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Predictive Factors of Renal Damage during Sickle Cell Disease at the Hematology-Oncology Department of Donka University Hospital

Predictive Factors of Renal Damage during Sickle Cell Disease at the Hematology-Oncology Department of Donka University Hospital

作     者:Moussa Traoré Ansoumane Sayon Kanté Marthe Sidibé Mamady Diakité Mohammed Lamine Tégui Camara Foussény Diakité Mamadou Saliou Baldé Ibrahima Chérif Mustapha Komrabai-Kanu Mohammed Lamine Kaba Moussa Traoré;Ansoumane Sayon Kanté;Marthe Sidibé;Mamady Diakité;Mohammed Lamine Tégui Camara;Foussény Diakité;Mamadou Saliou Baldé;Ibrahima Chérif;Mustapha Komrabai-Kanu;Mohammed Lamine Kaba

作者机构:Nephrology-Hemodialysis Department of Donka University Hospital Conakry Guinea Hematology-Oncology Department of Donka University Hospital Conakry Guinea Hematology-Oncology Department of Ignace Deen University Hospital Conakry Guinea Medical Care Clinic Freetown Sierra-Leone 

出 版 物:《Open Journal of Nephrology》 (肾脏病(英文))

年 卷 期:2024年第14卷第3期

页      面:302-312页

学科分类:1002[医学-临床医学] 100210[医学-外科学(含:普外、骨外、泌尿外、胸心外、神外、整形、烧伤、野战外)] 10[医学] 

主  题:Kidney Damage Predictive Factors Sickle Cell Disease Donka 

摘      要:Introduction: Sickle cell disease, which is the most common hereditary hemoglobinopathy in the world, attacks all body systems, particularly the kidneys. The view of this study was to investigate the predictive factors of kidney damage during sickle cell disease. Materials and methods: It was a retrospective, descriptive and analytical study on files of sickle cell patients hospitalized in the Hematology-Oncology Department of Donka University Hospital during a period from January 1, 2016 to December 31, 2019. Records of sickle cell patients with one or more renal abnormalities were retained. Sickle cell patients without kidney damage were also selected for a comparative study. Only patients without sickle cell disease were excluded. Results: Seventy-five (75) medical records were collected during the study period. From these cases, thirteen (13) records with kidney disease were observed, a frequency of 17%. The mean age of patients was 24.2 years for extremes of 10 and 65 years. The sex ratio was 1.6 in favor of men. The SSFA 2 form was the most represented with 92%. 24-hour proteinuria was measured in 13 patients between whom 6 patients (46.2%) had a proteinuria level ≤ 1 g. Eight (8) patients (61.5%) were in stage 1 of chronic kidney disease. The most common type of renal involvement was tubulo-interstitial nephropathy with 8 patients (61.5%). Bivariate analysis showed that elevated serum creatinine (P 0.001), elevated serum uremia (P 0.001) and the SSFA 2 form of the sickness (P 0.003) were the main factors linked with renal damage in sickle cell patients. Conclusio n: After the observation of an increased serum creatinine and urea, a predominance observation of the SSFA 2 form, it should be possible to target patients for whom screening for kidney damage should henceforth be systematic.

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