Constipation Clinical Trial
Official title:
An Evaluation of the Efficacy and Safety of a Polyethylene Glycol (PEG) Based Bowel Protocol for the Management of Constipation in Peritoneal Dialysis Patients: A Pilot Study
Constipation is a common condition, which occurs one in four Canadians. Maintaining regular
bowel movements is imperative because constipation can affect the quality of PD dialysate
flow and result in an unwanted effect on the dialysis adequacy.
There is limited data on how to best manage constipation in the peritoneal dialysis
population. Polyethylene glycol (PEG) is an osmotic laxative that is becoming popular for
prevention and treatment of constipation across Canada. Although some PD programs in Canada
have already converted to PEG for management of constipation, more research in this
population would help guide practice. For now, the current PD bowel regimen at the Nova
Scotia Health Authority (NSHA) includes daily preventative therapy using a stimulant
laxative, senna, along with an osmotic laxative, lactulose, for acute constipation.
The investigators will review all patients in the NSHA PD program who have regular or recent
laxative use for participation in this study. Patients included in this study will be
randomly assigned to the Current Bowel Protocol or the PEG Bowel Protocol for 8 weeks.
The goal is to determine if the PEG Bowel Protocol is as effective and safe for the
prevention of constipation as the Current Bowel Protocol used in the PD Program. The
investigators will use bowel function diaries and patient surveys to determine efficacy and
safety outcomes.
Constipation is a common condition, which impacts one in four Canadians Maintaining regular
bowel movements is important in the peritoneal dialysis (PD) population because constipation
can negatively impact the quality of dialysate flow and can result in impaired dialysis
adequacy. Unfortunately, treating constipation is challenging in PD patients because of the
diet and fluid restrictions required in this population, as well as the need for constipating
calcium based phosphate binders.
Constipation treatment can be administered orally or rectally. Although patients often prefer
oral therapy, there are occasions when rectal therapy is preferred (ie. rectal suppositories
and enemas). Oral laxatives include bulk, osmotic, stimulant, and lubricants.
In the Nova Scotia (NS) PD Program, patients are counseled to maintain a type 3-4 stool on
the Bristol Stool Chart (BSC). An ideal stool is a type 4, which appears like a sausage or
snake and is smooth and soft in consistency. To maintain a type 3-4 stool, current therapy
includes senna 8.6-17.2 g twice daily with the addition of lactulose 30-60 mL twice daily, as
needed. Rescue therapy in the Current Bowel Protocol is lactulose 30-60 mL every hour until
bowel movement.
There is limited evidence to guide the ideal bowel regimen in PD patients. Reasons to
consider PEG therapy include the evidence promoting PEG in the general population with
constipation, the positive outcomes found in a small population of PD patients (Mimidis
2005), as well as positive feedback from other provinces who currently recommend PEG in PD
patients. The investigators postulate the PEG protocol would be as effective and safe as the
Current Bowel Protocol, and thus will evaluate PEG in the PD population, the investigators
will conduct a prospective, interventional, randomized, open label, pilot study.
All patients with recent laxative use will be approached for inclusion. Patients will be
randomly assigned to the Current Bowel Protocol (senna/lactulose) or the PEG Bowel Protocol
(PEG/lactulose) for 8 weeks.
The primary objective is to compare the efficacy of the PEG Bowel Protocol in preventing
constipation to the Current Bowel Protocol. We will review the safety of the regimens by
monitoring for adverse events from all laxatives and explore the impact of constipation in
patients who experience PD treatment failure.
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