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Introduction: childhood tuberculosis continues to be a major public health problem, despite the fact that the visibility of the epidemic in this population group has increased, studies are still lacking that can resolve the gaps that persist.
Objective: To design, implement and evaluate an integrated care strategy for children under five years old household contacts of patients with smear positive pulmonary tuberculosis in Medellín and the Metropolitan Area.
Methodology: quasi-experimental study, in which around 300 children household contacts of patients with smear positive pulmonary tuberculosis from Medellín and the Metropolitan Area will be evaluated, who will be recruited in a period of one year. A subgroup of these children, estimated at 85, who require treatment for latent tuberculosis, will be offered to receive treatment for latent tuberculosis under a integrated care strategy that includes some modifications to the currently standardized scheme in Colombia, with rifampicin treatment daily oral route for four months, follow-up under the project scheme with the availability of a nurse, general practitioner, specialists, care by professionals from other disciplines such as social work, psychology, and nutritionist, and the provision of incentives (transport and food assistance). This strategy will be compared with isoniazid treatment according to the standardized scheme in the country, which was received by a cohort of children between 2015 and 2018. The study has the CIB Research Ethics Committee approval.
Expected results: this project is expected to contribute with greater local evidence of integrated care strategies that allow greater compliance with treatment for latent tuberculosis in children, so that there is a real impact in the control of childhood tuberculosis and in the reduction of tuberculosis reservoirs in order to achieve the goals proposed by the World Health Organization's End TB Strategy.
Full description
Objective:
To design, implement and evaluate an integrated care strategy for children under five years old household contacts of patients with smear positive pulmonary tuberculosis in Medellín and the Metropolitan Area.
Methodology:
Study design
Quasi-experimental study with a one-year follow-up, which will include a cohort of children household contacts of patients with smear positive pulmonary TB from Medellín and the Valle de Aburrá Metropolitan Area, to carry out the contact tracing and treatment for latent TB in those who is indicated, and who will receive the intervention of the integrated care strategy. Compliance with the treatment achieved with this strategy will be compared with compliance achieved with the treatment with isoniazid in the 2015-2018 cohort.
The integrated care strategy for contact children of patients with smear positive pulmonary TB will have the following components:
Operational hypothesis
The proportion of treatment compliance for latent TB in contact children of patients with smear positive pulmonary TB in Medellín and the Metropolitan Area who receive the integrated care strategy is greater than the proportion of treatment compliance for children who received isoniazid in the 2015-2018 cohort.
Study population
Sample: the sample will be children under five years old household contacts of patients with smear positive confirmed pulmonary TB from Medellín and the Metropolitan Area notified to the surveillance system during 2020, in whom treatment for latent TB is indicated.
Sample
Sampling type: it will correspond to an Incidental Sampling, since the children of the study will be recruited as new cases (incidents) of smear positive confirmed pulmonary TB identified in Medellín and the Metropolitan Area.
Sample size: all children household contacts of smear positive pulmonary TB patients from Medellín and the Metropolitan Area will be follow-up initially for a period of one year, according to previous studies it is estimated that around 250 to 300 children will be assessed with a proportion of estimated infection of 73.5%.
The complete intervention of the integrated care strategy (with medication, incentives and active follow-up) will be provided to a subgroup of children who require treatment for latent tuberculosis, and who will also be selected incidentally, according to their willingness to participate. To calculate the sample size of this subgroup, compliance with the treatment with isoniazid in the 2015-2018 cohort of 59% was considered, hoping that the proposed strategy achieves at least 80% of compliance (expected goal), with a confidence level of 95% and a power of 80%, it is estimated that a group of at least 75 children will be required in the proposed comprehensive care strategy (sample size calculated with Epidat version 4.2), an additional 10% will be estimated due to loss to follow-up, so the total number of children to enter the integrated care strategy will be 85.
Description of interventions
The intervention will be the integrated care strategy, in which the effects of interventions established in the regulations of the TB program at the national level will be observed, such as the diagnosis and administration of treatment for latent TB in children household contacts of patients with pulmonary TB, with two main modifications, the supply of daily oral rifampicin for four months self-administered scheme (instead of daily oral isoniazid for nine months self-administered scheme), and provision of incentives such as transport and food assistance (monthly food supplies). In addition to this, immune response tests will be performed measuring interferon gamma production levels (QuantiFERON®-TB Gold Plus - QFT Plus test) and tuberculin skin test (TST).
Procedures
Research site
Children will be assessed at CIB medical office for clinical and epidemiological conditions and to rule out the diagnosis of tuberculosis and confirm the diagnosis of latent TB; in those who enter the integrated care strategy, treatment compliance and side effects will be assessed, with a clinical assessment at the time of intake, monthly while receiving medication (rifampin four months) and 12 months after the initial assessment; immune response (TST and IGRA) at baseline will also be evaluated; as defined in the procedures.
Chest radiography (including standardized reading) and sampling of induced sputum and gastric juice aspirate will be performed at the Pablo Tobón Uribe Hospital, the samples will be processed at the Corporation for Biological Research (CIB). Liver function tests will be taken at CIB, and processed in Laboratorio Echavarría.
Data analysis To describe the characteristics of children's exposure to TB, a univariate analysis will be carried out, which will include the variables corresponding to the index case, the child's exposure, and other epidemiological variables. Frequencies distribution and proportions estimation will be carried out for the qualitative variables such as sex, socioeconomic stratum, system of affiliation to the social security system in health, history of BCG vaccination, bacteriological study and other variables.
The characteristics of the children in the 2015-2018 and 2020-2022 cohort will be compared using the Z test for the difference in proportions for the qualitative variables and using the Mann-Whitney U test for the quantitative variables according to the normality of those variables estimated with the Shapiro Wilk test. The characteristics of the index cases and the characteristics of the children household contacts will be analyzed separately.
To examine the cellular immune response to M. tuberculosis, a univariate analysis will be carried out. The proportion of response to the TST will be calculated according to categories in <5 mm, between 5 and 10 mm and ≥10 mm, and the prevalence of positive response with cutoff point ≥5 mm. Proportion of interferon gamma production (QuantiFERON®-TB Gold Plus - QFT Plus) will be calculated according to the categories of positive and negative results.
The total agreement between the two immunological tests will be analyzed, as well as the different possibilities of discordance. The kappa index will also be calculated. The prevalence ratio of TST ≥5 mm and / or positive QFT will be calculated, and a bivariate analysis will be made with the characteristics of exposure to TB in children, adjusting for the index case cluster using Poisson regression. Subsequently, the multivariate analysis will be performed adjusting for the variables that met the Hosmer-Lemeshow criterion in the bivariate analysis (p-value <0.25).
A description of the characteristics of the treatment for latent TB will be made, a univariate analysis of the characteristics of the treatment for latent TB will be made, by estimating proportions, the qualitative variables related to the characteristics of the administration of the treatment, side effects (appearance of symptoms such as gastrointestinal or allergic) and treatment compliance (temporary or permanent suspension, cause of treatment suspension).
The difference in treatment compliance proportions between the 2015-2018 and 2020-2022 cohorts will be calculated, with 95% confidence.
Enrollment
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Inclusion criteria
Inclusion criteria for initial evaluation (clinical and paraclinical)
Diagnostic criteria for latent tuberculosis
Inclusion criteria to start treatment for latent tuberculosis infection
Exclusion criteria
Exclusion criteria for receiving treatment for latent tuberculosis
Exclusion criteria for performing induced sputum
• Having severe asthma.
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Central trial contact
Dione Benjumea, Dr
Data sourced from clinicaltrials.gov
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