cite this article?
Chaudhary GS, KumarV, Chaurasiya O S, Singh M4. Evaluation of acid base
status and outcome of neonatal respiratory distress. Pediatr Rev: Int J
Pediatr Res 2016; 3(1): 32-35.doi: 10.17511/ijpr.2016.1.06.