Prerequisites for Xpert MTB/RIF Implementation
19 items · Health · Medium difficulty · 30 min
Key country-level steps to prepare for Xpert MTB/RIF rollout.
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Review national TB burden and testing gaps
Check recent case data and lab coverage to justify Xpert rollout.
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Secure government commitment and budget
Obtain formal approval and line items for equipment, cartridges, and operations.
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Update national diagnostic policy to include Xpert
Define who gets tested and how Xpert fits with existing algorithms.
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Identify priority health facilities and laboratories for rollout
Map high-burden areas and referral networks to choose initial sites.
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Verify power supply, lab space, and biosafety needs
Confirm reliable electricity, bench space, and basic biosafety measures.
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Plan procurement for machines and consumables
Decide models, quantities, and procurement timelines for devices and cartridges.
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Order GeneXpert machines
Place orders with approved suppliers and track delivery timelines.
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Order cartridges and laboratory consumables
Forecast initial and buffer stock levels; include shipment lead time.
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Arrange maintenance, warranty, and service contracts
Set up local support, spare parts, and a plan for device downtime.
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Train laboratory technicians on Xpert operation
Provide hands-on training covering test running, troubleshooting, and QC.
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Set up sputum collection, transport, and specimen handling
Define sample containers, labeling, and transport timing/conditions.
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Start a quality assurance program and enroll in EQA
Implement internal controls, periodic proficiency testing, and audits.
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Integrate Xpert results into national reporting systems
Ensure electronic or paper reporting feeds into surveillance and patient records.
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Define testing algorithms and clinical guidelines
Specify indications, confirmatory testing, and links to treatment pathways.
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Create a forecasting plan for cartridges and supplies
Use consumption data and buffer stock rules to prevent stockouts.
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Implement waste management and cartridge disposal procedures
Set safe disposal protocols for used cartridges and infectious waste.
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Set indicators and monitor test volumes, positivity, and errors
Track key metrics regularly to evaluate performance and quality.
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Inform clinicians, community workers, and partners about rollout
Share eligibility criteria, expected turnaround times, and referral paths.
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Develop a long-term scale-up and sustainability plan
Plan financing, training refreshers, and phased expansion.
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