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1 JNC-8: Process, Critical Questions and Future Reports Barry L. Carter, Pharm.D., FCCP, FAHA, FASH The Patrick E. Keefe Professor in Pharmacy Department of Pharmacy Practice and Science College of Pharmacy and Professor, Department of Family Medicine Roy J. and Lucille A. Carver College of Medicine University of Iowa Disclosure of Relationships Over the past 5 years Grant Support: NIH, AHRQ, VA HSR&D. I have had NONE of the following: Consultant, Speakers Bureau, Major Stock Shareholder, or Other Support from Industry. Learning Objectives At the complekon of the presentakon, parkcipants will be able to: 1. Describe the evidence quality grading and recommendakon strength process used by JNC- 8 which will be used to formulate the guidelines. 2. Compare and contrast the JNC- 8 systemakc review and guideline development process with previous hypertension guidelines. 3. Discuss the three main crikcal queskons being addressed by JNC- 8. 1

2 NHLBI Adult CVD Prevention Guidelines NHLBI-sponsored Adult CVD Prevention Guidelines Joint National Committee on Prevention, Detection, Evaluation, & Treatment of High Blood Pressure (JNC) JNC 7: 2003 JNC 6: 1997 JNC 5: 1992 JNC 4: 1988 JNC 3: 1984 JNC 2: 1980 JNC 1: 1976 Detection, Evaluation, &Treatment of High Blood Cholesterol in Adults (ATP, Adult Treatment Panel) ATP III Update: 2004 ATP III: 2002 ATP II: 1993 ATP I: 1988 Clinical Guidelines on the Identification, Evaluation, & Treatment of Overweight and Obesity in Adults Obesity: 1998 Hypertension: A Moving Target JNC BP Classifications: SBP SBP (mm Hg) No recommendations for SBP in JNC I or JNC II ISH Borderline ISH Borderline Normal Stage 4 Stage 3 Stage 2 Stage 1 Stage 1 Highnormal Normal Optimal Stage 3 Stage 2 Highnormal Normal Optimal Stage 2 Stage 1 Prehypertension Normal JNC I JNC II JNC III JNC IV JNC V JNC VI JNC 7 JNC I. JAMA. 1977;237: JNC II. Arch Intern Med. 1980;140: JNC III. Arch Intern Med. 1984;144: JNC IV. Arch Intern Med. 1988;148: JNC V. Arch Intern Med. 1993;153: JNC VI. Arch Intern Med. 1997;157: Chobanian AV et al. JAMA. 2003;289: JNC 7 Emphasizes Importance of Low BP Hypertension JNC VI (1997) OPTIMAL < 120 and < 80 NORMAL < 130 and < 85 HIGH NORMAL or STAGE or STAGE or STAGE or 110 JNC VI. Arch Intern Med. 1997;157: JNC 7 (2003) NORMAL < 120 and < 80 PREHYPERTENSION or STAGE or STAGE or 100 JNC 7. JAMA. 2003;289(19):

3 National Heart, Lung, and Blood Institute National High Blood Pressure Education Program Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7) EXPRESS My Observations About Previous Structure and Process JNC- V (1993): Chairman Ray Gifford, Jr. MD Subcommittee on Pharmacologic TX: Edward D. Frohlich, MD chair Started June 1991, published January 1993 JNC- VI (1997): Chairman Sheldon Sheps, MD Prevention and Treatment Chair: Norman Kaplan, MD Started September 1996, published November 1997 JNC-7 (2003): Chairman: Aram Chobanian, MD Started December 2002, published May 2003 JNC- 8 (pending): Co-Chairs: Paul James, MD, Suzanne Oparil, MD Prevention and Treatment Chairs: William Cushman, MD, Jackson Wright, MD Started August 2008, report for comment expected fall Institute of Medicine Report: Quality Chasm In its current form, habits, and environment, American health care is incapable of providing the public with the quality health care it expects and deserves. Current: Decision making is based on training and experience. New: Decision making is based on evidence. Patients should receive care based on the best available scientific knowledge. Care should not vary illogically from clinician to clinician or from place to place. Evidence-based Clinical Practice Guidelines can help make this vision a reality Institute of Medicine, Crossing the Quality Chasm: New Health System for the Twenty-first Century. Washington: National Academy Press,

