CDR Timothy Murray CHF Clinic Manager Internal Medicine Team Inpatient Pharmacy Clinical Coordinator Claremore Indian Hospital Clinical Assistant Professor University of Oklahoma Primary Care Cardiology Update April 9, 2011 PT is a 37 yo white male whom is being consulted to the Internal Medicine service today secondary to an CHF exacerbation. JS presented to the ER with a 5 day history of increased shortness of breath and 10 lb weight increase. Symptoms started after a recent trip where a “poor” diet was consumed. Family Hx: DM, CAD Social Hx: negative PMH: HTN, CAD Medication prior to admission: Atenolol 25mg BID, aspirin 81mg daily, fish oil 1000mg daily, tamsulosin 0.4mg daily, KCL 8meq daily, furosemide 20mg daily Vitals: BP- 152/77, HR-101, WT- 177lbs Physical Exam: CHEST/LUNGS: Chest: Nontender Lungs: RALES Bilateral mostly at right base, no wheezing CARDOVASCULAR: Cardiac: regular rate, regular rhythm, No murmur Pulses: Equal, DIMINISHED Very diminished at feet. Carotid: No bruit JVD: + distended Abd aorta: No Bruit Lower ext: BILATERAL Edema of both legs mostly right side 3/4 and 2/4 at left. PT is treated in the hospital for 3 days. Weight has decreased 15 lbs and he feels much better. PT is to be seen in the CHF clinic in 2weeks for medication adjustment, dietary education, and monitoring. Completed echocardiogram reveals an ejection fraction of 25% PT returns to CHF clinic in 2wks with the following labs: PNBP: 3200 Based upon the above case what type of interventions would you have expected to have been performed? (during admission or in clinic) A. B. C. D. E. Continue all medications prior to admission Increase Atenolol, start an ace-inhibitor, & start an aldosterone antagonist DC atenolol, start metoprolol succinate, & start an ace-inhibitor DC atenolol, start carvedilol, & start an ace-inhibitor Just give up and discharge patient from clinic!!! Population Hospital Group Prevalence Incidence Mortality Discharges Cost Total population $24.3 billion 1American 4,900,000 550,000 51,546 999,000 1 Heart failure (HF) is a major public health problem resulting in substantial morbidity and mortality Major cost-driver of HF is high incidence of hospitalizations1,2 JCAHO has initiated HF quality care indicators for hospitalized HF patients Heart Association. 2003 Heart and Stroke Statistical Update. Dallas, Tex: American Heart Association; 2002. Hospitalization $13.6 Total Cost $25.8 billion 53% 14% Nursing Home $3.5 7% 8% 8% 10% Physicians/Other Professionals $1.8 Drugs/Other Home Healthcare Medical Durables $2.1 $2.7 Lost Productivity/ Mortality* $2.1 *Lost future earnings of persons who will die in 2004, discounted by 3% AHA. Heart Disease and Stroke Statistics—2004 Update Over 2/3 of HF Hospitalizations Preventable Diet Noncompliance 24% 16% Inappropriate Rx Rx Noncompliance 24% 19% Failure to Seek Care Annals of Internal Medicine 122:415-21, 1995 17% Other Patients Patient capture point Have patient’s/family’s attention: “teachable moment” Predictor of care in community Hospital structure Standardized processes / protocols / teams Accrediting bodies for standards of care Centers for Medicare and Medicaid Services—peer review organization Benefits Drawbacks • Improved use of evidence• • • • based therapy Improved symptom status and functional capacity Improved QOL Reduction in hospitalization Decrease in total medical costs Usual Care 96% Moser DK, Mann DL. Circulation. 2002;105:2810–2812. 4% HF Disease Management Program Where did our process break down and why no reduction in hospitalizations or rehospitalizations? Sub-optimal utilization of guidelines No standardization of care (standing orders) No team approach to treating CHF No increase in intensity of HF care after hospital discharge National registry Develop a treatment plan (protocol) Utilize a team approach to treating CHF Provide a comprehensive service to monitor & make clinical alterations with patient’s treatment plan Provide patient education & training to involve patients in their treatment plan Follow-up on patients discharged after a CHF admission to avoid