Severe Anemia During Pregnancy: Prevalence, Risk Factors and Maternal-Fetal Prognosis

Lyande LB*1, Limbaya Ekanga NMJ2, Amisi BM1, Lokenye Kabinda A1, Kumiele PM1 and Bakulanga P1

1Higher Institute of Medical Techniques of Yangambi (ISTM – YBI), Democratic Republic of the Congo
2Higher Institute of Medical Techniques of Kisangani (ISTM – KIS), Democratic Republic of the Congo

*Correspondence: Ley Bafeno Lyande, Higher Institute of Medical Techniques of Yangambi (ISTM – YBI), Democratic Republic of the Congo

Received on 10 July 2023; Accepted on 09 August 2023; Published on 21 August 2023

Copyright © 2023 Lyande LB, et al. This is an open-access article and is distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Anemia is one of the most important public health problems in the world and concerns the World Health Organization (WHO) given its prevalence, its many etiologies but also the consequences for which it is responsible in mothers and young children. In pregnant women, the causes of anemia are multiple and often intertwined: iron deficiency (but also folic acid, vitamin, etc.), intestinal helminthiasis, malaria, other infections (HIV infection, etc.), and hemoglobinopathies are the main causes. But among these etiologies, it has been estimated that 75% of anemias are attributable to iron deficiency and remain a cause of considerable perinatal morbidity and mortality. To avoid this, health services should design and implement strategies to control anemia in pregnant women, including prevention, early diagnosis, and appropriate management. The objective is to contribute to improving the management of anemia during pregnancy in order to reduce maternal and fetal morbidity and mortality linked to anemia in pregnant women.

Keywords

severe anemia; pregnant; risk factors and foeto-maternal prognosis; Yangambi

Introduction

Anemia is one of the most important public health problems in the world and has been of concern to the World Health Organization (WHO) since 1949, taking into account its prevalence, its many etiologies but also the consequences for which it is responsible in the mother and the young child [1].

According to the WHO, anemia is defined during pregnancy by a hemoglobin level below 11 g/dL in the first and third trimester of pregnancy; less than 10.5 g/dL in the second [2].

According to a joint study conducted by the WHO and the CDC on the global prevalence of anemia between 1993 and 2005, Africa is the continent most affected by anemia during pregnancy with an average prevalence of 57%, while in Europe, the average is 25.1%, in Asia 48.2%, and in America 24.1%. On a global scale, this prevalence was 41.8% or 56.4 million pregnant women concerned [3].

A 2007 survey of maternal-fetal health in the DRC revealed that nearly 70% of pregnant women were anemic. The highest rates were reported in Bas-Congo and Maniema, respectively 90.4% and 77.5% [4].

In pregnant women, the causes of anemia are multiple and often intertwined: iron deficiency (but also folic acid, vitamin, etc.), intestinal helminthiasis, malaria, other infections (HIV infection, etc.), and hemoglobinopathies are the main causes. Among these etiologies, it has been estimated that 75% of anemias are attributable to iron deficiency [5]. This high prevalence of iron and other micronutrient deficiency among pregnant women in developing countries is a cause for concern, and maternal anemia still remains a cause of considerable perinatal morbidity and mortality [6, 7].

Presentation of Results

Prevalence of anemia among gestants

  • Overall prevalence of anemia during pregnancy

Table 1 shows us that the frequency of anemia during pregnancy is 55.67%.

Pregnant Number %
Anemia 167 55.67%
No anemia 133 44.33%
Total 300 100%

Table 1: Overall prevalence of anemia during pregnancy.

  • Type of anemia according to hemoglobin level

In the light of Table 2, we note only severe anemia presents 53.29% of cases.

Type of anemia Number %
Mild anemia 53 31.74%
Moderate anemia 25 14.97%
Severe anemia 89 53.29%
Total 167 100%

Table 2: Type of anemia according to hemoglobin level.

Factors associated with severe anemia

  • Socio-demographic characteristics

A. Age of patients

Table 3 shows that there is no statistically significant difference between the different age groups with regard to the occurrence of severe anemia during pregnancy.

Age (years) ≤20 21–25 26–30 30–35 30–35
n % n % n % n % n %
Mild anemia 0 0% 0 0% 0 0% 0 0% 0 0%
Moderate anemia 2 40% 17 42.5% 29 51.8% 18 42.9% 12 50%
Severe anemia 3 60% 23 57.5% 27 48.2% 24 57.1% 12 50%
Total 5 100% 40 100% 56 100% 42 100% 24 100%

Table 3: The influence of age on the occurrence of anemia during pregnancy; P-value = 0.8597.

