Term
| Indications for GI Prophylaxis |
|
Definition
Stress-related Mucosal Damage (SMRD - "stress ulcers"); NSAID-induced ulcers |
|
|
Term
| Stress-related Mucosal Damage (SMRD - "Stress Ulcers") |
|
Definition
occurs in critically ill pts; mucosal erosions begin w/in hrs of "stress"; increased gastric acid production, decreased protection; |
|
|
Term
|
Definition
best treatment for SMRD (stress ulcers); Indicated when: - if major risk factor present OR - if >2 minor risk factors present |
|
|
Term
|
Definition
MAJOR: mechanical ventilation; coagulopathy (Plt <50,000; INR >1.5; PTT >2 x control); Hx of GI ulceration w/in past year;
MINOR: Sepsis; ICU admission >1 wk; Occult GI bleeding lasting > or = 6 days; Glucocorticoid therapy (>250 mg hydrocortisone); |
|
|
Term
|
Definition
| restore mucosal blood flow |
|
|
Term
| Antisecretory Meds - PPI, H2RA |
|
Definition
| preferred option for tx/prophylaxis of SMRD |
|
|
Term
|
Definition
| antisecretory med preferred in ICU pts on PO medication |
|
|
Term
|
Definition
| preferred antisecretory med for ICU pts that are NPO (not by mouth) |
|
|
Term
|
Definition
most studied antisecretory med; found to be most effective; given BID most commonly |
|
|
Term
|
Definition
| 2 antisecretory meds that generally are NOT used for prophylaxis of SMRD |
|
|
Term
| Zegerid (IR omeprazole + NaHCO3) |
|
Definition
IR omeprazole 40 mg + NaHCO3 20 mEq; - give 40 mg q6-8 hr x 2 doses, then 40 mg/day x 14 days |
|
|
Term
|
Definition
| H2RA that can be given as IV infusion |
|
|
Term
| High Risk for NSAID-induced Ulcer |
|
Definition
Hx of complicated ulcer; More than 2 risk factors for NSAID-induced GI toxicity; Low dose ASA + (glucocorticoids OR warfarin OR clopidogrel OR prasugrel); |
|
|
Term
| Moderate Risk (1-2) for NSAID-induced Ulcers |
|
Definition
>65 yr old; High-dose NSAID; Previous uncomplicated ulcer;
**If you have ALL 3 of these --> HIGH RISK** |
|
|
Term
| Low CV Risk AND Low GI Toxicity Risk (no indication for ASA) |
|
Definition
| Can use lowest dose NSAID |
|
|
Term
| Low GI toxicity risk AND High CV Risk (need ASA for CV protection) |
|
Definition
| naproxen + (PPI or misoprostol) |
|
|
Term
| Moderate GI Toxicity Risk AND Low CV Risk (no need for ASA) |
|
Definition
| NSAID + (PPI or misoprostol) |
|
|
Term
| High GI Toxicity Risk AND Low CV Risk (no need for ASA) |
|
Definition
Alternative Tx OR COX-2 inhibitor + (PPI or misoprostol) |
|
|
Term
| Moderate GI Toxicity Risk AND High CV Risk (needs ASA) |
|
Definition
| naproxen + (PPI or misoprostol) |
|
|
Term
| High GI TOxicity Risk AND High CV Risk (ASA needed) |
|
Definition
Alternative Tx --> Use tramadol, then opiates if tramadol is not effective; **NO COX-2 inhibitors OR NSAIDs** |
|
|
Term
| naproxen + esomeprazole (Vimovo) |
|
Definition
| 375 mg/20 mg - 500 mg/20 mg BID |
|
|
Term
|
Definition
better than placebo at protecting gut; equivalent to PPI/H2RA at 200 mcg QID; use limited due to ADRs (GI side effects); |
|
|
Term
| PPI - esomeprazole [Nexium] 20-40 mg qday, lansoprazole [Prevacid] 15-30 mg qday |
|
Definition
| significantly reduced gastric & duodenal ulcer in pts taking NSAIDs & COX-2 inhibitors; |
|
|
Term
|
Definition
can use standard doses to relieve NSAID-induced dyspepsia; NOT recommended as prophylaxis for GI complications; use standard doses |
|
|
Term
| Secondary Prevention of GI Prophylaxis |
|
Definition
| Continued use of NSAID/low-dose ASA --> use PPI at lowest dose |
|
|
Term
| Improvement of Pt's Status |
|
Definition
| can stop prophylaxis when this occurs |
|
|
Term
|
Definition
CYP enzyme that metabolizes PPIs; Can have genetic polymorphisms (more common in Asians) |
|
|
Term
|
Definition
antiplatelet med activated by CYP 2C19 & 3A; PPIs cause decreased activation --> decreased efficacy; |
|
|
Term
|
Definition
another antiplatelet medication activated by CYP 3A, 2B6, 2C9, 2C19; PPIs decrease activation --> decreased efficacy; |
|
|
Term
|
Definition
antiplatelet medication activated via CYP 3A4; PPIs decrease activation --> decreased efficacy |
|
|
Term
|
Definition
antiviral w/ ADR & GI problems; Metabolized by CYP 2C19 & 3A4; If HIV pt is stable (no detectable VL), try to AVOID PPI** If you HAVE to use PPI, use for LESS than 14 days; |
|
|
Term
|
Definition
| anticoagulant that interacts w/ omeprazole --> PT decreases by 10% |
|
|
Term
|
Definition
| benzodiazepine that interacts w/ omeprazole --> increases T1/2 by 130% |
|
|
Term
|
Definition
| anticonvulsant that interacts w/ omeprazole --> T1/2 increased by 30% |
|
|
Term
|
Definition
| antiarrhythmic that interacts with omeprazole --> AUC increased by 10% |
|
|
Term
|
Definition
| anticonvulsant that interacts w/ omeprazole --> AUC increased by 75% |
|
|
Term
| Drug Interactions with PPIs |
|
Definition
decreased effectiveness of alendronate; decreased Mg absorption; increased risk of fractures; increased risk of C. diff infections; rebound hypersecretion; increased risk for nosocomial & community-acquired pneumonia; decreased Vit. B12 absorption; decreased Iron absorption |
|
|