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    Health & Fitness

    Family Medicine & Pharmacy Podcast

    priority topics for family medicine and community pharmacy

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    Latest Episodes:
    A Fib 4: Rhythm Control Medications Feb 24, 2014
    Show notes

    Tina discusses the following rhythm control medications for atrial fibrillation:

    Class 3 antiarrhythmics: blocks potassium channels and prolongs action potential duration

    • Amiodarone
    • Dronedarone
    • Sotalol

    Class 1 antiarrhythmics: blocks sodium channels, which results in a slowed atrial conduction, lengthens atrial refractoriness, and suppresses automaticity

    • propafenone
    • flecainide

    Indiana University’s P450 Drug Interaction Table: http://medicine.iupui.edu/clinpharm/ddis/clinical-table/

    References:

    • CCS Guideline www.onlinecjc.ca/article/S0828-282X(12)00046-3/fulltext
    • UptoDate uptodate.com
    • e-CPS www.e-therapeutics.ca/
    • RXFiles www.rxfiles.ca
    • Lexicomp www.lexi.com

    The post A Fib 4: Rhythm Control Medications appeared first on Family Pharm Podcast.


    A Fib 3: Rate Control Medications Feb 22, 2014
    Show notes

    Tina discusses the following rate control medications for atrial fibrillation:

    Beta blockers

    • Bisoprolol
    • Metoprolol
    • Atenolol

    Calcium channel blockers (non-dihydropyridines)

    • verapamil
    • diltiazem

    Digoxin

    References:

    • CCS Guideline www.onlinecjc.ca/article/S0828-282X(12)00046-3/fulltext
    • UptoDate uptodate.com
    • e-CPS www.e-therapeutics.ca/
    • RXFiles www.rxfiles.ca
    • Lexicomp www.lexi.com

    The post A Fib 3: Rate Control Medications appeared first on Family Pharm Podcast.


    A Fib 2: CCS 2012 Treatment Guidelines Feb 15, 2014
    Show notes

    The CHADS2 and HAS-BLED predictive index are useful in assessing a patient’s thromboembolic risk and in predicting which antithrombotic therapy is most suitable; and that is either aspirin, clopidogrel, or anticoagulants. The 3 new anticoagulants may be simpler to use and may have less intracranial hemorrhage side effect than warfarin, there has been longer clinical experience with warfarin and an antidote is present if needed.

    As for rate control and rhythm control, there is no significant difference in controlling survival and mortality between the two. Therapy is chosen based on patient’s symptoms and preference. Rate control medications include BB, non-dihydropyridine CCB, and digoxin. And rhythm control includes dronedarone, flecainide, sotalol, and amiodarone. We will go over details of these medications in the next episode.

    Catheter ablation is mainly for symptom control. It may be first line for highly selected patients, is often considered 2nd line after multiple drug therapy, or for patients who failed on multiple antiarrhythmic therapy and maintenance of sinus rhythm is still desired.

    • Focused 2012 Update of the Canadian Cardiovascular Society Atrial Fibrillation Guidelines: Recommendations for Stroke Prevention and Rate/Rhythm Control

    http://www.onlinecjc.ca/article/S0828-282X(12)00046-3/fulltext

    • The 2012 Canadian Cardiovascular Society Heart Failure Management Guidelines Update: Focus on Acute and Chronic Heart Failure

    http://www.onlinecjc.ca/article/S0828-282X%2812%2901379-7/abstract

    • Canadian Cardiovascular Society Atrial Fibrillation Guidelines 2010: Catheter Ablation for Atrial Fibrillation/Atrial Flutter

    http://www.onlinecjc.ca/article/S0828-282X(10)00012-7/fulltext

    The post A Fib 2: CCS 2012 Treatment Guidelines appeared first on Family Pharm Podcast.


