Selective prophylactic transfusion in sickle cell disease

被引:12
|
作者
Grossetti, Elizabeth [1 ]
Carles, Gabriel [2 ]
El Guindi, Wael [2 ]
Seve, Beatrice [2 ]
Montoya, Yohni [2 ]
Creveuil, Christian [3 ]
Dreyfus, Michel [1 ]
机构
[1] Univ Hosp Caen, Dept Gynecol & Obstet, Caen, France
[2] Hosp Franck Joly St Laurent Maroni, Dept Gynecol & Obstet, French Guyana, France
[3] Univ Hosp Caen, Dept Med Comp Technol, Caen, France
关键词
Sickle cell disease; pregnancy; prophylactic transfusion; BLOOD-TRANSFUSION; PREGNANT PATIENTS; MANAGEMENT; HEMOGLOBINOPATHIES; EXPERIENCE;
D O I
10.1080/00016340903134171
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective. To record feto-maternal complications following the use of selective prophylactic transfusions in women with major sickle cell disease (SCD) and determine whether selective prophylactic transfusion reduces these complications, through a comparison with a population of women who received transfusions for complications only. Design. A retrospective cohort study. Setting. Public regional referral hospital in western French Guyana. Population. Between 1992 and 2004, in all 29 women, 55 pregnancies, and 56 neonates. Methods. Close obstetric follow-up and selective prophylactic transfusions after 26 weeks. Main outcome measures. Adverse obstetric outcome (pre-eclampsia, preterm delivery, intrauterine growth restriction (IUGR), intrauterine fetal death (IUFD), cesarean delivery, neonatal and maternal mortality) and end-points for SCD outcome (vaso-occlusive crisis (VOC), acute chest syndrome, and infections). Results. Complications involved the different major SCD types to an equal extent. Comparison with the control group showed that women who had received prophylactic transfusions had lower rates of VOC (p=0.002) and preterm deliveries (p=0.036), but a significant increase in IUGR cases (p=0.048). Conclusion. Selective prophylactic transfusion seems to reduce certain maternal and fetal complications in women with severe forms of SCD. These results can only be confirmed through a randomized prospective study.
引用
收藏
页码:1090 / 1094
页数:5
相关论文
共 50 条
  • [31] Global burden of transfusion in sickle cell disease
    Inusa, Baba P. D.
    Atoyebi, Wale
    Andemariam, Biree
    Hourani, James N.
    Omert, Laurel
    [J]. TRANSFUSION AND APHERESIS SCIENCE, 2023, 62 (05)
  • [32] TRANSFUSION AND ALLOIMMUNIZATION IN SICKLE-CELL DISEASE
    NOROL, F
    NADJAHI, J
    BACHIR, D
    DESAINT, C
    BATAILLE, MG
    BEAUJEAN, F
    BIERLING, P
    BONIN, P
    GALACTEROS, F
    DUEDARI, N
    [J]. TRANSFUSION CLINIQUE ET BIOLOGIQUE, 1994, 1 (01) : 27 - 34
  • [33] TRANSFUSION MANAGEMENT OF SICKLE-CELL DISEASE
    WAYNE, AS
    KEVY, SV
    NATHAN, DG
    [J]. BLOOD, 1993, 81 (05) : 1109 - 1123
  • [34] TRANSFUSION AND ALLOIMMUNIZATION IN SICKLE-CELL DISEASE
    ROSSE, WF
    GALLAGHER, D
    KINNEY, TR
    CASTRO, O
    DOSIK, H
    MOOHR, J
    WANG, W
    LEVY, PS
    [J]. BLOOD, 1990, 76 (07) : 1431 - 1437
  • [35] Genotyping and the Future of Transfusion in Sickle Cell Disease
    Karafin, Matthew S.
    Howard, Jo
    [J]. HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2022, 36 (06) : 1271 - 1284
  • [36] Transfusion support for patients with sickle cell disease
    Wallace, Lisa R.
    Thibodeaux, Suzanne R.
    [J]. TRANSFUSION AND APHERESIS SCIENCE, 2022, 61 (05)
  • [37] TRANSFUSION THERAPY IN SICKLE-CELL DISEASE
    BELAS, F
    TRAINEAU, R
    LOKIECZERAH, MH
    BUNTHOR, H
    BONNETGAJDOS, M
    REVIRON, J
    [J]. ARCHIVES FRANCAISES DE PEDIATRIE, 1983, 40 (09): : 750 - 750
  • [38] TRANSFUSION, SURGERY, AND SICKLE-CELL DISEASE
    MCINTOSH, S
    PEARSON, HA
    [J]. PEDIATRICS, 1979, 63 (02) : 350 - 350
  • [39] Transfusion support in patients with sickle cell disease
    Sharma, Deva
    Ogbenna, Ann Abiola
    Kassim, Adetola
    Andrews, Jennifer
    [J]. SEMINARS IN HEMATOLOGY, 2020, 57 (02) : 39 - 50
  • [40] ADENOTONSILLECTOMY IN SICKLE CELL DISEASE: IS TRANSFUSION NEEDED?
    Elshinawy, M.
    Al Marhoobi, N.
    Wali, Y.
    [J]. HAEMATOLOGICA, 2016, 101 : 845 - 845