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Initial assessment pathway
The aim of the initial assessment is to identify the type of incontinence, find reversible causes and red flags, assess the impact on quality of life and start first-line treatment. For most patients, one or two visits without instrumental tests are enough.

Step 1. Ask actively
Many women don't raise incontinence themselves. Ask actively: at routine check-ups, postnatally, around menopause, and in women with obesity, diabetes or chronic cough. A simple question: "Do you ever leak urine when you cough, exercise or on the way to the toilet?"
Step 2. History
- Symptoms: leakage on effort, urgency, daytime frequency, nocturia, amount lost, pad use.
- Duration and course, relation to childbirth, menopause, surgery, new medicines.
- Voiding symptoms: weak stream, straining, feeling of incomplete emptying.
- Red flags: haematuria, pain, recurrent infections, neurological symptoms.
- Obstetric history: parity, mode of delivery, birth weight, instrumental delivery, multiple births.
- Comorbidities: diabetes, COPD, neurological disease, constipation, cognitive impairment, mobility.
- Medicines: diuretics, ACE inhibitors (cough), anticholinergics, sedatives.
- The patient's goals and impact on quality of life and sexual function.
Step 3. Questionnaire and diary
ICIQ-SF quantifies severity (0–21 points) and allows you to track change. Patients can complete it beforehand on this site. Klovning severity bands: 1–5 slight, 6–12 moderate, 13–18 severe, 19–21 very severe.
The bladder diary is kept for at least 3 days: time and volume of voids, fluid intake, episodes of urgency and leakage. It reveals polyuria (more than 40 ml/kg per 24 hours), nocturnal polyuria, low functional bladder capacity, and excessive or inadequate fluid intake.
Step 4. Examination
- abdominal palpation (masses, palpable bladder);
- perineal and vaginal examination: mucosal atrophy, pelvic organ prolapse (POP-Q where possible), fistulae;
- cough stress test with a full bladder;
- digital assessment of voluntary pelvic floor contraction (e.g. modified Oxford scale);
- brief neurological examination if a neurological cause is suspected.
Step 5. Laboratory tests
- urine dipstick for all patients; if infection is suspected, send a sample for culture before starting antibiotics;
- blood glucose if there is polyuria or risk factors for diabetes;
- renal function if chronic retention is suspected.
Step 6. Post-void residual
Measure (preferably with bladder ultrasound) if there are voiding symptoms, recurrent infections, neurological disease or prolapse, and before starting antimuscarinics in at-risk patients.
Step 7. Classification and plan
- Determine the predominant type: stress, urgency (OAB), mixed or overflow.
- Exclude and correct reversible causes: infection, constipation, medicines, hyperglycaemia, excessive fluid intake.
- If there are no red flags, start first-line treatment (see Management pathway).
- Agree a goal and a follow-up date with the patient.
Referral criteria
- Urgent: visible haematuria; microscopic haematuria in women 50 and over; suspected malignancy; acute retention; neurological symptoms with voiding dysfunction.
- Routine: bladder or urethral pain, recurrent infections, suspected fistula, significant residual urine, symptomatic prolapse, previous continence surgery or radical pelvic procedures, diagnostic uncertainty, failure of first-line treatment.
Sources
- NICE guideline NG123. 2019. nice.org.uk
- EAU Guidelines on Non-neurogenic Female LUTS. uroweb.org
- Avery K, et al. ICIQ. Neurourol Urodyn. 2004;23(4):322–330.
- Klovning A, et al. Comparison of two questionnaires for assessing the severity of urinary incontinence: The ICIQ-UI SF versus the incontinence severity index. Neurourol Urodyn. 2009;28(5):411–415.