IMR Press / CEOG / Volume 28 / Issue 1 / pii/2001012

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 47 Issue 1 (2020). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Original Research

A study report of 174 units of placental umbilical cord whole blood transfusion in 62 patients as a rich source of fetal hemoglobin supply in different indications of blood transfusion

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1 Principal Investigatorof the Project, Surgeon Superintendent, Bijoygarth State Hospital, Calcutta (India)
2 Emeritus Professor, Vivekananda Institute of Medical Sciences, Sarat Bose Road, Calcutta (India)
3 Former Director of Health Services, Govt. of West Bengal and of the Institute of Post Graduate Medical Education and Research (IPGMER), Emiritus Professor, Department of Medicine, IPGMER, Calcutta (India)
4 Principal Scientific Officer, Dept. of Science & Technology, Govt. of West Bengal, Salt Lake, Calcutta (India)
5 Research Associate in the project;'Reader, Jadavpur University, Calcutta (India)
Clin. Exp. Obstet. Gynecol. 2001, 28(1), 47–52;
Published: 10 March 2001
Abstract

Background: In the animal kingdom, even herbivorous animals swallow the placenta after the birth of the baby (for example, the cow). In the human system, we do mlt know about the proper utilization of the placenta and membranes although there are sugge­stions regarding this on the basis of research on placental umbilical cord blood stem cells as an alternative to bone marrow transplantation. In this present series of placental umbilical cord whole blood transfusions, we wanted to examine the safety aspect of other components of cord blood transfusion, e.g., fetal RBC, growth factors and cytokine filled plasma, etc., in different indications of blood transfusion, from the pediatric to the geriatric age group, in malignant and non-malignant disorders affecting our patients. Methods: One hundred and seventy-four units of umbilical cord whole blood were collected aseptically from the umbilical vein after caesarean section in standard pediatric blood transfusion bags*, after the removal of the baby from the operative field and after confirming the stable condition of the mother. The volume of cord blood varied from 50 ml to 140 mL with a mean of 86 mL ± 16 mL. Results and Analysis: The cord blood was transfused immediately (within three days of collection) to 62 patients from nine years to 78 years of age, of whom 32 were suffering from varying stages and grades of malignancy from 1 April 1999 till date i.e., 11 Aug 2000, after obtaining adequate consent and following the precautions of standard blood transfusion protocol. The remaining 30 patients included patients suffering from thalassemia major, aplastic anemia, systemic lupus erythematosus, chronic renal failure, rheumatoid arthritis, ankylosing spondylitis and a geriatric group of patients with benign prostatic hypertrophy. All have tolerated the procedure without any immunological or non-immunological reactions. Conclusion: On the basis of our experience with 174 units of placental umbilical cord whole blood transfusion in malignant and non-malignant conditions (within three days of collection and preservation at l–6 ℃ in a refrigerator), we are of the opinion that this is a safe transfusion protocol which takes advantage of the safety of nature's finest biological sieve, i.e., the placenta, as an alter­native to adult whole blood transfusion. It also has the advantage of a higher oxygen carrying capacity of fetal hemoglobin in addi­tion to many growth factors and other cytokine filled cord blood plasma along with its hypoantigenicity.

Keywords
Fetal hemoglobin
Placental umbilical cord whole blood
Safe transfusion
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