    A Fib 1: Etiology and Diagnosis Feb 09, 2014
    Show notes

    Canadian Cardiovascular Society Atrial Fibrillation Guidelines 2010: Etiology and Initial Investigations

    • http://www.onlinecjc.ca/article/S0828-282X(10)00016-4/fulltext

    CHADS2 Score

    • http://www.mdcalc.com/chads2-score-for-atrial-fibrillation-stroke-risk/

    HAS-BLED Score

    • http://www.mdcalc.com/has-bled-score-for-major-bleeding-risk/

    Mayo Clinic on A Fib

    • http://www.mayoclinic.org/diseases-conditions/atrial-fibrillation/basics/definition/con-20027014

    The post A Fib 1: Etiology and Diagnosis appeared first on Family Pharm Podcast.


    CHF 2: medications Jan 11, 2014
    Show notes

    Tina revisits ACEI, ARB, BB, and Thiazides, which were covered previously with the hypertension episodes, and introduces a few new medications as well:

    • Mineralocorticoid Receptor Antagonists: spironolactone and eplerenone
    • Loop diuretic: furosemide
    • Digoxin
    • Vasodilators: hydralazine and isosorbite dinitrate

    For a quick summary of the CCS 2013 recommendations:

    ACE inhibitors:

    • all asymptomatic patients with an EF < 35%
    • all symptomatic HF patients and EF < 40%

    ARB:

    • if intolerant to ACEI
    • add to ACEI if intolerant or contraindicated for BB
    • add to ACEI and BB if NYHA class II-IV HF and EF ≤ 40% deemed at increased risk of HF events

    BB:

    • all HF patients with an EF ≤ 40%
    • initiated at a low dose and titrated to the target dose or maximal tolerated dose

    MRA:

    • patients > 55 years with mild to moderate HF during standard HF treatments with EF ≤ 30% (or ≤ 35% if QRS duration > 130 ms) and recent (6 months) hospitalization for CV disease or
    • with elevated BNP or NT-proBNP levels
    • after an MI with EF ≤ 30% and HF or
    • EF ≤ 30% alone in the presence of diabetes
    • EF < 30% and severe chronic HF (NYHA IIIB-IV) despite optimization of other recommended treatments

    Diuretics:

    • for congestive symptoms
    • When acute congestion is cleared, the lowest dose should be used that is compatible with stable signs and symptoms
    • persistent volume overload despite optimal medical therapy and increases in loop diuretics, cautious addition of a second diuretic (a thiazide or low dose metolazone) may be considered as long as it is possible to closely monitor morning weight, renal function, and serum potassium

    Digoxin:

    • patients in sinus rhythm who continue to have moderate to severe symptoms, despite optimized HF therapy
    • patients with chronic atrial fibrillation (AF) and poor control of ventricular rate

    Isosorbide dinitrate and hydralazine:

    • black Canadians with HF-REF
    • non-black HF patients unable to tolerate an ACE inhibitor or ARB

    Drug information from:

    • Drug monographs
    • CPS: http://www.e-therapeutics.ca/
    • Therapeutic Choices: http://www.e-therapeutics.ca/
    • Rx Files: http://www.rxfiles.ca/rxfiles/modules/druginfoindex/druginfo.aspx

    The post CHF 2: medications appeared first on Family Pharm Podcast.


    CHF 1: CCS 2012 Guideline Jan 05, 2014
    Show notes

    We turned our attention to chronic congestive heart failure (CHF) and reviewed “The 2012 Canadian Cardiovascular Society Heart Failure Management Guidelines Update“.

    National Institute of Health provided a great summary on CHF for patients and the public: http://www.nhlbi.nih.gov/health/health-topics/topics/hf/

    For a basic anatomy review of the circulatory system:

    Anatomy of the heart. Source: Wikimedia.

    For another diagram showing the heart in relation to the body, click here.

    And an over-simplification of the pathophysiology of left vs right heart failure is that when the left ventricle fails, not enough oxygenated blood gets pumps to the body to meet its demand. Instead, blood gets backed up into the lungs and cause fluid buildup in the lungs. This pressure can further back up into the right heart, such that the right ventricle and right atrium cannot accommodate a normal amount of venous return, and fluid can accumulate in the body to cause edema. Wikipedia strikes a good balance of depth and readability on this topic: http://en.wikipedia.org/wiki/Heart_failure

    The CCS guideline suggests the following investigations for CHF:

    • CXR,
    • echocardiography,
    • BNP,
    • labs (CBC, electrolytes, creatinine, urinalysis, glucose, thyroid function), and
    • further testing (nuclear imaging, catheterization, stress test, MRI, CT, endomyocardial biopsy) if appropriate.