4 ACC/AHA Guidelines Grading Schema Level of Evidence A Evidence Quality Recommendation based on evidence from multiple randomized trials or meta analyses Level of Evidence B Recommendation based on evidence from a single randomized trial or nonrandomized studies Level of Evidence C Recommendation based on expert opinion, case studies, or standards of care 10 Scientific Evidence Underlying ACC/AHA Guidelines (JAMA. 2009; 301: ) AF Heart failure PAD STEMI Perioperative Secondary prevention Stable angina SV arrhythmias UA/NSTEMI Valvular disease VA/SCD PCI CABG Pacemaker Radionuclide imaging AHA Level of Evidence A in Current Guidelines* 0.3% 6.4% 6.1% 4.9% 4.8% 9.7% 11.7% 13.5% 12.0% 11.0% 15.3% 19.0% 22.9% 23.6% 26.4% 0% 10% 20% 30% *in guidelines with level of evidence NHLBI Evidence Quality Grading and Recommendation Strength High Evidence Quality Well-designed and conducted RCTs Moderate RCTs with minor limitations Well-conducted observational studies Low RCTs with major limitations Observational studies with major limitations Recommendation Strength A Strong B Moderate C Weak D Against E Expert Opinion N No Recommendation 12 4

5 Adult CVD Guidelines: NHLBI approach Advice to NHLBI from advisory groups: Update risk factor guidelines (hypertension, cholesterol, obesity) Develop an integrated guideline Use an evidence-based approach including systematic reviews The NHLBI guideline development process Was established to assure rigor and to minimize bias Methods being used meet many of the new IOM standards Two recent IOM reports set new standards Finding What Works in Health Care standards for systematic reviews Clinical Practice Guidelines We can Trust standards for developing trustworthy CPGs NHLBI Systematic Review and Guideline Development Process Topic Area Identified Evidence Tables Developed; Body of Evidence Summarized Graded Evidence Statements & Recommendations Developed Expert Panel Selected Studies Quality Rated; Data Abstracted External Review of Guideline Drafts; Revised as Needed Critical Questions & Study Eligibility Criteria Identified Literature Searched; Eligible Studies Identified Guidelines Disseminated & Implemented Expertise Represented Hypertension, primary care, cardiology, nephrology, clinical trials, research methodology, evidence-based medicine, epidemiology, guideline development and implementation, nutrition/lifestyle, nursing, pharmacy, systems of care, and informatics Panel also includes senior scientists from NHLBI and NIDDK with expertise in hypertension, clinical trials, translational research, nephrology, guideline development, and evidence-based methodology 5

6 JNC 8 CommiYee Members Co- Chair: Suzanne Oparil MD Jackson T. Wright, Jr. MD, PhD Sandra J. Taler, MD Joel Handler, MD Barry L. Carter, PharmD Daniel T. Lackland, DrPH Sidney C. Smith, Jr., MD Olugbenga Ogedegbe, MD, MPH, MS Lawrence J. Fine, MD, DrPH (Ex- Officio) Cheryl Dennison Himmelfarb, RN, ANP, PhD Co- Chair: Paul A. James MD Laura Svetkey, MD, MHS Michael L. LeFevre, MD, MSPH Raymond R. Townsend, MD William C. Cushman, MD Thomas D. MacKenzie, MD, MSPH Andrew S. Narva, MD (Ex- Officio) Eduardo OrKz, MD, MPH, NHLBI Lead, Ex- Officio, Non- VoKng Member * 4 members had relakonships to disclose; 13 had no relakonships to disclose. Panel members disclose their relakonships and recuse themselves from vokng on evidence statements and recommendakons relevant to their relakonships. How the Process Has Evolved Strictly evidence-based Focus only on randomized controlled trials assessing important health outcomes (no use of intermediate/surrogate measures) Every included study is rated for quality by two independent reviewers using standardized tools Evidence statements graded for quality using prespecified criteria Separate grading for recommendations Independent methodology team to ensure objectivity of the review Initial set of recommendations focused on 3 key questions How Were Questions Selected? Panel Chairs and NHLBI staff developed questions based on their expertise, brief literature review, and speaking with colleagues These questions were sent to panel members to review, revise, and add or delete questions Resulted in 23 questions, which were sent to all panel members Panel members discussed these questions on conference calls, then independently ranked the 3-5 questions felt to be of highest priority The five highest ranked questions discussed further and prioritized 6

