Nonpharmacologic management
›Lifestyle and behavioral therapy
›Weight reduction when overweight or obese
›Symptom improvement expectation
›Lower intra-abdominal pressure rationale
›Meal timing and portion adjustments
›Avoid large meals
›Avoid eating within 2 to 3 hours of bedtime
›Head-of-bed elevation for nocturnal symptoms
›Bed risers or wedge pillow
›Avoid stacked pillows only
›Trigger identification and reduction
›High-fat meals
›Caffeine if clearly linked
›Tobacco cessation
›LES tone improvement rationale
›Barrett and cancer risk reduction rationale
Acid suppression and mucosal protection
›Medication strategy selection
›Typical symptoms without alarm features
›Initial PPI trial
›Duration 8 weeks
›Dosing once daily before breakfast
›Step-down after response
›Lowest effective dose
›On-demand use option for nonerosive disease
›Mild intermittent symptoms
›Antacids or alginate-based therapy
›Rapid symptom relief role
›Breakthrough symptom use
›Proton pump inhibitors
›Omeprazole PO 20 mg daily
›If partial response, increase to 20 mg twice daily
›Second dose before dinner
›Reassess after 4 to 8 weeks
›Maximum typical outpatient dosing 40 mg twice daily
›Use for refractory or erosive disease phenotype
›De-escalate when controlled
›Pantoprazole PO 40 mg daily
›If partial response, increase to 40 mg twice daily
›Timing 30 to 60 minutes before meals
›Check adherence and timing before escalating
›Maximum typical outpatient dosing 40 mg twice daily
›Shortest effective duration principle
›Long-term risk counseling
›Esomeprazole PO 20 mg daily
›If partial response, increase to 20 mg twice daily
›Consider CYP2C19 variability context
›Avoid duplication with other PPIs
›Maximum typical outpatient dosing 40 mg twice daily
›Consider specialist input at high dose
›Objective testing for refractory symptoms
›H2 receptor antagonists
›Famotidine PO 10 mg to 20 mg as needed
›Breakthrough symptoms on PPI
›Bedtime dose for nocturnal acid breakthrough
›Tolerance with nightly use
›Renal impairment dose adjustment
›Lower dose with reduced eGFR
›Monitor confusion risk in older adults
›Famotidine PO 20 mg twice daily
›Mild to moderate symptoms alternative
›Less effective than PPI for erosive esophagitis
›Consider step-up to PPI if persistent
›Maximum typical dose 40 mg twice daily
›Avoid prolonged high-dose without reassessment
›Consider endoscopy if persistent symptoms
›Antacids and alginates
›Calcium carbonate PO 500 mg to 1000 mg as needed
›Rapid relief role
›Short duration effect
›Avoid overuse with hypercalcemia risk
›Constipation risk
›Hydration advice
›Alternative antacid selection
›Alginate-based therapy after meals and at bedtime
›Postprandial reflux barrier mechanism
›Useful for regurgitation phenotype
›Add-on to PPI for symptoms
›Sodium load consideration
›Heart failure patients caution
›Hypertension patients caution
›Sucralfate
›Sucralfate PO 1 g four times daily
›Pregnancy symptom option
›Minimal systemic absorption
›Constipation risk
›Drug interaction spacing
›Separate from other meds by 2 hours
›Reduced absorption risk
Refractory symptoms and optimization
›Optimization checklist before labeling refractory GERD
›Adherence verification
›Daily dosing
›Missed doses frequency
›Timing correction
›30 to 60 minutes before breakfast
›Before dinner for twice daily regimens
›Phenotype reassessment
›Functional heartburn possibility
›Reflux hypersensitivity possibility
›Next steps when persistent symptoms
›Objective testing consideration
›Endoscopy for alarm features or long-standing symptoms
›pH impedance testing for uncertain diagnosis
›Alternative diagnoses evaluation
›Eosinophilic esophagitis
›Achalasia
›Adjunctive therapies by phenotype
›Bedtime H2RA for nocturnal symptoms
›Alginate therapy for regurgitation
Procedural and surgical options
›Anti-reflux procedures
›Laparoscopic fundoplication
›Indications
›Objective GERD with persistent symptoms
›Preference to avoid long-term medication
›Preoperative workup
›pH testing confirmation when endoscopy nonerosive
›Manometry to exclude major motility disorder
›Evidence statement
›Class I recommendation for surgery in selected patients with objective reflux and appropriate workup
›Shared decision-making on dysphagia and gas-bloat risks
›Magnetic sphincter augmentation
›Indications
›Objective GERD with normal motility
›Regurgitation predominant phenotype
›Contraindications
›Severe esophagitis
›Large hiatal hernia without repair plan
›Endoscopic therapies
›Selected patient use
›Mild to moderate disease phenotype
›Not for high-grade esophagitis
›Counseling on durability limits
›Variable long-term outcomes
›Continue surveillance for complications