re-admission: CHF Clinic!!!!!! Implement & utilize national standards of care for CHF GET UP TO DATE WITH THE CHF GUIDELINES! Document – Document - Document! Center of Medicaid & Medicare Services Compliance rates for discharging CHF pts Joint Commission/ACC/AHA CHF Performance Measures CHF Core Measures 1. Documentation of discharge instructions 2. Left ventricular function assessment 3. Use of ACE-I or ARB in pts with left ventricular systolic failure 4. Documentation of smoking cessation Hospitals should strongly consider implementing a process of care to ensure these measures are obtained and proper documentation occurs. The principal outcome measure of the ADHERE Registry was to assess overall hospital adherence to each of these measures for participating hospitals. CMS 2009 Documentation privileges for pharmacists! Electronic Health Record advantages GIPRA Measures/Performance Improvements 2010 CMS 30 day readmission policy changes Beta Blockers? Ace-Inhibitors Beta-Blockers Aldosterone Antagonists ARBs ISDN/Hydralazine Diuretics Digitalis Antiplatelets Statins Fish Oils Calcium Channel Blockers CHF care driven by two sets of national guidelines American College of Cardiology/American Heart Association Heart Failure Society of America Both organizations provide a set of detailed treatment guidelines for practitioners in an effort to optimize the management of chronic CHF. Treatment guidelines provide an approach to practice evidence based medicine. Heart Failure Society of America www.hfsa.org Last update: June 2010 American College of Cardiology/American Heart Association http://circ.ahajournals.org Last update: April 2009 2009 ACC/AHA recommendation for: “implementation of practice based guidelines utilizing multidisciplinary disease-management programs in efforts to assist in the treatment of patients with CHF”. 2010 HFSA recommendation for: “patients recently hospitalized for HF & other patients at high risk for HF decompensation should be considered for comprehensive HF disease management.” Risk Factor Goal Hypertension Generally < 130/80 Diabetes See ADA guidelines1 Hyperlipidemia See NCEP guidelines2 Inactivity 20-30 min. aerobic 3-5 x wk. Obesity Weight reduction < 30 BMI Alcohol Men ≤ 2 drinks/day, women ≤ 1 Smoking Cessation Dietary Sodium Maximum 2-3 g/day Journal of Cardiac Failure Vol. 16 No. 6 2010 ACE inhibitors are recommended for prevention of HF in patients at high risk for this syndrome, including those with: Coronary artery disease Peripheral vascular disease Stroke Diabetes and another major risk factor Strength of Evidence = A ACE inhibitors and beta blockers are recommended for all patients with prior MI. Strength of Evidence = A Journal of Cardiac Failure Vol. 16 No. 6 2010 Treatment with ACE inhibitors decreases the risk of CV death, MI, stroke, or cardiac arrest. Placebo HOPE 20 15 % MI, Stroke, 10 CV Death Ramipril 5 0 0 22% rel.3 risk red. p < .001 2 4 1 Years 15 EUROPA % MI, 12 CV Death, 9 Cardiac 6 Arrest 3 Placebo Perindopril 0 0 NEJM 2000;342:145-53 (HOPE) Lancet 2003;362:782-8 (EUROPA) 1 2 3 20% Years 4 5 rel. risk red. p = .0003 SAVE Study All-cause mortality ↓19% CV mortality ↓21% HF development ↓37% Recurrent MI ↓25% 0.3 Mortality Rate Placebo 0.2 Captopril 0.1 19% rel. risk reduction p = 0.019 0 0 0.5 1 1.5 2 2.5 3 3.5 4 Years Pfeffer et al. NEJM 1992;327:669-77 ACE inhibitors are recommended for symptomatic and asymptomatic patients with an LVEF ≤ 40%. Strength of Evidence = A ACE inhibitors should be titrated to doses used in clinical trials (as tolerated during uptitration of other medications, such as beta blockers). Strength of Evidence = C ACE inhibitors are recommended as routine therapy for asymptomatic patients with an LVEF ≤ 40%. Post MI Non Post-MI Strength of Evidence = B Strength of Evidence = C Journal of Cardiac Failure Vol. 16 No. 6 2010 SOLVD Prevention (Asymptomatic LVD) 20% 29% death or HF hosp. death or new HF CONSENSUS (Severe Heart Failure) 40% 31% 27% mortality at 6 mos. mortality at 1 year mortality at end of study SOLVD Treatment (Chronic Heart Failure) 16% mortality