| Literature DB >> 32993713 |
Hojoon Sohn1, Austin Tucker2, Olivia Ferguson2, Isabella Gomes2, David Dowdy2.
Abstract
BACKGROUND: Failing to account for the resources required to successfully implement public health interventions can lead to an underestimation of costs and budget impact, optimistic cost-effectiveness estimates, and ultimately a disconnect between published evidence and public health decision-making.Entities:
Keywords: Costs of implementation; Decision-making; Economic evaluation; Implementation strategies; Tuberculosis
Year: 2020 PMID: 32993713 PMCID: PMC7526415 DOI: 10.1186/s13012-020-01047-2
Source DB: PubMed Journal: Implement Sci ISSN: 1748-5908 Impact factor: 7.327
Fig. 1Simplified illustration of stages, activities, resource classification, and assessment of costs of public health intervention implementation process. a A description of the implementation process listing key components of each phase that may carry additional resource requirements is provided. Light blue arrows represent potential feedback loops between phases. b An illustration of resource and cost classification of the public health intervention implementation process. At each phase, resource-use for relevant activities is classified based on the location (above site vs. site-specific) of activity and degree to which activities are programmatic versus research specific. Sizes of each square (different shades of blue)—arbitrarily assigned for the purposes of demonstration—represent the corresponding size of each activity category. The increasing size of light-shaded boxes to the right indicate an increasing programmatic component as the study progresses into the maintenance phase
Descriptions of key activities by study phases (XPEL study example)
| Classification of activities | Research or knowledge generation costsa | Programmatic costs | Shared research/program costs |
|---|---|---|---|
| Central | • Ministry of Health (MoH), provincial, and district level approvals for the research study • Institutional Review Board approvals • Development of study CRFs (clinical outcomes) • Development of research database (RedCap* program) • Development of study protocols • International collaborator site visits and periodic study calls | • Central procurement of GeneXpert machines, related equipment (e.g., solar panels and external batteries), Xpert Ultra cartridges, and associated supplies • Development of SOPs* for Xpert testing, troubleshooting and QA/QC manuals, and management of testing equipment | • Recruitment of study staff • Focus group discussions |
| Site-specific | • Site visits for site selection • Review of clinical and laboratory data | • N/A | • Sensitization meetings at district health office and potential study sites • Pilot studies conducted at select potential study sites |
| Central | • Establish clinical and laboratory data monitoring (including National TB Reference Laboratory) • Management of regulatory processes with MoH • Development of data collection plans for health economics study • International collaborator site visits and periodic study calls | • Development of plans and organization of site visit and training • Stock management (medical and laboratory consumables and Xpert cartridges) | • Study database management (clinical and programmatic) • Data quality checks • Weekly study call (implementation issues, study data checks, etc.) |
| Site-specific | • Management of provincial, district level regulatory processes | • Installation of solar panel and GeneXpert equipment (including GX Alert system) • Distribution of Xpert cartridges and laboratory consumables • Training of laboratory personnel and technical support for Xpert testing | • Site sensitization meetings (w/ routine clinic staff) at both intervention and control sites • Initial participant enrolment • Establishment of data collection and follow-up plans • Interim adjustments in implementation plans (including addition or exclusion of sites) • Recruitment of study contact persons at each site (for data monitoring and study logistics purposes) |
| Central | • Management and monitoring of study data • International collaborator site visits and periodic study calls • Data analyses and reporting | • Stock management (medical and laboratory consumables and Xpert cartridges) • Site visit organizations and communications | • Study database management (clinical and programmatic) • Central database data review and quality checks • Weekly study call (implementation issues, study data checks, etc.) • Central study team human resource management |
| Site-specific | • Site-specific data issue troubleshooting | • Ongoing technical support and troubleshooting (for GeneXpert and Solar panel equipment) • Distribution of Xpert cartridges and laboratory consumables • Procurement and replacement of key equipment (if broken) • QA/QC of Xpert testing • Review of GX Alert data • Periodic EQA and re-training for Xpert testing | • Quarterly site visit • Participant enrolment • Adjustments in site-specific operations • Ongoing human resource management at study sites • Data monitoring and quality checks |
aResearch or knowledge generation costs that would be required for programmatic implementation in other settings (for example, ongoing monitoring and evaluation) should be clearly delineated and considered as programmatic costs in most analyses
SOP Standard operation procedure, QA Quality assurance, QC Quality control, EQA External quality control, GX Alert System software system to centrally report site-specific Xpert testing statistics, equipment and testing troubleshooting, and testing operations
Interventions for peripheral diagnosis of tuberculosis (TB) likely to incur large costs in each phase of implementation
| Implementation phase | Application | Example |
|---|---|---|
| Design phase | Interventions needing large capital outlay for design and adaptation with uncertain scale-up | Implementation of mHealth-facilitated contact investigation for TB requiring procurement and tailoring of software packages |
| Initiation phase | Simple interventions with low consumable costs that require changes in policy and workflow | Low-cost lateral-flow LAM assay for TB that necessitates a new supply chain, clinical algorithms, and training of personnel |
| Maintenance phase | Interventions that require continued infrastructure support and quality control | Molecular diagnosis of TB with equipment (e.g., Xpert MTB/RIF®) that necessitates service contracts for equipment failure and external quality assurance of test results |