Mayo Clinic Arizona, Department of Urology, Phoenix, AZ, USA.
Phoenix Children's Hospital, Department of Research, Phoenix, AZ, USA.
J Pediatr Urol. 2024 Jun;20(3):487.e1-487.e6. doi: 10.1016/j.jpurol.2024.02.011. Epub 2024 Feb 15.
Hemorrhagic cystitis (HC) is a devastating complication of bone marrow (BMT) and stem cell transplant (SCT). Much of the literature has focused on exclusively adult patient populations, with limited evidence regarding risk factors for mortality and morbidity among pediatric HC patients.
To examine factors associated with all-cause mortality in children with HC after BMT/SCT.
The Pediatric Health Information System database was queried for patients with ICD-9/10 codes for hematopoietic transplant and gross hematuria, hematuria unspecified, or cystitis with hematuria. Multivariable logistic regression examined association of medical and surgical interventions frequently employed for hemorrhagic cystitis with mortality and genitourinary morbidity, defined as having received instillation of any bladder medication or having undergone any genitourinary procedure.
A total of 811 patients, mean age of 12.4 years and 62% male, were included. Primary diagnosis included 388 (49%) leukemia/lymphoma, 182 (22%) blood dyscrasia, 99 (12%) solid organ tumor, 27 (3%) metabolic disease, 115 (14%) unknown. Transplant type included 377 (46%) bone marrow, 329 (41%) stem cell, 105, and (13%) unknown. Performing any bladder instillation (p < 0.0001) or any type of GU procedure (p < 0.0001) was significantly associated with mortality. On multivariate analysis, dialysis (OR = 10.7, 95% CI = 5.7-20.2), genitourinary morbidity (OR = 4, 95% CI = 2.2-6.8) and intravenous cidofovir (OR = 2.0, 95% CI = 1.2-3.3) were significantly associated with all cause mortality. Having an underlying diagnosis of blood dyscrasia was protective against mortality (OR = 0.425, CI = 0.205-0.88).
In this large retrospective study evaluating factors associated with mortality in children with HC, all cause mortality was found to be 11%. This is probably an underrepresentation of true mortality in this population, as many patients discharged from the hospital likely die outside the hospital at home or hospice care. This study supports the current literature that invasive GU procedures are not associated with increased survival in patients with severe HC. This study is limited by retrospective use of a billing database that has the potential for errors in data entry and missing data. Patients who were discharged from the hospital were not captured by the PHIS which only collects data from inpatient stays.
Patients with HC who received dialysis, intravenous cidofovir, or underwent GU intervention had significantly higher all-cause mortality. High grade HC is a marker of disease severity and efforts should be made by urologists and oncologists to maximize quality of life and limit futile treatments in this patient population.
骨髓(BMT)和干细胞移植(SCT)后的出血性膀胱炎(HC)是一种毁灭性的并发症。大多数文献都集中在专门的成年患者群体上,关于儿科 HC 患者的死亡率和发病率的风险因素的证据有限。
检查与 BMT/SCT 后儿童 HC 全因死亡率相关的因素。
通过 ICD-9/10 代码查询儿科健康信息系统数据库,用于造血移植和肉眼血尿、血尿不明或伴有血尿的膀胱炎。多变量逻辑回归检查了频繁用于治疗出血性膀胱炎的医疗和手术干预措施与死亡率和泌尿生殖系统发病率(定义为接受任何膀胱药物灌注或接受任何泌尿生殖系统手术)之间的关联。
共纳入 811 例患者,平均年龄 12.4 岁,男性占 62%。主要诊断包括 388 例(49%)白血病/淋巴瘤、182 例(22%)血液系统疾病、99 例(12%)实体器官肿瘤、27 例(3%)代谢疾病、115 例(14%)未知。移植类型包括 377 例(46%)骨髓、329 例(41%)干细胞、105 例(13%)未知。进行任何膀胱灌注(p<0.0001)或任何类型的 GU 手术(p<0.0001)与死亡率显著相关。多变量分析显示,透析(OR=10.7,95%CI=5.7-20.2)、泌尿生殖系统发病率(OR=4,95%CI=2.2-6.8)和静脉注射更昔洛韦(OR=2.0,95%CI=1.2-3.3)与全因死亡率显著相关。存在血液系统疾病的基础诊断可降低死亡率(OR=0.425,CI=0.205-0.88)。
在这项评估儿童 HC 相关死亡率因素的大型回顾性研究中,全因死亡率为 11%。这可能是该人群实际死亡率的低估,因为许多从医院出院的患者很可能在家或临终关怀中死于医院外。本研究支持目前的文献,即严重 HC 患者的侵入性 GU 手术与生存率的提高无关。本研究的局限性在于使用计费数据库进行回顾性研究,该数据库可能存在数据录入错误和数据缺失的可能性。出院患者未被 PHIS 捕获,PHIS 仅收集住院患者的数据。
接受透析、静脉注射更昔洛韦或接受 GU 干预的 HC 患者全因死亡率显著升高。高级别 HC 是疾病严重程度的标志,泌尿科医生和肿瘤学家应努力提高该患者群体的生活质量并限制无效治疗。