    The CCS guideline on treatment of chronic CHF:

    ACE inhibitors for:

    • all symptomatic HF patients and EF < 40%.
    • all patients with an EF < 35%

    Angiotensin receptor blocker:

    • if patient intolerant to ACEI
    • add to ACEI if intolerant or contraindicated for BB
    • add to ACEI and BB if patient has NYHA class II-IV HF and EF ≤ 40% deemed at increased risk of HF events

    Beta blocker:

    • all HF patients with an EF ≤ 40%
    • initiated at a low dose and titrated to the target dose or maximal tolerated dose

    Mineralocorticoid receptor antagonist:

    • EF <30% and one of the following:
      • past MI and HF
      • diabetes
      • severe chronic HF (NYHA IIIB-IV) despite optimized treatment
      • age >55 with HF symptoms on treatment and recent hospitalization for CV disease in the past 6 months (or if QRS duration > 130ms and EF <35%)
    • with elevated BNP or NT-proBNP levels

    Diuretics:

    • loop diuretic, such as furosemide, for most patients with HF and congestive symptoms. When acute congestion is cleared, the lowest dose should be used that is compatible with stable signs and symptoms
    • persistent volume overload despite optimal medical therapy and increases in loop diuretics, cautious addition of a second diuretic (a thiazide or low dose metolazone) may be considered as long as it is possible to closely monitor morning weight, renal function, and serum potassium

    Digoxin:

    • patients in sinus rhythm who continue to have moderate to severe symptoms, despite optimized HF therapy
    • patients with chronic atrial fibrillation (AF) and poor control of ventricular rate

    Isosorbide dinitrate and hydralazine:

    • black Canadians with HF-REF
    • non-black HF patients unable to tolerate an ACE inhbitor or ARB

    The post CHF 1: CCS 2012 Guideline appeared first on Family Pharm Podcast.


    Diabetes 3: Insulin and Official Launch Dec 27, 2013
    Show notes

    Classes of insulin and different treatment regimens are discussed in the third episode of a 3-part series on diabetes. This episode also marks the conclusion of our coverage of the “Big Three” of modern medicine (hypertension, dyslipidemia, and diabetes), and with it, we make an official announcement of the launch of the Family Pharm Podcast to the world (aka Facebook)!

    Class Drug Onset Peak Duration
    Very Rapid-acting Insulin Analogues insulin aspart
    (NovoRapid)
    10–15 min 60–90 min 4–5 h
    insulin glulisine
    (Apidra)
    insulin lispro
    (Humalog)
    Rapid-acting Insulin insulin regular
    (Humulin R, Novolin ge Toronto)
    30–60 min 2–4 h 5–8 h
    Intermediate-acting Insulin insulin NPH
    (Humulin N, Novolin ge NPH)
    1–2 h 5–8 h 14–18 h
    Long-acting Insulin Analogues insulin detemir
    (Levemir)
    1.5 h Flat, no discernible peak 24 h
    insulin glargine
    (Lantus)
    Mixed (regular/NPH) Human Insulin insulin regular/insulin NPH
    Humulin 30/70,
    Novolin ge 30/70, 40/60, 50/50
    Combination of individual components
    Mixed Insulin Analogues insulin lispro/lispro protamine
    Humalog Mix25, Humalog Mix50
    10–15 min Not available Not available
    Mixed Insulin Analogues insulin aspart/aspart protamine
    NovoMix 30
    10–15 min 60–90 min 15–18 h

    Classes of insulin preparations. Adapted from Therapeutic Choices 6th edition.

    CDA guideline on insulin for Type 1 diabetes, including description of basal-bolus regimen by carb counting:

    • http://guidelines.diabetes.ca/Browse/Chapter12

    Examples of insulin regimens from CDA:

    • http://guidelines.diabetes.ca/Browse/Appendices/Appendix3

    Self monitoring:

    • http://guidelines.diabetes.ca/executivesummary/ch9

    The post Diabetes 3: Insulin and Official Launch appeared first on Family Pharm Podcast.


