Abstract
Background
Complete blood count is one of the routinely advised blood investigation during pregnancy. It is also utilized as a diagnostic tool for neonatal anemia, sepsis and determining hemostatic status of the newborn. The present study aims at estimating the complete blood count of maternal and umbilical cord blood at the time of delivery and to establish its correlation.
Method
This cross sectional study included 114 mothers and their healthy neonates born through normal vaginal delivery. Complete blood count of umbilical cord blood and maternal blood was estimated using automatic hematology analyzer.
Results
The mean maternal and neonatal hemoglobin concentration was 11.14 ± 1.39 g/dL and 16.34 ± 2.01 g/dL respectively. A significant positive correlation was found between maternal and fetal hemoglobin concentration (p < 0.001 and Pearson R = 0.496). The correlation between maternal and fetal WBC, RBC and Platelet count was not statistically significant. A significant positive correlation was found between maternal and fetal MCV and MCH while PCV showed a non-significant positive correlation.
Conclusion
There was moderately positive correlation between maternal and fetal hemoglobin, MCV and MCH. The cord blood hemoglobin was lower in babies born to anemic mothers. The decrease in hemoglobin followed the severity of anemia, however, the correlation did not exist in anemic mothers. It suggested that fetal hematological parameters are not reflective of maternal hemogram.
Keywords: Hematology, Umbilical cord blood, Hemoglobin, Mother
Background
Maternal physiology endures several alterations in hematological parameters with an average rise of 40–50% in blood and plasma volume during pregnancy [1]. This hemodilution produces pronounced effect in hematocrit values. Complete blood count is the most commonly advised blood investigation. It is often the first step in evaluating hematologic function and diagnosis of related diseases [2]. During embryonic period, hematopoiesis occurs in different parts of the developing fetus. It starts initially in the embryonic yolk sack migrating to the fetal liver and preterm marrow. However, hematopoiesis is primarily restricted to the bone marrow in adults [3].
Anemia is a clinical condition in which the number of circulating red blood cells is insufficient to meet the body’s physiologic demands. WHO classifies anemia [4] in pregnancy as non-anemic (> 11 g/dL), mild anemia (10–10.9 g/dL), moderate anemia (7–9.9 g/dL) and severe anemia (< 7 g/dL).
Umbilical cord blood hemoglobin is a dominant hematologic parameter of newborns at birth. Hemoglobin along with hematocrit values together have been customarily used in the diagnosis and follow-up of the neonatal anemia [5]. Besides this, other hematologic parameters like white blood cell count and platelet count are worthwhile in assessing neonatal sepsis and hemostatic status of infant [5]. Studies have shown some relationships between maternal and fetal hemogram but the extent of effect on maternal and neonatal health is still uncertain. This study was conducted to assess the effect of maternal hematologic profile during normal pregnancy on cord blood hematology.
In an attempt to achieving Millennium Development Goals (MDG) 4 and 5 Nepal has made noteworthy progress in the field of maternal, newborn and child health. Nepal Government has implemented certain health related policies like free ion supplementation and ANC visits even in the remote parts of the country. The policy also includes rewards for delivering babies in health care facilities. As a result, substantial improvement has been observed in maternal mortality rate plummeting from 450 in 2004 to 260 in 2014 [6]. As of yet, no studies have been conducted in Pokhara Valley of Nepal on maternal and neonatal hemogram. The present study aims at obtaining a complete picture of maternal and fetal hemogram thereby enabling to maintain referencing in the general population of this region. The anticipated advantage of this study was to determine the fetal outcomes beforehand and building up a strategy in order to prevent adverse outcomes.
Methods
This was a hospital based cross-sectional study conducted from April 2014 to March 2015 at Manipal Teaching Hospital, Pokhara (827 m above sea level), Nepal. A total of 114 normal singleton pregnant mothers and their healthy newborn babies were included in the study. All pregnant women were residents of Pokhara Valley. They all have had 4 routine antenatal checkups during the course of pregnancy and all of them were supplemented with iron and folic acid. A written consent was obtained from the mother for participation in the study for both the mother and their newborn child. A brief history of the mother was taken during presentation for delivery. 3 ml of blood was collected in a sterile syringe from ante cubital vein and stored in an EDTA containing vial. After 2 min of delivery of the baby, 3 ml of umbilical cord blood was collected and was stored in an EDTA containing vial. Upon collection of the sample, it was analyzed within 3–6 h using an automatic hematology analyzer (Diagnova RFCL lablife h3d premier). Appropriate internal quality controls were run before assay of samples. Statistical analysis was performed by using the program Statistical Packages of Social Sciences (SPSS) version 20.0. The results were evaluated by using Pearson correlation test and Independent sample ‘t’ test. Shapiro Wilk test was done to check the normality of distribution of different variables. Multiple regression analysis was performed for multivariate analysis. Statistical significance was considered at p < 0.05.
