摘要
目的探讨三联药物膀胱灌注联合生物反馈治疗女性间质性膀胱炎/膀胱疼痛综合征(IC/PBS)的临床疗效。方法选取26例女性IC/PBS患者为研究对象,均行三联药物混合溶液(2%利多卡因20ml+肝素钠10万U+5%碳酸氢钠10ml+0.9%氯化钠溶液20ml)膀胱灌注,膀胱内保留1h后自行排出,1次/周,疗程2个月;同时联合生物反馈治疗,第1个月强化治疗(5次/周),第2个月间断治疗(3次/周),疗程2个月。比较治疗前与治疗1、2个月时O'Le a ry-Sa nt间质性膀胱炎症状评分(ICSI)、问题评分标准(ICPI)、盆腔疼痛及尿频评分(PUF)、焦虑自评量表评分(SAS)、24h日间及夜间排尿次数、平均每次排尿量、不良反应发生情况等。结果26例患者均完成全部治疗过程。治疗1、2个月时ICSI、ICPI、PUF、SAS、24h日间及夜间排尿次数、平均每次排尿量均较治疗前明显改善(均P<0.05)。治疗期间有1例患者首次膀胱灌注后出现轻度体温升高,未予特殊处理,后续灌注无明显不适;2例患者首次灌注后出现膀胱区疼痛加重,可耐受,继续接受第2次膀胱灌注后上述感觉逐渐消失。所有患者均未发生严重不良反应。结论三联药物膀胱灌注联合生物反馈治疗女性IC/PBS安全有效,易被患者接受。
引文
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