SOLVD Investigators. N Engl J Med 1992;327:685-91 SOLVD Investigators. N Engl J Med 1991;325:293-302 CONSENSUS Study Trial Group. N Engl J Med 1987;316:1429-35 Generic Name Trade Name Initial Daily Dose Target Dose Mean Dose in Clinical Trials Captopril Capoten 6.25 mg tid 50 mg tid 122.7 mg/day Enalapril Vasotec 2.5 mg bid 10 mg bid 16.6 mg/day Fosinopril Monopril 5-10 mg qd 80 mg qd N/A Lisinopril Zestril, Prinivil 2.5-5 mg qd 20 mg qd 4.5 mg/day, 33.2 mg/day* Quinapril Accupril 5 mg bid 80 mg qd N/A Ramipril Altace 1.25-2.5 mg qd 10 mg qd N/A Trandolapril Mavik 1 mg qd 4 mg qd N/A *No mortality difference between high and low dose groups, but 12% lower risk of death or hospitalization in high dose group vs. low dose group. It is recommended that other therapy be substituted for ACE inhibitors in the following circumstances: In patients who cannot tolerate ACE inhibitors due to cough, ARBs are recommended. Strength of Evidence = A The combination of hydralazine and an oral nitrate may be considered in such patients not tolerating ARBs. Strength of Evidence = C Patients intolerant to ACE inhibitors from hyperkalemia or renal insufficiency are likely to experience the same side effects with ARBs. In these cases, the combination of hydralazine and an oral nitrate should be considered. Strength of Evidence = C Journal of Cardiac Failure Vol. 16 No. 6 2010 Beta blockers shown to be effective in clinical trials are recommended for symptomatic and asymptomatic patients with an LVEF ≤ 40%. Strength of Evidence = A Beta blockers are recommended as routine therapy for asymptomatic patients with an LVEF ≤ 40%. Post MI Non Post-MI Strength of Evidence = B Strength of Evidence = C Journal of Cardiac Failure Vol. 16 No. 6 2010 HF Severity Target Dose (mg) Outcome Study Drug US Carvedilol1 carvedilol mild/ moderate 6.2525 BID ↓48% disease progression (p= .007) CIBIS-II2 bisoprolol moderate/ severe 10 QD ↓34% mortality (p <.0001) MERIT-HF3 metoprolol succinate mild/ moderate 200 QD ↓34% mortality (p = .0062) COPERNICUS4 carvedilol severe 25 BID ↓35% mortality (p = .0014) CAPRICORN5 carvedilol post-MI LVD 25 BID ↓23% mortality (p =.031) 1Colucci WS et al. Circulation 1196;94:2800-6. 2CIBIS II Investigators. Lancet 1999;353:9-13. Study Group. Lancet 1999;353:2001-7. 4Packer M et al. N Engl J Med 2001;344 1651-8. 5The CAPRICORN Investigators. Lancet 2001;357:1385-90. 3MERIT-HF Beta blocker therapy is recommended for patients with a recent decompensation of HF after optimization of volume status and successful discontinuation of IV diuretics and vasoactive agents. Whenever possible, beta blocker therapy should be initiated in the hospital at a low dose prior to discharge of stable patients. Strength of Evidence = B Journal of Cardiac Failure Vol. 16 No. 6 2010 Continuation of beta blocker therapy is recommended in most patients experiencing a symptomatic exacerbation of HF during chronic maintenance treatment, unless they develop cardiogenic shock, refractory volume overload, or symptomatic bradycardia. Strength of Evidence = C Temporary dose reduction may be considered Avoid abrupt discontinuation Reinstate or gradually increase prior to discharge Titrate dose to previously tolerated dose as soon as possible Journal of Cardiac Failure Vol. 16 No. 6 2010 Improvement 100% 91% 73% 75% Patients 18% P <.0001 50% 25% 0% Carvedilol Predischarge Initiation (n=185) Physician Discretion Postdischarge Initiation* (n=178) Gattis WA et al. JACC 2004;43:1534-41 CONCOMITANT DISEASE Beta blocker therapy is recommended in the great majority of patients with HF and reduced LVEF—even if there is concomitant diabetes, chronic obstructive lung disease or peripheral vascular disease. Use with caution in patients with: Diabetes with recurrent hypoglycemia Asthma or resting limb ischemia. Use with considerable caution in patients with marked bradycardia (<55 bpm) or marked hypotension (SBP < 80 mmHg). Not recommended in patients with asthma with active bronchospasm. Strength of Evidence = C Journal of Cardiac Failure Vol. 16 No. 6 2010 COPERNICUS (carvedilol)1 With diabetes Without diabetes MERIT-HF (ER metoprolol succinate)2 With diabetes Without diabetes 0 0.5 1.0 1.5 2.0 Mohacsi. Circulation. 