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镰状细胞病患儿肾脏并发症的早期检测:一项单中心前瞻性研究

Early Detection of Renal Complication in Children With Sickle Cell Disease: A Single Center Prospective Study.

作者信息

Alghorayed Raghad, Alsubayni Bashaer, Hanafy Ehab, Mustafa Mohammed, Albalawi Naif, El-Shereif Shimaa, Ahmed Muawia, M B Yassir, Moustafa Yassin, Al Blewi Sawsan M

机构信息

Pediatrics, King Salman Armed Forces Hospital, Tabuk, SAU.

Prince Sultan Oncology Center, King Salman Armed Forces Hospital, Tabuk, SAU.

出版信息

Cureus. 2024 Jul 8;16(7):e64058. doi: 10.7759/cureus.64058. eCollection 2024 Jul.

Abstract

INTRODUCTION

This observational cross-sectional study aimed to identify predictors of renal complications in pediatric patients with sickle cell disease (SCD) at King Salman Armed Forces Hospital, Tabuk, Saudi Arabia, over six months from February 2023 to July 2023. The study evaluated microalbuminuria as an early indicator of renal injury and explored its correlations with clinical and laboratory parameters and abdominal ultrasound (US) findings.

METHODS

Included were pediatric patients aged 1 to 14 years with confirmed SCD, excluding those with acute infections or pre-existing renal diseases. Data from 100 patients' electronic medical records were analyzed using IBM SPSS Statistics for Windows, Version 26 (Released 2019; IBM Corp., Armonk, New York, United States), with a significance set at p ≤ 0.05.

RESULTS

The mean age was 7.6 ± 3.3 years, with 51 males and 49 females; 11 were diagnosed with Hb-S-beta thalassemia. Hydroxyurea (HU) compliance was high, with only four non-compliant patients, though all took folic acid. Among 42 tested for albuminuria, all had negative results (<30 mg/g creatinine). A significant association was found between SCD diagnosis and kidney, ureter, and bladder (KUB) US results (p=0.008), with abnormal KUB findings more prevalent in the Hb-S-beta thalassemia group. Patients with abnormal KUB results had significantly lower mean weight (p=0.024). Additionally, Hb-S-beta thalassemia patients had lower mean weight than hemoglobin SS (HGSS) patients (p=0.04). Though not statistically significant, Hb-S-beta thalassemia patients had higher mean systolic blood pressure (p=0.053).

CONCLUSION

Significant associations were identified between SCD diagnosis type and renal US results, with lower body weight emerging as a potential predictor of renal complications. High HU compliance and its impact on renal outcomes warrant further investigation. Routine monitoring of microalbuminuria and KUB US may aid early detection of renal complications in pediatric SCD patients. Further studies with larger sample sizes are recommended to validate these findings and develop comprehensive renal protective strategies.

摘要

引言

这项观察性横断面研究旨在确定2023年2月至2023年7月在沙特阿拉伯塔布克的国王萨勒曼武装部队医院中镰状细胞病(SCD)儿科患者发生肾脏并发症的预测因素。该研究评估了微量白蛋白尿作为肾损伤的早期指标,并探讨了其与临床和实验室参数以及腹部超声(US)检查结果的相关性。

方法

纳入年龄在1至14岁之间确诊为SCD的儿科患者,排除患有急性感染或既往有肾脏疾病的患者。使用IBM SPSS Statistics for Windows 26版(2019年发布;IBM公司,美国纽约州阿蒙克)对100例患者的电子病历数据进行分析,显著性设定为p≤0.05。

结果

平均年龄为7.6±3.3岁,其中男性51例,女性49例;11例被诊断为血红蛋白S-β地中海贫血。羟基脲(HU)的依从性较高,只有4例不依从患者,不过所有患者都服用了叶酸。在42例接受蛋白尿检测的患者中,所有结果均为阴性(<30mg/g肌酐)。发现SCD诊断与肾脏、输尿管和膀胱(KUB)超声结果之间存在显著关联(p=0.008),KUB检查异常结果在血红蛋白S-β地中海贫血组中更为普遍。KUB结果异常的患者平均体重显著较低(p=0.024)。此外,血红蛋白S-β地中海贫血患者的平均体重低于血红蛋白SS(HGSS)患者(p=0.04)。尽管无统计学意义,但血红蛋白S-β地中海贫血患者的平均收缩压较高(p=0.053)。

结论

确定了SCD诊断类型与肾脏超声结果之间存在显著关联,较低的体重成为肾脏并发症的潜在预测因素。高HU依从性及其对肾脏结局的影响值得进一步研究。对微量白蛋白尿和KUB超声进行常规监测可能有助于早期发现儿科SCD患者的肾脏并发症。建议进行更大样本量的进一步研究以验证这些发现并制定全面的肾脏保护策略。

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