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Department of General Internal Medicine, Johns Hopkins Hospital, Baltimore, Maryland
Given name(s)
Naveen
Family name
Pemmaraju
Degrees
MD

Solifenacin‐Induced Small Bowel Pseudo‐Obstruction

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Solifenacin‐induced small bowel pseudo‐obstruction

Solfenacin succinate, an antimuscarinic agent, is approved for the treatment of overactive bladder and described as well tolerated in the elderly.1 We present the case of solifenacin‐induced small bowel pseudo‐obstruction in an 89‐year‐old woman.

FINDINGS

An 89‐year‐old woman with untreated stage 0 chronic lymphocytic leukemia and a history of stage III colorectal cancer treated with hemicolectomy and adjuvant capecitabine in 2003 was admitted to Johns Hopkins Hospital in 2006. She reported feeling dehydrated, nauseated, and constipated, with decreased output from her colostomy. She also noted no urine output for 4 days and felt that she had to urinate, but I can't. This coincided with a decrease in fluid intake. She denied fevers, chills, abdominal pain, or loss of appetite. While waiting to be seen in the emergency department, the patient was finally able to urinate.

She had no evidence of colon cancer recurrence, with a normal postoperative positron‐emission tomography (PET) scan in 2003, colonoscopy in 2005, and screening computerized tomography (CT) scan in 2005. She also had a history of well‐controlled hypertension and hypothyroidism, hyperlipidemia, chemotherapy‐induced neuropathy, and anxiety.

Her home medication regimen included solifenacin 5 mg once daily (started 10 days prior to her admission) for bladder overactivity, buspirone 5 mg 3 times a day, metoprolol 25 mg twice a day, pantoprazole 40 mg once daily, levothyroxine 100 g once daily, lisinopril/hydrochlorathiazide 20 mg/25 mg twice daily, gabapentin 300 mg twice a day, and fenofibrate 145 mg nightly.

The patient appeared nontoxic. Her exam was remarkable only for hypoactive bowel sounds and mild diffuse abdominal tenderness without distension or peritoneal signs. A Foley catheter was placed, and her postvoid residual was only 50 cc of urine. Her admission serum blood urea nitrogen and creatinine were 90 and 3.4 mg/dL, respectively, as compared with 18 and 0.8 mg/dL 2 months prior to presentation. A CT scan of the abdomen (Figure 1) revealed multiple dilated loops of small bowel with a transition point at the left lower quadrant ostomy site, consistent with a small bowel obstruction. A PET scan revealed no evidence of malignancy. A renal ultrasound showed no evidence of obstruction.

Figure 1
Long arrow: dilated loop of small bowel with air fluid levels. Short arrow: decompressed loop of small bowel distal to the obstruction.

With cessation of solifenacin and lisinopril/hydrochlorothiazide and hydration with normal saline, her constipation resolved, as did her acute renal failure and perception of urinary retention. She began to tolerate a regular diet after 4 days of hospitalization, and her colostomy output normalized. At follow‐up 8 months after admission, her creatinine was 0.8 mg/dL, and a screening abdominal CT showed complete resolution of the small bowel obstruction.

DISCUSSION

We believe that this patient developed small bowel pseudo‐obstruction as well the feeling of urinary retention because of treatment with solifenacin, an antimuscarinic agent approved for the treatment of bladder overactivity. Her acute renal failure was a result of prerenal azotemia. This particular patient was at increased risk for developing antimuscarinic‐induced bowel obstruction because of her previous surgery and exposure to chemotherapy.

In the 4 randomized trials cited in the prescribing information for solifenacin,2 only 189 patients of the 1811 who received the active drug were greater than 75 years old. Healthy elderly patients ranging from 64 to 78 years of age (mean 68.0 years) who received 2 weeks of treatment with solifenacin 5 and 10 mg had a mean AUC024 that was approximately 20% higher than that of younger subjects.3 In the 4 12‐week double‐blind clinical trials in which 1158 patients were treated with solifenacin 10 mg, there were 3 serious intestinal adverse events: 1 patient had a fecal impaction, 1 patient had a colonic obstruction, and 1 patient had an intestinal obstruction.2 Patients receiving solifenacin 5 and 10 mg were more likely to experience constipation than those receiving placebo (5.4%, 13.4%, and 2.9%, respectively).2 Given the dearth of clinical data on patients greater than 75 years old, the effects of age on the pharmacokinetics, the higher likelihood of bowel pathology in the elderly, the increased risk of solifenacin‐induced side effects in the elderly as reported in the pooled analysis of patients at least 65 years old,4 and the small clinical benefit of solifenacin,46 physicians should seriously consider whether the benefits of solifenacin outweigh both the known and the possible risks. 0

Randomized Placebo‐Controlled Double‐Blind Studies of Solifenacin
Patients in safety analysis (n) Constipation, n (%) Micturition/24 hours
Placebo 5 mg 10 mg Placebo 5 mg 10 mg Baseline Mean decrease from baseline
Placebo 5 mg 10 mg
  • Trials lasted 12 weeks and did not utilize an intention‐to‐treat analysis.

