Home Family Medicine Constipation

Constipation

📋 Key Information Summary

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  • Prevalence: Constipation affects approximately 1 in 7 Australian adults and up to 30% of children, with higher rates in Aboriginal and Torres Strait Islander communities and the elderly.
  • Diagnostic model: Apply the Bristol Stool Form Scale, Rome IV criteria, and a structured history to distinguish functional (idiopathic) constipation from secondary and drug-related causes before initiating treatment.
  • Red flags: New-onset constipation >50 years, rectal bleeding, unexplained weight loss, iron-deficiency anaemia, family history of colorectal cancer, and progressive symptoms warrant urgent colonoscopy referral.
  • Drug-related causes are common: Opioids, anticholinergics, calcium-channel blockers, iron supplements, and serotonergic agents are frequent offenders — always review the medication chart before diagnosing idiopathic constipation.
  • First-line pharmacotherapy: Osmotic laxatives (macrogol 3350, lactulose) are first-line for all age groups; bulk-forming agents (psyllium) suit those with low-fibre intake. Stimulant laxatives (senna, sodium picosulfate) are second-line or adjunctive.
  • Lifestyle measures are foundational: Adequate fluid intake (≥1.5 L/day), dietary fibre (25–30 g/day for adults), and regular physical activity should accompany all pharmacotherapy.
  • Children: Functional constipation accounts for >95% of paediatric cases. Macrogol 3350 (Movicol®) is first-line; disimpaction doses are higher than maintenance doses. Avoid lactulose in infants <1 month.
  • Slow-transit constipation should be suspected when patients fail to respond to adequate fibre, fluids, and osmotic laxatives — refer to a gastroenterologist for colonic transit studies or anorectal manometry.
  • Pelvic floor dyssynergia presents with incomplete evacuation and straining despite soft stools; biofeedback therapy is the evidence-based treatment, available through specialist continence services.
  • Opioid-induced constipation (OIC): Prophylactic laxatives (macrogol + stimulant) should be co-prescribed with all opioid prescriptions. Peripherally-acting mu-opioid receptor antagonists (PAMORAs) e.g. naloxegol, are PBS-listed for refractory OIC.
  • Aboriginal and Torres Strait Islander populations: Higher prevalence due to reduced fibre intake in remote communities, polypharmacy, and limited access to specialist services — use culturally safe communication and community-controlled health services.
  • When to refer: Failure of 4–8 weeks of optimised therapy, suspected Hirschsprung disease in children, red-flag features, need for biofeedback, or consideration of surgical intervention.

Introduction & Australian Epidemiology

Constipation is one of the most common gastrointestinal complaints presenting in Australian primary care, affecting an estimated 14% of adults and up to 30% of children. It is characterised by infrequent bowel movements (typically <3 per week), straining, hard stools, incomplete evacuation, and/or the need for manual manoeuvres during defecation. While often considered a benign, self-limiting condition, chronic constipation significantly impairs quality of life, increases healthcare utilisation, and carries substantial economic costs estimated at over AUD 450 million annually in the Australian healthcare system.

The burden of constipation is not evenly distributed across the population. Prevalence is highest in women (approximately 2:1 female-to-male ratio), adults aged over 65 years, Aboriginal and Torres Strait Islander peoples, nursing home residents, and those with physical or intellectual disabilities. In children, functional constipation is the most common diagnosis, accounting for at least 95% of presentations, with a peak incidence during toilet training (ages 2–4 years).

A structured, evidence-based approach to diagnosis is essential. The Rome IV diagnostic criteria (2016) provide the international standard for functional constipation, while the Bristol Stool Form Scale remains a practical clinical tool. Australian general practitioners (GPs) play a central role in initial assessment, exclusion of secondary causes, medication review, and initiation of treatment. Escalation to gastroenterology or colorectal surgery is reserved for refractory cases, alarm features, or diagnostic uncertainty.

This guideline provides a comprehensive overview of the diagnostic model for constipation, common drug-related and secondary causes, evidence-based management of idiopathic constipation in adults, and the specific considerations for constipation in children. Recommendations are aligned with Australian Therapeutic Guidelines, the RACGP Red Book, NHMRC standards, and international consensus frameworks.

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Key epidemiological fact: In Australian nursing homes, up to 50–74% of residents use regular laxatives. Inadequate management of constipation in this setting contributes to faecal impaction, bowel obstruction, urinary retention, and avoidable hospitalisations.

Australian Prevalence Data

Population Estimated Prevalence Key Risk Factors
Australian adults (general) 12–17% Female sex, low fibre, sedentary lifestyle, polypharmacy
Adults ≥65 years 30–40% Reduced mobility, medications, comorbidities, dehydration
Nursing home residents 50–74% Institutionalised care, immobility, anticholinergic burden
Children (general paediatrics) 10–30% Toilet training, dietary factors, pain avoidance, withholding behaviour
Aboriginal and Torres Strait Islander adults Up to 20–25% (estimated) Remote living, reduced fresh food access, chronic disease burden
Pregnant women ~40% Hormonal changes, iron supplements, reduced physical activity

Constipation Diagnostic Model

A systematic diagnostic approach is essential to avoid the twin pitfalls of over-investigating simple functional constipation and missing serious secondary causes. The diagnostic model proceeds through four sequential steps: symptom characterisation using Rome IV criteria, structured history and medication review, targeted examination, and selective investigation.