7 Rationale for the Questions Interest in assessing the evidence to support 140/90 mm Hg as a treatment threshold or goal Should the treatment threshold / goal be lower in populations with diabetes, chronic kidney disease, coronary artery disease, stroke, and other co-morbidities or characteristics? Should the treatment threshold / goal be different in older adults? Use of different treatment thresholds and goals is confusing Is there evidence that treatment to lower BP with a particular drug or drug class improves outcomes compared to another? Critical Questions and I/E Criteria Critical Question (CQ) in PICO format Population Intervention/Exposure Control/Comparator Outcomes Study Inclusion/ Exclusion criteria: Types of studies (e.g., RCTs, epidemiology, systematic reviews) Subgroups (e.g., elderly, diabetes) Specific outcomes (e.g., CVD mortality, MI, stroke, HF) Execu)ve CommiBee Sidney Smith Jr. MD BP Panel Paul James MD Suzanne Oparil MD Cholesterol Panel Neil Stone MD Alice Lichtenstein DSc Jennifer Robinson MD Obesity Panel Michael Jensen MD Donna Ryan MD Lifestyle WG Robert Eckel MD John Jakicic PhD Risk Assessment WG David Goff Jr. MD, PhD Donald M. Lloyd- Jones MD, ScD Implementa)on WG Thomas Pearson MD, PhD Wiley Chan MD Expert Panel Composition Diversity and balance of expertise Diversity of demographics Conflict of interest management 7

8 NHLBI Adult CVD Prevention Guidelines Expert Panels and WorkGroups BP Panel Evidence Review on BP Tx 3 CQs Cholesterol Panel Evidence Review on Cholesterol Tx 3 CQs Obesity Panel Evidence Review on Obesity 5 CQs (2 SRs) Lifestyle WG Evidence Review on Diet & Physical Activity 3 CQs (1 SR) Risk Assessment WG Evidence Review & Risk Prediction Model 2 CQs+model (1 SR) Five draft reports released for public comment, one at a time Implementation WG Implementability Guidance (GLIA) Implementation Science Review 22 Question 1 Among adults with hypertension, does initiating antihypertensive pharmacological therapy at specific BP thresholds improve health outcomes? When to initiate drug treatment? Question 2 Among adults, does treatment with antihypertensive pharmacological therapy to a specified BP goal lead to improvements in health outcomes? How low should you go? 8

9 Question 3 In adults with hypertension, do various antihypertensive drugs or drug classes differ in comparative benefits and harms on specific health outcomes? How do you get there? Inclusion/Exclusion Criteria Randomized Controlled Trials RCTs are subject to less bias and represent the gold standard for determining efficacy and effectiveness 1 Search dates: 1966 to present Minimum one-year follow-up period Studies with sample sizes less than 100 excluded 1 Institute of Medicine Finding What Works In Health Care. Standards For Systematic Reviews. Washington, DC: The National Academies Press. Populations Included Adults 18 years of age and older Prespecified subgroups including: Diabetes Chronic kidney disease Proteinuria Coronary artery disease Peripheral artery disease Previous stroke Heart Failure Older Adults Men and women Racial and ethnic groups 9

10 Outcomes Overall mortality, CVD-related mortality, CKD-related mortality, myocardial infarction, heart failure, hospitalization for heart failure, stroke Coronary revascularization (includes coronary artery bypass surgery, coronary angioplasty and coronary stent placement), peripheral revascularization (includes carotid, renal, and lower extremity revascularization) End stage renal disease (i.e., kidney failure resulting in dialysis or transplant), doubling of creatinine, halving of egfr Literature Review and Assessment Process Systematic search of literature for the CQ Citations found using inclusion/exclusion criteria Papers screened and reviewed for inclusion Result: unbiased list of studies based on a priori criteria Quality of each included study rated Good, Fair, Poor NHLBI study rating instruments Controlled intervention studies Cohort and cross-sectional studies Case-control studies Systematic reviews and meta-analyses NHLBI Study Assessment Tool: Controlled Intervention Studies Criteria 1.Was the study described as randomized, a randomized trial, a randomized clinical trial, or an RCT? 5. Were the people assessing the outcomes blinded to the participants group assignments? 7. Was the overall drop-out rate from the study at its endpoint 20% or less than the number originally allocated to treatment? 14. Were all randomized participants analyzed in the group to which they were originally assigned (i.e., did they use an intention-to-treat analysis)? Quality Rating (Good, Fair, Poor) (see guidance) Rater #1 initials: Rater #2 initials: Additional Comments (If POOR, please state why): Yes No Other 10