  • Inclusion criteria: men and women at least 18 years old, symptoms of overactive bladder syndrome for at least 3 months, average frequency of at least 8 voids/24 hours.

  • Exclusion criteria included significant bladder outlet obstruction, postvoid residual > 200 mL, presence of a neurological cause for detrusor muscle overactivity, any medical condition contraindicating the use of antimuscarinic medication, diabetic neuropathy, and use of any drugs with cholinergic or anticholinergic side effects.

  • Pooled analysis of patients at least 65 years old in Chapple et al.,6 Cardozo et al.,4 and 2 unpublished studies.1

Chapple et al.6* 267 279 268 5 (1.9) 20 (7.2) 21 (7.8) 12.0812.32 1.2 2.19 2.61
Cardozo et al.4* 301 299 307 6 (2.0) 11 (3.7) 28 (9.1) 12.0512.31 1.59 2.37 2.81
Wagg3 422 192 431 18 (4.3) 18 (9.4) 78 (18.1) 11.611.7 1.1 2.0 2.5
References
  1. Chapple CR.Solifenacin provides effective antimuscarinic therapy for the complete management of overactive bladder.Expert Opin Pharmacother.2006;7:24212434.
  2. Yamanouchi Pharma America, Inc.United States prescribing information for solifenacin succinate (Vesicare®), November2004.
  3. Krauwinkel WJ,Smulders RA,Mulder H,Swart PJ,Taekema‐Roelvink ME.Effect of age on the pharmacokinetics of solifenacin in men and women.Int J Clin Pharmacol Ther.2005;43:227238.
  4. Wagg A,Wyndaele JJ,Sieber P.Efficacy and tolerability of solifenacin in elderly subjects with overactive bladder syndrome: a pooled analysis.Am J Geriatr Pharmacother.2006;4(1):1424.
  5. Cardozo L,Lisec M,Millard R, et al.Randomized, double‐blind placebo controlled trial of the once daily antimuscarinic agent solifenacin succinate in patients with overactive bladder.J Urol.2004;172(5 Pt 1):19191924.
  6. Chapple CR,Rechberger T,Al‐Shukri S, et al.Randomized, double‐blind placebo‐ and tolterodine‐controlled trial of the once‐daily antimuscarinic agent solifenacin in patients with symptomatic overactive bladder.BJU Int.2004;93:303310.
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Journal of Hospital Medicine - 3(2)
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176-178
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solifenacin, Vesicare, small bowel obstruction, urinary retention, intestinal pseudo‐obstruction
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Solfenacin succinate, an antimuscarinic agent, is approved for the treatment of overactive bladder and described as well tolerated in the elderly.1 We present the case of solifenacin‐induced small bowel pseudo‐obstruction in an 89‐year‐old woman.

FINDINGS

An 89‐year‐old woman with untreated stage 0 chronic lymphocytic leukemia and a history of stage III colorectal cancer treated with hemicolectomy and adjuvant capecitabine in 2003 was admitted to Johns Hopkins Hospital in 2006. She reported feeling dehydrated, nauseated, and constipated, with decreased output from her colostomy. She also noted no urine output for 4 days and felt that she had to urinate, but I can't. This coincided with a decrease in fluid intake. She denied fevers, chills, abdominal pain, or loss of appetite. While waiting to be seen in the emergency department, the patient was finally able to urinate.

She had no evidence of colon cancer recurrence, with a normal postoperative positron‐emission tomography (PET) scan in 2003, colonoscopy in 2005, and screening computerized tomography (CT) scan in 2005. She also had a history of well‐controlled hypertension and hypothyroidism, hyperlipidemia, chemotherapy‐induced neuropathy, and anxiety.

