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Treating constipation during pregnancy
Magan Trottier, MSc, Aida Erebara, MD and Pina Bozzo
August 2012
QUESTION
Many of my patients experience constipation during pregnancy, even after increasing dietary fibre and fluids. Are there any safe treatments I can recommend to them?
ANSWER
Although the recommended first-line therapy for constipation includes increasing fibre, fluids, and exercise, these are sometimes ineffective. Therefore, laxatives such as bulk-forming agents, lubricant laxatives, stool softeners, osmotic laxatives, and stimulant laxatives might be considered. Although few of the various types of laxatives have been assessed for safety in pregnancy, they have minimal systemic absorption. Therefore, they are not expected to be associated with an increased risk of congenital anomalies. However, it is recommended that osmotic and stimulant laxatives be used only in the short term or occasionally to avoid dehydration or electrolyte imbalances in pregnant women.
QUESTION
Beaucoup de mes patientes enceintes souffrent de constipation, même si elles consomment plus de fibres alimentaires et de liquides. Existe-t-il des traitements sécuritaires que je pourrais leur recommander?
RÉPONSE
Bien que le traitement de première intention recommandé pour la constipation préconise l'ajout de fibres, de liquides et d'activité physique, ces moyens demeurent parfois inefficaces. Par conséquent, on peut envisager des laxatifs comme les laxatifs de lest, les lubrifiants, les émollients, les laxatifs osmotiques et les laxatifs stimulants. L'innocuité durant la grossesse de bon nombre de ces types de produits n'a pas été étudiée, mais leur absorption systémique est minime. On ne s'attend donc pas à ce qu'ils soient associés à un risque accru d'anomalies congénitales. Cependant, il est recommandé de n'utiliser les laxatifs osmotiques ou stimulants qu'à court terme ou qu'à l'occasion pour éviter la déshydratation ou les déséquilibres des électrolytes chez les femmes enceintes.
Treating constipation during pregnancy
Many of my patients experience constipation during pregnancy, even after increasing dietary fibre and fluids. Are there any safe treatments I can recommend to them?
Although the recommended first-line therapy for constipation includes increasing fibre, fluids, and exercise, these are sometimes ineffective. Therefore, laxatives such as bulk-forming agents, lubricant laxatives, stool softeners, osmotic laxatives, and stimulant laxatives might be considered. Although few of the various types of laxatives have been assessed for safety in pregnancy, they have minimal systemic absorption. Therefore, they are not expected to be associated with an increased risk of congenital anomalies. However, it is recommended that osmotic and stimulant laxatives be used only in the short term or occasionally to avoid dehydration or electrolyte imbalances in pregnant women.
It has been estimated that approximately 11% to 38% of pregnant women experience constipation, 1 which is generally described as infrequent bowel movements or difficult evacuation. 2 Pregnancy predisposes women to developing constipation owing to physiologic and anatomic changes in the gastrointestinal tract. For instance, rising progesterone levels during pregnancy and reduced motilin hormone levels lead to increases in bowel transit time. 2,3 Also, there is increased water absorption from the intestines, which causes stool to dry out. Decreased maternal activity and increased vitamin supplementation (eg, iron and calcium) can further contribute to constipation. 3 Later in pregnancy, an enlarging uterus might slow onward movement of feces. 4 Constipation can result in serious complications such as fecal impaction, but such complications are rare. It is important to note that constipation negatively affects patients' daily lives and is second only to nausea as the most common gastrointestinal complaint in pregnancy. 2,4
Treatment
Many patients find relief from constipation with an increase in dietary fibre and fluids, as well as daily exercise. Probiotics that alter the colonic flora might also improve bowel function. 3 If these are ineffective, laxatives are the second line of therapy (Table 1). 2,5,6 In general, there are insufficient data on the use of laxatives in pregnancy; however, limited studies have been performed for specific laxatives, and the safety of others can be inferred from information about their systemic absorption (Table 2). 7-16
Table 1
Types of laxatives
| Treatment | Mechanism of Action | Examples |
|---|---|---|
| Bulk-forming agents | Luminal water binding increases stool's bulk, making it easier to pass 5 | Psyllium, bran |
| Stool softeners | Stimulates net secretion of water, sodium, chloride, and potassium and inhibits net absorption of glucose and bicarbonate in the jejunum 6 | Docusate sodium or calcium |