11 Data Abstraction and Evidence Tables Information from individual studies Key data abstracted into a database Evidence table for each study/paper: subjects, sample size, intervention, comparison, results Evidence summaries by Critical Question Tables and text of major elements relevant to the CQ Graded evidence statements Multiple ESs for each CQ Graded recommendations based on the evidence Multiple ESs could result in a single recommendation 31 Question 1: Among adults with hypertension, does initiating antihypertensive pharmacological therapy at specific BP thresholds improve health outcomes? ArEcles Screened = 1496 Good = 8 Included = 44 Fair = 18 Poor = 18 Excluded = 1452 (Did not meet prespecified inclusion criteria) Total Abstracted = 26 Question 2: Among adults, does treatment with antihypertensive pharmacological therapy to a specified BP goal lead to improvements in health outcomes? ArEcles Screened = 1978 Good = 17 Included = 92 Fair = 39 Poor = 36 Excluded = 1886 (Did not meet prespecified inclusion criteria) Total Abstracted = 56 11

12 Question 3: In adults with hypertension, do various antihypertensive drugs or drug classes differ in comparative benefits and harms on specific health outcomes? ArEcles Screened = 2662 Good = 15 Included = 101 Fair = 51 Poor = 35 Excluded = 2561 (Did not meet prespecified inclusion criteria) Total Abstracted = 66 Methods description Critical questions Adult CV Guideline Report Content With study eligibility criteria and rationale Summary of evidence for each CQ Summary tables and text ( e.g. 24 studies, 10 RCTs ) Graded evidence statements (ES) Rationale for ES based on specific studies or previous systematic reviews Graded High, Medium, Low Graded recommendations Rationale for the recommendation based on the evidence Graded A, B, C, D, E, or N Reference citations 35 Conclusion The new NHLBI-sponsored adult CV guideline reports Are strictly evidence based Will not look like the previous guidelines Will have more depth and rigor; will have less breadth Will be released in 2012, one at a time as they are ready Will use evidence based strategies for Implementation 36 12

13 New reports vs Previous reports The new guideline reports will not look like the previous guidelines! Recommendations are based on systematic reviews of RCTs Restricted to a few critical questions More depth, less breadth (More rigor, less comprehensive) The new guideline reports will look more similar to each other than in the past Previous reports used different methods and structure New reports are using the same methods and structure 37 Next Steps Evidence statements and recommendations (in progress) Draft report (in progress) Review of the draft report by: Other federal agencies (CDC, CMS, AHRQ, HRSA, VA, etc.) Invited organizations and individuals Public Revisions based on comments received Final report Summary JNC 8 is close Hope to build on the current effort for future guidelines While there is a need for a complete evidence- based document, there will be areas where evidence is lacking IntegraKon of experts/specialists with primary care providers to facilitate true change 13

14 Active Learning Example You are a reviewer for a study in hypertension. The study is described as a randomized, controlled trial comparing two different drugs on major cardiovascular events. In your review you find that: 1. the paper describes there are about 33% who dropped out. 2. You also find that despite proper design, 20% in each study arm actually crossed over to other arm. It is not clear in the methods how these crossovers were analyzed. 3. When subjects had a heart ayack or stroke, or other event, the individual who determined if an event actually occurred was aware which treatment the subject received. Questions 1. How do you think you would rate the quality of this study (Good, Fair, or Poor)? 2. How likely do you think this study will carry significant weight in making treatment recommendakons? 3. If this is the only study in the literature that could be used to answer one of your crikcal queskons and you must make a specific recommendakon or statement, what strength do you think this recommendakon might have? (Strong, Moderate, Weak, Against, Expert Opinion, No RecommendaKon) Thank You Contact Information: barry-carter@uiowa.edu 14

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