Verne G N, Eaker E Y, Hardy E, Sninsky C A
Gainesville Veterans Affairs Medical Center, Florida 32608-1197, USA.
Dig Dis Sci. 1995 Sep;40(9):1892-901. doi: 10.1007/BF02208652.
Treatment of chronic intestinal pseudoobstruction with prokinetic agents has been disappointing. Our study was designed to determine if octreotide and erythromycin would provide sustained relief from nausea, abdominal pain, and bloating in pseudoobstruction. Using gastrointestinal manometry, quantitative parameters of the activity front of the migrating motor complex at baseline and after prokinetic therapy with erythromycin and octreotide were determined in 14 patients with intestinal pseudoobstruction who had nausea, abdominal pain, and bloating. Patients were treated with erythromycin and octreotide for 20-33 weeks. Octreotide increased the frequency, duration, and motility index of activity fronts (AFs) from 1.2 +/- 0.3 AFs/4 hr, 2.7 +/- 0.7 min, and 85 +/- 23 min mm Hg to 4.1 +/- 0.8 AFs/4 hr, 5.5 +/- 0.7 min, and 152 +/- 24 min mm Hg, respectively (P < 0.05). Antral activity was decreased from 63 +/- 14 to 23 +/- 8% by octreotide (P < 0.05). Erythromycin induced antral activity; however, small intestinal motor activity was suppressed. While on erythromycin and octreotide, five patients had long-term improvement of nausea and abdominal pain. All responders had at least 5 AFs/4 hr induced by octreotide. We conclude that octreotide and erythromycin relieve abdominal pain and nausea in pseudoobstruction. Patients who have at least 5 AFs/4 hr after octreotide administration are most likely to clinically respond.
使用促动力剂治疗慢性肠道假性梗阻一直不尽人意。我们的研究旨在确定奥曲肽和红霉素是否能持续缓解假性梗阻患者的恶心、腹痛和腹胀症状。通过胃肠测压法,测定了14例伴有恶心、腹痛和腹胀的肠道假性梗阻患者在基线时以及接受红霉素和奥曲肽促动力治疗后的移行性运动复合波活动前沿的定量参数。患者接受红霉素和奥曲肽治疗20 - 33周。奥曲肽使活动前沿(AFs)的频率、持续时间和动力指数分别从1.2±0.3次AFs/4小时、2.7±0.7分钟和85±23分钟毫米汞柱增加至4.1±0.8次AFs/4小时、5.5±0.7分钟和152±24分钟毫米汞柱(P < 0.05)。奥曲肽使胃窦活动从63±14%降至23±8%(P < 0.05)。红霉素诱导胃窦活动;然而,小肠运动活动受到抑制。在使用红霉素和奥曲肽期间,5例患者的恶心和腹痛得到长期改善。所有有反应者在使用奥曲肽后至少有5次AFs/4小时。我们得出结论,奥曲肽和红霉素可缓解假性梗阻患者的腹痛和恶心。奥曲肽给药后至少有5次AFs/4小时的患者最有可能出现临床反应。