๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Use of continuous flow erythrocytapheresis in pregnant patients with sickle cell disease

โœ Scribed by John C. Morrison; Francis S. Morrison; Randall C. Floyd; William E. Roberts; L. Wayne Hess; Winfred L. Wiser


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
612 KB
Volume
6
Category
Article
ISSN
0733-2459

No coin nor oath required. For personal study only.

โœฆ Synopsis


The role of partial prophylactic red cell exchange transfusion in the management of pregnant patients with major sickle hemoglobinopathies is unclear. Over a I0-year period, 13 1 pregnant patients with major hemoglobinopathies (HbS 101, HbS-C 30) were managed by the same group of physicians. Of these, 103 received partial prophylactic exchange transfusion early during prenatal care while 28 received blood only when serious complications developed (control group). Patients treated with exchange transfusion received continuous flow erythrocytapheresis on an outpatient basis. The results indicate that there were fewer crises (P = .0001), a reduction in other significant medical complications ( P = .002), and a decrease in maternal hospital days ( P = .05) in those receiving prophylactic transfusions compared to women in the control group. The number of preterm delivcries ( P = .004), the prevalence of low birthweight infants ( P = .01), and the perinatal death rate ( P = .01) were significantly lower among those who were routinely transfused. Two patients developed hepatitis, five had transfusion reactions, and I 1 were found to have alloantibodies among those receiving prophylactic transfusions versus one, two, and fivc patients, respectively, in the control group. The results indicate a benefit of this methodology in the treatment of pregnant sickle cell patients in our population. However, a national collaborative randomized study is needed to adequately address the controversy regarding the use of red cell exchange in the pregnant sickler.


๐Ÿ“œ SIMILAR VOLUMES


Use of erythrocytapheresis in the treatm
โœ Dr. Steven H. Kleinman; Carole G. Hurvitz; Dennis Goldfinger ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 651 KB

We perfornied exchange transfusions. utilizing the technique of automated crythrocytaphcresk. for the treatment of patients with sickle cell anemia. In an attempt to determine guideline5 for the use of erythrocytapheresis, we studied the use of this procedure i n three distinct clinical situations i

Effect of erythrocytapheresis on arteria
โœ Uchida, Kou; Rackoff, Wayne R.; Ohene-Frempong, Kwaku; Kim, Haewon C.; Reilly, M ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 27 KB ๐Ÿ‘ 2 views

An important purpose of blood transfusion in patients with sickle cell disease is to improve arterial oxygen saturation (SaO 2 ) and thereby reduce red cell sickling. To investigate the degree of improvement in SaO 2 by blood transfusion, we determined the hemoglobin oxygen affinity, transcutaneous

Malignancy in patients with sickle cell
โœ William H. Schultz; for the International Association of Sickle Cell Nurses; Phy ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 66 KB ๐Ÿ‘ 2 views