Is IPT more effective in high-burden settings? Modelling the effect of tuberculosis incidence on IPT impact

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Ragonnet, R; Trauer, JM; McBryde, ES; Houben, RMGJ; Denholm, JT; Handel, A; Sumner, TDate
2017-01-01Source Title
International Journal of Tuberculosis and Lung DiseasePublisher
INT UNION AGAINST TUBERCULOSIS LUNG DISEASE (I U A T L D)University of Melbourne Author/s
McBryde, Emma; Denholm, Justin; Trauer, James; Ragonnet, Romain Frederic CorneilleAffiliation
Medicine and RadiologyMicrobiology and Immunology
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Ragonnet, R., Trauer, J. M., McBryde, E. S., Houben, R. M. G. J., Denholm, J. T., Handel, A. & Sumner, T. (2017). Is IPT more effective in high-burden settings? Modelling the effect of tuberculosis incidence on IPT impact. INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 21 (1), pp.60-66. https://doi.org/10.5588/ijtld.16.0297.Access Status
Open AccessAbstract
SETTING: Isoniazid preventive therapy (IPT) is effective for preventing active tuberculosis (TB), although its mechanism of action is poorly understood and the optimal disease burden for IPT use has not been defined. OBJECTIVE: To describe the relationship between TB incidence and IPT effectiveness. METHODS: We constructed a model of TB transmission dynamics to investigate IPT effectiveness under various epidemiological settings. The model structure was intended to be highly adaptable to uncertainty in both input parameters and the mechanism of action of IPT. To determine the optimal setting for IPT use, we identified the lowest number needed to treat (NNT) with IPT to prevent one case of active TB. RESULTS: We found that the NNT as a function of TB incidence shows a 'U-shape', whereby IPT impact is greatest at an intermediate incidence and attenuated at both lower and higher incidence levels. This U-shape was observed over a broad range of parameter values; the optimal TB incidence was between 500 and 900 cases per 100 000 per year. CONCLUSIONS: TB burden is a critical factor to consider when making decisions about communitywide implementation of IPT. We believe that the total disease burden should not preclude programmatic application of IPT.
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