Marciniak Christina M, Toledo Santiago, Lee Jungwha, Jesselson Michael, Bateman Jillian, Grover Benjamin, Tierny Joy
Christina M Marciniak, Santiago Toledo, Department of Physical Medicine and Rehabilitation, School of Medicine, Northwestern University, Chicago, IL 60611, United States.
World J Gastroenterol. 2014 Nov 21;20(43):16323-33. doi: 10.3748/wjg.v20.i43.16323.
To investigate the efficacy of lubiprostone compared to Senna on bowel symptoms and constipation in post-operative orthopedic patients treated with opioids.
In this double blind, randomized, active comparator trial, adults who required opioids for analgesia following orthopedic procedures and who were admitted in inpatient rehabilitation were randomized following baseline assessments to lubiprostone (Amitza(®)), orally twice a day or Senna (generic) two capsules administered daily for six days. Subjects were assessed using the patient assessment of constipation (PAC)-symptoms (PAC-SYM) and the PAC-quality of life (PAC-QOL) scales measured at baseline and Day 7; Subjects were assessed daily for secondary measures included the Bristol stool scale bowel consistency, specific bowel symptom score (Nausea, cramping, straining, completeness, abdominal pain, time per lavatory attempt, assistance needed), adverse events and rescue medications required. Function was measured using the functional independence measure (FIM) at admission and discharge; length of stay (LOS) and missed treatments due to gastrointestinal symptoms were also assessed.
64 adults were enrolled; 56 participants (28 in each group) had baseline and follow up measures and were included in the intention to treat (ITT) analyses. 43 participants completed the study, 21 in the active lubiprostone and 22 in the active Senna group. The mean age of the participants was 71.5 years (SD = 11.4 years, range: 28-96 years). In the ITT analyses, participants showed significant improvement in bowel symptoms as measured by the PAC-SYM (mean ± SD, -0.28 ± 0.60, range: -1-2.33) and PAC-QOL (mean ± SD, 0.33 ± 0.81, range: -1.5-2.0) over time, but there were no significant differences between the lubiprostone and Senna groups in mean change in the PAC-SYM (-0.20 ± 0.60 vs -0.36 ± 0.61, P = 0.61 respectively) or the PAC-QOL (0.29 ± 0.76 vs 0.37 ± 0.87, P = 0.61 respectively). The mean change in each bowel symptom also did not significantly differ between treatment groups on ITT analyses, except for completeness of bowel movement, with the Senna group showing greater negative mean change in bowel movement completeness (-0.56 ± 1.01 vs -2.00 ± 1.41, P = 0.03) and for reduction of abdominal pain, favoring Senna (-0.14 ± 0.73 vs -0.73 ± 1.08, P = 0.04). Fifteen (75%) participants in the lubiprostone and in the Senna group requested rescue treatments. Participants made significant functional improvement from admission to discharge over a median LOS of 12 d, with a mean FIM change of 29.13 ± 13.58 and no significant between group differences (27.0 ± 9.2 vs 31.5 ± 16.6, P = 0.27).
Both lubiprostone and Senna improved constipation-related symptoms and QOL in opioid-induced constipation, with no significant between-group differences.
研究鲁比前列酮与番泻叶相比,对接受阿片类药物治疗的骨科术后患者肠道症状和便秘的疗效。
在这项双盲、随机、活性对照试验中,骨科手术后需要使用阿片类药物镇痛且入住住院康复病房的成年人,在基线评估后被随机分为两组,一组每日口服两次鲁比前列酮(Amitza(®)),另一组每日服用两粒番泻叶(非专利药),共服用六天。使用患者便秘评估(PAC)-症状(PAC-SYM)量表和PAC-生活质量(PAC-QOL)量表在基线和第7天对受试者进行评估;每天对受试者进行次要指标评估,包括布里斯托大便分类法的大便稠度、特定肠道症状评分(恶心、绞痛、用力、排便完全感、腹痛、每次如厕尝试时间、所需协助)、不良事件和所需的解救药物。在入院时和出院时使用功能独立性测量(FIM)评估功能;还评估住院时间(LOS)和因胃肠道症状而错过的治疗。
共纳入64名成年人;56名参与者(每组28名)有基线和随访测量数据,并纳入意向性分析(ITT)。43名参与者完成了研究,鲁比前列酮活性组21名,番泻叶活性组22名。参与者的平均年龄为71.5岁(标准差=11.4岁,范围:28-96岁)。在ITT分析中,随着时间的推移,参与者的肠道症状通过PAC-SYM(平均值±标准差,-0.28±0.60,范围:-1至2.33)和PAC-QOL(平均值±标准差,0.33±0.81,范围:-1.5至2.0)测量有显著改善,但鲁比前列酮组和番泻叶组在PAC-SYM的平均变化(分别为-0.20±0.60和-0.36±0.61,P=0.61)或PAC-QOL的平均变化(分别为0.29±0.76和0.37±0.87,P=0.61)方面没有显著差异。在ITT分析中,除排便完全感外,各治疗组之间每种肠道症状的平均变化也没有显著差异,番泻叶组在排便完全感方面的平均负变化更大(-0.56±1.01对-2.00±1.41,P=0.03),在腹痛减轻方面,番泻叶组更具优势(-0.14±0.73对-0.73±1.08,P=0.04)。鲁比前列酮组和番泻叶组各有15名(75%)参与者请求解救治疗。参与者从入院到出院功能有显著改善,中位住院时间为12天,FIM平均变化为29.13±13.58,组间无显著差异(27.0±9.2对31.5±16.6,P=0.27)。
鲁比前列酮和番泻叶均可改善阿片类药物引起的便秘相关症状和生活质量,组间无显著差异。