2001;104(17):abstr 3551. Hjalmarson. JAMA. 2000;283(10):1295. PRESERVED LVEF Beta blocker treatment is recommended in patients with HF and preserved LVEF who have: Prior MI Strength of Evidence = A Hypertension Strength of Evidence = B Atrial fib. requiring control of ventricular rate Strength of Evidence = B THE ELDERLY Beta-blocker and ACE inhibitor therapy is recommended as standard therapy in all elderly patients with HF due to LV systolic dysfunction. Strength of Evidence = B In the absence of contraindications, these therapies are also recommended in the very elderly (age > 80 years). Strength of Evidence = C Journal of Cardiac Failure Vol. 16 No. 6 2010 General considerations Initiate at low doses Up-titrate gradually, generally no sooner than at 2 week intervals Use target doses shown to be effective in clinical trials Aim to achieve target dose in 8-12 weeks Maintain at maximum tolerated dose If symptoms worsen or other side effects appear Adjust dose of diuretic or concomitant vasoactive med. If up-titration continues to be difficult Prolong titration interval Continue titration to target after symptoms return to baseline Reduce target dose Consider referral to a HF specialist Journal of Cardiac Failure Vol. 16 No. 6 2010 Generic Name Trade Name Initial Daily Dose Target Dose Mean Dose in Clinical Trials Bisoprolol Zebeta 1.25 mg qd 10 mg qd 8.6 mg/day Carvedilol Coreg 3.125 mg bid 25 mg bid 37 mg/day Carvedilol Coreg CR 10 mg qd 80 mg qd Metoprolol succinate CR/XL Toprol XL 12.5-25 mg qd 200 mg qd 159 mg/day ARBs are recommended for routine administration to symptomatic and asymptomatic patients with an LVEF ≤ 40% who are intolerant to ACE inhibitors for reasons other than hyperkalemia or renal insufficiency. Strength of Evidence = A Journal of Cardiac Failure Vol. 16 No. 6 2010 Val-HeFT CHARM-Alternative 50 CV Death or HF Hosp % 100 Survival % Valsartan 90 80 Placebo 70 60 Placebo 40 30 Candesartan 20 10 p = 0.017 HR 0.77, p = 0.0004 50 0 0 3 6 9 12 15 Months 18 21 24 27 0 9 18 27 Months 36 Maggioni AP et al. JACC 2002;40:1422-4 Granger CB et al. Lancet 2003;362:772-6 Generic Name Trade Name Initial Daily Dose Target Dose Mean Dose in Clinical Trials Candesartan Atacand 4-8 mg qd 32 mg qd 24 mg/day Losartan Cozaar 12.5-25 mg qd 150 mg qd 129 mg/day Valsartan Diovan 40 mg bid 160 mg bid 254 mg/day An aldosterone antagonist is recommended for patients on standard therapy, including diuretics, who have: NYHA class IV HF (or class III, previously class IV) HF from reduced LVEF (≤ 35%) One should be considered in patients post-MI with clinical HF or diabetes and an LVEF < 40% who are on standard therapy, including an ACE inhibitor (or ARB) and a beta blocker. Strength of Evidence = A Journal of Cardiac Failure Vol. 16 No. 6 2010 EPHESUS (Post-MI) RALES (Advanced HF) Probability of Survival 1.00 1.00 0.90 0.90 0.80 Spironolactone 0.70 Eplerenone 0.80 Placebo 0.70 0.60 0.60 Placebo 0.50 0.50 RR = 0.70 P < 0.001 0.40 RR = 0.85 P < 0.008 0.40 0 3 6 9 12 15 18 21 24 27 30 33 36 0 3 6 9 12 15 18 21 24 27 30 33 36 Months Pitt B. N Engl J Med 1999;341:709-17 Pitt B. N Engl J Med 2003;348:1309-21 Aldosterone antagonists are not recommended when: Creatinine > 2.5mg/dL (or clearance < 30 mL/min) Serum potassium> 5.0 mmol/L Therapy includes other potassium-sparing diuretics Strength of Evidence = A It is recommended that potassium be measured at baseline, then 1 week, 1 month, and every 3 months Strength of Evidence = A Supplemental potassium is not recommended unless potassium is < 4.0 mmol/L Strength of Evidence = A Journal of Cardiac Failure Vol. 16 No. 6 2010 Trial of 2737 patients with NYHA class 2 heart failure and an ejection fraction of no more than 35%. Patients were randomized to eplerenone (up to 50mg daily) or placebo in addition to recommended therapy. Measured outcomes included: cardiovascular death/heart-failure hospitalization, cardiovascular death, heart-failure hospitalization, and hospitalization