A 58 yo American female presents to establish care. She has a history of exercise induced asthma and HTN but is otherwise healthy without bad habits. What test should be part of your health maintenance screening?
a. DEXA
b. Hep C- Correct Answer
c. Zoster Vaccine
d. TSH
The Centers for Disease Control and Prevention (CDC) now recommends screening for all persons in the United States born between 1945 and 1965. This is a new recommendation as of 2012. This was based on a mathematical model that showed theapproach of 1-time screening for hepatitis C in this birth cohort followed by treatment was cost-effective.
Annals of Internal Medicine February 2012
Dexa scan is recommended in females >65: The USPSTF recommends screening for osteoporosis in women aged
65 years or older and in younger women whose fracture risk is equal to or greater than that of a 65-year-old white woman who has no additional
risk factors. The patient has no additional risk factors so should NOT be screened
USPSTF- Osteoporosis Screening
Zoster Vaccine in recommended by the CDC in patients without contraindications. This patient does not meet criteria based on age.
Shingles
There is insufficient evidence for thyroid screening in asymptomatic adults
USPSTF- TSH
Friday, October 26, 2012
Saturday, October 20, 2012
COW Week 12
64 yo M presents to establish care. Has CAD, HTN,
DM-II. He feels well, had recent
negative stress test with his cardiologist, has good exercise tolerance. Meds are metofromin/glipizide, metoprolol, ASA, lisinopril,
fish oil and atorvastatin. Labs: Cr 1.1, A1c 7.1, HDL 30, LDL 68, U protein/CR
Ratio 450mg/day. Echo shows EF 40%.
What should you do:
Add Niacin
Change MTP to Coreg
Add Losartan- Correct Answer
Change glipizide to insulin basal/bolus
This patient's CAD is well controlled and though he has a low EF he does not have clinical evidence of CHF. The patient's EF does not necessitate a change to carvedilol
. The landmark Comet Trial compared long-acting Metoprolol (Toprol XL) to Carvedilol (Coreg) in NYHA Class II-V CHF with EF 35% or less. The results showed improvement in these patients with Carvedilol. This patient does not have symptomatic CHF and his EF is 40% so he does not meet inclusion criteria for this trial and thus does not have in indication for a change in Beta Blocker Therapy.
The patient's LDL is a at goal, and he is on fish oil, however he has low HDL. Currently there are limited effective therapy to raise HDL other than statins and fish oil. Niacin is controversial.
The patient's A1c is at/near goal, there is no indication to change his hypoglycemics to insulin at this time. However, the patient has evidence of nephropathy, and his proteinuria is not controlled by his ACE-I. Thus he requires dual RAAS inhibition, which will confer now additional anti-hypertensive benefit but will decrease his proteiuria,.
The patient's LDL is a at goal, and he is on fish oil, however he has low HDL. Currently there are limited effective therapy to raise HDL other than statins and fish oil. Niacin is controversial.
The patient's A1c is at/near goal, there is no indication to change his hypoglycemics to insulin at this time. However, the patient has evidence of nephropathy, and his proteinuria is not controlled by his ACE-I. Thus he requires dual RAAS inhibition, which will confer now additional anti-hypertensive benefit but will decrease his proteiuria,.
Adding an ARB is currently not recommended in patients with CHF on an ACEi + BB but still symptomatic. A Cochrane review of outcomes of ARB plus ACE inhibitor therapy to ACE inhibitor therapy alone in patients with HF was dominated by the Val-HeFT and CHARM-Added results [3,12,13]. There were no statistically significant differences in total mortality (RR 0.98, 0.90-1.06), cardiovascular mortality, or non-cardiovascular mortality between combined ARB plus ACE inhibitor and ACE inhibitor monotherapy. Combination therapy reduced hospitalization for HF compared to ACE inhibitor therapy (RR 0.81, 95% CI .074, 0.89) but did not reduce total hospitalizations. Withdrawals due to adverse effects were more frequent with combination therapy
Poole-Wilson PA et al Comparison of carvedilol and metoprolol on clinical outcomes in patients with chronic heart failure in the Carvedilol Or Metoprolol European Trial (COMET): randomised controlled trial.
Lancet. 2003 Jul 5;362(9377):7-13.
Cohen DL, and Townsend RR Is There Added Value to Adding ARB to ACE Inhibitors in the Management of CKD?JASN August 1, 2009 vol. 20 no. 8 1666-1668
Monday, October 8, 2012
COW Week 11
Your 60yo male patient has COPD (FEV1 50%, FEV1/FVC 60%). He is compliant with his Advair and prn Combivent (with good technique) and stopped smoking 2 years ago. He is enrolled in pulmonary rehab and has a normal resting and ambulatory oxygen saturation. He has had 4 exacerbations in the past year. His other medications include lisinopril and atorvastatin and he has no cardiac history. What should be your next step?
a. Azithromycin 250mg MWF
b. EKG
c. Lung Reduction Surgery
d. Oxygen
Acute exacerbations of COPD portend to further morbidity. Each exacerbation increases the rate of FEV1 decline by an additional 2ml or 7ml per year in non-smokers and smoker respectively. The cost to society is also high. Treatment of COPD includes smoking cessation, pulmonary rehab, anti-cholinergics, beta-agonists, and glucocorticoids. Some patients, despite maximal therapy, may still have uncontrolled disease. Macrolides have anti-inflammatory and immune-modultating effects and may decrease the production of cytokines in the lungs (Role of Macrolide therapy in COPD. Int J Chron Obstruc Pulmon Dis 2008;3:331-50). Thus, these have been studied in COPD.