    Diabetes 2: antihyperglycemics Dec 22, 2013
    Show notes

    We reviewed the CDA 2013 guidelines on antihyperglycemic therapy for type 2 diabetes (http://guidelines.diabetes.ca/executivesummary/ch13), and explored the pharmacological properties of each of the major classes:

    • Biguanides: Metformin
    • Sulfonylureas: chlorpropamide, gliclazide, glimepiride, glyburide, and tolbutamide
    • Thiazolidinediones: pioglitazone and rosiglitazone
    • Meglitinides: Nateglinide and repaglinide
    • Alpha-glucosidase inhibitors: Acarbose
    • Dipeptidyl Peptidase-4 inhibitors (DPP4 inhibitors): Saxagliptin and sitagliptin
    • Glucagon Like Peptide-1 Analogues (GLP-1 analogues): Liraglutide and Exenatide

    Drug information:

    • Drug monographs
    • CPS: http://www.e-therapeutics.ca/
    • Therapeutic Choices: http://www.e-therapeutics.ca/
    • Rx Files: http://www.rxfiles.ca/rxfiles/modules/druginfoindex/druginfo.aspx

    The post Diabetes 2: antihyperglycemics appeared first on Family Pharm Podcast.


    Diabetes 1: CDA 2013 Guideline Dec 16, 2013
    Show notes

    To round up the “Big Three”, we turned out attention on diabetes. We reviewed the CDA guidelines on diabetes management and summarized the most relevant points that we think all family doctors and pharmacists would find interesting.

    http://guidelines.diabetes.ca/

    The CDA also prepared many apps and calculators that help HCPs make clinical decisions. As well, there are many other clinical practice guidelines on many different aspects of the care of diabetes that we cannot cover in this podcast. We recommend listeners to visit the CDA website to get a fuller picture than our synopsis here.

    The post Diabetes 1: CDA 2013 Guideline appeared first on Family Pharm Podcast.


    Dyslipidemia 4: EBM Special Dec 15, 2013
    Show notes

    We explore pieces of important evidence that offer a contrasting view on lipid control from the national guidelines.

    We are also introducing a new EBM resource available to CMA members: InfoPOEMs, which highlights clinical studies that the editorial team finds relevant. http://www.cma.ca/clinicalresources/infopoems

    Treatment group

    Tools for Practice 2013: “Is Diabetes a Coronary Heart Disease Equivalent?” http://www.acfp.ca/Portals/0/docs/TFP/20131021_093004.pdf

    “Though diabetes does confer an increased risk of CV events, it is not automatically equivalent to having experienced a myocardial infarction (MI) (and thus does not always warrant aggressive pharmacotherapy).

    CV risk should be predicted, and therapy guided, by taking into account individual risk factors.”

    InfoPOEM: “Limited data to guide lipid lowering in octogenarians” http://www.ncbi.nlm.nih.gov/pubmed/20952373

    either extremes of cholesterol levels (low or high) are associated with increased mortality in patients >80 years old

    Non statin lipid medications

    Tools for Practice 2010: “Ezetimibe: Lowers LDL cholesterol but what else?” http://www.acfp.ca/Portals/0/docs/TFP/20111028_105411.pdf

    “Eight years after being licensed by the FDA, there is still no evidence that ezetimibe reduces cardiovascular outcomes. It may be worse than niacin and there is concern about a potential increased cancer mortality risk.”

    Tools for Practice 2012: “Niacin added to statins for cardiovascular disease? 1 + 1 = 1” http://www.acfp.ca/Portals/0/docs/TFP/20120502_095745.pdf

    “In patients with cardiovascular disease already on statin therapy, adding niacin does not improve cardiovascular events. Among lipid treatments, only statin monotherapy has strong evidence for CVD prevention (regardless of lipid levels).”