B. Marital status

Table 4 shows the influence of marital status on the occurrence of anemia during pregnancy.

Single Married
n % n %
Moderate anemia 6 50% 72 46.5%
Severe anemia 6 50% 83 53.5%
Total 12 100% 155 100%

Table 4: Influence of marital status on the occurrence of anemia during pregnancy; P-value = 0.8123.

C. Profession

Table 5 shows that there is no statistical difference between the profession of the patients with regard to the occurrence of severe anemia during pregnancy.

Profession Civil servant Shopkeeper Housewife Pupils/students
n % n % n % n %
Severe anemia 13 46.4% 11 36.7% 50 36.7% 15 68.2%
Moderate anemia 15 53.6% 19 63.3% 37 63.3% 7 31.8%
Total 28 100% 30 100% 87 100% 23 100%

Table 5: Influence of profession on the onset of anemia during pregnancy; P-value = 0. 0924.

D. Level of education

Table 6 shows that the risk of study does not influence the severity of anemia during pregnancy.

Primary/secondary University/higher
n % n %
Severe anemia 59 53.6% 30 52.6%
Moderate anemia 51 46.4% 27 47.4%
Total 110 100% 57 100%

Table 6: Influence of patient education and the occurrence of severe anemia during pregnancy; P-value = 0.9097.

  • Gyneco-obstetric history

A. Parity

It appears from Table 7 that there is no statistical difference between the parities with regard to the occurrence of severe anemia during pregnancy.

Parity Nulliparous Primiparous Pauciparian Multiparous Grand multiparous
n % n % n % n % n %
Moderate anemia 10 30.3% 20 58.8% 12 46.2% 33 47.2% 3 60%
Severe anemia 23 69.7% 14 41.2% 14 53.8% 36 52.8% 2 40%
Total 33 100% 34 100% 26 100% 69 100% 5 100%

Table 7: Influence of parity on the occurrence of anemia during pregnancy; P-value = 0.2017.

B. Inter-birth interval

Table 8 shows that there is no statistical difference between the inter-birth interval of less than 2 years with severe anemia during pregnancy and those with moderate anemia.

Less than 2 years More than 2 years
n % n %
Moderate anemia 47 52.2% 21 47.7%
Severe anemia 43 47.8% 23 52.3%
Total 90 100% 44 100%

Table 8: The influence of the inter-birth interval on the occurrence of anemia during pregnancy; P-value = 0.6250.

C. History of postpartum hemorrhage

Table 9 shows that patients who had postpartum hemorrhage during their previous delivery are significantly more likely to have severe anemia, 66.7% against 42.3% in the moderate anemia group.

Postpartum hemorrhage No postpartum hemorrhage
n % n %
Moderate anemia 13 33.3% 55 57.9%
Severe anemia 26 67.7% 40 42.1%
Total 39 100% 95 100%

Table 9: Influence of history of postpartum hemorrhage; P-value = 0.0098.

Maternal-fetal prognosis

  • Maternal prognosis

A. Transfusion

We note that patients with severe anemia during pregnancy are significantly more likely to have been transfused (97.9%), as shown in Table 10.

Transfusion No transfusion
n % n %
Moderate anemia 1 2.1% 77 64.2%
Severe anemia 46 97.9% 43 35.8%
Total 47 100% 95 100%

Table 10: The impact of transfusion of patients with severe anemia during pregnancy; P-value = 0.0000.

  • Fetal prognosis

A. Low birth weight

Table 11 shows that low birth weight newborns from patients with severe anemia during pregnancy (87.5%) are significantly more numerous compared to 51.6% in the group with moderate anemia.

Low birth weight Normal birth weight
n % n %
Moderate anemia 1 12.5% 77 48.4%
Severe anemia 7 87.5% 82 51.6%
Total 8 100% 159 100%

Table 11: Relationship between anemia during pregnancy and birth weight; P-value = 0.0468.

B. APGAR from newborn to 5th minute

Table 12 shows that the APGAR less than or equal to 6 are significantly more likely to have newborns with a low APGAR score (67.6%) vs. 49.8% severe anemia during pregnancy.