Step 1: Symptom Characterisation — Rome IV Criteria

The Rome IV criteria for functional constipation require the presence of ≥2 of the following symptoms for at least 3 months, with symptom onset at least 6 months prior to diagnosis:

  • Straining during >25% of defecations
  • Lumpy or hard stools (Bristol Stool Form Scale types 1–2) in >25% of defecations
  • Sensation of incomplete evacuation in >25% of defecations
  • Sensation of anorectal obstruction/blockage in >25% of defecations
  • Manual manoeuvres to facilitate >25% of defecations (e.g. digital evacuation, pelvic floor support)
  • Fewer than 3 spontaneous bowel movements per week

Loose stools should rarely be present without the use of laxatives, and the patient should not meet criteria for irritable bowel syndrome (IBS). The Bristol Stool Form Scale is a validated tool freely available for use in Australian practice, classifying stool from type 1 (separate hard lumps) to type 7 (watery, no solid pieces).

Bristol Type Description Clinical Significance
Type 1 Separate hard lumps (nuts) Severe constipation — significant transit delay
Type 2 Sausage-shaped but lumpy Constipation — moderate transit delay
Type 3 Sausage-shaped with cracks Borderline / normal — mild transit delay possible
Type 4 Smooth, soft sausage or snake Normal — ideal stool form
Type 5 Soft blobs with clear-cut edges Lacking fibre — borderline normal or diarrhoea
Types 6–7 Mushy to watery Diarrhoea — consider alternative diagnosis

Step 2: Structured History & Medication Review

A thorough history should cover onset and duration, stool frequency and consistency, associated symptoms (pain, bloating, nausea, mucus or blood per rectum), dietary fibre and fluid intake, physical activity level, toileting habits, psychological factors (anxiety, depression, history of abuse), and a complete medication review including over-the-counter and complementary medicines.

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Alarm features requiring urgent investigation:
  • New-onset constipation in a patient aged ≥50 years without prior colonoscopy
  • Rectal bleeding or blood mixed in stool
  • Unintentional weight loss (>5% body weight in 6 months)
  • Iron-deficiency anaemia on FBE
  • Family history of colorectal cancer or hereditary polyposis syndromes
  • Progressive worsening despite treatment
  • New-onset change in bowel habit in any age group — consider colorectal cancer until proven otherwise

Step 3: Physical Examination

A focused examination should include abdominal palpation (masses, faecal loading, tenderness), digital rectal examination (DRE) to assess anal tone, stool consistency in the rectal vault, rectal masses, and assessment of perineal descent during simulated straining. DRE is recommended in all patients presenting with constipation and is particularly important in children to exclude anorectal malformations.

Step 4: Selective Investigation

Most patients with typical functional constipation and no alarm features do not require investigations beyond basic blood work. The following investigations are indicated when secondary causes are suspected or alarm features are present:

Essential Full blood examination (FBE) Exclude iron-deficiency anaemia; MBS Item 66512
Essential Serum calcium, TSH, glucose Screen for hypothyroidism, hypercalcaemia, diabetes; MBS Item 66512
Available Colonoscopy Indicated with alarm features or age ≥50 with new symptoms; MBS Item 32222
Available Colonic transit study (radiopaque marker) Suspected slow-transit constipation; available at major centres
Specialist Anorectal manometry & balloon expulsion test Suspected pelvic floor dyssynergia; gastroenterology/colorectal referral
Specialist Defecography (MR or conventional) Rectocele, intussusception, or dyssynergia assessment; tertiary centres
Referral Rectal biopsy (full-thickness or suction) Suspected Hirschsprung disease in children; absence of ganglion cells

Diagnostic Algorithm Summary

1
Characterise Symptoms
Apply Rome IV criteria; document Bristol stool types; duration >6 months
2
Identify Secondary Causes
Full medication review; screen for metabolic, endocrine, neurological causes
3
Examine the Patient
Abdominal exam; digital rectal examination; perineal assessment
4
Investigate Selectively
FBE, calcium, TSH if indicated; colonoscopy if alarm features; specialist tests for refractory cases

Idiopathic Constipation Management

Idiopathic (functional) constipation is diagnosed when no secondary structural, metabolic, or drug-related cause has been identified and Rome IV criteria are met. Management follows a stepwise approach from lifestyle modification through pharmacotherapy to specialist referral.

Step 1: Lifestyle & Dietary Modification

All patients with idiopathic constipation should receive counselling on the following measures, which form the foundation of treatment:

  • Dietary fibre: Aim for 25–30 g/day. Increase gradually over 2–4 weeks to minimise bloating. Sources include wholegrain cereals, fruits (pears, prunes, kiwifruit), vegetables, legumes, and psyllium husk.
  • Fluid intake: ≥1.5 L/day (6–8 glasses). Increased intake is particularly important when increasing fibre. In elderly and institutionalised patients, ensure assisted access to fluids.
  • Physical activity: ≥150 minutes of moderate-intensity activity per week (walking, cycling). Even gentle daily walking improves bowel transit time.
  • Toilet routine: Encourage a regular toileting schedule, ideally 15–30 minutes after meals (to exploit the gastrocolic reflex). Use a footstool to achieve a squatting position (knees above hips). Avoid straining — take time, relax, breathe.
  • Kiwifruit: Two green kiwifruit daily has demonstrated efficacy comparable to psyllium in randomised trials and is recommended as a first-line dietary intervention in Australian practice.
Evidence spotlight — Green kiwifruit: A 2023 meta-analysis of 9 RCTs (n = 477) found that consuming 2 green kiwifruit daily significantly increased stool frequency by 1.5 bowel movements/week and improved stool consistency (Bristol types 3–4). This intervention is low-cost, well-tolerated, and suitable for most patients including pregnant women and the elderly.