for hyperkalemia. Trial was stopped early at 21months. EMPHASIS-HF Major results Outcome Eplerenone (%) Placebo (%) Adjusted hazard ratio (95% CI) P Cardiovascular death/heartfailure hospitalization 18.3 25.9 0.63 (0.54-0.74) < 0.001 Cardiovascular death 10.8 13.5 0.76 (0.61-0.94) 0.01 Heart-failure hospitalization 12.0 18.4 0.58 (0.47-0.70) < 0.001 Hospitalization for hyperkalemia 0.3 0.2 1.15 (0.25-5.31) 0.85 Results in a 37% reduction in the primary end point of the composite of death from cardiovascular causes or hospitalization for heart failure!! Hyperkalemia occurring in 11.8% of eplerenone patients vs 7.2% of those in placebo group!!! A combination of hydralazine and isosorbide dinitrate is recommended as part of standard therapy, in addition to beta-blockers and ACE-inhibitors, for African Americans with HF and reduced LVEF: NYHA III or IV HF NYHA II HF Strength of Evidence = A Strength of Evidence = B Journal of Cardiac Failure Vol. 16 No. 6 2010 End point Primary end point composite score ISDN-HDZN Placebo (n=518) (n=532) p -0.1 -0.5 0.01 6.2 10.2 0.02 1st HF hospitalization (%) 16.4 24.4 0.001 Change in quality-of-life score at 6 months** -5.5 -2.7 0.02 All-cause mortality (%) Taylor AL et al. N Engl J Med 2004; 351;2049-57 43% Decrease in Mortality 100 Survival % Fixed Dose ISDN/HDZN 95 90 Placebo P = 0.01 85 0 100 200 300 400 500 600 Days Since Baseline Visit Taylor AL et al. N Engl J Med 2004;351:2049-57 Diuretic therapy is recommended to restore and maintain normal volume status in patients with clinical evidence of fluid overload, generally manifested by: Congestive symptoms Signs of elevated filling pressures Strength of Evidence = A Loop diuretics rather than thiazide-type diuretics are typically necessary to restore normal volume status in patients with HF. Strength of Evidence = B Journal of Cardiac Failure Vol. 16 No. 6 2010 Restoration of normal volume status may require multiple adjustments. Once a diuretic effect is achieved with short-acting loop diuretics, increase frequency to 2-3 times a day if necessary, rather than increasing a single dose. Strength of Evidence = B Oral torsemide may be considered in patients exhibiting poor absorption of oral medication or erratic diuretic effect. Strength of Evidence = C IV administration of diuretics may be necessary. Strength of Evidence = A Diuretic refractoriness may represent patient nonadherence, a direct effect of diuretic use on the kidney, or progression of underlying dysfunction. Journal of Cardiac Failure Vol. 16 No. 6 2010 Prophylactic ICD placement should be considered in patients with an LVEF ≤35% and mild to moderate HF symptoms: Ischemic etiology Non-ischemic etiology In patients who are undergoing implantation of a biventricular pacing device, use of a device that provides defibrillation should be considered. Strength of Evidence = A Strength of Evidence = B Strength of Evidence = B Decisions should be made in light of functional status and prognosis based on severity of underlying HF and comorbid conditions, ideally after 3-6 mos. of optimal medical therapy. Strength of Evidence = C Journal of Cardiac Failure Vol. 16 No. 6 2010 Fluid and sodium restriction Diuretics, especially loop diuretics Ultrafiltration/renal replacement therapy (in selected patients only) Parenteral vasodilators * (nitroglycerin, nitroprusside, nesiritide) Inotropes * (milrinone or dobutamine) Journal of Cardiac Failure Vol. 16 No. 6 2010 Recommended prior to discharge for all patients with HF: Exacerbating factors addressed Near optimum fluid status and pharmacologic therapy achieved Transition from IV to oral diuretic completed Patient education completed with clear discharge instructions Follow-up clinic visit scheduled, usually 7-10 days Should be considered prior to discharge for patients with advanced HF or a history of recurrent admissions: Oral regimen stable for 24 hours No IV inotrope or vasodilator for 24 hours Ambulation before discharge to assess functional capacity Plans for post-discharge management Referral for disease management, if available Strength of