Recambio de Hematíes en gestante con Anemia de Células Falciformes: reporte de un caso en el Hospital Regional de Talca / Red blood cell exchange in pregnant women with Sickle Cell Anemia: report of a case in the Regional Hospital of Talca
Rev. méd. Maule
; 36(2): 69-73, dic. 2021.
Article
de Es
| LILACS
| ID: biblio-1378547
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CL1.1
ABSTRACT
Sickle cell anemia or sickle cell disease is an autosomal recessive disease, caused by a mutation in the hemoglobin gene, where glutamic acid is substituted for valine at position 6 of the beta chain of hemoglobin, resulting in hemoglobin S The diagnosis is made with electrophoresis. The clinical manifestations are varied, the most frequent being the vaso-occlusive crisis, which can increase in pregnancy, during which sickle cell disease also increases the risk of maternal-fetal complications, caused by pre-eclampsia infections, intrauterine growth restriction, and premature delivery. and miscarriage. The usual treatment for the management of seizures is hydroxyurea, a drug that is teratogenic, so its use is contraindicated during pregnancy. Other treatment alternatives are red blood cell transfusion and red blood cell exchange. Next, the first case of red blood cell exchange or exchange transfusion in a pregnant patient with sickle cell anemia at the Hospital Regional de Talca is presented.
Mots clés
Texte intégral:
1
Indice:
LILACS
Sujet Principal:
Complications hématologiques de la grossesse
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Exsanguinotransfusion
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Transfusion d'érythrocytes
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Drépanocytose
Limites du sujet:
Adult
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Female
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Humans
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Male
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Newborn
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Pregnancy
langue:
Es
Texte intégral:
Rev. méd. Maule
Thème du journal:
MEDICINA
Année:
2021
Type:
Article