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Global Tuberculosis Control 2010 - Florida Department of Health

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α=Ī Ī (1– Ī )<br />

– 1<br />

V<br />

β=(1– Ī ) Ī (1– Ī )<br />

– 1<br />

V<br />

ĪNV<br />

<br />

V= 0.3<br />

4<br />

N<br />

2<br />

<br />

<br />

α= – x – x (1– – x )<br />

V<br />

– 1<br />

β=(1– – x ) – x (1– – x )<br />

V<br />

– 1<br />

x – V<br />

(u – l) 2<br />

V=<br />

4<br />

l = 1, u = 4<br />

<br />

l = 0.01, u = 0.2<br />

<br />

l = 0.2, u = 2<br />

<br />

l = 0.01, u = 1<br />

<br />

<br />

<br />

ƒ (x; α, β) =<br />

x α–1 (1– x) β–1<br />

u α–1 (1– u) β–1 du<br />

1<br />

0<br />

<br />

<br />

<br />

<br />

Data were assessed using a three-step process. This<br />

started with a systematic assessment <strong>of</strong> data quality,<br />

including an assessment <strong>of</strong> the over-dispersion <strong>of</strong> count<br />

data over time and across regions/districts (or similar<br />

geographical areas). This was followed by exploration <strong>of</strong><br />

potential factors driving time-changes in case notifications<br />

(such as improvements in diagnostic capacity and<br />

the HIV epidemic), and then by assessment <strong>of</strong> the likely<br />

number <strong>of</strong> TB cases that are not notified. To facilitate<br />

the documentation <strong>of</strong> expert opinion, an “onion” framework<br />

1 was used. In this framework, different “layers”<br />

<strong>of</strong> the onion represent distinct populations <strong>of</strong> TB cases<br />

that are not captured by national TB information systems<br />

(for example, cases with no access to health care<br />

and cases with access to private health-care services but<br />

not reported to NTPs – see ).<br />

These methods are documented in a workbook available<br />

on the web site <strong>of</strong> the WHO <strong>Global</strong> Task Force on TB<br />

Impact Measurement. 2<br />

Distributions <strong>of</strong> CDRs for the three years for which<br />

they were estimated were assumed to follow a Beta distribution<br />

( ). Reasons for using Beta distributions<br />

include the following:<br />

They are continuous and defined on the interval (0,<br />

1). Since the variance <strong>of</strong> CDR distributions tend to be<br />

large as a result <strong>of</strong> high uncertainty, random draws<br />

<strong>of</strong> numbers from a normal distribution would yield<br />

numbers outside the interval (0, 1). The use <strong>of</strong> truncated<br />

normal distributions may result in excess density<br />

towards one <strong>of</strong> the bounds.<br />

They are not necessarily symmetrical.<br />

They are defined with two parameters that can be<br />

estimated from available data using the method <strong>of</strong><br />

moments.<br />

The two shape parameters necessary to define the<br />

Beta distribution were computed using the method <strong>of</strong><br />

moments, as follows:<br />

1<br />

TB impact measurement: policy and recommendations for how to assess<br />

the epidemiological burden <strong>of</strong> TB and the impact <strong>of</strong> TB control. Geneva,<br />

World <strong>Health</strong> Organization, 2009 (Stop TB policy paper no 2; WHO/<br />

HTM/TB/2009.416. The onion framework is described on pages<br />

19–24). The policy paper is available on the Task Force’s website<br />

http://www.who.int/tb/advisory_bodies/impact_measurement_<br />

taskforce/en/index.html.<br />

2<br />

http://www.who.int/tb/advisory_bodies/impact_measurement_<br />

taskforce/en/index.html.

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