APGAR less than or equal to 6 APGAR greater than 6
n % n %
Moderate anemia 12 32.4% 66 50.8%
Severe anemia 25 67.6% 64 49.8%
Total 37 100% 130 100%

Table 12: Relationship between the APGAR of newborns at the 5th minute less than or equal to 6 and the occurrence of severe anemia during pregnancy; P-value = 0.0485.

C. Perinatal mortality

Table 13 shows that there is no statistical difference with regard to perinatal mortality.

Yes No
n % n %
Moderate anemia 2 20% 76 48.4%
Severe anemia 8 80% 81 51.6%
Total 10 100% 157 100%

Table 13: The influence of perinatal mortality on the occurrence of anemia in pregnancy; P-value = 0.0808.

Discussion

Prevalence of anemia in pregnant women

In our series, we found a prevalence of anemia in pregnancy of 55.7%. Anemia during pregnancy is very common, especially in developing countries, where it affects 50–80% of pregnant women [8, 9]. This figure is close to that found by Esike et al. [10] and Okube et al. [1]; on the other hand, this figure is higher than that found in Gombe in northern Nigeria [11–15] and that found by Alem et al. [16] and is higher than that found by the WHO and CDC [5]. We believe that this result is due to the high incidence of poverty in Democratic Republic of the Congo of 71.3% of the population, which imposes on many families a monotonous diet responsible for nutritional deficiency at the base of certain forms of deficiency anemia and also the situation of Yangambi which is highly endemic for malaria, where malaria is responsible for anemia in pregnant women. Promiscuity exposes to water diseases, ankylostomiasis, and amoebiasis, which are responsible for anemia by blood depletion.

Factors associated with severe anemia

  • Maternal age

We noted in our series that there is no statistically significant difference between the different age groups in the occurrence of anemia during pregnancy. Obai et al. [17] made the same observation as us; on the other hand, Ma et al. [18] found that patients aged 45–49 had a risk of severe anemia during pregnancy.

  • Marital status

In our series, we noted that there is no statistical difference between married and single women with regard to the occurrence of anemia during pregnancy; the same observation was made by Obai et al. [17] and Lokare et al. [19]. We think that this result would be justified by the poverty which lives in our environment of Yangambi in particular and of DR Congo in general; indeed, single people by the fact that they are abandoned to their sad fate without employment can develop deficiency anemia due to lack of means. The same is true for brides who generally abandon themselves to their spouses to meet their needs because they do not have a profit-making initiative.

  • Profession

It appears from our study that there is no statistical difference between the professions of patients in relation to the occurrence of anemia during pregnancy. Lokare et al. [19] made the same observation as us; on the other hand, Obai et al. [17] found that housewives were exposed to the risk of anemia, justifying this by the fact that they only had as a source of survival their spouses.

  • Level of education

We found that there is no statistical difference between levels of education with regard to the occurrence of severe anemia during pregnancy. Obai et al. [17] found that education was a factor that reduced the risk of anemia. They justified their result by the fact that pregnant women with a low level of education understand less well the recommendations made during the prenatal consultation, and they have difficulty observing the recommendations given to them during the health education sessions [20, 21].

  • Parity

We found in our series that there is no statistical difference between parity with regard to the occurrence of anemia during pregnancy. Our results agree with those of Ahmad et al. [22]. However, Obai et al. [17] found that compared to nulliparous, pauciparous, or multiparous women increases the risk of the onset of anemia during pregnancy.

  • Inter-birth interval

In our series, we found that there is no statistical difference between patients with an inter-birth space of less than 2 years and those with an interval greater than or equal to 2 years with regard to the occurrence of severe anemia during pregnancy. Contrary to our series, Kassa et al. [21] found that a short inter-birth interval doubles the risk of severity of anemia.

According to Labama [23–25], anemia during pregnancy is more linked to close parity because the maternal organism did not have sufficient time to compensate for previous anemia before the new pregnancy.

  • History of postpartum hemorrhage

Note that in our series, patients who had postpartum hemorrhage during their previous deliveries were more likely to have severe anemia compared to those in the moderate anemia group. This same observation has been made by other authors. Ma et al. [18] found that significant previous bleeding increases the risk of severe anemia 5-fold. This risk is due to the fact that the maternal organism deficient by a prior nutritional deficit has not had enough time to reconstitute itself when the woman becomes pregnant. The needs of pregnancy will only increase the risk [26, 27].