| Lubricant laxatives | Decreases surface tension of bowel's liquid contents so that more liquid remains in the stool, thereby facilitating evacuation and decreasing straining 2 | Mineral oil |
| Osmotic laxatives | Increases osmolar tension, resulting in increased water collection, distention, peristalsis, and evacuation 2 | Salts (eg, sodium chloride, potassium chloride), magnesium sulfate or citrate, lactulose, sorbitol, polyethylene glycol |
| Stimulant laxatives | Acts locally to stimulate colonic motility and decrease water absorption from large intestine 5 | Bisacodyl, senna |
Table 2
Studies examining safety in pregnancy and systemic absorption of commonly used laxatives
| Drug | Type of Study | Details | Outcomes |
|---|---|---|---|
| Psyllium | Surveillance | 100 > N < 199 during first trimester | No increased risk of malformations 7 |
| Docusate sodium | Prospective | N = 116 anytime during pregnancy | No increased risk of malformations 8 |
| Surveillance | N = 473 during first trimester | No increased risk of malformations (1/473 = 0.2%) 7 | |
| Surveillance | N = 319 during first trimester | No increased risk of malformations (3/319 = 0.9%) 9 | |
| Surveillance | N = 232 during first trimester | No increased risk of malformations (9/232 = 3.9%) 10 | |
| Lactulose | Pharmacokinetics | N = 6 adults given lactulose | Systemic bioavailability < 3% 11 |
| Polyethylene glycol | Pharmacokinetics | N = 11 adults given polyethylene glycol | Not absorbed 12 |
| Bisacodyl | Pharmacokinetics | N = 12 adults given oral and rectal bisacodyl | Minimal absorption 13 |
| Pharmacokinetics | N = 16 adults given bisacodyl suppository | Systemic bioavailability < 5% 14 | |
| Senna | Case-control | N = 506 cases (260 during first trimester) | No increased risk of malformations (OR 0.8; 95% CI 0.4-1.4) or adverse pregnancy outcomes 15 |
| Pharmacokinetics | N = 937 control (500 during first trimester); N = 10 adults given senna | Systemic bioavailability < 5% 16 |
- ORodds ratio.
- Data from Jick et al, 7 Heinonen et al, 8 Aselton et al, 9 Briggs et al, 10 Carulli et al, 11 Wilkinson, 12 Roth and Beschke, 13 Flig et al, 14 Acs et al, 15 and Krumbiegel and Schulz. 16
Bulk-forming agents
Bulk-forming agents are not absorbed 4 or associated with increased risk of malformations 7; therefore, they are considered safe for long-term use during pregnancy. However, they are not always effective and might be associated with unpleasant side effects such as gas, bloating, and cramping. 4
Stool softeners
Docusate sodium has not been associated with adverse effects in pregnancy in a number of studies, and it is thus also considered safe to use. 7-10 There is one case report of maternal chronic use of docusate sodium throughout pregnancy, which was associated with symptomatic hypomagnesemia in the neonate. 17
Lubricant laxatives
Mineral oil is poorly absorbed from the gastrointestinal tract 18 and does not appear to be associated with adverse effects. 19 There is controversy about whether prolonged use reduces the absorption of fat-soluble vitamins, although this appears to be a theoretical rather than actual risk. 20
Osmotic laxatives
Lactulose and polyethylene glycol are poorly absorbed systemically. 11,12 Their use has not been associated with adverse effects; however, individuals might experience side effects such as flatulence and bloating. 3 Theoretically, prolonged use of osmotic laxatives might lead to electrolyte imbalances. 3
Stimulant laxatives
Absorption of bisacodyl is minimal as it has poor bioavailability. 13,14 Senna does not appear to be associated with increased risk of malformations 15 and is not readily absorbed systemically. 16 However, women might experience unpleasant side effects such as abdominal cramps with the use of stimulant laxatives. 2 Similar to osmotic laxatives, prolonged use might theoretically lead to electrolyte imbalances. 3
Conclusion
The first line of therapy for constipation includes increasing dietary fibre and water intake and moderate amounts of daily exercise. 3 If these are ineffective, laxatives are the second line of therapy. Because most laxatives are not absorbed systemically, short-term use has not been, and is not expected to be, associated with an increased risk of malformations. However, as with the general population, it is recommended that osmotic and stimulant laxatives be used only in the short term or occasionally to avoid dehydration or electrolyte imbalances and the theoretical risk of "athartic colon." 21
Motherisk questions are prepared by the Motherisk Team at The Hospital for Sick Children in Toronto, ON. Ms. Trottier and Dr. Erebara are counselors and Ms. Bozzo is Assistant Director of the Motherisk Program.
