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Rob van Hest Capture-recapture Methods in Surveillance - RePub ...

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Chapter 8<br />

bacteriological confirmation, records three months before and after the study period were<br />

also exam<strong>in</strong>ed.<br />

Record-l<strong>in</strong>kage<br />

Duplicate entries with<strong>in</strong> each of the three data sources were excluded. Hospital records<br />

were l<strong>in</strong>ked to the previously l<strong>in</strong>ked Notification and Laboratory records. Record-l<strong>in</strong>kage<br />

software developed by the Centre for Infections establishes a likelihood of association<br />

between two records based on a core set of identifiers (date of birth, age, full postcode<br />

and sex of the patient and proximity of date of notification, <strong>in</strong>itial mycobacterial isolate or<br />

hospital admission). It allows for visual <strong>in</strong>spection of available additional <strong>in</strong>formation on<br />

geographical location, site of disease, ethnicity and smear, culture or histopathology<br />

results (when performed). All cases with <strong>in</strong>complete or miss<strong>in</strong>g <strong>in</strong>formation on both the<br />

date of birth and age were labelled as “<strong>in</strong>sufficient identifiers” and excluded.<br />

The software allocates an a priori determ<strong>in</strong>ed maximum number of po<strong>in</strong>ts to<br />

each core identifier for complete agreement, reflect<strong>in</strong>g the perceived relative importance<br />

of that identifier. Record-pairs with full agreement of all core identifiers are automatically<br />

assigned as true l<strong>in</strong>ks. Po<strong>in</strong>ts are deducted proportionally to the presumed loss of<br />

<strong>in</strong>formation for <strong>in</strong>creas<strong>in</strong>g deviation from perfect l<strong>in</strong>kage of each identifier to generate an<br />

aggregate score, reflect<strong>in</strong>g the likelihood of association between two patient records. All<br />

categories of candidate-l<strong>in</strong>ks other than automatically assigned l<strong>in</strong>ks were visually<br />

<strong>in</strong>spected and either accepted or rejected. L<strong>in</strong>ked cases were allocated to the year of first<br />

known date of notification, culture-confirmation or hospital admission.<br />

False-positive records and correction<br />

All laboratory-confirmed cases reported through MycobNet were assumed true<br />

tuberculosis cases, as previously found <strong>in</strong> a local capture-<strong>recapture</strong> study <strong>in</strong> England. 17<br />

Notification and Hospital records not l<strong>in</strong>ked with Laboratory could potentially <strong>in</strong>clude<br />

three groups of false-positive records:<br />

1. Cases ultimately diagnosed with an <strong>in</strong>fection with Mycobacteria Other Than<br />

Tuberculosis (MOTT)<br />

2. Cases with a f<strong>in</strong>al diagnosis other than tuberculosis or MOTT <strong>in</strong>fection.<br />

3. Cases misclassified or miscoded.<br />

The proportion of unl<strong>in</strong>ked Hospital cases attributable to MOTT <strong>in</strong>fection was<br />

estimated by l<strong>in</strong>k<strong>in</strong>g Hospital data from 2003 with a MOTT database which began <strong>in</strong> that<br />

same year and used to correct the number of unl<strong>in</strong>ked Hospital cases <strong>in</strong> all years under<br />

study us<strong>in</strong>g a formula expla<strong>in</strong>ed below, assum<strong>in</strong>g the annual proportion is similar.<br />

In order to estimate the proportion of cases with a f<strong>in</strong>al diagnosis other than<br />

tuberculosis or MOTT <strong>in</strong>fection Notification cases not known to Laboratory were l<strong>in</strong>ked<br />

with Treatment Outcome Monitor<strong>in</strong>g data, conta<strong>in</strong><strong>in</strong>g data on Notification cases with a<br />

f<strong>in</strong>al diagnosis other than tuberculosis. At the time of this study Treatment Outcome<br />

Monitor<strong>in</strong>g data were only available for 2001. The proportion of false-positive<br />

112

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