Post-Coital Bleeding: Evaluation and Management
All women presenting with post-coital bleeding should be tested for Chlamydia trachomatis and undergo speculum examination to assess for visible cervical lesions, with urgent referral if malignancy is suspected on examination. 1
Initial Clinical Assessment
History and Physical Examination
- Confirm the bleeding source is truly post-coital and not from the sexual partner, as partner bleeding can be mistaken for the patient's own bleeding 2
- Assess cervical appearance during speculum examination for ulcerating or fungating lesions that suggest malignancy 1
- Document associated symptoms including intermenstrual bleeding, post-menopausal bleeding, menstrual abnormalities (present in 39% of cases), and dyspareunia (present in 13% of cases) 3
- Evaluate for trauma, particularly in nulliparous women, as 89.7% of post-coital trauma cases occur in this population 4
Immediate Testing
- Test for Chlamydia trachomatis in all women with post-coital bleeding and treat if positive 1
- Do not perform unscheduled Pap smears outside the routine screening program, as this is not recommended 1
Risk Stratification
Low-Risk Features
- Age under 40 years: The probability of cervical cancer in women aged 20-24 with post-coital bleeding is 1 in 44,000, increasing to 1 in 2,400 for women aged 45-54 1
- Multiparity: Multiparous women have significantly lower risk (OR 0.39,95% CI 0.22-0.88) compared to nulliparous women 5
- Normal recent cervical cytology within the past year 5
High-Risk Features Requiring Urgent Referral
- Visible cervical lesion on examination (ulcerating or fungating appearance) warrants immediate referral for biopsy 1
- Abnormal Pap smear within the past year increases risk 3.3-fold (95% CI 1.31-8.35) 5
- Nulliparity is an independent risk factor for dysplasia 5
- Age over 40 years increases cancer probability 1
Diagnostic Workup
Colposcopy Indications
- Refer for colposcopy if abnormal cervical cytology is present, especially in nulliparous women 5
- Consider colposcopy even with normal cytology in persistent or recurrent post-coital bleeding, as the positive predictive value for koilocytosis/CIN 1 or higher is 15.6% 5
- Colposcopy findings in women with post-coital bleeding reveal pathology in approximately 48.9% of cases undergoing directed biopsy 5
Expected Findings
The most common etiologies identified at colposcopy include:
- Cervicitis (33.8% of biopsied cases) 5
- Koilocytosis/CIN 1/condyloma (30.3%) 5
- Cervical polyps (12.4%) 5
- Cervical ectropion (25% in general PCB population) 3
- CIN 2/3 or cancer (1.5% combined) 5
Treatment Based on Etiology
Infectious Causes
- Treat Chlamydia with appropriate antibiotics if testing is positive 1
- Manage cervicitis based on identified organism 5
Benign Structural Lesions
- Remove cervical polyps if identified, as they account for 20% of cases 3
- Consider endometrial polyp evaluation with hysteroscopy if bleeding persists despite normal cervical examination, as endometrial polyps can contribute to post-coital bleeding 3
- Cervical ectropion may be managed expectantly or with cryotherapy/thermal ablation if symptomatic 3
Dysplasia/Malignancy
- Refer to gynecologic oncology for CIN 2/3 or invasive cancer 1
- Multidisciplinary team management is essential for confirmed cervical cancer 1
Special Considerations
Natural History Without Identifiable Cause
- Reassurance is appropriate when examination, Chlamydia testing, and age-appropriate cervical cancer screening are normal 2
- The incidence of cervical cancer is low (0.5%) even among women presenting with post-coital bleeding who undergo colposcopy 5
Common Pitfalls to Avoid
- Do not rely solely on cervical cytology to exclude significant pathology, as CIN may not always be asymptomatic 3
- Do not dismiss post-coital bleeding in younger women, though cancer risk is lower, dysplasia can still occur 5
- Do not perform unscheduled Pap smears as they are not recommended and may delay appropriate evaluation 1
- Do not assume all bleeding is benign in nulliparous women, as they have higher risk for dysplasia 5