Rifampicin Resistant Tuberculosis, Tuberculosis, Pulmonary
Conditions
Keywords
tuberculosis, implementation science, point-of-care, diagnostics, GeneXpert, Uganda
Brief summary
The investigators' overall objective is to assess the effectiveness, implementation and costs of a streamlined TB diagnostic evaluation strategy based around rapid, onsite molecular testing. The intervention strategy was developed based on theory-informed assessment of barriers to TB diagnostic evaluation at community health centers in Uganda and a process of engagement with local stakeholders. It includes: 1) Point-of-care molecular testing using GeneXpert as a replacement for sputum smear microscopy; 2) Re-structuring of clinic-level procedures to facilitate same-day TB diagnosis and treatment; and 3) Quarterly feedback of TB evaluation metrics to health center staff. The investigators' central hypothesis is that the intervention strategy will have high uptake and increase the number of patients diagnosed with and treated for active pulmonary TB. To test this hypothesis, the investigators will conduct a pragmatic cluster-randomized trial at community health centers that provide TB microscopy services in Uganda in partnership with the National TB Program (NTP). The investigators utilize an effectiveness-implementation hybrid design in which, concurrent with the clinical trial, the investigators will conduct nested mixed methods, health economic and modeling studies to assess 1) whether the intervention strategy modifies targeted barriers to TB diagnostic evaluation; 2) fidelity of implementation of the intervention components (i.e, the degree to which intervention components were implemented as intended vs. adapted across sites); and 3) cost-effectiveness and public health impact.
Detailed description
Aim 1: To compare patient outcomes at health centers randomized to intervention vs. standard-of-care TB diagnostic evaluation strategies. The investigators will randomize 20 community health centers to continue standard TB evaluation (routine microscopy plus referral of patients for Xpert testing per existing processes of care) or to implement the intervention strategy (1. Onsite molecular testing; 2. Re-structuring clinic-level procedures to facilitate same-day TB diagnosis and treatment; and 3. Performance feedback). The investigators will compare reach and effectiveness based on the numbers and proportions of patients (N=5500) who complete TB testing, are found to have TB, and have treatment initiated within one week of specimen provision. Aim 2: To identify processes and contextual factors that influence the effectiveness and fidelity of the intervention TB diagnostic evaluation strategy. The investigators will use quantitative process metrics to assess the adoption and maintenance over time of the core components of the intervention strategy. The investigators will also collect quantitative and qualitative data to describe the fidelity of implementation of each component and faithfulness to the conceptual model. Aim 3: To compare the costs and epidemiological impact of intervention vs. standard-of-care TB diagnostic evaluation strategies. The investigators will model the incremental costs and cost-effectiveness of intervention relative to standard-of-care TB diagnostic evaluation from the health system and patient perspective. The investigators will then construct an epidemic model of the population-level impact of the intervention strategy on TB incidence and mortality.
Interventions
Onsite molecular testing with GeneXpert I as a replacement for microscopy
Research and Uganda NTLP staff will engage health center staff in a discussion of how to re-organize clinical, laboratory and pharmacy services to enable same-day TB diagnosis and treatment.
Feedback of TB diagnostic evaluation quality indicators to health center staff
Sponsors
Study design
Eligibility
Inclusion criteria
* Site-level: Use standard (multi-day) sputum smear microscopy as the primary method of TB diagnosis * Site-level: Participate in NTP-sponsored external quality assurance (EQA) for sputum smear microscopy * Site-level: Send samples to a district or regional hospital/health center for Xpert testing * Patient-level: Initiate evaluation for active TB at a study health center
Exclusion criteria
* Site-level: Do not agree to be randomized to standard-of-care vs. intervention arms * Site-level: Perform sputum smear examination on \<150 patients per year (based on 2015 data) * Site-level: Diagnose \<15 smear-positive TB cases per year (based on 2015 data) * Patient-level: Have sputum collected for monitoring of response to anti-TB therapy * Patient-level: Have sputum collected as part of active, community-based case finding (e.g., contact tracing, community outreach campaign) * Patient-level: Referred to a study health center for TB treatment after a diagnosis is established elsewhere * Patient-level: Started on TB treatment for extra-pulmonary TB only
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number Treated for Microbiologically-confirmed TB Within 14 Days After Presentation to the Health Center for TB Evaluation | Within 14 days after presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to Microbiologically-confirmed TB | Within 6 months of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. Time-to-diagnosis if microbiologically-confirmed TB. |
| Number Treated for TB | Within 14 days of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Time-to-treatment of Microbiologically-confirmed TB | Days from initial health center visit to initiation of treatment if diagnosed, up to 6 months. | Effectiveness outcome. Time-to-treatment if microbiologically-confirmed TB and treated. |
| Number Who Died Within 6 Months | Within 6 months of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Number Diagnosed With Microbiologically-confirmed TB | Within 14 days after presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Number Tested for TB According to National Guidelines | Within 6 months of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Number Suspected/Diagnosed With Rifampin-resistant TB | Within 6 months of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Number Diagnosed and Treated for Microbiologically-confirmed TB | On the same-day of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Number Diagnosed AND Treated for TB | On the same-day of presentation to the health center for tuberculosis evaluation | Effectiveness outcome. |
| Number of Patients Enrolled | Presentation to the health center for tuberculosis evaluation during the 16-month study time frame | Effectiveness outcome. |
Countries
Uganda
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Control Group Onsite ZN or LED fluorescence microscopy + hub-based GeneXpert testing per existing protocols | 5,098 |
| Intervention Onsite molecular testing for TB with GeneXpert + process redesign to facilitate same-day TB diagnosis and treatment + performance feedback
GeneXpert: Onsite molecular testing with GeneXpert as a replacement for microscopy
Process re-design: Research and Uganda NTLP staff will engage health center staff in a discussion of how to re-organize clinical, laboratory and pharmacy services to enable same-day TB diagnosis and treatment.
