Confounding: what it is and how to deal with it Kitty J. Jager¹, Carmine Zoccali 2, Alison MacLeod 3 and Friedo W. Dekker 1,4 1 ERA–EDTA Registry, Dept.

Slides:



Advertisements
Similar presentations
Measures of effect: relative risks, odds ratios, risk difference and number needed to treat Giovanni Tripepi, Kitty J. Jager 1, Friedo W. Dekker 1,2, Christoph.
Advertisements

Measures of Disease Occurrence Kitty J. Jager¹, Carmine Zoccali², Reinhard Kramar³ and Friedo W. Dekker 1,4 1 ERA–EDTA Registry, Dept. of Medical Informatics,
The analysis of survival data: the Kaplan Meier method Kitty J. Jager¹, Paul van Dijk 1,2, Carmine Zoccali 3 and Friedo W. Dekker 1,4 1 ERA–EDTA Registry,
The valuable contribution of observational studies to nephrology Kitty J. Jager¹, Vianda S. Stel¹, Christoph Wanner², Carmine Zoccali³ and Friedo W. Dekker.
The analysis of survival data in nephrology. Basic concepts and methods of Cox regression Paul C. van Dijk 1-2, Kitty J. Jager 1, Aeilko H. Zwinderman.
The randomized clinical trial: an unbeatable standard in clinical research? Vianda S. Stel¹, Kitty J. Jager¹, Carmine Zoccali², Christoph Wanner³, Friedo.
Agreement between Methods Karlijn J. van Stralen¹, Kitty J. Jager¹, Carmine Zoccali², and Friedo W. Dekker 1,3 1 ERA–EDTA Registry, Dept. of Medical Informatics,
June 25, 2006 Propensity Score Adjustment in Survival Models Carolyn Rutter Group Health Cooperative AcademyHealth, Seattle WA.
Analytical epidemiology
ESPN/ERA-EDTA registry Karlijn van Stralen Enrico Verrina, Jane Tizard, Kitty Jager Status.
Multicenter database of clinical course of CKD patients Internal Medicine Jang Hye Ryoun.
How would you explain the smoking paradox. Smokers fair better after an infarction in hospital than non-smokers. This apparently disagrees with the view.
M2 Medical Epidemiology
Deriving Biological Inferences From Epidemiologic Studies.
This Power Point presentation belongs to the Danish Renal Registry, which owns the copyright. It can be freely used for non-commercial study and educational.
Chance, bias and confounding
Estimation and Reporting of Heterogeneity of Treatment Effects in Observational Comparative Effectiveness Research Prepared for: Agency for Healthcare.
Elements of a clinical trial research protocol
Confounding And Interaction Dr. L. Jeyaseelan Department Of Biostatistics CMC, Vellore.
NHANES III Prevalence of Hypertension* According to BMI
Journal Club Alcohol, Other Drugs, and Health: Current Evidence July-August 2007.
Journal Club Alcohol and Health: Current Evidence July–August 2004.
CKD Conservative care and preparation for dialysis UK Renal Registry 2013 Annual Audit Meeting Dr Anirudh Rao Registrar, UK Renal Registry.
RENAL DISEASE IN DIABETES
Cohort Study.
INTRODUCTION TO EPIDEMIOLO FOR POME 105. Lesson 3: R H THEKISO:SENIOR PAT TIME LECTURER INE OF PRESENTATION 1.Epidemiologic measures of association 2.Study.
Multiple Choice Questions for discussion
6 / 5 / RENAL DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED INTO 3 GROUPS BY BASELINE GLOMERULAR FILTRATION RATE (GFR) ALLHAT.
Evidence-Based Medicine 4 More Knowledge and Skills for Critical Reading Karen E. Schetzina, MD, MPH.
Epidemiology The Basics Only… Adapted with permission from a class presentation developed by Dr. Charles Lynch – University of Iowa, Iowa City.
AETIOLOGY Case control studies (also RCT, cohort and ecological studies)
Evidence-Based Medicine 3 More Knowledge and Skills for Critical Reading Karen E. Schetzina, MD, MPH.
Biostatistics Case Studies Peter D. Christenson Biostatistician Session 5: Analysis Issues in Large Observational Studies.
Lecture 6 Objective 16. Describe the elements of design of observational studies: (current) cohort studies (longitudinal studies). Discuss the advantages.
Amsterdam Rehabilitation Research Center | Reade Multiple regression analysis Analysis of confounding and effectmodification Martin van de Esch, PhD.