NEJM published a study in 2011 showing daily use of azithromycin 250mg reduced the frequency of acute exacerbations of COPD (NEJM Article). The median time to the first acute exacerbation was increased by 92 days compared to the placebo group (266 days compared to 174 days). Quality of life was also improved per the St. George's Respiratory Questionnaire. There was no statistically significant difference in mortality. Similar results were found in a trial using erythromycin (Am J Respir Crit Care Med 2008; 178:1139-47).
Long-term use of azithromycin comes with many concerns including prolonged QT (greater than 450), ototoxicity, drug interactions, and possible antibiotic resistance. The risk of torsades is of great concern. It is because of these side-effecs that the GOLD report guidelines stated that despite it's proven efficacy azithromycin is "not recommended because of an unfavorable balance between benefits and side effects" (GOLD Report).
Many expert believe it is still safe and reasonable to add azithromycin if proper baseline screening is done. Important baseline tests include heart-rate, QTc, audiography, LFTs, and medicationreview. If the patient is taking a QTc prolonging agent, has a baseline QTc greater than 450, or has a significant cardiac history (CHF, hx of stroke) then azithromycin is not recommended. Additionally it is not recommended if the patient has an abnormal audiogram or LFTs greater then 3x the ULN. If these tests are normal then it is reasonable to start a trial of azithromycin, but only in those patients who continue to have frequent COPD exacerbations despite being on maximal therapy (~ 2 or more a year). Expert opinion favors three times a week dosing, despite the trials using a daily dose based on pharmacokinietics of the drug. This may also minimize the side effects. (NEMJ Clinical Therueptucis article). They also recommend repeating EKG, audiography, and labs every three months to monitor for side effects. Some experts suggest obtaining a baseline sputum culture to asses for nontuberculous mycobactermia as well.
Therefore, for this patient the answer is to obtain a baseline EKG and hearing test. If normal, it is reasonable to start azithromycin three times a week with monitoring of side effects.
This case is based on the following article: NEJM Clinical Therapeutics of COPD:
a. Azithromycin 250mg MWF
b. EKG
c. Lung Reduction Surgery
d. Oxygen
Acute exacerbations of COPD portend to further morbidity. Each exacerbation increases the rate of FEV1 decline by an additional 2ml or 7ml per year in non-smokers and smoker respectively. The cost to society is also high. Treatment of COPD includes smoking cessation, pulmonary rehab, anti-cholinergics, beta-agonists, and glucocorticoids. Some patients, despite maximal therapy, may still have uncontrolled disease. Macrolides have anti-inflammatory and immune-modultating effects and may decrease the production of cytokines in the lungs (Role of Macrolide therapy in COPD. Int J Chron Obstruc Pulmon Dis 2008;3:331-50). Thus, these have been studied in COPD.
NEJM published a study in 2011 showing daily use of azithromycin 250mg reduced the frequency of acute exacerbations of COPD (NEJM Article). The median time to the first acute exacerbation was increased by 92 days compared to the placebo group (266 days compared to 174 days). Quality of life was also improved per the St. George's Respiratory Questionnaire. There was no statistically significant difference in mortality. Similar results were found in a trial using erythromycin (Am J Respir Crit Care Med 2008; 178:1139-47).
Long-term use of azithromycin comes with many concerns including prolonged QT (greater than 450), ototoxicity, drug interactions, and possible antibiotic resistance. The risk of torsades is of great concern. It is because of these side-effecs that the GOLD report guidelines stated that despite it's proven efficacy azithromycin is "not recommended because of an unfavorable balance between benefits and side effects" (GOLD Report).
Many expert believe it is still safe and reasonable to add azithromycin if proper baseline screening is done. Important baseline tests include heart-rate, QTc, audiography, LFTs, and medicationreview. If the patient is taking a QTc prolonging agent, has a baseline QTc greater than 450, or has a significant cardiac history (CHF, hx of stroke) then azithromycin is not recommended. Additionally it is not recommended if the patient has an abnormal audiogram or LFTs greater then 3x the ULN. If these tests are normal then it is reasonable to start a trial of azithromycin, but only in those patients who continue to have frequent COPD exacerbations despite being on maximal therapy (~ 2 or more a year). Expert opinion favors three times a week dosing, despite the trials using a daily dose based on pharmacokinietics of the drug. This may also minimize the side effects. (NEMJ Clinical Therueptucis article). They also recommend repeating EKG, audiography, and labs every three months to monitor for side effects. Some experts suggest obtaining a baseline sputum culture to asses for nontuberculous mycobactermia as well.
Therefore, for this patient the answer is to obtain a baseline EKG and hearing test. If normal, it is reasonable to start azithromycin three times a week with monitoring of side effects.
This case is based on the following article: NEJM Clinical Therapeutics of COPD:
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