Epistaxsis causes, bleeding site( how to differentiate ), risk factors, investigations, management in emergency opd and age wise

| Feature | Anterior Epistaxis | Posterior Epistaxis |
|---|---|---|
| Frequency | >90% of cases | ~10% |
| Source | Kiesselbach's plexus (Little's area) | Woodruff plexus / sphenopalatine branches |
| Age group | Children, young adults | Elderly (>50 years) |
| Laterality | Usually unilateral | Often bilateral or non-localizable |
| Severity | Mild to moderate, self-limiting | Severe, arterial, profuse |
| Visibility | Visible on anterior rhinoscopy | Not visible anteriorly |
| Blood flow direction | Predominantly out of nostril | Down posterior pharynx (patient swallows blood, nausea, haematemesis) |
| Response to pressure | Stops with external pressure | Does NOT stop with external pressure |
| Responds to anterior pack | Yes | No - needs posterior pack |
| Associated features | Dry mucosa, nose picking | Hypertension, arteriosclerosis, anticoagulants |
| Category | Specific Causes |
|---|---|
| Traumatic | Nose picking (most common), vigorous nose blowing, nasal/facial fractures, foreign body, chemical injury, piercings, skull base fractures involving anterior ethmoidal arteries |
| Mucosal irritation | Cold/dry weather, low humidity, CPAP/nasal cannula, septal deviation, septal perforation |
| Infections | Viral/bacterial/fungal rhinosinusitis, granulomatous disorders |
| Neoplastic | Juvenile angiofibroma (adolescent boys, life-threatening), haemangioma, pyogenic granuloma, inverted papilloma, carcinoma, sarcoma, lymphoma |
| Vascular | HHT (Osler-Weber-Rendu disease) - autosomal dominant, recurrent multifocal bleeds from thin-walled telangiectasias |
| Iatrogenic | Post-nasal/sinus/septal surgery, NG tube placement |
| Category | Specific Causes |
|---|---|
| Cardiovascular | Hypertension, arteriosclerosis |
| Coagulation disorders | Haemophilia A/B, von Willebrand disease, thrombocytopenia (primary, drug-induced, leukaemia/lymphoma), DIC |
| Medications | Warfarin, NOACs (rivaroxaban, apixaban), heparin, aspirin, clopidogrel, topical nasal steroids, chronic nasal vasoconstrictors |
| Liver disease | Chronic liver disease / cirrhosis (impaired clotting factor synthesis) |
| Renal disease | CKD (platelet dysfunction) |
| Nutritional | Vitamin K deficiency, folic acid deficiency |
| Drug/toxin | Cocaine abuse (mucosal destruction), chronic alcohol use |
| Haematologic malignancy | Leukaemia, lymphoma |
| Chemotherapy | Thrombocytopenia |
| Investigation | Indication |
|---|---|
| FBC (CBC) | Assess Hb (transfuse if <7 g/dL, or <8 g/dL with cardiovascular disease), platelet count |
| Coagulation screen (PT, aPTT, INR) | Anticoagulant use, liver disease, DIC |
| Blood group and crossmatch | Severe haemorrhage |
| Liver function tests | Suspected liver disease |
| Renal function | CKD |
| Blood film | Suspected leukaemia/haematologic malignancy |
| vWF antigen/activity | Recurrent epistaxis in young patient |
| Nasal endoscopy | Identify source, especially posterior bleeds |
| CT sinuses/nose | Suspected tumour, trauma, vascular malformation |
| Contrast CT/MRI | Juvenile angiofibroma (anterior bowing of posterior antral wall = Holman-Miller / antral sign) |
| Angiography | Pre-embolisation workup for refractory cases |
| Procedure | Indication |
|---|---|
| Endoscopic sphenopalatine artery ligation (ESPAL) | Posterior epistaxis failing packing; safe, effective, avoids posterior packing morbidity |
| Anterior/posterior ethmoidal artery ligation | Superior/posterior bleeds; endoscopic or transorbital approach |
| Internal maxillary artery ligation | In pterygopalatine fossa (endoscopic approach) |
| External carotid artery ligation | Above origin of lingual artery; last resort |
| Interventional radiology (embolisation) | Refractory epistaxis, nasopharyngeal carcinoma, tumours, carotid injury, facial trauma; pre-operative vascular control for juvenile angiofibroma |