Do you have questions about the effects of drugs, chemicals, radiation, or infections in women who are pregnant or breastfeeding? We invite you to submit them to the Motherisk Program by fax at 416 813-7562; they will be addressed in future Motherisk Updates.
Published Motherisk Updates are available on the Canadian Family Physician website (www.cfp.ca) and also on the Motherisk website.
Competing interests
None declared
Copyright © the College of Family Physicians of Canada
Can Fam Physician
Vol. 58, No. 8, August 2012 836-838
Copyright © 2012 by The College of Family Physicians of Canada
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- West L, Warren J, Cutts T. Diagnosis and management of irritable bowel syndrome, constipation, and diarrhea in pregnancy. Gastroenterol Clin North Am 1992;21(4):793-802. Medline
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- Jick H, Holmes LB, Hunter JR, Madsen S, Stergachis A. First-trimester drug use and congenital disorders. JAMA 1981;246(4):343-6. CrossRef | Medline
- Heinonen OP, Slone D, Shapiro S Birth defects and drugs in pregnancy: maternal drug exposure and congenital malformations. Littleton, MA: Publishing Sciences Group; 1977. p. 442.
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- Briggs GG, Freeman RK,n Yaffe SJ. Drugs in pregnancy and lactation. 9th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2011. p. 439.
- Carulli N, Salvioli GF, Manenti F. Absorption of lactulose in man. Digestion 1972;6(3):139-45. Medline
- Wilkinson R. Polyethylene glycol 4000 as a continuously administered nonabsorbable faecal marker for metabolic balance studies in human subjects. Gut 1971;12(8):654-60. Abstract/FREE Full Text
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- Flig E, Hermann TW, Zabel M. Is bisacodyl absorbed at all from suppositories in man? Int J Pharm 2000;196(1):11-20. CrossRef | Medline
- Acs N, Bánhidy F, Puhó EH, Czeizel AE. Senna treatment in pregnant women and congenital abnormalities in their offspringa population-based case-control study. Reprod Toxicol 2009;28(1):100-4. Epub 2009 Feb 24. Medline
- Krumbiegel G, Schulz HU. Rhein and aloe-emodin kinetics from senna laxatives in man. Pharmacology 1993;47(Suppl 1):120-4. Medline
- Schindler AM. Isolated neonatal hypomagnesaemia associated with maternal overuse of stool softener. Lancet 1984;2(8406):822. Medline
- Hazardous Substances Data Bank [website]. Mineral oil. CASRN: 8012-95-1. Bethedsa, MD: U.S. National Library of Medicine; 2005. Available from: http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB. Accessed 2012 Jun 26.
- Sharif F, Crushell E, O'Driscoll K, Bourke B. Liquid paraffin: a reappraisal of its role in the treatment of constipation. Arch Dis Child 2001;85(2):121-4. FREE Full Text
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- Joo JS, Ehrenpreis ED, Gonzalez L, Kaye M, Breno B, Wexner SD, et al. Alterations in colonic anatomy induced by chronic stimulant laxatives: the cathartic colon revisited. J Clin Gastroenterol 1998;26(4):283-6. CrossRef | Medline












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