Step 2: Pharmacotherapy — First-Line (Osmotic Laxatives)

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Macrogol 3350 (Polyethylene Glycol)
Movicol® · Molaxole® · Osmolax® · Osmotic laxative
Adult dose 1–3 sachets daily (each sachet dissolved in 125 mL water). Start with 1 sachet daily, titrate up.
Paediatric dose ≥2 years: 1 sachet daily (Movicol®-Half for children); titrate to effect. See Paediatric section.
Route Oral (dissolved in water)
Duration Short or long-term use as required; dose titrated to 1–2 soft stools daily
Renal adjustment Use with caution in severe renal impairment (CrCl <30) due to electrolyte risk; monitor UEC
Hepatic adjustment No adjustment required
Key advantages No significant electrolyte disturbance; safe in pregnancy; well-tolerated; titratable
PBS status ✔ PBS General Benefit
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Lactulose
Duphalac® · Actilax® · Osmotic laxative (synthetic disaccharide)
Adult dose 15–30 mL PO once or twice daily. Titrate to produce 1–2 soft stools daily.
Paediatric dose 1 month–1 year: 2.5 mL BD; 1–5 years: 2.5–10 mL BD; 5–18 years: 5–20 mL BD
Route Oral
Duration May be used short- or long-term
Renal adjustment Use with caution; may precipitate hepatic encephalopathy in severe liver disease (avoid)
Cautions Flatulence, bloating; contains galactose — avoid in galactosaemia; sweet taste poorly tolerated by some children
PBS status ✔ PBS General Benefit
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Psyllium (Ispaghula husk)
Metamucil® · Fybogel® · Bulk-forming laxative / Fibre supplement
Adult dose 3.5 g (1 sachet) PO once or twice daily with ≥250 mL water
Paediatric dose 6–12 years: half adult dose; not recommended <6 years
Route Oral (dissolved in water)
Cautions Must be taken with adequate fluid; risk of faecal impaction if taken without sufficient water; may worsen bloating initially
PBS status ✔ PBS General Benefit

Step 3: Pharmacotherapy — Second-Line (Stimulant Laxatives)

Stimulant laxatives are used when osmotic laxatives alone are insufficient, or as rescue therapy. They act by stimulating the myenteric plexus to increase intestinal motility and secretion. Short-term use is generally safe; chronic daily use should be avoided where possible, although evidence for the traditional concern about "cathartic colon" is weak.

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Senna
Senokot® · Stimulant laxative (anthraquinone glycoside)
Adult dose 15–30 mg (1–2 tablets) PO at night. Effect in 8–12 hours.
Paediatric dose 2–6 years: 7.5 mg nocte; 6–12 years: 7.5–15 mg nocte; ≥12 years: adult dose
Renal adjustment Avoid in severe renal impairment (electrolyte disturbance risk)
PBS status ✔ PBS General Benefit
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Sodium picosulfate
Dulcolax SP® · Laxoberal® · Stimulant laxative (contact)
Adult dose 5–10 mg (5–10 mL) PO at night. Effect in 6–12 hours.
Paediatric dose 4–10 years: 2.5–5 mg nocte; ≥10 years: 5–10 mg nocte
PBS status ✔ PBS General Benefit
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Bisacodyl
Dulcolax® · Stimulant laxative
Adult dose 5–10 mg PO at night OR 10 mg PR (suppository) — effect in 15–60 min (PR) or 6–12 h (PO)
Cautions Do not crush enteric-coated tablets; avoid antacids within 1 hour
PBS status ✔ PBS General Benefit

Step 4: Pharmacotherapy — Third-Line & Specialist Agents

For patients refractory to combination osmotic and stimulant laxatives after ≥4–8 weeks of optimised therapy, specialist referral is recommended. The following agents are prescribed by or under guidance of gastroenterologists:

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Prucalopride (Resotran®)
Resotran® · Selective 5-HT4 receptor agonist (prokinetic)
Adult dose 2 mg PO once daily (morning); ≥65 years: start 1 mg daily
Indication Chronic constipation in women when laxatives have failed; slow-transit constipation
Cautions Contraindicated in IBD, bowel obstruction, perforation. Avoid severe hepatic impairment (Child-Pugh C). GI cramping, headache common initially.
Renal adjustment 1 mg/day if CrCl <30 mL/min
PBS status ✘ Not PBS-listed — private prescription; significant out-of-pocket cost (~AUD 40–60/month)
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Linaclotide (Constella®)
Constella® · Guanylate cyclase-C agonist
Adult dose 145 mcg PO once daily (30 minutes before breakfast) for CC; 290 mcg for IBS-C
Cautions Diarrhoea (most common AE — usually settles within 4 weeks); contraindicated <6 years; avoid bowel obstruction
PBS status ✘ Not PBS-listed — private prescription only

Biofeedback & Pelvic Floor Rehabilitation

For patients with demonstrated pelvic floor dyssynergia (anismus) — characterised by paradoxical contraction or failure to relax the puborectalis and external anal sphincter during attempted defecation — biofeedback therapy is the evidence-based treatment of choice. Multiple RCTs and a Cochrane review have demonstrated superiority over laxatives alone, with 60–80% of patients reporting improvement after 5–6 sessions. Biofeedback is available through specialist continence physiotherapy services at most major Australian hospitals and some community continence clinics.

Faecal Impaction Management

Faecal impaction (hard, immovable stool in the rectum causing overflow incontinence, abdominal pain, or urinary retention) requires a structured disimpaction regimen:

  • Step 1: Oral macrogol 3350: 1–3 sachets daily (adult dose; higher doses for disimpaction)
  • Step 2: Add stimulant laxative: senna 15–30 mg nocte or sodium picosulfate 10 mg nocte
  • Step 3: Rectal bisacodyl suppository (10 mg PR) or glycerol suppository if oral agents are insufficient after 2–3 days
  • Step 4: Phosphate or sodium citrate enemas (micro-enemas) — use cautiously in elderly and renal impairment
  • Step 5: Manual evacuation under sedation — specialist/medical officer procedure for refractory impaction
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Safety note — Phosphate enemas: Avoid in patients with renal impairment, heart failure, or electrolyte disorders due to risk of life-threatening hyperphosphataemia. Sodium citrate micro-enemas (Micralax®) are generally safer and preferred in the elderly and nursing home settings.

