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OtherPractice

Understanding and communicating risk

Measures of outcome and the magnitude of benefits and harms

Neil R. Bell, James A. Dickinson, Roland Grad, Harminder Singh, Danielle Kasperavicius and Brett D. Thombs
Canadian Family Physician March 2018; 64 (3) 181-185;
Neil R. Bell
Professor in the Department of Family Medicine at the University of Alberta in Edmonton.
MD SM CCFP FCFP
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  • For correspondence: nrbell@telusplanet.net
James A. Dickinson
Professor in the Department of Family Medicine and the Department of Community Health Sciences at the University of Calgary in Alberta.
MB BS PhD CCFP FRACGP
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Roland Grad
Associate Professor in the Department of Family Medicine at McGill University and Senior Investigator at the Lady Davis Institute in Montreal, Que.
MD CM MSc CCFP FCFP
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Harminder Singh
Associate Professor in the Department of Internal Medicine and the Department of Community Health Sciences at the University of Manitoba in Winnipeg and the Department of Hematology and Oncology for CancerCare Manitoba.
MD MPH FRCPC
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Danielle Kasperavicius
Research Coordinator for the Knowledge Translation Program at St Michael’s Hospital in Toronto, Ont.
MPH
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Brett D. Thombs
Professor and William Dawson Scholar in the Faculty of Medicine at McGill University and Chair of the Canadian Task Force on Preventive Health Care.
PhD
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    Table 1.

    Outcome measures encountered in preventive screening

    MEASUREHOW TO CALCULATEADVANTAGES AND DISADVANTAGES IN PATIENT RISK COMMUNICATION
    Mortality (overall and disease specific)The number of patients who died divided by the total number of patients in the study population.
    Mortality would be calculated separately for the control and intervention groups in randomized controlled trials
    • Provides the highest-quality estimate of the benefits of cancer screening

    • Results unaffected by lead-time, length-time, or overdiagnosis bias

    5- or 10-year survival rates (absolute rate)The number of individuals who are alive at 5 or 10 years after the time of diagnosis of disease divided by the total number diagnosed with the disease
    • Provides exaggerated estimates of the benefits of preventive screening owing to lead-time, length-time, and overdiagnosis bias

    Incidence (new cases)The number of new events or cases that develop during a given time period in the total population at risk
    • Provides exaggerated estimates of benefits of preventive screening owing to overdiagnosis

    • View popup
    Table 2.

    Measures of magnitude or effect size encountered in preventive screening

    MEASUREABBREVIATIONHOW TO CALCULATEADVANTAGES AND DISADVANTAGES IN PATIENT RISK COMMUNICATIONEXAMPLE* (REDUCTION IN LUNG CANCER MORTALITY)
    Natural frequencyNFNumber of persons with events in a population
    • Highest levels of patient understanding and satisfaction

    • Denominator of 1000 people increases patient understanding of harms and benefits

    • Understanding increased when baseline risk is included

    13 of 1000 people died of lung cancer with screening; 16 of 1000 people died from lung cancer without screening.
    Thus, there were 3 of 1000 fewer deaths from lung cancer with screening
    Absolute riskARThe number of events in the screened or control groups divided by the number of people in that group
    • Increases patient understanding of risk

    • Understanding increased when baseline risk is included

    AR in control group = 1.66%
    AR in screened group = 1.33%
    Absolute risk reductionARRDifference in the event rates between the screened and control arms of the studyARR = 1.66% − 1.33% = 0.33%
    Relative riskRRRatio of the outcome measure (eg, overall mortality) in the screened group compared with the unscreened group
    • Can cause exaggerated perceived screening or treatment effects

    RR = 0.80
    Relative risk reductionRRRThe difference in event rates between the screened and control groups divided by the event rate in the control group
    • Can exaggerate the perceived treatment effect for both physicians and patients. Often presented as percentage without baseline risk

    RRR = 1.66 − 1.33/1.66 = 0.20
    RRR = 20%
    Number needed to screenNNSReciprocal of the ARR
    • Decreased level of patient understanding compared with other measures of magnitude or effect size

    NNS = 308†
    • ↵* All measures describe the same reduction in lung cancer mortality.

    • ↵† Differs slightly from 1/ARR in this example owing to rounding.

    • All examples are taken from the National Lung Screening Trial.24

    • Estimates were taken from the Canadian Task Force on Preventive Health Care systematic review and meta-analysis on screening for lung cancer.25,26

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Canadian Family Physician: 64 (3)
Canadian Family Physician
Vol. 64, Issue 3
1 Mar 2018
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Understanding and communicating risk
Neil R. Bell, James A. Dickinson, Roland Grad, Harminder Singh, Danielle Kasperavicius, Brett D. Thombs
Canadian Family Physician Mar 2018, 64 (3) 181-185;

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Neil R. Bell, James A. Dickinson, Roland Grad, Harminder Singh, Danielle Kasperavicius, Brett D. Thombs
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