Her home medication regimen included solifenacin 5 mg once daily (started 10 days prior to her admission) for bladder overactivity, buspirone 5 mg 3 times a day, metoprolol 25 mg twice a day, pantoprazole 40 mg once daily, levothyroxine 100 g once daily, lisinopril/hydrochlorathiazide 20 mg/25 mg twice daily, gabapentin 300 mg twice a day, and fenofibrate 145 mg nightly.

The patient appeared nontoxic. Her exam was remarkable only for hypoactive bowel sounds and mild diffuse abdominal tenderness without distension or peritoneal signs. A Foley catheter was placed, and her postvoid residual was only 50 cc of urine. Her admission serum blood urea nitrogen and creatinine were 90 and 3.4 mg/dL, respectively, as compared with 18 and 0.8 mg/dL 2 months prior to presentation. A CT scan of the abdomen (Figure 1) revealed multiple dilated loops of small bowel with a transition point at the left lower quadrant ostomy site, consistent with a small bowel obstruction. A PET scan revealed no evidence of malignancy. A renal ultrasound showed no evidence of obstruction.

Figure 1
Long arrow: dilated loop of small bowel with air fluid levels. Short arrow: decompressed loop of small bowel distal to the obstruction.

With cessation of solifenacin and lisinopril/hydrochlorothiazide and hydration with normal saline, her constipation resolved, as did her acute renal failure and perception of urinary retention. She began to tolerate a regular diet after 4 days of hospitalization, and her colostomy output normalized. At follow‐up 8 months after admission, her creatinine was 0.8 mg/dL, and a screening abdominal CT showed complete resolution of the small bowel obstruction.

DISCUSSION

We believe that this patient developed small bowel pseudo‐obstruction as well the feeling of urinary retention because of treatment with solifenacin, an antimuscarinic agent approved for the treatment of bladder overactivity. Her acute renal failure was a result of prerenal azotemia. This particular patient was at increased risk for developing antimuscarinic‐induced bowel obstruction because of her previous surgery and exposure to chemotherapy.

In the 4 randomized trials cited in the prescribing information for solifenacin,2 only 189 patients of the 1811 who received the active drug were greater than 75 years old. Healthy elderly patients ranging from 64 to 78 years of age (mean 68.0 years) who received 2 weeks of treatment with solifenacin 5 and 10 mg had a mean AUC024 that was approximately 20% higher than that of younger subjects.3 In the 4 12‐week double‐blind clinical trials in which 1158 patients were treated with solifenacin 10 mg, there were 3 serious intestinal adverse events: 1 patient had a fecal impaction, 1 patient had a colonic obstruction, and 1 patient had an intestinal obstruction.2 Patients receiving solifenacin 5 and 10 mg were more likely to experience constipation than those receiving placebo (5.4%, 13.4%, and 2.9%, respectively).2 Given the dearth of clinical data on patients greater than 75 years old, the effects of age on the pharmacokinetics, the higher likelihood of bowel pathology in the elderly, the increased risk of solifenacin‐induced side effects in the elderly as reported in the pooled analysis of patients at least 65 years old,4 and the small clinical benefit of solifenacin,46 physicians should seriously consider whether the benefits of solifenacin outweigh both the known and the possible risks. 0

Randomized Placebo‐Controlled Double‐Blind Studies of Solifenacin
Patients in safety analysis (n) Constipation, n (%) Micturition/24 hours
Placebo 5 mg 10 mg Placebo 5 mg 10 mg Baseline Mean decrease from baseline
Placebo 5 mg 10 mg
  • Trials lasted 12 weeks and did not utilize an intention‐to‐treat analysis.

  • Inclusion criteria: men and women at least 18 years old, symptoms of overactive bladder syndrome for at least 3 months, average frequency of at least 8 voids/24 hours.

  • Exclusion criteria included significant bladder outlet obstruction, postvoid residual > 200 mL, presence of a neurological cause for detrusor muscle overactivity, any medical condition contraindicating the use of antimuscarinic medication, diabetic neuropathy, and use of any drugs with cholinergic or anticholinergic side effects.

  • Pooled analysis of patients at least 65 years old in Chapple et al.,6 Cardozo et al.,4 and 2 unpublished studies.1

Chapple et al.6* 267 279 268 5 (1.9) 20 (7.2) 21 (7.8) 12.0812.32 1.2 2.19 2.61
Cardozo et al.4* 301 299 307 6 (2.0) 11 (3.7) 28 (9.1) 12.0512.31 1.59 2.37 2.81
Wagg3 422 192 431 18 (4.3) 18 (9.4) 78 (18.1) 11.611.7 1.1 2.0 2.5

Solfenacin succinate, an antimuscarinic agent, is approved for the treatment of overactive bladder and described as well tolerated in the elderly.1 We present the case of solifenacin‐induced small bowel pseudo‐obstruction in an 89‐year‐old woman.

