The Management of Priapism in Sickle Cell Anemia
- 1 May 1978
- journal article
- research article
- Published by Wolters Kluwer Health in Journal of Urology
- Vol. 119 (5), 610-611
- https://doi.org/10.1016/s0022-5347(17)57565-5
Abstract
After assessing the data currently available on the multiple modalities used to manage priapism secondary to sickle cell disease a specific therapeutic regimen for the treatment of this problem was adopted. Early non-surgical measures, including hydration, alkalization and analgesics, rapid red cell infusion to double the hematocrit and late shunting procedures in conjunction with exchange transfusion, offer the soundest approach on pathophysiological grounds. There is currently no evidence to support early surgical intervention as the best approach to conserve potency in this problem.This publication has 16 references indexed in Scilit:
- Priapism in boysUrology, 1975
- Priapism in association with sickle hemoglobinopathies in childrenThe Journal of Pediatrics, 1975
- Priapism: A Review of 46 CasesJournal of Urology, 1974
- Management Of Priapism In Patients With Chronic Granulocytic LeukemiaJournal of Urology, 1974
- Intensive Transfusion Therapy for Priapism in Boys with Sickle Cell AnemiaJournal of Urology, 1973
- Priapism in sickle cell disease: report of five casesThe American Journal of the Medical Sciences, 1972
- Priapism in Children with Sickle Cell AnemiaClinical Pediatrics, 1971
- Priapism in Children: a Complication of Sickle Cell DiseaseJournal of Urology, 1971
- Surgical Management of Priapism and Its Sequelae in Sickle Cell DiseaseSouthern Medical Journal, 1966
- Studies in sickle cell anemia: XIX. Priapism as a complication in childrenThe Journal of Pediatrics, 1962