Maternal-fetal prognosis

  • Maternal transfusion

We found during our study that patients with severe anemia during pregnancy were significantly more likely to have been transfused, i.e., 51.7% against 1.9% in the moderate anemia group. Childbirth is a situation that is always accompanied by hemorrhage. The good maternal tolerance to hemorrhage is linked to its state of hypovolemia, the hemoglobin level, and the passage in the general circulation of the blood contained in the uterine muscle during its retraction; this volume can reach up to 500 ml. We are talking about physiological transfusion. The physiological responses to hemorrhage vary according to its severity and the patient’s condition: either the hemorrhage occurs on the normal ground or an anemic ground preexisting at delivery.

Patients with severe anemia are, therefore, more likely to decompensate much more easily regardless of the amount of blood lost and therefore benefit from a transfusion, which justifies our results.

  • Maternal mortality

We did not record any cases of death during our study series. According to the United Nations, severe anemia, as defined by the WHO (Hb less than 7 g/dL), is responsible for more than half of the cases of maternal death worldwide [28, 29]. We believe that the results observed in our series of studies could be justified by good management in Yangambi of patients showing signs of anemia decompensation.

  • Low birth weight

It emerged from our study that patients with severe anemia during pregnancy were significantly more likely to have low birth weight newborns, i.e., 7.8% vs. 1.9% in the moderate anemia group. In 2011, Ndeye [30] listed 30 cases of fetal distress, including 17 in the anemia group. Also, in Nablus, the rate of low birth weight found by the authors in the population of anemic women was 56.6% [31–34].

We believe, like Beucher et al. [35], that the risk of low birth weight and suffering fetus increases with the severity and duration of the anemia as a consequence of nutritional deficiency and lack of oxygen for metabolism.

  • Newborn APGAR

We found in our series that patients with severe anemia during pregnancy are significantly more likely to have newborns with a low APGAR score. As said before, we think, like Beucher et al. [35], that the risk of low birth weight and fetal distress increases with the severity and the length of the anemia as a consequence of nutritional deficiency and lack of oxygen for the metabolism.

  • Perinatal mortality

We found in our series that the perinatal mortality of newborns from pregnant women who presented severe anemia is 8.9%, while those who presented moderate anemia is 2.6%. The difference is not statistically significant. We believe that these results are due to the fact that at the time of our study, the hospital had a high technical platform in equipment and personnel in neonatology who promptly took care of newborns.