FINDINGS

An 89‐year‐old woman with untreated stage 0 chronic lymphocytic leukemia and a history of stage III colorectal cancer treated with hemicolectomy and adjuvant capecitabine in 2003 was admitted to Johns Hopkins Hospital in 2006. She reported feeling dehydrated, nauseated, and constipated, with decreased output from her colostomy. She also noted no urine output for 4 days and felt that she had to urinate, but I can't. This coincided with a decrease in fluid intake. She denied fevers, chills, abdominal pain, or loss of appetite. While waiting to be seen in the emergency department, the patient was finally able to urinate.

She had no evidence of colon cancer recurrence, with a normal postoperative positron‐emission tomography (PET) scan in 2003, colonoscopy in 2005, and screening computerized tomography (CT) scan in 2005. She also had a history of well‐controlled hypertension and hypothyroidism, hyperlipidemia, chemotherapy‐induced neuropathy, and anxiety.

Her home medication regimen included solifenacin 5 mg once daily (started 10 days prior to her admission) for bladder overactivity, buspirone 5 mg 3 times a day, metoprolol 25 mg twice a day, pantoprazole 40 mg once daily, levothyroxine 100 g once daily, lisinopril/hydrochlorathiazide 20 mg/25 mg twice daily, gabapentin 300 mg twice a day, and fenofibrate 145 mg nightly.

The patient appeared nontoxic. Her exam was remarkable only for hypoactive bowel sounds and mild diffuse abdominal tenderness without distension or peritoneal signs. A Foley catheter was placed, and her postvoid residual was only 50 cc of urine. Her admission serum blood urea nitrogen and creatinine were 90 and 3.4 mg/dL, respectively, as compared with 18 and 0.8 mg/dL 2 months prior to presentation. A CT scan of the abdomen (Figure 1) revealed multiple dilated loops of small bowel with a transition point at the left lower quadrant ostomy site, consistent with a small bowel obstruction. A PET scan revealed no evidence of malignancy. A renal ultrasound showed no evidence of obstruction.

Figure 1
Long arrow: dilated loop of small bowel with air fluid levels. Short arrow: decompressed loop of small bowel distal to the obstruction.

With cessation of solifenacin and lisinopril/hydrochlorothiazide and hydration with normal saline, her constipation resolved, as did her acute renal failure and perception of urinary retention. She began to tolerate a regular diet after 4 days of hospitalization, and her colostomy output normalized. At follow‐up 8 months after admission, her creatinine was 0.8 mg/dL, and a screening abdominal CT showed complete resolution of the small bowel obstruction.

DISCUSSION

We believe that this patient developed small bowel pseudo‐obstruction as well the feeling of urinary retention because of treatment with solifenacin, an antimuscarinic agent approved for the treatment of bladder overactivity. Her acute renal failure was a result of prerenal azotemia. This particular patient was at increased risk for developing antimuscarinic‐induced bowel obstruction because of her previous surgery and exposure to chemotherapy.

In the 4 randomized trials cited in the prescribing information for solifenacin,2 only 189 patients of the 1811 who received the active drug were greater than 75 years old. Healthy elderly patients ranging from 64 to 78 years of age (mean 68.0 years) who received 2 weeks of treatment with solifenacin 5 and 10 mg had a mean AUC024 that was approximately 20% higher than that of younger subjects.3 In the 4 12‐week double‐blind clinical trials in which 1158 patients were treated with solifenacin 10 mg, there were 3 serious intestinal adverse events: 1 patient had a fecal impaction, 1 patient had a colonic obstruction, and 1 patient had an intestinal obstruction.2 Patients receiving solifenacin 5 and 10 mg were more likely to experience constipation than those receiving placebo (5.4%, 13.4%, and 2.9%, respectively).2 Given the dearth of clinical data on patients greater than 75 years old, the effects of age on the pharmacokinetics, the higher likelihood of bowel pathology in the elderly, the increased risk of solifenacin‐induced side effects in the elderly as reported in the pooled analysis of patients at least 65 years old,4 and the small clinical benefit of solifenacin,46 physicians should seriously consider whether the benefits of solifenacin outweigh both the known and the possible risks. 0

Randomized Placebo‐Controlled Double‐Blind Studies of Solifenacin
Patients in safety analysis (n) Constipation, n (%) Micturition/24 hours
Placebo 5 mg 10 mg Placebo 5 mg 10 mg Baseline Mean decrease from baseline
Placebo 5 mg 10 mg
  • Trials lasted 12 weeks and did not utilize an intention‐to‐treat analysis.

