Effectiveness and safety of lubiprostone after switching from stimulant laxatives in elderly patients with chronic constipation

Author:

Maruyama Masaki1ORCID,Miida Suguru1,Sato Toshihiro2,Kimura Takazumi3,Watanabe Azuma4,Watanabe Hideo5,Nishizawa Masafumi6,Horikawa Kyohei7,Kajiwara Takahiro8,Karasawa Yusuke9ORCID,Hasebe Yuko9,Nozawa Kazutaka9ORCID,Terai Shuji10ORCID

Affiliation:

1. Department of Internal Medicine Kashiwazaki General Hospital and Medical Center Kashiwazaki Niigata Japan

2. Sato Clinic Kashiwazaki Niigata Japan

3. Kimura Internal Medicine Clinic Yokohama Kanagawa Japan

4. Department of Gastroenterology Kameda Daiichi Hospital Niigata Japan

5. Department of Surgery Watanabe Hospital Matsuyama Ehime Japan

6. Department of Internal Medicine Minamisanriku Hospital Motoyoshi‐gun Miyagi Japan

7. Wakamatsuen Health Care Facility for the Elderly Okinawa Japan

8. Lotus Care Center, Health Care Facility for the Elderly Chiba Japan

9. Medical Affairs, Viatris Pharmaceuticals Japan Inc. Tokyo Japan

10. Division of Gastroenterology & Hepatology, Graduate School of Medical and Dental Sciences Niigata University Niigata Japan

Abstract

AbstractBackground and AimStimulant laxatives may cause electrolyte abnormalities, dehydration, and abdominal pain; their long‐term use can lead to tolerance and subsequent refractory constipation. We investigated the effectiveness, safety, and quality of life after switching from stimulant laxatives to lubiprostone in elderly patients with chronic constipation (CC).MethodsThis multicenter, interventional, open‐label, single‐arm, before‐and‐after comparison study enrolled 99 Japanese patients aged 65–90 years with CC who took stimulant laxatives for ≥2 weeks prior to switching to lubiprostone monotherapy.ResultsThe mean ± SD spontaneous defecations at Week 1 of 7.8 ± 6.2 times/week was not significantly different from that at baseline (8.3 ± 4.7). Spontaneous defecations were significantly reduced at Weeks 2 (−1.5 ± 4.0, P < 0.001) and 4 (−1.5 ± 3.7, P < 0.001). The Bristol Stool Form Scale score did not change from baseline (4.7 ± 0.9) at Weeks 1 (4.5 ± 1.3) or 4 (4.3 ± 1.3), but it did at Week 2 (4.3 ± 1.5, P < 0.05). The Patient Assessment of Constipation Quality of Life questionnaire score increased (0.36 ± 0.07, P < 0.001) after 28 days. Nausea was the only symptom that worsened from baseline and was the most frequently reported adverse drug reaction (15.2%).ConclusionSwitching to lubiprostone monotherapy for CC was not associated with significant concerns in short‐term spontaneous defecation frequency and safety, but it might affect the efficacy and patient quality of life over 2 weeks. Careful treatment strategies facilitating gradual switching to lubiprostone monotherapy may be needed in patients using stimulant laxatives.

Publisher

Wiley

Subject

Gastroenterology,Hepatology

Reference28 articles.

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2. Evaluation of efficacy and safety of lubiprostone in patients with chronic constipation

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