Department of Endocrinology, Austin Health, Melbourne, VIC, Australia.
Med J Aust. 2014 Aug 18;201(4):224-6. doi: 10.5694/mja13.00193.
To investigate the safety, tolerability and efficacy of combination phentermine and topiramate therapy for maintenance of weight loss.
DESIGN, SETTING AND PATIENTS: Retrospective audit of patients attending the Austin Health Weight Control Clinic who were dispensed phentermine-topiramate between 22 January 2010 and 16 July 2012 and after reaching a target weight by following a very low energy diet (VLED). Data collection continued until July 2013.
Number of patients who ceased pharmacotherapy; duration of use of pharmacotherapy; types and numbers of adverse effects; and mean weight and blood pressure measurements at the initial visit, the end of the VLED and the last observation during pharmacotherapy.
Data were available for 103 patients who were dispensed phentermine-topiramate; 61 patients ceased combination pharmacotherapy before the end of the data collection period, 41 due to adverse effects (eg, paraesthesia, cognitive changes, dry mouth and depression). The mean duration of use of pharmacotherapy was 10 months. Mean weight decreased by 10% due to the VLED (from 135.5 kg to 122.5 kg) and this loss was maintained. For 30 patients who continued on phentermine-topiramate, the mean duration of pharmacotherapy was 22 months and the mean weight decreased by 6.7 kg between the end of the VLED and the last observation during pharmacotherapy.
Phentermine-topiramate therapy was not well tolerated; more than half of the patients in our study stopped taking it because of adverse effects, and more than half of the adverse events reported were ascribed to topiramate. However, in those able to continue with pharmacotherapy, the combination was efficacious for both maintenance of weight loss and ongoing weight loss.
研究联合应用安非他酮和托吡酯治疗对维持减肥效果的安全性、耐受性和疗效。
设计、地点和患者:对 2010 年 1 月 22 日至 2012 年 7 月 16 日期间在奥斯汀健康体重控制诊所就诊并在遵循极低能量饮食(VLED)达到目标体重后开出处方安非他酮-托吡酯的患者进行回顾性审计。数据收集持续到 2013 年 7 月。
停止药物治疗的患者数量;药物治疗的持续时间;不良反应的类型和数量;以及初始就诊、VLED 结束时和药物治疗期间最后一次观察时的平均体重和血压测量值。
103 名患者的数据可用,他们开出处方安非他酮-托吡酯;41 名患者因不良反应(如感觉异常、认知改变、口干和抑郁)在数据收集结束前停止联合药物治疗,61 名患者停止联合药物治疗。药物治疗的平均持续时间为 10 个月。由于 VLED,平均体重下降 10%(从 135.5 公斤降至 122.5 公斤),且这一降幅得以维持。对于继续服用安非他酮-托吡酯的 30 名患者,药物治疗的平均持续时间为 22 个月,且 VLED 结束与药物治疗期间最后一次观察之间的平均体重下降 6.7 公斤。
安非他酮-托吡酯治疗耐受性差;我们研究中的一半以上患者因不良反应停止服用该药,报告的一半以上不良反应归因于托吡酯。然而,对于能够继续药物治疗的患者,该联合疗法对维持减肥效果和持续减肥均有效。