| Literature DB >> 27391996 |
Kevin Fiori1,2,3, Jennifer Schechter1, Monica Dey4, Sandra Braganza2,3, Joseph Rhatigan5,6, Spero Houndenou4, Christophe Gbeleou4, Emmanuel Palerbo4, Elfamozo Tchangani4, Andrew Lopez1,4, Emily Bensen1,4, Lisa R Hirschhorn5,6,7.
Abstract
Providing quality care for all children living with HIV/AIDS remains a global challenge and requires the development of new healthcare delivery strategies. The care delivery value chain (CDVC) is a framework that maps activities required to provide effective and responsive care for a patient with a particular disease across the continuum of care. By mapping activities along a value chain, the CDVC enables managers to better allocate resources, improve communication, and coordinate activities. We report on the successful application of the CDVC as a strategy to optimize care delivery and inform quality improvement (QI) efforts with the overall aim of improving care for Pediatric HIV patients in Togo, West Africa. Over the course of 12 months, 13 distinct QI activities in Pediatric HIV/AIDS care delivery were monitored, and 11 of those activities met or exceeded established targets. Examples included: increase in infants receiving routine polymerase chain reaction testing at 2 months (39-95%), increase in HIV exposed children receiving confirmatory HIV testing at 18 months (67-100%), and increase in patients receiving initial CD4 testing within 3 months of HIV diagnosis (67-100%). The CDVC was an effective approach for evaluating existing systems and prioritizing gaps in delivery for QI over the full cycle of Pediatric HIV/AIDS care in three specific ways: (1) facilitating the first comprehensive mapping of Pediatric HIV/AIDS services, (2) identifying gaps in available services, and (3) catalyzing the creation of a responsive QI plan. The CDVC provided a framework to drive meaningful, strategic action to improve Pediatric HIV care in Togo.Entities:
Keywords: Pediatric HIV; Togo; care delivery value chain; global healthcare delivery; implementation science
Mesh:
Year: 2016 PMID: 27391996 PMCID: PMC4991220 DOI: 10.1080/09540121.2016.1176678
Source DB: PubMed Journal: AIDS Care ISSN: 0954-0121
Quality improvement objectives and associated target values, organized by CDVC area.
| No. | CDVC Area | QI Objective and target value |
|---|---|---|
| 1 | Prevention and Screening | >90% of HIV+ pregnant women enrolled in pMTCT program initiate ART within first trimester |
| 2 | Prevention and Screening | <5% of HIV+ expecting mothers lost to follow-up |
| 3 | Prevention and Screening | >85% of infants screened for HIV by PCR method within first six weeks of life |
| 4 | Prevention and Screening | >80% of medicines on “essential medication” list available at all times |
| 5 | Diagnosing and Staging | >90% of mother/infant pairs identified as late for medical consultations receive monthly home visit |
| 6 | Diagnosing and Staging | >85% of HIV+ children screened for: (1) Tuberculosis and (2) Hepatitis B |
| 7 | Pre-antiretroviral Medical and Psychosocial Care | >95% infants (of mothers initially enrolled in pMTCT program) tested for HIV at 18 months |
| 8 | Pre-antiretroviral Medical and Psychosocial Care | Improved clinical integration developed between wrap-around support services and clinical program |
| 9 | Pre-antiretroviral Medical and Psychosocial Care | >75% of pediatric patients receive “disclosure counseling” by age 13 |
| 10 | Intervening and ARV Initiation | >95% of patients receive initial CD4 test within 3 months of HIV diagnosis |
| 11 | Intervening and ARV Initiation | >95% of pediatric patients initiate ART within 3 months of date of eligibility for treatment |
| 12 | Intervening and ARV Initiation | >75% of “new caretakers” receive counseling sessions |
| 13 | Continuous Management | >85% of cohort of “high risk” patients adherent to ART |
| 14 | Management of Complications | >95% of “high risk” pediatric patients receive recommended periodicity for: (1) home visits and (2) medical consultations |
| 15 | Management of Complications | Quarterly morbidity and mortality sessions conducted |
Note: PCR, polymerase chain reaction.
Figure 1. Care delivery value chain for pediatric HIV services in Kara, Togo in 2014–2015.
Accomplished QI objectives with target, baseline and year-end values.
| No. | QI Prioritized objectives | Baseline | 12 month |
|---|---|---|---|
| Target achieved | |||
| 1 | >90% of HIV+ pregnant women enrolled in pMTCT program initiate ART within first trimester | 20% | 100% |
| 2 | <5% of HIV+ expecting mothers lost to follow-up | a | <1% (one pair loss-to-follow-up) |
| 3 | >85% of infants screened for HIV by PCR method within first six weeks of life | 39% | 95% |
| 4 | >80% of medicines on “essential medication” list available at all times | a | 97% |
| 5 | >90% of mother/infant pairs identified as late for medical consultations receive monthly home visit | a | >98% (only one pair identified) |
| 7 | >95% infants (of mothers initially enrolled in pMTCT program) tested for HIV at 18 months | 66.70% | 100% |
| 8 | Improved clinical integration developed between wrap-around support services and clinical program | No plan | Plan created and implemented |
| 10 | >95% of patients receive initial CD4 test within 3 months of HIV diagnosis | 66.70% | 100% |
| 12 | >75% of “new caretakers” receive counseling sessions | <5% | 95% |
| 13 | >85% of cohort of “high risk” patients adherent to ART | <5% | 94% |
| 14 | >95% of “high risk” pediatric patients receive recommended periodicity for: (1) home visits and (2) medical consultations | (1) 85% | (1) 97% |
| Target not met | |||
| 11 | >95% of pediatric patients initiate ART within 3 months of date of eligibility for treatment | 60% | 75% |
| 15 | Quarterly morbidity and mortality sessions conducted | 2 | 1 over 12-month period |
| Insufficient data collection | |||
| 6 | >85% of HIV+ children screened for: (1) Tuberculosis and (2) Hepatitis B | NA | NA |
| 9 | >75% of pediatric patients receive “disclosure counseling” by age 13 | NA | NA |
Note: PCR, polymerase chain reaction.
aBaseline data did not exist for this area, in process of QI efforts, developed strategy for capturing data.
Figure 2. Schematic model for CDVC/quality improvement integration.