Results
The study included a total of 114 pregnant women and their newborns (86 males and 28 females). Of the total participants, 68(59.64%) were multi gravida and 46 (40.36%) were primigravida. The mean age of pregnancy was 26.04 ± 3.47 years with 86% (98/114) between the age of 21–30 years. The result presented here affirms the existence of variations in red cell indices of umbilical cord blood reported for Pokhara valley of Nepal. These results could be helpful in providing a baseline data for further studies as to establish a reference value for maternal and umbilical cord hemogram in the locality.
The result showed no significant correlation between total white blood cell count of mother with that of the fetus (p > 0.01). The normally distributed variables were hemoglobin, RBC count, hematocrit, MCV and platelets while the remaining variables were non-normally distributed.
The mean maternal hemoglobin concentration was 11.14 ± 1.39 g/dL. According to the WHO classification of anemia in pregnant women, 46.49% of the participants were found to be anemic. The mean hemoglobin concentration of umbilical cord blood was found to be 16.34 ± 2.01 g/dL. The mean cord blood hemoglobin concentration in anemic and non-anemic mothers was 15.38 ± 1.7 g/dL and 17.21 ± 1.87 g/dL respectively. Figure 1 represents the scatter plot of mean hemoglobin of mother with that of the umbilical cord blood showing a linear correlation which was found to be statistically significant (p < 0.05). Likewise, Fig. 2 shows the scatter plot of mean MCH of mother with that of the umbilical cord blood indicating a linear correlation and was also found to be statistically significant (Tables 1 and 2).
Table 1.
Maternal Hemoglobin g/dL (WHO Classification) |
Mean maternal Hemoglobin g/dL |
No of patients | Pearson’s correlation coefficient R | p value |
---|---|---|---|---|
Non anemic Hb > 11 g/dL |
12.17 ± 0.81 | 60 | 0.460 | p < 0.05 |
Mild anemia Hb = 10–10.9 g/dL |
10.57 ± 0.27 | 33 | 0.456 | p < 0.05 |
Moderate Anemia Hb = 7–9.9 g/dL |
9.18 ± 0.65 | 20 | 0.499 | p < 0.05 |
Severe anemia Hb < 7 g/dL |
………. | 1 | ……. | ……… |
Table 2.
Parameters | Mother | Fetal | Pearson’s correlation coefficient R | p-value |
---|---|---|---|---|
WBC (X 103/mm3) | 10.20 ± 3.36 | 15.52 ± 5.60 | −0.040 | NS |
Hb (g/dL) | 11.14 ± 1.39 | 16.34 ± 2.01 | 0.496 | p < 0.001 |
RBC X 106/mm3) | 4.04 ± 0.46 | 4.72 ± 0.59 | 0.083 | NS |
Hematocrit (%) | 33.29 ± 4.02 | 48.79 ± 6.88 | 0.109 | NS |
MCV (fL) | 82.33 ± 6.46 | 102.85 ± 8.58 | 0.058 | NS |
MCH (pg) | 33.34 ± 5.94 | 34.70 ± 4.73 | 0.478 | p < 0.001 |
MCHC (g/dL) | 33.40 ± 1.25 | 33.26 ± 1.09 | −0.069 | NS |
Platelets (X 104/mm3) | 22.29 ± 6.61 | 229.20 ± 73.39 | 0.005 | NS |
Multivariate analysis showed maternal factors like age, gravida and smoking history did not influence the hematological parameters of the fetus. As all pregnant mothers were supplemented with iron and folic acid, ion supplementation was not considered as a confounding factor to umbilical cord hemogram.
Discussion
The mean age of pregnancy was found to be 26.04 ± 3.47 years and the median age was 26 years which was slightly above the national data of census of Nepal 2011. WHO’s [4] report of 44% prevalence of anemia in Nepal was consistent with the present study. The result of the present study was homogenous to WHO survey for mean hemoglobin concentration of average Nepali pregnant women estimated at 11.1 g/dL (10.8–11.5 g/dL with 95% credibility interval) [4]. Similar to studies in other parts of the country, [7–10] 45.61% of pregnant women were found to have hemoglobin concentrations less than 10 g/dL and 0.8% with hemoglobin concentration less than 7 g/dL. This finding was far from similar to the 2016 Nepal DHS Key indicators [11] which reported anemia in this part of Nepal to be around 28%. The prevalence of anemia throughout the country is however similar to the present study (46%). [10].
The present study showed significant positive correlation between maternal and fetal hemoglobin concentrations like Dapper DV et al. [12] in Nigeria, McElroy PD et al. [13] in Kenya, and Alizadeh L et al. [14] in Iran. No significant correlation was observed between maternal and fetal white cell count and MCHC [12–14]. A positive linear Pearson correlation was observed between mean hemoglobin and PCV of cord blood and maternal blood. All these results were similar to the ones observed by Nneli R et al. [15] Singla PN et al. [16] and Al-hilli NM et al. [17]. In contrast to the present study, some previous investigators including Qaiser DH et al., [18] Kilbride J et al., [19] and Mamoury GH et al. [20] have failed to find a relationship between the maternal and cord blood hemoglobin.