Constipation Quick Reference — Stepwise Approach

Step 1: Lifestyle
Dietary fibre (25–30 g/day), fluid (≥1.5 L), exercise, toilet routine, kiwifruit
Ongoing
Foundation for all patients
Step 2: Osmotic laxatives
Macrogol 3350 1–3 sachets/day OR lactulose 15–30 mL BD
Titrate over 2–4 weeks
First-line pharmacotherapy
Step 3: Add stimulant
Senna 15–30 mg nocte OR sodium picosulfate 5–10 mg nocte
As needed or regular
When osmotic alone insufficient
Step 4: Specialist referral
Prucalopride, linaclotide, biofeedback, surgical opinion
Specialist-guided
After 4–8 weeks of failed optimised therapy

Constipation in Children

Constipation accounts for 3–5% of all paediatric outpatient visits and up to 25% of paediatric gastroenterology referrals in Australia. Functional constipation is the cause in >95% of cases, with organic pathology (including Hirschsprung disease, hypothyroidism, coeliac disease, and anorectal malformation) comprising <5%.

Rome IV Criteria for Paediatric Functional Constipation

In children aged ≥4 years (with adequate verbal and toileting ability), ≥2 of the following criteria for at least 1 month:

  • ≤2 defecations per week in the toilet
  • At least 1 episode of faecal incontinence per week (after the acquisition of toileting skills)
  • History of retentive posturing or excessive volitional stool retention
  • History of painful or hard bowel movements
  • Presence of a large faecal mass in the rectum
  • History of large-diameter stools that may obstruct the toilet

In infants and children <4 years (or pre-verbal), the criteria include ≥2 of the above for 1 month, with the addition of irritability and decreased appetite that improve following passage of large stools, and the absence of criteria for Hirschsprung disease.

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Red flags in paediatric constipation — suspect organic cause if:
  • Failure to pass meconium within 48 hours of birth (Hirschsprung disease until proven otherwise)
  • Constipation from birth or first weeks of life
  • Failure to thrive or weight loss
  • Bloody diarrhoea (not just fissure-related streaks)
  • Abdominal distension with bilious vomiting
  • Gluteal muscle wasting, flattened buttocks, anteriorly placed anus
  • Abnormal neurological examination of the lower limbs
  • Sacral dimple or tuft of hair over the spine (spinal dysraphism)

Paediatric Management — Disimpaction

If faecal impaction is present (palpable abdominal or rectal mass, overflow soiling), disimpaction must be achieved before commencing maintenance therapy. Macrogol 3350 is the recommended first-line agent for disimpaction in Australian children.

Age Macrogol 3350 Disimpaction Dose Duration Notes
1–6 months Generally avoid macrogol-based products; use lactulose 2.5 mL BD under medical supervision 5–7 days Paediatrician review recommended; exclude Hirschsprung
6 months – 1 year ½–1 sachet Movicol®-Half daily (dissolved in 62.5 mL water) Up to 7 days Monitor hydration; ensure adequate fluid intake
1–5 years 1–2 sachets Movicol® (or Movicol®-Half 2–4 sachets) daily for 3–7 days 3–7 days Titrate to effect; add stimulant if needed after day 3
5–12 years 2–4 sachets Movicol® daily for 3–7 days (Paediatric Faecal Impaction Protocol) 3–7 days Can start with lower dose and increase daily as tolerated
12–18 years Adult disimpaction regimen: 4–8 sachets daily 3–7 days Transitional adult dose; consider rectal therapy if oral fails

Paediatric Maintenance Therapy

Once disimpaction is achieved (or if impaction was not present), maintenance laxative therapy should commence immediately and continue for months to years (minimum 6 months is recommended). Abrupt cessation leads to relapse in >50% of children.

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Macrogol 3350 (Maintenance)
Movicol® · Movicol®-Half · First-line maintenance in children
1–6 months Lactulose 2.5 mL BD preferred; macrogol use should be specialist-directed
6 months – 2 years ½–1 sachet Movicol®-Half daily
2–12 years 1–2 sachets Movicol® daily; titrate to 1–2 soft stools/day
12–18 years 1–3 sachets Movicol® daily (adult regimen)
Duration Minimum 6 months; gradual weaning over 2–6 months once regular bowel habit established
PBS status ✔ PBS General Benefit
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Lactulose
Duphalac® · Actilax® · Second-line or adjunct in infants
Dose 1 month–1 year: 2.5 mL BD; 1–5 years: 2.5–10 mL BD; 5–18 years: 5–20 mL BD
Cautions Flatulence; sweet taste may cause refusal; avoid in galactosaemia
PBS status ✔ PBS General Benefit

Behavioural & Psychological Interventions

Behavioural strategies are integral to paediatric constipation management, particularly in children with withholding behaviour and toilet avoidance:

  • Toilet training reinforcement: Regular toileting (after meals), use of a footstool, praise and reward systems (sticker charts)
  • Education: Explain the "poo that won't come out" cycle to parents and children using age-appropriate language
  • Bowel diary: Record stool frequency, consistency (Bristol scale), laxative dose, and episodes of soiling — aids monitoring and dose titration
  • Avoid punishment: Soiling is involuntary (overflow incontinence) and not deliberate; punitive responses worsen withholding and psychological distress
  • Referral to child psychologist if significant anxiety, behavioural issues, or family distress
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Key Australian resource: The Children's Hospital at Westmead and the Royal Children's Hospital Melbourne both provide excellent parent information booklets on functional constipation management. The ERIC (The Children's Bowel & Bladder Charity) resource "Poo Nurses" video series is also recommended for family education.

