Evaluation of outcomes of clinical phenotyping-based treatment for bladder pain syndrome/interstitial cystitis.

Bladder (San Francisco, Calif.) Pub Date : 2024-08-23 eCollection Date: 2024-01-01 DOI:10.14440/bladder.2024.0010
Ankur Sharma, Rajesh Taneja, Apeksha Raheja, Kanishak Mehta, Nilesh Taneja, Ashutosh Singh
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Abstract

Introduction: Bladder pain syndrome/Interstitial cystitis (BPS/IC) is clinically of diverse types because different causes contribute to the development of their symptoms. It is important to classify patients into various groups based on the possible etiopathogenesis of their condition. Treatment may be tailored to each specific group according to the possible cause.

Methodology: Twenty-five patients diagnosed with BPS/IC were categorized into four different clinical phenotypes (CP) based on their history of symptoms, allergy, dysfunctional voiding, neuropathic pain, and the presence of Hunner's ulcer. Some patients could be classified into multiple groups. The patients were given oral pentosan polysulfate, and treatment specific to their CP. Patients in CP1, CP2, and CP3 groups received, respectively hydroxyzine, clonazepam, and amitriptyline. Patients with Hunner's lesions (HL) (CP4) underwent hydro distension and ablation of the lesion, followed by intravesical instillation of heparin and hydrocortisone. The patients were evaluated using the Apollo clinical scoring (ACS) system and their clinical scores were recorded at 1, 3, and 6 month(s).

Results: Among the 25 patients, 5, 7, 4, and 9 patients were classified into CP 1 - CP4 groups respectively, and were all subjected to ACS assessment. In CP1 group (allergy group), 80% (4/5) of patients responded well to the treatment and 20% (1/5) had unsatisfactory responses. In CP2 group (dysfunctional voiding group), 71.42% (5/7) patients had good, and 28.57% (2/7) had excellent responses. In CP3 group (neuropathic pain group), 28.57% (3/4) patients had excellent, and 75% (1/4) patients had good responses. In CP4 group (HL group), 33.33% (3/9) patients had unsatisfactory, 44.44% (4/9) achieved good, and 22.22% (2/9) had excellent responses. Overall, 16% (4/25) patients had unsatisfactory, 56% (14/25) attained good, and 28% (7/25) had an excellent response at the completion of the study.

Conclusion: Using clinical phenotyping-based features indicative of etiology could potentially improve treatment outcomes by targeting the specific pathological processes contributing to the patients' symptoms.

基于临床表型的膀胱疼痛综合征/间质性膀胱炎治疗效果评估。
导言:膀胱疼痛综合征/间质性膀胱炎(BPS/IC)在临床上有多种类型,因为不同的病因会导致不同的症状。根据可能的发病机制将患者分为不同的组别非常重要。治疗方法:根据患者的症状史、过敏史、排尿功能障碍、神经性疼痛以及是否存在亨纳氏溃疡,将 25 名确诊为 BPS/IC 的患者分为四种不同的临床表型(CP)。有些患者可分为多组。患者口服多硫酸戊聚糖,并接受针对其 CP 的治疗。CP1、CP2 和 CP3 组患者分别接受羟嗪、氯硝西泮和阿米替林治疗。有亨纳氏病变(HL)的患者(CP4)接受了肾积水扩张和病变消融术,然后膀胱内灌注肝素和氢化可的松。采用阿波罗临床评分(ACS)系统对患者进行了评估,并记录了1、3和6个月的临床评分:结果:在 25 名患者中,分别有 5、7、4 和 9 名患者被分为 CP1 - CP4 组,并全部接受了 ACS 评估。在 CP1 组(过敏组)中,80%(4/5)的患者对治疗反应良好,20%(1/5)的患者反应不理想。在 CP2 组(排尿功能障碍组)中,71.42%(5/7)的患者反应良好,28.57%(2/7)的患者反应极佳。在 CP3 组(神经性疼痛组)中,28.57%(3/4)的患者反应极佳,75%(1/4)的患者反应良好。在 CP4 组(HL 组)中,33.33%(3/9)的患者反应不满意,44.44%(4/9)的患者反应良好,22.22%(2/9)的患者反应优秀。总体而言,在研究结束时,16%(4/25)的患者反应不满意,56%(14/25)的患者反应良好,28%(7/25)的患者反应优秀:结论:利用基于临床表型的病因学特征,针对导致患者症状的特定病理过程进行治疗,有可能提高治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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