Abstract
Amaç: Bu çalışmada ağrılı krizle gelen orak hücreli anemi hastalarımızın hastaneye yatış sıklığını etkileyen faktörleri bulmayı amaçladık. Materyal ve Metod: Yetmiş i homozigot, 14'ü orak-beta talasemi olan 84 orak hücreli anemi hastası stabil durumdayken çalışmamıza katıldı. Bu çalışmada aynı zamanda 2010 ve 1012 yılları arasında hastalarımızın demografik ve klinik verilerini bildirdik. Bulgular ve Sonuç: Hidroksiüre alan hastaların hastaneye daha sık yattıklarını ve hastaneye yatışla diğer değişkenler arasında bir ilişki olmadığı saptanmıştır. Hastaneye yatış açısından diğer değişkenler yönünden fark bulunamadı.
References
- Carroll CP, Haywood C Jr, Lanzkron S. Prediction of onset and course of high hospital utilization in sickle cell disease. J Hosp Med. 2011;6:248-55.
- Raphael JL, Mei M, Mueller BU, Giordano T. High resource hospitalizations among children with vaso-occlusive crises in sickle cell disease. Pediatr Blood Cancer. 2012;58:584-90.
- Epstein K, Yuen E, Riggio JM, Ballas SK, Moleski SM. Utilization of the office, hospital and emergency department for adult sickle cell patients: a five-year study. J Natl Med Assoc. 2006;98:1109-13.
- Carool CP, Haywood C Jr, Fagan P et al. The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization. Am J Hematol..2009;84:666-70.
- Steinberg MH. Predicting clinical severity in sickle cell anaemia. Br J Haematol. 2005;129:465-81.
- Sebastiani P, Nolan VG, Baldwin CT. A network model to predict the risk of death in sickle cell disease. Blood. 2007;110:2727-35.
- Yazışma Adresi / Address for Correspondence: Dr. Gül İlhan Hatay Antakya Government Hospital Hematology Department ç Hastalıkları Anabilim Dalı HATAY/ANTAKYA E mail: gullhan2002@yahool.com geliş tarihi/received :19.08.2013 kabul tarihi/accepted:16.09.2013
Abstract
Purpose: In this study, we aimed to find factors effecting hospitalization frequency of our sickle cell anemia (SCA) patients with painful crisis. Material and Methods: Eighty four SCA patients in steady-state condition participated to the study: Seventy with homozygous, and 14 with sickle cell-beta thalassemia disease. In this study we also reported demographic and clinical data of our patients from February 2010 to October 2012. Results and Conclusion: We found that patients using hydroxyurea and penicillin prophylaxis stayed in hospital more times than the others. No relationship between high hospitalization and other variables have been found. However genetic differences may be present among these patients which warrant further studies.
References
- Carroll CP, Haywood C Jr, Lanzkron S. Prediction of onset and course of high hospital utilization in sickle cell disease. J Hosp Med. 2011;6:248-55.
- Raphael JL, Mei M, Mueller BU, Giordano T. High resource hospitalizations among children with vaso-occlusive crises in sickle cell disease. Pediatr Blood Cancer. 2012;58:584-90.
- Epstein K, Yuen E, Riggio JM, Ballas SK, Moleski SM. Utilization of the office, hospital and emergency department for adult sickle cell patients: a five-year study. J Natl Med Assoc. 2006;98:1109-13.
- Carool CP, Haywood C Jr, Fagan P et al. The course and correlates of high hospital utilization in sickle cell disease: Evidence from a large, urban Medicaid managed care organization. Am J Hematol..2009;84:666-70.
- Steinberg MH. Predicting clinical severity in sickle cell anaemia. Br J Haematol. 2005;129:465-81.
- Sebastiani P, Nolan VG, Baldwin CT. A network model to predict the risk of death in sickle cell disease. Blood. 2007;110:2727-35.
- Yazışma Adresi / Address for Correspondence: Dr. Gül İlhan Hatay Antakya Government Hospital Hematology Department ç Hastalıkları Anabilim Dalı HATAY/ANTAKYA E mail: gullhan2002@yahool.com geliş tarihi/received :19.08.2013 kabul tarihi/accepted:16.09.2013
Details
| Primary Language | Turkish |
|---|---|
| Journal Section | Research |
| Authors | |
| Publication Date | July 22, 2014 |
| Published in Issue | Year 2014 Volume: 39 Issue: 1 |