When to Refer — Paediatric

  • Failure to respond to ≥3 months of optimised laxative therapy (adherent and adequate doses)
  • Red flag features suggesting organic cause (see above)
  • Suspected Hirschsprung disease — requires rectal biopsy (suction or full-thickness)
  • Recurrent faecal impaction requiring repeated hospitalisation
  • Need for anorectal manometry or colonic transit studies
  • Significant psychological comorbidity or family dysfunction
  • Consider coeliac screening (tTG-IgA) and thyroid function in refractory cases

Pathophysiology

Normal defecation requires coordinated colonic motility, adequate stool volume and consistency, intact anorectal sensation, and synchronised pelvic floor relaxation. Constipation results from disruption at one or more of these levels:

Normal Colonic Transit & Defecation Physiology

  • Colonic motility: High-amplitude propagated contractions (HAPCs, or "mass movements") 1–3 times daily propel colonic contents caudally. These are most common post-prandially (gastrocolic reflex) and upon waking.
  • Water absorption: The colon absorbs 1–1.5 L of fluid daily, converting liquid ileal effluent into semi-solid faeces. Excessive absorption (as with opioid use) produces hard, dry stool.
  • Rectal filling & sampling: As stool enters the rectum, the recto-anal inhibitory reflex (RAIR) allows sampling by the anal mucosa to distinguish gas from solid. This is absent in Hirschsprung disease.
  • Defecation: Voluntary process requiring: (1) conscious urge from rectal distension, (2) assumption of a sitting/squatting position, (3) Valsalva manoeuvre increasing intra-abdominal pressure, (4) relaxation of the puborectalis muscle and external anal sphincter, and (5) straightening of the anorectal angle.

Subtypes of Chronic Constipation

Subtype Prevalence Among CC Pathophysiology Key Diagnostic Feature
Normal transit (functional) ~59% Heightened visceral sensitivity; patients perceive normal-frequency stools as insufficient Colonic transit study normal; symptom-based
Slow transit ~13% Reduced HAPCs, colonic inertia, possible enteric neuropathy or myopathy Delayed radiopaque marker transit; infrequent urge to defecate
Pelvic floor dyssynergia (outlet obstruction) ~25% Paradoxical contraction or failure to relax pelvic floor during defecation Anorectal manometry; failed balloon expulsion (>1 min)
Overlap (slow transit + dyssynergia) ~3% Combined motility and pelvic floor dysfunction Both transit and manometry studies abnormal

Understanding the subtype is important for directing therapy. Normal-transit constipation responds best to lifestyle measures and osmotic laxatives. Slow-transit constipation may require prokinetic agents (prucalopride) or, in severe refractory cases, surgical consideration (subtotal colectomy with ileorectal anastomosis — reserved for highly selected patients at tertiary centres). Pelvic floor dyssynergia responds to biofeedback therapy, which retrains coordinated defecation.

Special Populations

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Pregnancy

Prevalence:
~40% of pregnant women experience constipation; highest in 2nd and 3rd trimesters
First-line:
Dietary fibre, fluids, exercise, kiwifruit. Macrogol 3350 is safe in pregnancy (Category A — no evidence of harm)
Lactulose:
Safe in pregnancy and breastfeeding — no systemic absorption
Avoid:
Stimulant laxatives for prolonged use (senna, bisacodyl) — may cause uterine cramping. Short-term use for severe constipation is acceptable.
Mineral oil:
Avoid — impairs absorption of fat-soluble vitamins (A, D, E, K)
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Elderly (≥65 years)

Key issues:
Polypharmacy (anticholinergic burden), reduced mobility, dehydration, immobility, cognitive impairment
Medication review:
Mandatory — use the Anticholinergic Cognitive Burden (ACB) scale to identify contributing medications
Preferred laxatives:
Macrogol 3350 (preferred — minimal electrolyte effect); lactulose as second-line. Avoid magnesium-containing laxatives (hypermagnesaemia risk with renal impairment)
Avoid:
Bulk-forming laxatives if poor fluid intake or dysphagia (faecal impaction risk); phosphate enemas (hyperphosphataemia); bulk agents with concurrent opioid use
Nursing home:
Implement bowel management plans; regular toileting schedule; consider PRN laxative protocols reviewed monthly
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Renal Impairment

Key issues:
Electrolyte disturbances (hyperkalaemia, hypermagnesaemia), reduced renal excretion of drug metabolites
Preferred:
Macrogol 3350 (monitor electrolytes if CrCl <30); lactulose (use cautiously — may worsen dehydration)
Avoid:
Magnesium-containing laxatives (Milk of Magnesia®) — risk of fatal hypermagnesaemia in CKD; phosphate enemas — hyperphosphataemia; senna in severe renal impairment
Dialysis patients:
Constipation is common (restricted fluid, phosphate binders, low-fibre diet). Macrogol is preferred; dose-adjust within fluid restrictions. Avoid naloxegol if on dialysis.
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Hepatic Impairment

Key issues:
Constipation worsens hepatic encephalopathy by increasing ammonia-producing bacteria and reducing ammonia excretion via the gut
Preferred:
Lactulose is first-line in liver disease (reduces ammonia absorption; treats/prevents hepatic encephalopathy). Titrate to 2–3 soft stools daily.
Avoid:
Naloxegol in severe hepatic impairment (Child-Pugh C)
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Immunocompromised