    Tools for Practice 2013: “Fibrates: Statin’s Trusty Sidekick or Lackluster Fallback?” http://www.acfp.ca/Portals/0/docs/TFP/20131007_090323.pdf

    “When used alone, fibrates reduce non-fatal coronary events, but have no effect on mortality or other CV events, including stroke. Current evidence suggests fibrates provide no advantage when added to statin therapy.”

    InfoPOEM: “Statins but not fibrates associated with lower risk of pancreatitis” http://www.ncbi.nlm.nih.gov/pubmed/22910758

    statins significantly reduced risk of pancreatitis, where as fibrates did not

    Statin dosing and efficacy

    Cochrane 2014: “Statins for the primary prevention of cardiovascular disease” http://summaries.cochrane.org/CD004816/statins-for-the-primary-prevention-of-cardiovascular-disease

    “All-cause mortality was reduced by statins (OR 0.86, 95% CI 0.79 to 0.94); as was combined fatal and non-fatal CVD RR 0.75 (95% CI 0.70 to 0.81), combined fatal and non-fatal CHD events RR 0.73 (95% CI 0.67 to 0.80) and combined fatal and non-fatal stroke (RR 0.78, 95% CI 0.68 to 0.89). Reduction of revascularisation rates (RR 0.62, 95% CI 0.54 to 0.72) was also seen. [...] Evidence available to date showed that primary prevention with statins is likely to be cost-effective and may improve patient quality of life. Recent findings from the Cholesterol Treatment Trialists study using individual patient data meta-analysis indicate that these benefits are similar in people at lower (< 1% per year) risk of a major cardiovascular event.”

    InfoPOEM: “Statins of modest benefit for low- to moderate-risk persons (NNT ~ 80)” http://www.ncbi.nlm.nih.gov/pubmed/21989464

    for a patient group with a mean 10-year risk of cardiovascular death or MI around 6.2%, the NNT for all-cause mortality was 80, for any MI was 72, and for any stroke was 97 over 10 years of statin treatment

    InfoPOEM: “Statins for hyperlipidemia reduce all-cause mortality” http://www.ncbi.nlm.nih.gov/pubmed/20934984

    for patients with hyperlipidemia (LDL 180 mg/dL or 4.6mmol/L), and a mean follow up of 2.7 years, number needed to treat [NNT] to reduce 1 death = 67

    Tools for Practice 2012: “How does high dose statin compare to low dose in people with heart disease?” http://www.acfp.ca/Portals/0/docs/TFP/20120522_090852.pdf

    “In patients with coronary heart disease, using high dose statins (compared to low-moderate dose) prevents one CHD event for every 91 patients but results in one in 47 patients discontinuing therapy due to adverse events.

    However, low-moderate dose statin (compared to placebo) provides 2-3 times greater benefit than increasing to high dose statin. Therefore, getting and keeping patients on any statin is key, with dose adjusted up to tolerable levels”

    Statin side effects

    InfoPOEM: “Does statins cause cognitive decline?” http://www.ncbi.nlm.nih.gov/pubmed/24000778

    No. Statins are not associated with cognitive decline. Actually, in patients without baseline cognitive impairment, statin use is associated with slower cognitive decline.

    Tools for Practice 2013: “Statin-Induced Diabetes: Too Sweet a Deal?” http://www.acfp.ca/Portals/0/docs/TFP/20130527_014005.pdf

    “Statins modestly increase blood glucose, which leads to 1 in 250 or so patients crossing the “diabetic threshold” over 5 years. Pre-existing elevated sugars, other diabetes risk factors or higher doses may slightly increase the risk. This should not change statin prescribing as they reduce cardiovascular events and all-cause mortality in appropriate patients.”

    Additional tests

    InfoPOEM: “CRP of little value for risk stratification” http://www.ncbi.nlm.nih.gov/pubmed/23034020

    “In patients with an intermediate 10-year risk of a cardiovascular event (10% – 20%), you would have to screen more than 440 with a C-reactive protein (CRP) test to prevent 1 [cardiovascular] event. This test is quite expensive: in the neighborhood of $100 or more at many laboratories (LOE = 2a)“

    (Originally published on February 1, 2014)

    The post Dyslipidemia 4: EBM Special appeared first on Family Pharm Podcast.


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