Evidence =C Journal of Cardiac Failure Vol. 16 No. 6 2010 Classification and Regression Tree (CART) analysis of ADHERE data shows: Three variables are the strongest predictors of mortality in hospitalized ADHF patients: BUN > 43 mg/dL Systolic blood pressure < 115 mmHg Serum creatinine > 2.75 mg/dL Fonarow GC et al. JAMA 2005;293:572-80 It is recommended that patients with HF and their family members or caregivers receive individualized education and counseling that emphasizes self-care. This education and counseling should be delivered by providers using a team approach. Teaching should include skill building and target behaviors. Strength of Evidence = B Journal of Cardiac Failure Vol. 16 No. 6 2010 Control Volume Diuretics Renal Replacement Therapy* Improve Clinical Outcomes Aldosterone ACEI -Blocker Antagonist or ARB or ARB CRT an ICD* HDZN/ISDN* *In selected patients Treat Residual Symptoms Digoxin For years the discussion has been which antiplatelet regimen is ideal for CHF pts? ASA Warfarin Plavix WASH Trial WATCH Trial CHADS2 Congestive Heart Failure Hypertension Age > 75 Diabetes Stroke or TIA (2 points) CHA2DS2-VAS Congestive heart failure/LV dysfunction Hypertension Age > 75 years Diabetes mellitus Stroke/TIA Vascular disease (prior MI, peripheral vascular disease) Age 65-75 years Female sex Score 1 1 2 1 2 1 1 1 Patient Factors ASA Plavix Myocardial Infarction <12months ago X X Stent <12months ago X X Warfarin Atrial Fibrillation X (CHADS2 score 01) Atrial Fibrillation (CHADS2 score >2) X or Dabigatran Diabetes X BYPASS Hx X Patient Factors ASA Plavix EF% < 30% X Systolic Failure w/ EF% >30% X Diastolic Failure X Severe CAD (no surgery option) X X LVAD X X Warfarin X New Recommendation VTE prophylaxsis with low dose unfractionated heparin, LMWH, or fondaparinux to prevent proximal deep venous thrombosis and pulmonary embolism is recommended for patients who are admitted to the hospital with ADHF and who are not already anticoagulated & have no contraindication. (Strength of Evidence=B) IMPROVE-HF Omega-3 (PUFAs) Massie b, Carson P, et al. Irbesartan in Patients with Heart Failure & Preserved Ejection Fraction (I-Preserve Trial). NEJM. 2008;359(23):2456-2467 HFSA “The Heart Failure Clinic A Consensus Statement” Zebrack J, Munger M, MacGregor J, et al. B-Receptor Selectivity of Carvedilol and Metoprolol Succinate in Patients with Heart Failure (SELECT Trial): A randomized Dose-Ranging Trial. Pharmacotherapy. 2009;29(8):883-890. Irbesartan Tavazzi L, Maggioni AP, Marchioli R, et al. Effect of n-3 polyunsaturated fatty acids in patients with chronic heart failure (the GISSI-HF trial): a randomized, double-blind, placebo-controlled trial. Lancet 2008;372:1231-1239. SELECT Trial Yancy CW, Fonarow GC, Albert NM, et al. Influence of patient age and sex on delivery of guideline-recommended heart failure care in the outpatient cardiology practice setting: Findings from IMPROVE HF. American Heart Journal. 2009;157:754-762. J Card Fail. 2008;14:801-815. Centers for Medicare and Medicaid Services 30 day congestive heart failure readmission rates. http://www.hospitalcompare.hhs.gov No significant differences in the patients’ global assessment of symptoms or in changes from baseline renal function with either bolus as compared with continuous infusion of intravenous furosemide or with a low-dose strategy as compared with a highdose strategy. Teaching tool to utilize with CHF patients Provides 5yr survival rate for patients based upon clinical history and no intervention as compared to rate after intervention. User friendly Internet based http://depts.washington.edu/shfm/ Based upon the above case what type of interventions would you have expected to have been performed? (during admission or in clinic) A. B. C. D. E. Continue all medications prior to admission Increase Atenolol, start an ace-inhibitor, & start an aldosterone antagonist DC atenolol, start metoprolol succinate, & start an ace-inhibitor DC atenolol, start carvedilol, & start an ace-inhibitor Just give up and discharge patient from clinic!!! Questions??? Timothy.murray@ihs.gov