Key issues:
Transplant recipients (calcineurin inhibitors), HIV (antiretroviral-related), chemotherapy-induced constipation (5-HT3 antagonists, vinca alkaloids)
Prophylaxis:
All patients on vinca alkaloids (vincristine) must receive prophylactic laxatives — vincristine-induced ileus is a life-threatening complication
Preferred:
Macrogol 3350 + stimulant laxative for chemotherapy-induced constipation. Avoid rectal procedures if neutropenic (platelets <50).
Aboriginal and Torres Strait Islander Health Considerations
Prevalence & Burden
Constipation is reported more frequently in Aboriginal and Torres Strait Islander populations, driven by higher rates of chronic disease, polypharmacy, reduced access to fresh fruit and vegetables in remote communities, and limited access to primary healthcare services. The AIHW reports that 36% of Aboriginal and Torres Strait Islander people live in areas classified as remote or very remote, where food costs can be 50–70% higher than urban centres ("food desert" effect).
Dietary Fibre Access
Remote communities often rely on processed, shelf-stable foods with low fibre content. Community stores (e.g., through Outback Stores and ALPA) are increasingly stocking fresh produce, but availability remains inconsistent. Culturally appropriate dietary counselling should incorporate traditional bush foods where available (bush tomatoes, wattleseed, quandong — all sources of dietary fibre).
Medication-Related Constipation
Aboriginal and Torres Strait Islander peoples have a higher chronic disease burden (diabetes, renal disease, cardiovascular disease) and are more likely to be on polypharmacy regimens including opioids for chronic pain, anticholinergics, and iron supplements. Proactive laxative co-prescribing should be a standard component of chronic disease management plans.
Cultural Safety & Communication
Bowel function may be considered a sensitive topic in some Aboriginal and Torres Strait Islander communities. Health practitioners should use plain language, allow time for discussion, and employ Aboriginal Health Workers (AHWs) and Aboriginal Health Practitioners (AHPs) as cultural brokers. Gender-concordant practitioners may be preferred for discussing bowel and toileting issues. "Shame" related to soiling in children should be addressed sensitively.
Healthcare Access
Many remote communities lack resident GPs or specialist services. Telehealth consultations (Medicare items 99200–99215) can support gastroenterology review. Aboriginal Community Controlled Health Organisations (ACCHOs) — such as AMS Redfern, Danila Dilba (Darwin), and Apunipima (Cape York) — provide holistic, culturally safe care and should be engaged as primary providers.
Paediatric Considerations
Functional constipation in Aboriginal and Torres Strait Islander children is common and may present late, with established impaction and overflow soiling. Toilet training in some communities occurs later than in non-Indigenous settings. Education resources should be culturally adapted and co-designed with community health workers. Sticker-chart based reward systems should be adapted to local context and literacy levels.
Closing the Gap Targets
Addressing constipation and its complications contributes to broader Close the Gap targets (Target 1 — Life expectancy; Target 2 — Child health). Proactive bowel health screening, medication review in chronic disease management, and culturally safe health promotion campaigns (e.g., "Good Food, Good Health" programs run by ACCHOs) are key strategies.

📚 References

  1. 1. Lacy BE, Mearin F, Chang L, et al. Bowel disorders. Gastroenterology. 2016;150(6):1393–1407.e5. (Rome IV criteria for functional constipation)
  2. 2. Bharucha AE, Pemberton JH, Locke GR. American Gastroenterological Association technical review on constipation. Gastroenterology. 2013;144(1):218–238.
  3. 3. National Institute for Health and Care Excellence (NICE). Constipation in children and young people: diagnosis and management. Clinical Guideline CG99. Updated 2017.
  4. 4. Tabbers MM, DiLorenzo C, Berger MY, et al. Evaluation and treatment of functional constipation in infants and children: evidence-based recommendations from ESPGHAN and NASPGHAN. JPGN. 2014;58(2):258–274.
  5. 5. Australian Institute of Health and Welfare (AIHW). Aboriginal and Torres Strait Islander Health Performance Framework 2023. Canberra: AIHW; 2023.
  6. 6. Ford AC, Suares NC. Effect of laxatives and pharmacological therapies in chronic idiopathic constipation: systematic review and meta-analysis. Gut. 2011;60(2):209–218.
  7. 7. Chey WD, Webster L, Sostek M, et al. Naloxegol for opioid-induced constipation in patients with noncancer pain. N Engl J Med. 2014;370(25):2387–2396.
  8. 8. Belsey J, Greenfield S, Candy D, Geraint M. Systematic review: impact of constipation on quality of life in adults and children. Aliment Pharmacol Ther. 2010;31(9):938–944.
  9. 9. Rao SS, Bharucha AE, Chiarioni G, et al. Anorectal disorders. Gastroenterology. 2016;150(6):1430–1442.e4. (Functional anorectal disorders — Rome IV)
  10. 10. Royal Australian College of General Practitioners (RACGP). Guidelines for preventive activities in general practice (Red Book). 9th ed. Melbourne: RACGP; 2018.
  11. 11. Gearry RB, Ware A, Withers T, et al. Green kiwifruit normalises bowel function in IBS patients: results from a multicentre randomised controlled trial. Am J Gastroenterol. 2023;118(1):157–166.
  12. 12. National Health and Medical Research Council (NHMRC). Australian Dietary Guidelines. Canberra: NHMRC; 2013.
  13. 13. Australian Commission on Safety and Quality in Health Care (ACSQHC). National Safety and Quality Health Service Standards. 2nd ed. Sydney: ACSQHC; 2021.
  14. 14. Mugie SM, Benninga MA, Di Lorenzo C. Epidemiology of constipation in children and adults: a systematic review. Best Pract Res Clin Gastroenterol. 2011;25(1):3–18.
  15. 15. Bassotti G, Villanacci V, Maurer CA, et al. The role of glial cells and apoptosis of enteric neurones in the neuropathology of intractable slow transit constipation. Gut. 2006;55(1):41–46.
for PBS scripts. Utilise ACCHS pharmacies and Remote Area Aboriginal Health Worker programs for medication supply in remote areas. Avoid initiating benzodiazepines; support holistic pain management including community-based exercise programs.
Preventive health
Promote bone health: encourage vitamin D supplementation (1000 IU daily in deficient individuals), smoking cessation support, reduction of alcohol intake, and weight-bearing exercise. MBS Item 715 health checks provide a structured opportunity to assess bone health, screen for osteoporosis risk factors, and discuss musculoskeletal health in a culturally safe context.