  • Inclusion criteria: men and women at least 18 years old, symptoms of overactive bladder syndrome for at least 3 months, average frequency of at least 8 voids/24 hours.

  • Exclusion criteria included significant bladder outlet obstruction, postvoid residual > 200 mL, presence of a neurological cause for detrusor muscle overactivity, any medical condition contraindicating the use of antimuscarinic medication, diabetic neuropathy, and use of any drugs with cholinergic or anticholinergic side effects.

  • Pooled analysis of patients at least 65 years old in Chapple et al.,6 Cardozo et al.,4 and 2 unpublished studies.1

Chapple et al.6* 267 279 268 5 (1.9) 20 (7.2) 21 (7.8) 12.0812.32 1.2 2.19 2.61
Cardozo et al.4* 301 299 307 6 (2.0) 11 (3.7) 28 (9.1) 12.0512.31 1.59 2.37 2.81
Wagg3 422 192 431 18 (4.3) 18 (9.4) 78 (18.1) 11.611.7 1.1 2.0 2.5
References
  1. Chapple CR.Solifenacin provides effective antimuscarinic therapy for the complete management of overactive bladder.Expert Opin Pharmacother.2006;7:24212434.
  2. Yamanouchi Pharma America, Inc.United States prescribing information for solifenacin succinate (Vesicare®), November2004.
  3. Krauwinkel WJ,Smulders RA,Mulder H,Swart PJ,Taekema‐Roelvink ME.Effect of age on the pharmacokinetics of solifenacin in men and women.Int J Clin Pharmacol Ther.2005;43:227238.
  4. Wagg A,Wyndaele JJ,Sieber P.Efficacy and tolerability of solifenacin in elderly subjects with overactive bladder syndrome: a pooled analysis.Am J Geriatr Pharmacother.2006;4(1):1424.
  5. Cardozo L,Lisec M,Millard R, et al.Randomized, double‐blind placebo controlled trial of the once daily antimuscarinic agent solifenacin succinate in patients with overactive bladder.J Urol.2004;172(5 Pt 1):19191924.
  6. Chapple CR,Rechberger T,Al‐Shukri S, et al.Randomized, double‐blind placebo‐ and tolterodine‐controlled trial of the once‐daily antimuscarinic agent solifenacin in patients with symptomatic overactive bladder.BJU Int.2004;93:303310.
References
  1. Chapple CR.Solifenacin provides effective antimuscarinic therapy for the complete management of overactive bladder.Expert Opin Pharmacother.2006;7:24212434.
  2. Yamanouchi Pharma America, Inc.United States prescribing information for solifenacin succinate (Vesicare®), November2004.
  3. Krauwinkel WJ,Smulders RA,Mulder H,Swart PJ,Taekema‐Roelvink ME.Effect of age on the pharmacokinetics of solifenacin in men and women.Int J Clin Pharmacol Ther.2005;43:227238.
  4. Wagg A,Wyndaele JJ,Sieber P.Efficacy and tolerability of solifenacin in elderly subjects with overactive bladder syndrome: a pooled analysis.Am J Geriatr Pharmacother.2006;4(1):1424.
  5. Cardozo L,Lisec M,Millard R, et al.Randomized, double‐blind placebo controlled trial of the once daily antimuscarinic agent solifenacin succinate in patients with overactive bladder.J Urol.2004;172(5 Pt 1):19191924.
  6. Chapple CR,Rechberger T,Al‐Shukri S, et al.Randomized, double‐blind placebo‐ and tolterodine‐controlled trial of the once‐daily antimuscarinic agent solifenacin in patients with symptomatic overactive bladder.BJU Int.2004;93:303310.
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Solifenacin‐induced small bowel pseudo‐obstruction
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Solifenacin‐induced small bowel pseudo‐obstruction
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solifenacin, Vesicare, small bowel obstruction, urinary retention, intestinal pseudo‐obstruction
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solifenacin, Vesicare, small bowel obstruction, urinary retention, intestinal pseudo‐obstruction
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