Performance Feedback: Feedback of TB diagnostic evaluation quality indicators to health center staff | 5,546 |
| Total | 10,644 |
Baseline characteristics
| Characteristic | Control Group | Intervention | Total |
|---|---|---|---|
| Age, Continuous | 38 years | 40 years | 40 years |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 5098 Participants | 5546 Participants | 10644 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| HIV infection | 1905 Participants | 2285 Participants | 4190 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 5098 Participants | 5546 Participants | 10644 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 0 Participants | 0 Participants | 0 Participants |
| Region of Enrollment Uganda | 5098 participants | 5546 participants | 10644 participants |
| Sex: Female, Male Female | 3112 Participants | 3289 Participants | 6401 Participants |
| Sex: Female, Male Male | 1986 Participants | 2257 Participants | 4243 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 154 / 3,857 | 145 / 4,556 |
| other Total, other adverse events | 0 / 0 | 0 / 0 |
| serious Total, serious adverse events | 0 / 0 | 0 / 0 |
Outcome results
Number Treated for Microbiologically-confirmed TB Within 14 Days After Presentation to the Health Center for TB Evaluation
Effectiveness outcome.
Time frame: Within 14 days after presentation to the health center for tuberculosis evaluation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Treated for Microbiologically-confirmed TB Within 14 Days After Presentation to the Health Center for TB Evaluation | 220 Participants |
| Intervention | Number Treated for Microbiologically-confirmed TB Within 14 Days After Presentation to the Health Center for TB Evaluation | 342 Participants |
Number Diagnosed and Treated for Microbiologically-confirmed TB
Effectiveness outcome.
Time frame: On the same-day of presentation to the health center for tuberculosis evaluation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Diagnosed and Treated for Microbiologically-confirmed TB | 106 Participants |
| Intervention | Number Diagnosed and Treated for Microbiologically-confirmed TB | 251 Participants |
Number Diagnosed AND Treated for TB
Effectiveness outcome.
Time frame: On the same-day of presentation to the health center for tuberculosis evaluation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Diagnosed AND Treated for TB | 199 Participants |
| Intervention | Number Diagnosed AND Treated for TB | 362 Participants |
Number Diagnosed With Microbiologically-confirmed TB
Effectiveness outcome.
Time frame: Within 14 days after presentation to the health center for tuberculosis evaluation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Diagnosed With Microbiologically-confirmed TB | 299 Participants |
| Intervention | Number Diagnosed With Microbiologically-confirmed TB | 389 Participants |
Number of Patients Enrolled
Effectiveness outcome.
Time frame: Presentation to the health center for tuberculosis evaluation during the 16-month study time frame
Population: All eligible were enrolled as there was a waiver of informed consent
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number of Patients Enrolled | 5098 Participants |
| Intervention | Number of Patients Enrolled | 5546 Participants |
Number Suspected/Diagnosed With Rifampin-resistant TB
Effectiveness outcome.
Time frame: Within 6 months of presentation to the health center for tuberculosis evaluation
Population: The data analyzed included all adult patients in the target population. Those with rifampin-resistant tuberculosis, extrapulmonary tuberculosis and/or missing age data were excluded from the trial population. Therefore, the number of participants analyzed for this measure differs from other parts of the record.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Suspected/Diagnosed With Rifampin-resistant TB | 5 Participants |
| Intervention | Number Suspected/Diagnosed With Rifampin-resistant TB | 2 Participants |
Number Tested for TB According to National Guidelines
Effectiveness outcome.
Time frame: Within 6 months of presentation to the health center for tuberculosis evaluation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Tested for TB According to National Guidelines | 2687 Participants |
| Intervention | Number Tested for TB According to National Guidelines | 5108 Participants |
Number Treated for TB
Effectiveness outcome.
Time frame: Within 14 days of presentation to the health center for tuberculosis evaluation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Treated for TB | 339 Participants |
| Intervention | Number Treated for TB | 485 Participants |
Number Who Died Within 6 Months
Effectiveness outcome.
Time frame: Within 6 months of presentation to the health center for tuberculosis evaluation
Population: Includes those with vital status follow-up at six months post-visit to health center
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Control Group | Number Who Died Within 6 Months | 123 Participants |
| Intervention | Number Who Died Within 6 Months | 116 Participants |
Time to Microbiologically-confirmed TB
Effectiveness outcome. Time-to-diagnosis if microbiologically-confirmed TB.
Time frame: Within 6 months of presentation to the health center for tuberculosis evaluation
Population: All participants' data was analyzed to determine who had confirmed TB.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Control Group | Time to Microbiologically-confirmed TB | 0 days |
| Intervention | Time to Microbiologically-confirmed TB | 0 days |
Time-to-treatment of Microbiologically-confirmed TB
Effectiveness outcome. Time-to-treatment if microbiologically-confirmed TB and treated.
Time frame: Days from initial health center visit to initiation of treatment if diagnosed, up to 6 months.
Population: All participants' data was analyzed to determine who had confirmed TB and treatment initiated.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Control Group | Time-to-treatment of Microbiologically-confirmed TB | 1 days |
| Intervention | Time-to-treatment of Microbiologically-confirmed TB | 0 days |