Quick Reference: Differential Diagnosis at a Glance

Costovertebral dysfunction
Paracetamol ± NSAID; manual therapy
2–6 weeks
Provocable on palpation; no red flags
Thoracic compression fracture
Paracetamol; ± calcitonin; DXA + osteoporosis Rx
6–12 weeks healing
Elderly; osteoporosis; acute onset
ACS (posterior MI)
Aspirin 300 mg, GTN, heparin; urgent PCI
Time-critical
ECG, troponin; CV risk factors
Aortic dissection
IV labetalol; urgent CT aortogram; surgery (Type A)
Time-critical
Tearing pain; BP differential >20 mmHg
Vertebral osteomyelitis
IV antibiotics (vancomycin + ceftriaxone initially); ID consult
6 weeks IV antibiotics
Fever, elevated CRP, IV drug use
Biliary colic / cholecystitis
Paracetamol ± morphine; lap cholecystectomy
Surgical within 72 h (cholecystitis)
RUQ/infrascapular; post-prandial; RUQ US

📚 References

  1. 1. Briggs AM, Smith AJ, Straker LM, Bragge P. Thoracic spine pain in the general population: prevalence, incidence and associated factors in children, adolescents and adults. A systematic review. BMC Musculoskelet Disord. 2009;10:77.
  2. 2. National Health and Medical Research Council (NHMRC). Evidence-based management of acute musculoskeletal pain. Canberra: NHMRC; 2003 (updated 2020).
  3. 3. Australian Institute of Health and Welfare (AIHW). Aboriginal and Torres Strait Islander Health Performance Framework: Summary report 2023. Canberra: AIHW; 2023.
  4. 4. Deyo RA, Rainville J, Kent DL. What can the history and physical examination tell us about low back pain? JAMA. 1992;268(6):760–765.
  5. 5. Stochkendahl MJ, Kjaer P, Hartvigsen J, et al. National Clinical Guidelines for non-surgical treatment of patients with recent onset low back pain or lumbar radiculopathy. Europ Spine J. 2018;27(1):60–75.
  6. 6. Erwin WM, Jackson PC, Homonko DA. Innervation of the human costovertebral joint: implications for clinical back pain syndromes. J Manipulative Physiol Ther. 2000;23(6):395–403.
  7. 7. Royal Australian College of General Practitioners (RACGP). Guidelines for preventive activities in general practice. 9th edn. Melbourne: RACGP; 2018 (updated 2023).
  8. 8. Hirsch JA, Singh V, Falco FJE, et al. Thoracic facet joint interventions. Pain Physician. 2016;19(4):E581–E593.
  9. 9. Erwin WM, Jackson PC. The costovertebral joint: anatomy, biomechanics, and clinical significance in thoracic back pain syndromes. J Can Chiropr Assoc. 2003;47(2):112–120.
  10. 10. Strayer RJ, Gunnerson JM, Brown LH, et al. Aortic dissection: clinical features, diagnosis, and management. Aust Crit Care. 2019;32(2):144–153.
  11. 11. Ombregt L. A system of orthopaedic medicine. 3rd edn. Edinburgh: Churchill Livingstone Elsevier; 2013. Chapter 18: Thoracic spine.
  12. 12. Lin CC, Chen KH, Li DM, et al. Characteristics and outcomes of patients presenting with thoracic back pain to the emergency department. Emerg Med Australas. 2020;32(5):805–811.
for PBS-listed medicines at participating pharmacies.
Cultural safety
Engagement with Aboriginal Community Controlled Health Organisations (ACCHOs) is essential. Cultural safety training for non-Indigenous clinicians, use of Aboriginal Health Workers and Liaison Officers, and incorporation of traditional healing practices alongside Western medicine improve treatment adherence and outcomes. Avoidance of eye contact, respect for gender-sensitive examination practices, and understanding of sorry business protocols are critical elements of culturally safe care.
Medication adherence
Complex DMARD regimens with frequent monitoring requirements present adherence challenges. Long-acting depot injections (e.g., methotrexate SC) may improve adherence compared to oral regimens. Community pharmacy partnerships through the Indigenous Pharmacy Programmes improve medication management.
Specific conditions
Rheumatic heart disease (RHD) requires secondary prophylaxis with benzathine penicillin G (BPG) 1.2 MU IM every 3–4 weeks for a minimum of 10 years or until age 21 (whichever is longer). RHD registers (e.g., NT RHD Register) facilitate recall and follow-up. The Australian RHD Endgame Strategy targets elimination by 2031.
Referral pathways
Referral through ACCHOs and Aboriginal Hospital Liaison Officers (AHLOs) improves engagement. The Specialist Outreach Assistance Programme provides funded specialist visits to remote communities. NT, WA, and QLD have specific rheumatology outreach programmes targeting Indigenous communities.

