How are anal fissures diagnosed and treated in a clinical setting?
Executive summary
Anal fissures are diagnosed primarily by history and direct inspection of the anoderm, and are managed stepwise from conservative measures—diet, sitz baths and stool softeners—to topical pharmacologic sphincter relaxants, botulinum toxin injection, and, for refractory chronic cases, surgical options such as lateral internal sphincterotomy (LIS) or fissurectomy [1] [2] [3]. Guidelines from multiple professional societies emphasize nonoperative first-line care for acute fissures and reserve surgery for chronic or treatment‑resistant disease because of both good healing rates with medical therapy and the long‑term risks of incontinence after surgery [3] [4] [5].
1. Diagnosis is clinical, not high‑tech
The typical patient history—severe tearing pain during and after defecation often with bright red bleeding—combined with direct visualization of a linear posterior midline tear usually establishes the diagnosis in the clinic; inspection is the cornerstone of evaluation and usually suffices to exclude other causes such as thrombosed external hemorrhoids or abscess [1] [2] [6]. Atypical presentations—multiple fissures, ulcers off the midline, or fissures in patients with systemic symptoms—trigger further workup for secondary causes like Crohn disease, infection or malignancy and may require referral and additional testing [1] [6] [7].
2. Classifying acute versus chronic changes what clinicians do next
Fissures are often categorized as acute (symptoms <6 weeks) or chronic (>6 weeks), and that distinction guides treatment choice because acute fissures frequently heal with conservative measures while chronic fissures are less likely to resolve without targeted pharmacologic or procedural therapy [1] [5]. Professional guidelines recommend trying nonoperative therapy first for acute fissures and warn that healing rates decline as symptom duration increases—one series showed near‑universal healing when treated within a month versus much lower rates after six months [3] [5].
3. First‑line conservative care: stool form, hygiene, sitz baths
Initial management in the clinic focuses on reducing trauma and spasm: fiber or bulk-forming agents and stool softeners to prevent hard stools, sitz baths and topical emollients to improve hygiene and decrease spasm and pain; about half of patients with acute fissures improve with these measures alone [8] [5] [9]. These interventions are low‑risk and form the base of guideline‑recommended stepwise care [3] [9].
4. Topical medicine and minimally invasive injections for chronic fissures
When conservative measures fail, topical pharmacologic sphincter relaxants are standard: nitroglycerin (nitrates) and topical calcium‑channel blockers such as diltiazem or nifedipine reduce internal sphincter tone and promote healing, with CCBs often preferred because they cause fewer headaches than nitrates [4] [5] [10]. For patients who do not respond to topical therapy, botulinum toxin injected into the internal sphincter can induce temporary chemical denervation and has documented efficacy as a second‑line, less invasive option than surgery [10] [9].
5. When surgery is considered — types and tradeoffs
Surgical management, most commonly lateral internal sphincterotomy (LIS), is the definitive treatment for many refractory chronic fissures and has high healing rates, but it carries real long‑term risks including fecal incontinence; therefore guidelines advise reserving LIS for selected patients who have failed medical therapy and who have no baseline incontinence [4] [7] [5]. Fissurectomy and other operative techniques are alternatives in specific contexts, and most consensus documents recommend exploring surgical options only after 6–8 weeks of unsuccessful topical treatment [7] [9].
6. Controversies, evidence gaps and clinician judgement
Although multiple international guidelines harmonize around a stepwise approach, nuances remain—uncertainty persists about oral versus topical CCBs, optimal botulinum dosing and long‑term comparative trials of surgical techniques versus medical therapy—and clinical judgment tied to symptom duration, sphincter function and patient priorities remains essential [5] [10]. Some guideline panels explicitly note limitations of the evidence base and emphasize individualized decisions; clinicians should also investigate secondary causes when features are atypical to avoid missing systemic disease [6] [1].