Antenatal screening for hemoglobinopathies with HPLC and their fetomaternal outcome

https://doi.org/10.53730/ijhs.v6nS9.13186

Authors

  • Bandita Priyadarsini Senior Resident, Department of Obstretics and Gynecology, SCB Medical College, Cuttack, Odisha, India.
  • Kirtirekha Mohapatra Professor and HOD, Department of Obstretics and Gynecology, S.C.B. Medical College Cuttack, Odisha, India
  • Madhushree Naik Assistant Professor, Department of Obstretics and Gynecology, S.C.B. Medical College, Cuttack, Odisha, lndia.
  • Sasmita Behuria Associate professor, Department of Obstetrics and Gynaecology, S.C.B. Medical College, Cuttack, Odisha, India

Keywords:

Fetomaternal Outcome, Antenatal screening, Hemoglobinopathies

Abstract

Introduction: Hemoglobinopathies are diverse group of inherited disorders of hemoglobin production and function. They represent the most common single-gene disorders that are found in humans and are distributed in various frequencies throughout the world. Pregnancy in women with sickle cell disease can increase the risk of maternal and perinatal mortality. HPLC offers the advantages over the routine Hemoglobin electrophoresis as it can more accurately identify and quantitate abnormal hemoglobin. HPLC forms an accurate, rapid and reproducible tool for early detection and management of thalassemia and abnormal hemoglobin variants.   Material and Methods: This is an observational study was undertaken in the Department of Obstetrics & Gynaecology and Department of Hematology of S.C.B Medical College, Cuttack. During this period those pregnant women, who attended gynaecology OPD of SCB medical college, Cuttack were investigated during various months of gestations. All pregnant women were counselled and offered screening for hemoglobinopathies after informed and written consent. Results: Among the antenatal women with hemoglobinopathy, 90.91% were anemic, 09.09% were not anemic. Among the normal group 71.06% were anemic, 28.94% were not anemic. So, there was more prevalence of anaemia among hemoglobinopathy than normal subjects which was statistically significant. (p=0.004).

Downloads

Download data is not yet available.

References

Daigavane M, Kar T, Jena R K. Perinatal outcome in sickle cell disease Randomized controlled study, Hemoglobin journal, vol. -6, 2013.

Balgir RS. The genetic burden of hemoglobinopathies with special reference to community health in India and the challenges ahead.Indian J Hemat Blood Transfus2002;20:2-7.

Weatherall1 D.J., Clegg J.B. Inherited haemoglobin disorders: an increasing global health problem. Bulletin of the World Health Organization, 2001, 79: 704-7128.

Balgir RS. The burden of hemoglobinopathies in India and the challenges ahead. Curr Sci 2000;79:1536-47.

Wainscoat JS. The haemoglobinopathies. In: Hoffbrand AV, Lewis SM, editors. Postgraduate Haemotology. 1988 3rd ed. London: Heinemann. pp 121 – 1451

Feng CS, Tsoi WC. A survey of pregnancy that ended in Haemoglobin Bart’s hydropsfoetalis and Cooley’s anemia, HJMK, 1995, 1:22-6.

Rappaport VJ, Velazquez M, Williams K. Hemoglobinopathies in pregnancy. Obstet Gynecol Clin N Am 2004; 31: 287-317.

Kobak AJ, Stien PJ, Daro AF.Sickle cell anemia in pregnancy.A review of the literature and report of six cases. Am J Obstet Gynecol 1941; 41:811-21.

Powars DR. Yaster M et al. Pregnancy in sickle cell disease. Obstet Gynecol1986;67:217-28.

Hassell K. Pregnancy and sickle cell disease. Hematol Oncol Clin North Am 2005:19:903-16.

Russel RV, Lal H. Tribes and castes of the central provinces of India. Four Volumes. London, Macmillan Company, 1916.

Balgir RS, Dash BP, Murmu B. Blood groups, hemoglobinopathy and G-6- PD enzyme investigations among fifteen major scheduled tribes of Orissa, India. Anthropologist, 2004; 6:69-75

Mellissa C, Roberts I, Koshy M et al. Sickle cell disease: Current activities, public health implications, and future directions. Journal of Women’s. Health, 2007, Volume 16, Number 5.

Baill IC, Kazazian HH, Sun PB et al. Sickle trait and its association with birth weightand urinary tract infections in pregnancy. Int J GynaecolObstet 1990, 33:19-21

Bryant AS, Cheng YW, Lyell DJ, Laros RK, Caughey AB, Presence of the sickle celltrait and preterm delivery in African-American ObstetGynecol2007;109:870-4.

Tita TNA, Biggio RJ, Chapman V et al. Perinatal and Maternal Outcomes in women. Women With Sickle ör Hemoglobin C Trait ObstetGynecol 2007; 110:1113-9

Larrabee K, Molitierno JA, Carson CC. et al. Women with sickle cell trait are atincreased risk for pre-eclampsia. Am J Obstet Gynecol 1997, 177:425-8.

Thurman AR, Steed LL, Hulsey T, David ES. Bacteriuria in pregnant women withsickle cell trait. American Journal of Obstetrics and Gynecology (2006) 194, 1366-70.

Panda A. Praveen B, Bisht SS. Clinical & pathological status of haemoglobinopathies among pregnant women in southern Orissa. Indian Journal of Biotechnology 2009;8(4):456-57.

Herrick, J.B. 1910.Peculiar elongated and sickle-shaped red blood corpuscules in a case of severe anemia. Arch. Int. Med. 6:517-521.

Afolabi BB., IwualaNC.,Iwuala IC. & Ogedengbe OK. Morbidityand mortality in sickle cell pregnancies in Lagos, Nigeria: A case control study. Journal of Obstetrics and Gynaecology, 2009, 29(2): 104-106

Serjeant GR, Serjeant GR, Sandu M et al. Outcome of pregnancy in homozygous sickle cell disease. ObstetGynecol 2004; 103(6):1278-85.

Villers MS, Jamison MG, DeCastro LM, et al. Morbidity associated with SSD in pregnancy. Am J ObstetGynecol 2008;1:e1-5.

Al Jama FE, Gasem T, Burshaid S et al. Pregnancy outcome in patients with homozygous sickle cell disease in a university hospital, Eastern Saudi Arabia, ArchGynecolObstet 2009; 280:793-7971

Blattner P, Dar H, Nitowsky HM. Pregnancy outcome in women with sickle cell trait Journal of American Medical Association 1977; 238:1392- 1394

Published

02-10-2022

How to Cite

Priyadarsini, B., Mohapatra, K., Naik, M., & Behuria, S. (2022). Antenatal screening for hemoglobinopathies with HPLC and their fetomaternal outcome. International Journal of Health Sciences, 6(S9), 2958–2968. https://doi.org/10.53730/ijhs.v6nS9.13186

Issue

Section

Peer Review Articles