Secondary causes of constipation should be treated. If possible, the concurrent use of constipating drugs should be avoided. Most patients will have idiopathic constipation, or constipation-predominant irritable bowel syndrome. The initial approach in this condition should be diet and non-drug treatment. If this fails, drugs can be used.
Non-drug treatment
Reassurance can be offered if there are no alarm symptoms. Simple education about a normal stool habit may help. The timing of bowel motions should be as regular as possible. Defecation should not be postponed unnecessarily when the urge arises. Patients can be reminded that colonic motility is maximal after meals and that this is a good time to try to plan regular defecation. If the disorder is defecatory, then biofeedback is effective in up to 75% of cases.
There is a reliable dose-response between fibre and water intake and stool bulk and frequency. A dietary history will determine whether there is sufficient fibre in the diet in the form of cereals, grains, and fruit and vegetables. Increasing dietary fibre to the recommended daily intake of approximately 30 g or the use of fibre supplements such as psyllium should help in those patients with fibre deficiency. Adequate daily fluid intake is also important to maximise the benefit of fibre. However, increasing fibre intake beyond the required amount results in bloating or flatulence in many patients without relieving constipation, and may even aggravate it. Similarly, merely increasing the daily fluid intake in the absence of adequate fibre will not improve constipation.
Increasing physical activity can promote colonic motility, so an active lifestyle can be encouraged. As constipation may be exacerbated by stress and depression, these factors should be addressed if they are present.
Pharmacological measures
Many patients who present with constipation will have already tried a variety of non-prescription remedies. Enquire about the use of these remedies before deciding the best approach to treatment.
The numerous agents commonly used to treat constipation can be classified according to their mechanism of action (Table 1). Their relative efficacy and tolerability has generally not been well studied. The choice of treatment is therefore based on the mechanism of action, required onset, duration of action and patient preference. Trial and error is often required to determine the optimal management plan.
Bulking agents
Hydrophillic organic polymers (including psyllium and bran) function by sequestering extra water in the stools. The resulting increase in the volume of luminal contents is thought to stimulate intestinal activity and thereby enhance the speed of transit. A change in stool consistency associated with the increased water content may also ease defecation. The bulking agents are often the first line of treatment. However, fermentation of fibre in the colon can result in bloating and flatulence, particularly if the patient's diet already has sufficient fibre.
Osmotic laxatives
The capacity of the intestine to absorb some molecules and ions, such as magnesium salts, is limited. Other molecules, such as lactulose and sorbitol, are completely unabsorbed. To maintain an iso-osmolar state, these substances draw water into the intestinal lumen resulting in a laxative effect. Osmotic laxatives can be tried if the bulking agents are not appropriate or are ineffective.
The non-absorbable sugars are fermented in the colon so they can cause bloating, distension and flatulence which may limit their use. They should not be used by people with diabetes. Long-term use of magnesium salts is not recommended, particularly in patients with renal impairment.
Another approach is the use of large osmotically active polymers such as polyethylene glycol (PEG or macrogol). They are made iso-osmolar with intestinal contents so the water ingested with them is retained in the gut. The polymers are not absorbed, making them more suitable for long-term use in low volume. They can be used if simpler measures are ineffective, and are also used to prepare patients for colonoscopy.
Table 1 Treatments for constipation in adults
Constituent
|
Dose
|
Time to onset
|
Bulking agents
|
Ispaghula
|
1 sachet or teaspoon in water
|
24 hours, maximum effect at 2–3 days
|
Psyllium (multiple formulations and additives)
|
Per packet* – two teaspoons 1–3/day
|
24 hours, maximum effect at 2–3 days
|
Sterculia
|
1–2 teaspoons 1–2/day
|
24 hours, maximum effect at 2–3 days
|
Osmotic agents
|
Oral
|
|
Lactulose
|
15–30 mL 1–2/day
|
1–2 days
|
|
Macrogol (PEG 3350) with electrolytes
|
1–2 sachets each in 125 mL water, can give up to 8 for faecal impaction
|
Variable
|
|
Magnesium sulfate
|
15 g in 250 mL water daily
|
1 hour
|
|
Sorbitol liquid
|
20 mL 1–3/day
|
2–3 days
|
|
Sodium phosphate
|
Per packet*
|
½–6 hours
|
|
Sodium picosulfate (multiple formulations and additives)
|
Per packet*
|
Variable
|
Rectal
|
|
Sodium phosphate
|
133 mL single dose
|
2–5 minutes
|
|
Sodium citrate/sorbitol/sodium lauryl sulfoacetate
|
5 mL
|
30 minutes
|
Stool softeners
|
Docusate
|
2 x 120 mg tablets daily
|
1–3 days
|
Stimulant laxatives
|
Oral
|
|
Bisacodyl
|
1–2 x 5 mg tablets daily
|
6–12 hours
|
|
Senna/sennosides (multiple formulations and additives)
|
Per packet*
|
6–12 hours
|
Rectal
|
|
Bisacodyl (multiple formulations)
|
Per packet*
|
15–60 minutes
|
Lubricants
|
Oral
|
|
Paraffin emulsion
|
15–30 mL two hours before lying down
|
2–3 days
|
Rectal
|
|
Glycerol suppository
|
1 daily
|
5–30 minutes
|
Stimulant laxatives
Stimulant laxatives are often combined with stool softeners and may be useful in patients with poor colonic motility.
Diphenylmethane derivatives inhibit water absorption after activation, by endogenous esterases in the case of bisacodyl, or by colonic flora in the case of sodium picosulfate. These laxatives can precipitate cramping and electrolyte wasting.
Anthraquinones are available as mixtures of compounds (such as senna) and lead to water secretion following mucosal contact as well as direct stimulation of enteric nerve endings. There is a suggestion of a damaging effect on the colonic mucosa and increasing doses are often needed over time. The chronic use of stimulant laxatives should be avoided.
Stool softeners and lubricants
Stool softeners such as docusate are detergents that facilitate the interaction between colonic water and stool. Lubricants, such as paraffin, have no pharmacological interaction with colonic mucosa, but alter stool composition in addition to their lubricating effect. Prolonged use of paraffin may cause malabsorption of fat soluble vitamins and should be used only in special circumstances, for example in some patients with cystic fibrosis. Liquid paraffin should not be used by patients at risk of aspiration.
Neuromuscular drugs
The benefit of these drugs is in their known adverse effect of diarrhoea, but they are not available primarily for this purpose and there are no clinical trials supporting their use. Local chloride channel activators (lubiprostone) and 5HT4 receptor modulators like cisapride, prucalopride and tegasarod, are not available in Australia.
Methylnaltrexone
Methylnaltrexone is a peripherally acting mu opioid receptor antagonist. It is administered subcutaneously, and is used in patients with opioid-induced constipation. It is only approved for use in the setting of palliation, and is contraindicated in malignant bowel obstruction.