Mouchli M A, Camilleri M, Lee T, Parthasarathy G, Vijayvargiya P, Halland M, Acosta A, Bharucha A E
Clinical Enteric Neuroscience Translational and Epidemiological Research (C.E.N.T.E.R.), Mayo Clinic, Rochester, MN, USA.
Institute for Digestive Research, Soonchunhyang University, Seoul Hospital, Seoul, Korea.
Neurogastroenterol Motil. 2016 Jun;28(6):871-8. doi: 10.1111/nmo.12786. Epub 2016 Feb 3.
Neostigmine, an acetyl cholinesterase inhibitor, stimulates colonic motor activity and may induce vagally mediated cardiovascular effects. Our aim was to evaluate effects of i.v. neostigmine on colonic compliance and its safety in patients with chronic constipation.
We retrospectively reviewed medical records of a selected group of 144 outpatients with chronic constipation who were refractory to treatment. These patients had undergone intracolonic motility and compliance measurements with an infinitely compliant balloon linked to a barostat. Data abstracted included barostat balloon mean volumes with increases in pressure (4 mmHg steps from 0 to 44 mmHg) before and after i.v. neostigmine. Vital signs and oxygen saturation before and after neostigmine were recorded.
Of the 144 patients, 133 were female, mean age was 41.0 ± 15.4 years (SD), and duration of constipation was 12.9 ± 13.8 years. Among patients who had undergone colonic transit measurement by scintigraphy, the overall colonic transit at 24 h (geometric center, GC24 [n = 115]) was 1.5 ± 0.7 (normal >1.3), and at 48 h (GC48 [n = 75]) it was 2.3 ± 0.9 (normal >1.9). Neostigmine decreased colonic compliance at lower distension pressures (e.g., 12 and 20 mmHg [both p < 0.001]), but not at 40 mmHg. There were expected minor changes in vital signs in response to neostigmine in 144 patients; however, one patient developed unresponsiveness, significant bradycardia, hypotension, and muscular rigidity that responded to 400 mcg i.v. atropine.
CONCLUSIONS & INFERENCES: Neostigmine significantly decreases colonic compliance in patients with refractory chronic constipation. Symptomatic bradycardia in response to neostigmine should be promptly reversed with atropine.
新斯的明是一种乙酰胆碱酯酶抑制剂,可刺激结肠运动活性,并可能诱发迷走神经介导的心血管效应。我们的目的是评估静脉注射新斯的明对慢性便秘患者结肠顺应性的影响及其安全性。
我们回顾性分析了一组144例对治疗无效的慢性便秘门诊患者的病历。这些患者接受了通过与恒压器相连的无限顺应性球囊进行的结肠动力和顺应性测量。提取的数据包括静脉注射新斯的明前后,恒压器球囊在压力增加时(从0至44 mmHg,每次增加4 mmHg)的平均容积。记录新斯的明前后的生命体征和血氧饱和度。
144例患者中,133例为女性,平均年龄为41.0±15.4岁(标准差),便秘持续时间为12.9±13.8年。在通过闪烁扫描法进行结肠转运测量的患者中,24小时时的总体结肠转运(几何中心,GC24 [n = 115])为1.5±0.7(正常>1.3),48小时时(GC48 [n = 75])为2.3±0.9(正常>1.9)。新斯的明在较低扩张压力下(例如12和20 mmHg [均p < 0.001])降低了结肠顺应性,但在40 mmHg时未降低。144例患者中,新斯的明引起的生命体征出现了预期的轻微变化;然而,有1例患者出现无反应、显著心动过缓、低血压和肌肉强直,静脉注射400 mcg阿托品后症状得到缓解。
新斯的明显着降低难治性慢性便秘患者的结肠顺应性。新斯的明引起的症状性心动过缓应立即用阿托品逆转。