Haemodialysis Vascular Access: Recent Trends From ANZDATA Dr Kevan Polkinghorne Monash Medical Centre ANZSN September 2007.
 Exemplary Care  Cutting-edge Research  World-class Education  Raghavan Murugan MD, MS, FRCP Associate Professor Dept. of Critical Care Medicine Clinical.
Article Review Cara Carty 09-Mar-06. “Confounding by indication in non-experimental evaluation of vaccine effectiveness: the example of prevention of.
Data completeness reporting Alex Hodsman, David Bull, Paul Dawson UK Renal Registry.
Literature searching & critical appraisal Chihaya Koriyama August 15, 2011 (Lecture 2)
UK Renal Registry 10th Annual Report 2007 Fig 3.1 Incident rates in the countries of the UK:
Association between Systolic Blood Pressure and Congestive Heart Failure Complication among Hypertensive and Diabetic Hypertensive Patients Mrs. Sutheera.
Case-control study Chihaya Koriyama August 17 (Lecture 1)
Design and Analysis of Clinical Study 2. Bias and Confounders Dr. Tuan V. Nguyen Garvan Institute of Medical Research Sydney, Australia.
UK Renal Registry 17th Annual Report Figure 1.1. RRT incidence rates in the countries of the UK 1990–2013.
Study Designs for Clinical and Epidemiological Research Carla J. Alvarado, MS, CIC University of Wisconsin-Madison (608)
Instructor Resource Chapter 14 Copyright © Scott B. Patten, Permission granted for classroom use with Epidemiology for Canadian Students: Principles,
Raghavan Murugan, MD, MS, FRCP Associate Professor of Critical Care Medicine, and Clinical & Translational Science Core Faculty, Center for Critical Care.
ALLHAT 6/5/ CARDIOVASCULAR DISEASE OUTCOMES IN HYPERTENSIVE PATIENTS STRATIFIED BY BASELINE GLOMERULAR FILTRATION RATE (3 GROUPS by GFR)
Instructor Resource Chapter 15 Copyright © Scott B. Patten, Permission granted for classroom use with Epidemiology for Canadian Students: Principles,
The Databases: Successes and Shortcomings in Renal Replacement Therapy Since 1989 European Renal Association and European Dialysis and Transplant Association.
Matching. Objectives Discuss methods of matching Discuss advantages and disadvantages of matching Discuss applications of matching Confounding residual.
Unit 11: Evaluating Epidemiologic Literature. Unit 11 Learning Objectives: 1. Recognize uniform guidelines used in preparing manuscripts for publication.
What happens to patients returning to dialysis after transplant failure? Data from the UK Renal Registry Dr Lynsey Webb 1, Dr Anna Casula 1, Dr Charlie.
Carina Signori, DO Journal Club August 2010 Macdonald, M. et al. Diabetes Care; Jun 2010; 33,
Date of download: 6/2/2016 Copyright © 2016 American Medical Association. All rights reserved. From: Similar Outcomes With Hemodialysis and Peritoneal.
The SYMPHONY Trial Reference Reddan DN, et al. Renal function, concomitant medication use and outcomes following acute coronary syndromes. Nephrol Dial.
Am J Kidney Dis. 2014;63(6): R3 박세정 /prof. 이태원 Comparative Effectiveness of Early Versus Conventional Timing of Dialysis Initiation in Advanced.
Is it possible to predict New Onset Diabetes After Transplantation (NODAT) in renal recipients using epidemiological data alone? Background NODAT is an.
Date of download: 7/1/2016 From: Time-Updated Systolic Blood Pressure and the Progression of Chronic Kidney Disease: A Cohort Study Ann Intern Med. 2015;162(4):
- Higher SBP visit-to-visit variability (SBV) has been associated
Alcohol, Other Drugs, and Health: Current Evidence July–August 2017
FIGURE 1 Flow chart of the study population
UK Renal Registry 16th Annual Report
Presenter: Wen-Ching Lan Date: 2018/03/28
Confounding: What it is and how to deal with it
Evaluating Effect Measure Modification
UK Renal Registry 14th Annual Report
(A) Kaplan-Meier renal survival estimates of patients with diabetic nephropathy (DN), non-diabetic renal disease (NDRD) and mixed groups, adjusting for.
Adjusted relative risk for developing end-stage renal disease (ESRD) associated with blood-pressure level BP level (mm Hg) Adjusted relative risk 95%
Presentation transcript:

Confounding: what it is and how to deal with it Kitty J. Jager¹, Carmine Zoccali 2, Alison MacLeod 3 and Friedo W. Dekker 1,4 1 ERA–EDTA Registry, Dept. of Medical Informatics, Academic Medical Center, Amsterdam, The Netherlands 2 CNR–IBIM Clinical Epidemiology and Pathophysiology of Renal Diseases and Hypertension, Renal and Transplantation Unit, Ospedali Riuniti, Reggio Cal., Italy 3 University of Aberdeen Medical School, Aberdeen, United Kingdom 4 Department of Clinical Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands Kidney International: ABC on epidemiology

Confounding Mixing or blurring of effects In studies investigating disease etiology and causal relationships, confounding is regarded as undesirable, as it obscures the real effect of an exposure. This presentation will explain the concept of confounding and describe a number of ways in which it can be addressed: –randomization, restriction, matching and stratification

When are variables potential confounders? Properties of a potential confounder (1)the variable must have an association with the disease, i.e. it should be a risk factor for the disease; (2) it must be associated with the exposure, i.e. it must be unequally distributed between the exposed and non-exposed groups; and (3) it must not be an effect of the exposure, nor (linked to this) be a factor in the causal pathway of the disease

Association between initial dialysis modality and patient survival Is GFR a potential confounder? 1 Couchoud C, Moranne O, Frimat L, Labeeuw M, Allot V, Stengel B. Associations between comorbidities, treatment choice and outcome in the elderly with end-stage renal disease. Nephrol Dial Transplant Advance Access published July 5, Example 1 – Association between treatment choice and outcome in the elderly with end-stage renal disease (ESRD). Couchoud et al. 1 studied the association between initial dialysis modality and 2-year patient survival in a cohort of 3512 elderly ESRD patients. After adjustment for eGFR at dialysis initiation and a number of other factors, unplanned HD was associated with a 50% increased risk of death and PD with a 30% increased risk of death compared with planned HD. GFR is a potential confounder

Association between body mass index and the risk of ESRD Is blood pressure a potential confounder? 2 Hsu C, McCulloch CE; Iribarren C, Darbinian J, Go AS. Body Mass Index and Risk for End-Stage Renal Disease. Ann Intern Med 2006;144: Example 2 - BMI and the risk for ESRD Hsu et al. 2 investigated the relationship between BMI and the risk for ESRD using data of more than 320,000 members of Kaiser Permanente. They were able to show that, adjusted for a number of confounders like age, sex and race (but not for blood pressure), increased BMI was strongly associated with an increased risk for ESRD. Blood pressure is not a potential confounder

How to address confounding? During study design by randomization, restriction or matching During data analysis by adjustment for confounding using stratification or multivariate analysis

Randomization Random assignment of patients to experimental group or a control group Helps to prevent selection bias / confounding by indication by the clinician Any remaining differences between the groups are due to chance Large study size helps randomization process to be successful If important differences remain, investigators may adjust for these confounders in their analysis

Other ways to address confounding Restriction: e.g. perform only in patients above 65 years of age Matching: e.g. in a cohort study for each exposed person with DM the investigator may select an unexposed person without DM of the same age -Cave:in case-control studies the choice of matching variables requires careful attention Stratification: e.g. calculate relative risks in subgroups according to age and then calculate an adjusted relative risk by pooling or standardization

Commonly made errors - I Over-adjustment is a commonly made error It takes away part of the real effect In this example adjustment for blood pressure is incorrect from the perspective of confounding Adjustment may however be useful to explore potential causal pathways Example 2 - BMI and the risk for ESRD 2 Relative Risk of BMI kg/m2 adjusted model without blood pressure 6.12 (CI, 4.97 to 7.54) after additional adjustment for blood pressure 4.68 (CI, 3.79 to 5.79)

Commonly made errors - II Example 3 - CNDP1 - Mannheim variant and the susceptibility to diabetic nephropathy (DN) Janssen et al. 3 performed a case-control study using diabetic patients with DN as cases and diabetic patients without DN as controls. They showed that the CNDP1 - Mannheim variant was more common in the absence of DN (odds ratio 2.56 (CI, 1.36 to 4.84)). 3 Janssen B, Hohenadel D, Brinkkoetter P et al. Carnosine as a protective factor in diabetic nephropathy. Association with a leucine repeat of the carnosinase gene CNDP1. Diabetes 2005;54:2320–2327. Would it have been useful if Janssen et al. would have matched for BMI? Matching for body mass index would have been incorrect, as body mass index is not a potential confounder

Commonly made errors - III The use of statistical significance tests to detect confounding is incorrect The amount of confounding is the result of the strength of the associations between the confounder on the one hand and the exposure and the disease on the other hand P-values will not provide information if a particular variable is a confounder The amount of confounding caused by a variable that satisfies all criteria for a potential confounder can be measured by looking at the difference between the crude and adjusted effect size: If these are almost equal there is no confounding If the difference between is important there is confounding

Conclusion Confounding is a mixing of effects distorting the real effect of an exposure Before adjusting for confounding all criteria for a possible confounder should be carefully checked in order to prevent the introduction of new bias through over-adjustment for variables that do not satisfy all criteria for confounding