TY - JOUR
T1 - Poor record linkage sensitivity biased outcomes in a linked cohort analysis
AU - Moore, Cecilia L.
AU - Gidding, Heather F.
AU - Law, Matthew G.
AU - Amin, Janaki
PY - 2016/7/1
Y1 - 2016/7/1
N2 - Objectives To examine the validity of deterministic compared to probabilistic record linkage in the ascertainment of hospitalizations in two linked cohorts. Study Design and Setting HIV-negative (HIV-ve) (n = 1,325) and HIV-positive (HIV+ve) gay and bisexual men (n = 557) recruited in Sydney, Australia, were probabilistically and deterministically linked to a statewide hospital registry (July 2000–June 2012). Results Using probabilistic linkage as the reference standard, deterministic linkage had higher specificity but much lower sensitivity [34.67% (95% confidence interval: 33.44, 35.92)]. A disproportionate number of links missed were individuals with poorer socioeconomic and health indicators, including HIV status. Risk of hospitalization compared to the general male population [HIV+ve standardized incidence ratio (SIR) = 1.45 (1.33–1.59); HIV-ve SIR = 0.72 (0.67–0.78)] was significantly underestimated when deterministic linkage was used [HIV+ve SIR = 0.46 (0.37–0.58); HIV-ve SIR = 0.29 (0.24–0.35)]. The impact of linkage strategy on the calculation of incidence rate ratios (IRRs) was less, but a greater discrepancy in IRRs was seen for diagnostic categories where event rates were low or where the sensitivity of the deterministic linkage was differential between the two cohorts. Conclusion Linkage without proven high sensitivity and specificity should be carefully considered. In circumstances of undetermined sensitivity, SIRs should not be calculated as the extent of underestimation is unknown. The comparison of linked events within or between cohorts is more robust to linkage misclassification; however, selection bias does affect estimates and should be considered before linkage.
AB - Objectives To examine the validity of deterministic compared to probabilistic record linkage in the ascertainment of hospitalizations in two linked cohorts. Study Design and Setting HIV-negative (HIV-ve) (n = 1,325) and HIV-positive (HIV+ve) gay and bisexual men (n = 557) recruited in Sydney, Australia, were probabilistically and deterministically linked to a statewide hospital registry (July 2000–June 2012). Results Using probabilistic linkage as the reference standard, deterministic linkage had higher specificity but much lower sensitivity [34.67% (95% confidence interval: 33.44, 35.92)]. A disproportionate number of links missed were individuals with poorer socioeconomic and health indicators, including HIV status. Risk of hospitalization compared to the general male population [HIV+ve standardized incidence ratio (SIR) = 1.45 (1.33–1.59); HIV-ve SIR = 0.72 (0.67–0.78)] was significantly underestimated when deterministic linkage was used [HIV+ve SIR = 0.46 (0.37–0.58); HIV-ve SIR = 0.29 (0.24–0.35)]. The impact of linkage strategy on the calculation of incidence rate ratios (IRRs) was less, but a greater discrepancy in IRRs was seen for diagnostic categories where event rates were low or where the sensitivity of the deterministic linkage was differential between the two cohorts. Conclusion Linkage without proven high sensitivity and specificity should be carefully considered. In circumstances of undetermined sensitivity, SIRs should not be calculated as the extent of underestimation is unknown. The comparison of linked events within or between cohorts is more robust to linkage misclassification; however, selection bias does affect estimates and should be considered before linkage.
KW - Australia
KW - Cohort study
KW - Deterministic record linkage
KW - Evaluation
KW - Hospital discharge
KW - Probabilistic record linkage
UR - http://www.scopus.com/inward/record.url?scp=84959440575&partnerID=8YFLogxK
U2 - 10.1016/j.jclinepi.2016.01.023
DO - 10.1016/j.jclinepi.2016.01.023
M3 - Article
C2 - 26836255
AN - SCOPUS:84959440575
SN - 0895-4356
VL - 75
SP - 70
EP - 77
JO - Journal of Clinical Epidemiology
JF - Journal of Clinical Epidemiology
ER -