The present study showed 5.7% of the fetuses had low hemoglobin concentration, 23.94% had low MCV, 18.24% had low MCH and none of the fetuses had low MCHC which was a constant finding with Abdelgader EA et al. [21] and Steer PJ [22]. The cord blood hemoglobin (16.8 g/dL) of healthy term neonates in this study was uniform with those reported from studies in the west [23, 24].
Qaiser DH et al. [25] measured the mean of all CBC parameters aiming to maintain refrencing, and found the mean hemoglobin = 14.99 ± 1.47 g/dL, RBC = 4.29 ± 0.44, PCV = 45.65 ± 4.83, MCV = 105.81 ± 6.24, MCH = 34.96 ± 2.11, MCHC = 32.47 ± 2.12, TC = 13.61 ± 4.23 and platelet count = 256.25 ± 76.54 in the umbilical cord blood. The result showed similar findings with the present study but with a slightly higher total WBC count.
As the study was conducted in only one tertiary care center and that too with a limited number of patients, the result does not represent the pregnant women in Western Development Region of Nepal. Also, the study only included the patients attending hospital for delivery so the results cannot be generalized as it may not be a true reflection of the general population. However researchers have found the increasing trend of hospital based deliveries in urban population and Pokhara being an urban city, the data and results presented could actually represent the urban population of Pokhara valley. Socioeconomic status of the pregnant women was also not considered in the study. Moreover, further studies are to be conducted in the field to achieve complete results.
Conclusions
There was moderately positive correlation between maternal and fetal hemoglobin, MCV and MCH. There was a decrease in the cord blood hemoglobin in different severities of anemia, however, the correlation between maternal and fetal hemoglobin did not exist. It suggested that the fetal hematological parameters are not reflective of maternal hemogram.
Anemia in pregnancy should be properly evaluated and treated accordingly in order to avoid unwanted fetal and maternal outcomes.
Acknowledgements
We would like to thank the ethical committee of Manipal College of Medical Sciences for providing us the consent to conduct this study at this esteemed institute. We would also like to whole heartedly thank the participants of the study without whom the study would not have been possible. We are highly indebted to Prof Dr. C G Saha, HOD and all faculties of Department of Physiology, Manipal College of Medical Sciences for their continuous encouragement and support in the field of research. We would also like to thank Dr. Indu Tiwari, Mr. Bhuwan Baskota and Mr. Madhav Poudel for their help and support. Our sincere gratitude to Dr. Santosh Timalsina for his untiring and ever encouraging words during data analysis. Also, we would like to thank Dr. Nikki Shrestha for her English language assistance.
Funding
No funding of any sort was received for the study.
Availability of data and materials
The datasets obtained and/or analyzed during the current study are not publicly available due to confidentiality consent of the study but can be obtained from the corresponding author on reasonable request.
Abbreviations
- ANC
Ante-natal Checkup
- CBC
Complete Blood Count
- EDTA
Ethylene Di-amine Tetra Acetic acid
- Hb
Hemoglobin
- MCH
Mean Corpuscular Hemoglobin
- MCHC
Mean Corpuscular Hemoglobin Concentration
- MCV
Mean Corpuscular Volume
- MDG
Millennium Development Goals
- PCV
Packed Cell Volume
- RBC
Red Blood Cells
- SPSS
Statistical Package for Social Sciences
- TC
Total Count
- WBC
White Blood Cells
- WHO
World Health Organization
Authors’ contributions
ST wrote the proposal, participated in data collection, analyzed the data and drafted the paper. SK assisted in data collection, laboratory procedures and helped in revising the draft. AG and PB helped in the analysis of the data and writing manuscript. GP and DS participated in manuscript editing and final writing. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Ethical approval was obtained from the Ethics and Research Committee, Manipal College of Medical Sciences, Pokhara, Nepal. A written consent was obtained from the mother for participation in the study of both the mother and their newborn child. It was clearly informed verbally and in written that there would be no potential harm to the mother or the newborn baby while performing the blood tests. The consent also informed the participants that the data obtained could be used and made public under anonymity. All procedures were in accordance with the Helsinki declaration and its later amendments.
Consent for publication
Not Applicable
Competing interests
The authors declare that they have no competing interests.
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Contributor Information
Sameer Timilsina, Email: timilsina.sameer@cmc.edu.np, Email: sawmer@gmail.com.
Sirisa Karki, Email: sirisa.karki@gmail.com.
Aajeevan Gautam, Email: gautamaajeevan@gmail.com.
Pujan Bhusal, Email: poojanbhusal@gmail.com.
Gita Paudel, Email: medrgita@gmail.com.
Deepak Sharma, Email: drdeepakphysiology@gmail.com.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets obtained and/or analyzed during the current study are not publicly available due to confidentiality consent of the study but can be obtained from the corresponding author on reasonable request.