📚 References

  1. 1. Australian Institute of Health and Welfare (AIHW). Autoimmune disease in Australia. Cat. no. PHE 312. Canberra: AIHW; 2023.
  2. 2. Fraenkel L, Bathon JM, England BR, et al. 2021 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Care Res. 2021;73(7):924–939.
  3. 3. Fanouriakis A, Kostopoulou M, Alber K, et al. 2019 update of the EULAR recommendations for the management of systemic lupus erythematosus. Ann Rheum Dis. 2019;78(6):736–745.
  4. 4. Chung SA, Langford CA, Maz M, et al. 2021 American College of Rheumatology/Vasculitis Foundation guideline for the management of antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Care Res. 2021;73(11):1583–1599.
  5. 5. Smolen JS, Landewé RBM, Bijlsma JWJ, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2022 update. Ann Rheum Dis. 2023;82(1):3–18.
  6. 6. Australian Technical Advisory Group on Immunisation (ATAGI). Australian Immunisation Handbook. Australian Government Department of Health; 2024. Available from: immunisationhandbook.health.gov.au.
  7. 7. Rheumatic Heart Disease Australia (RHDAustralia). The 2020 Australian guideline for prevention, diagnosis, and management of acute rheumatic fever and rheumatic heart disease. 3rd ed. Darwin: Menzies School of Health Research; 2020.
  8. 8. Pharmaceutical Benefits Scheme (PBS). PBS Schedule. Australian Government Department of Health. Available from: pbs.gov.au. Accessed 2024.
  9. 9. Agarwal S, Cunnington J, Nossent J. Autoimmune disease in Indigenous Australians: a systematic review. Int J Rheum Dis. 2021;24(12):1487–1498.
  10. 10. Pisetsky DS. Antinuclear antibody testing — misunderstood or misused? Clin Immunol. 2023;255:109717.
  11. 11. Bertsias GK, Tektonidou M, Amoura Z, et al. Joint European League Against Rheumatism and European Renal Association–European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations for the management of adult and paediatric lupus nephritis. Ann Rheum Dis. 2012;71(11):1771–1782.
  12. 12. Ledingham J, Deighton C; British Society for Rheumatology Standards, Audit and Guidelines Working Group. Update on the British Society for Rheumatology guidelines for prescribing TNFα blockers in adults with rheumatoid arthritis. Rheumatology. 2005;44(2):155–158.
  13. 13. National Health and Medical Research Council (NHMRC). National statement on ethical conduct in human research. Canberra: NHMRC; 2023 (updated).
for PBS-listed medicines at participating pharmacies.
Cultural safety
Engagement with Aboriginal Community Controlled Health Organisations (ACCHOs) is essential. Cultural safety training for non-Indigenous clinicians, use of Aboriginal Health Workers and Liaison Officers, and incorporation of traditional healing practices alongside Western medicine improve treatment adherence and outcomes. Avoidance of eye contact, respect for gender-sensitive examination practices, and understanding of sorry business protocols are critical elements of culturally safe care.
Medication adherence
Complex DMARD regimens with frequent monitoring requirements present adherence challenges. Long-acting depot injections (e.g., methotrexate SC) may improve adherence compared to oral regimens. Community pharmacy partnerships through the Indigenous Pharmacy Programmes improve medication management.
Specific conditions
Rheumatic heart disease (RHD) requires secondary prophylaxis with benzathine penicillin G (BPG) 1.2 MU IM every 3–4 weeks for a minimum of 10 years or until age 21 (whichever is longer). RHD registers (e.g., NT RHD Register) facilitate recall and follow-up. The Australian RHD Endgame Strategy targets elimination by 2031.
Referral pathways
Referral through ACCHOs and Aboriginal Hospital Liaison Officers (AHLOs) improves engagement. The Specialist Outreach Assistance Programme provides funded specialist visits to remote communities. NT, WA, and QLD have specific rheumatology outreach programmes targeting Indigenous communities.

📚 References

  1. 1. Australian Institute of Health and Welfare (AIHW). Autoimmune disease in Australia. Cat. no. PHE 312. Canberra: AIHW; 2023.
  2. 2. Fraenkel L, Bathon JM, England BR, et al. 2021 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Care Res. 2021;73(7):924–939.
  3. 3. Fanouriakis A, Kostopoulou M, Alber K, et al. 2019 update of the EULAR recommendations for the management of systemic lupus erythematosus. Ann Rheum Dis. 2019;78(6):736–745.
  4. 4. Chung SA, Langford CA, Maz M, et al. 2021 American College of Rheumatology/Vasculitis Foundation guideline for the management of antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Care Res. 2021;73(11):1583–1599.
  5. 5. Smolen JS, Landewé RBM, Bijlsma JWJ, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2022 update. Ann Rheum Dis. 2023;82(1):3–18.
  6. 6. Australian Technical Advisory Group on Immunisation (ATAGI). Australian Immunisation Handbook. Australian Government Department of Health; 2024. Available from: immunisationhandbook.health.gov.au.
  7. 7. Rheumatic Heart Disease Australia (RHDAustralia). The 2020 Australian guideline for prevention, diagnosis, and management of acute rheumatic fever and rheumatic heart disease. 3rd ed. Darwin: Menzies School of Health Research; 2020.
  8. 8. Pharmaceutical Benefits Scheme (PBS). PBS Schedule. Australian Government Department of Health. Available from: pbs.gov.au. Accessed 2024.
  9. 9. Agarwal S, Cunnington J, Nossent J. Autoimmune disease in Indigenous Australians: a systematic review. Int J Rheum Dis. 2021;24(12):1487–1498.
  10. 10. Pisetsky DS. Antinuclear antibody testing — misunderstood or misused? Clin Immunol. 2023;255:109717.
  11. 11. Bertsias GK, Tektonidou M, Amoura Z, et al. Joint European League Against Rheumatism and European Renal Association–European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations for the management of adult and paediatric lupus nephritis. Ann Rheum Dis. 2012;71(11):1771–1782.
  12. 12. Ledingham J, Deighton C; British Society for Rheumatology Standards, Audit and Guidelines Working Group. Update on the British Society for Rheumatology guidelines for prescribing TNFα blockers in adults with rheumatoid arthritis. Rheumatology. 2005;44(2):155–158.
  13. 13. National Health and Medical Research Council (NHMRC). National statement on ethical conduct in human research. Canberra: NHMRC; 2023 (updated).