References

  1. Okube OT, Mirie W, Odhiambo E, et al. Prevalence and Factors Associated with Anaemia among Pregnant Women Attending Antenatal Clinic in the Second and Third Trimesters at Pumwani Maternity Hospital, Kenya. Open J Obstet Gynecol. 2016;6(1):16-27.
  2. Organisation mondiale de la sante. Le dossier mère-enfant: Guide pour une maternité sans risque. 1996.
  3. OMS : enquête mondiale sur l’anémie de 1993-2005.
  4. Ministère National de la Santé Publique de la RDC, politique nationale de la santé de reproduction.
  5. Nokia K. La prévalence de l’anémie chez la femme enceinte en Kisangani. 2013.
  6. Baidy BLO, Kone Y, Bassirou EL. Anémie nutritionnelle de la grossesse a Nouakchott. Médecine d’Afrique Noire. 1996;43(3):355-59.
  7. Kremed C: impact des carences nutritionnelles sur l’anémie de la femme enceinte session de réseau matermip. Anémie et grossesse. 2010 ;10 :1.
  8. Caroff-Pétillon A. État des lieux du dépistage de l’anémie pendant la grossesse. Étude rétrospective réalisée au centre hospitalier universitaire de Brest. Sage-Femme. 2008;7(2):51-55.
  9. Bitam A, Belkadi N. Prévalence de l’anémie ferriprive au cours de la grossesse dans la wilaya de Blida (Nord de l’Algérie). Nutrition Clinique et Métabolisme. 2008;22(3):100-07.
  10. Esike CO, Anozie OB, Onoh RC, et al. The prevalence of anemia in pregnancy at booking in Abakaliki, Nigeria. Trop J Obstet Gynaecol. 2016;33(3):332-36.
  11. Vanderjagt DJ, Brock HS, Melah GS, et al. Nutritional factors associated with anaemia in pregnant women in northern Nigeria. J Health Popul Nutr. 2007;25(1):75-81.
  12. Coll MT. Profil épidémiologique des interdictions alimentaires chez la femme enceinte dans la ville province de KINSHASA. 2008.
  13. Organisation mondiale de la Santé‎. Rôle de la supplémentation hebdomadaire en fer et en acide folique chez la femme en âge de procréer pour favoriser une santé optimale de la mère et de l’enfant. 2009.
  14. Rotsart H, Courte JJ. Maternité et santé. 2001.
  15. Jahier J, Giraud JR. Anémie et grossesse. Encycl Med Chir. 1978;5043(A):10-12.
  16. Alem M, Enawgaw B, Gelaw A, et al. Prevalence of Anemia and Associated Risk Factors among Pregnant Women Attending Antenatal Care in Azezo Health Center Gondar Town, Northwest Ethiopia. J Interdiscip Histopathol. 2013;1(3):137-44.
  17. Obai G, Odongo P, Wanyama R. Prevalence of anaemia and associated risk factors among pregnant women attending antenatal care in Gulu and Hoima Regional Hospitals in Uganda: A cross sectional study. BMC Pregnancy Childbirth. 2016;16:76.
  18. Ma Q, Zhang S, Liu J, et al. Study on the Prevalence of Severe Anemia among Non-Pregnant Women of Reproductive Age in Rural China: A Large Population-Based Cross-Sectional Study. Nutrients. 2017;9(12):1298.
  19. Lokare PO, Karanjekar VD, Gattani PL, et al. A study of prevalence of anemia and sociodemographic factors associated with anemia among pregnant women in Aurangabad city, India. Annals of Nigerian Medicine. 2012;6(1):30-34.
  20. Wilunda C, Massawe S, Jackson C. Determinants of moderate-to-severe anaemia among women of reproductive age in Tanzania: analysis of data from the 2010 Tanzania Demographic and Health Survey. Trop Med Int Health. 2013;18(12):1488-497.
  21. Kassa GM, Muche AA, Berhe AK, et al. Prevalence and determinants of anemia among pregnant women in Ethiopia; a systematic review and meta-analysis. BMC Hematol. 2017;17:17.
  22. Ahmad N, Kalakoti P, Bano R, et al. The prevalence of anaemia and associated factors in pregnant women in a rural Indian community. AMJ. 2010;3(5);276-80.
  23. Kanku T, Labama L, Wembodinga U, et al. Anémie de la femme enceinte à Kisangani: prévalence et risques liés à quelques indicateurs de risque. Congo Médical. 2000:2(13);915-920.
  24. Molina RA, Diez-Ewald M, Fernández G, et al. Nutritional anaemia during pregnancy. A comparative study of two socio-economic classes. J Obstet Gynaecol Br Commonw. 1974;81(6):454-58.
  25. Labama L. Particularites de la grossesse et de l’accouchement chez la grande multipare a Kinsangani. Artigo em Francês. 1993;1(1):637-641.
  26. Politique Nationale de la Sante de Reproduction. 2008.
  27. Allen LH. Iron-deficiency anemia increases risk of preterm delivery. Nutr Rev. 1993;51(2):49-52.
  28. Coulybaly M. Anémie et grossesse : Pronostic materno-fœtal dans le service de gynéco-obstétrique du centre de référence de la commune iv du district de Bamako, thèse de médecine, FM et pharmacie, Université de BAMAKO. 2005.
  29. Jeune L. Anémie en cours de grossesse : conduite à tenir, www performances-médicales. Gynéco Encours. 2008:13606.
  30. Ndeye SD. Prévalence de l’anémie au cours de l’état gravido- puerpéral, FM et pharmacie, thèse de doctorat de médecine. 2011.
  31. Abu-Hasira AWM. Iron Deficiency Anemia among Pregnant Women in Nablus District; Prevalence, Knowledge, Attitude and Practices. An-Najah National University Faculty of Graduate Studies. 2007;1-50.
  32. Macron WM, et al. Médecine de la femme enceinte, Flammarion Médecine-science, Paris:1990.
  33. World Health Organization. The global prevalence of anaemia in 2011. 2015.
  34. Walraven G. : traitement de l’anémie ferriprive au cours de la grossesse. Commentaire de la bibliothèque de santé génésique de l’OMS : 2007.
  35. Beucher G, Grossetti E, Simonet T, et al. Anémie par carence martiale et grossesse. Prévention et traitement. J Gynecol Obstet Biol Reprod (Paris). 2011;40(3):185-200.