|The Tingathe programme: a pilot intervention using community health workers to create a continuum of care in the prevention of mother to child transmission of HIV (PMTCT) cascade of services in Malawi.|
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|PMID: 22789644 Owner: NLM Status: MEDLINE|
|INTRODUCTION: Loss to follow-up is a major challenge in the prevention of mother to child transmission of HIV (PMTCT) programme in Malawi with reported loss to follow-up of greater than 70%. Tingathe-PMTCT is a pilot intervention that utilizes dedicated community health workers (CHWs) to create a complete continuum of care within the PMTCT cascade, improving service utilization and retention of mothers and infants. We describe the impact of the intervention on longitudinal care starting with diagnosis of the mother at antenatal care (ANC) through final diagnosis of the infant.
METHODS: PMTCT service utilization, programme retention and outcomes were evaluated for pregnant women living with HIV and their exposed infants enrolled in the Tingathe-PMTCT programme between March 2009 and March 2011. Multivariate logistic regression was done to evaluate maternal factors associated with failure to complete the cascade.
RESULTS: Over 24 months, 1688 pregnant women living with HIV were enrolled. Median maternal age was 27 years (IQR, 23.8 to 30.8); 333 (19.7%) were already on ART. Among the remaining women, 1328/1355 (98%) received a CD4 test, with 1243/1328 (93.6%) receiving results. Of the 499 eligible for ART, 363 (72.8%) were successfully initiated. Prior to, delivery there were 93 (5.7%) maternal/foetal deaths, 137 (8.1%) women transferred/moved, 51 (3.0%) were lost and 58 (3.4%) refused ongoing PMTCT services. Of the 1318 live births to date, 1264 (95.9%) of the mothers and 1285 (97.5%) of the infants received ARV prophylaxis; 1064 (80.7%) infants were tested for HIV by PCR and started on cotrimoxazole. Median age at PCR was 1.7 months (IQR, 1.5 to 2.5). Overall transmission at first PCR was 43/1047 (4.1%). Of the 43 infants with positive PCR results, 36 (83.7%) were enrolled in ART clinic and 33 (76.7%) were initiated on ART.
CONCLUSIONS: Case management and support by dedicated CHWs can create a continuum of longitudinal care in the PMTCT cascade and result in improved outcomes.
|Maria H Kim; Saeed Ahmed; W Chris Buck; Geoffrey A Preidis; Mina C Hosseinipour; Avni Bhalakia; Debora Nanthuru; Peter N Kazembe; Frank Chimbwandira; Thomas P Giordano; Elizabeth Y Chiao; Gordon E Schutze; Mark W Kline|
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|Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. Date: 2012-07-11|
|Title: Journal of the International AIDS Society Volume: 15 Suppl 2 ISSN: 1758-2652 ISO Abbreviation: J Int AIDS Soc Publication Date: 2012|
|Created Date: 2012-07-13 Completed Date: 2012-11-19 Revised Date: 2013-07-12|
Medline Journal Info:
|Nlm Unique ID: 101478566 Medline TA: J Int AIDS Soc Country: Switzerland|
|Languages: eng Pagination: 17389 Citation Subset: IM; X|
|Baylor College of Medicine International Pediatric AIDS Initiative at Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Anti-HIV Agents / therapeutic use
Community Health Workers
HIV Infections / drug therapy, prevention & control*, transmission*
Infectious Disease Transmission, Vertical / prevention & control*
Pregnancy Complications / prevention & control*
Journal ID (nlm-ta): J Int AIDS Soc
Journal ID (iso-abbrev): J Int AIDS Soc
Journal ID (publisher-id): JIAS
Publisher: International AIDS Society
© 2012 Kim MH et al; licensee International AIDS Society
Received Day: 17 Month: 12 Year: 2011
Accepted Day: 16 Month: 5 Year: 2012
Electronic publication date: Day: 11 Month: 7 Year: 2012
collection publication date: Year: 2012
Volume: 15 Issue: 4(Suppl 2)
E-location ID: 17389
PubMed Id: 22789644
Publisher Id: 17389
|The Tingathe programme: a pilot intervention using community health workers to create a continuum of care in the prevention of mother to child transmission of HIV (PMTCT) cascade of services in Malawi|
|Maria H Kim*§1|
|W Chris Buck2|
|Geoffrey A Preidis1|
|Mina C Hosseinipour34|
|Peter N Kazembe2|
|Thomas P Giordano6|
|Elizabeth Y Chiao6|
|Gordon E Schutze1|
|Mark W Kline1|
1Baylor College of Medicine International Pediatric AIDS Initiative at Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA
2Baylor College of Medicine-Abbott Fund Children's Clinical Center of Excellence, Lilongwe, Malawi
3UNC Project, Lilongwe, Malawi
4University of North Carolina School of Medicine Chapel Hill, NC, USA
5Malawi Ministry of Health, Lilongwe, Malawi
6Department of Medicine, Baylor College of Medicine, Houston, TX, USA
|§Corresponding author: Maria H Kim, Baylor College of Medicine International Pediatric AIDS Initiative at Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA. Tel: 832-822-1038. (firstname.lastname@example.org)
*These authors contributed equally to this work.
In 2011, UNAIDS announced a call to eliminate new paediatric HIV infections among children by 2015 . Effective medical interventions for prevention of mother to child transmission of HIV (PMTCT) have been known since the late 1990s, and in developed countries, almost no new paediatric HIV infections occur [2,3]. Globally, though, an estimated 370,000 children acquired HIV in 2009, the vast majority through vertical transmission . This disparity in outcomes has not been due to a lack of effective medications or tools. The World Health Organization (WHO) PMTCT guidelines detail simple and effective interventions that make transmission rates of less than 5% feasible, even among breastfeeding populations . Rather, persistent poor outcomes in developing countries are the result of mothers living with HIV and exposed infants not receiving the full array of available services [5–8].
Figure 1 provides details on the full PMTCT cascade and current utilization rates in sub-Saharan Africa. National guidelines and programs in high burden countries, including Malawi, often subdivide aspects of this cascade into separate PMTCT (vertical transmission), antiretroviral therapy (ART), early infant diagnosis (EID) and paediatric HIV programs, frequently with different providers and service locations for each component. Resulting poor utilization of available services, lack of coordination between providers and high rates of loss to follow-up have led to persistent high infection rates in exposed children [1,8,9]. It has been shown that, even with highly efficacious combination antiretroviral interventions, only marginal reductions in childhood HIV infections can be achieved without improved retention of pregnant mothers and infants within the PMTCT cascade of services . Human resource shortages in high burden countries further compound programme inefficiencies and limit the ability of the healthcare system to make improvements. If the goal of eliminating new paediatric infections is to be reached, interventions to improve health systems performance and to address human resource needs are required. Task shifting with the use of community health workers (CHWs) has been suggested as one strategy to address these challenges within resource-limited settings [11–15].
In March 2009, Baylor College of Medicine Children's Foundation Malawi, in collaboration with the Malawi Ministry of Health (MOH), initiated a pilot community-based intervention in Lilongwe that uses lay CHWs as a bridge linking the government PMTCT, EID and paediatric HIV programs. Called Tingathe-PMTCT (meaning “yes we can” in the local Chichewa language), the intervention was designed to create a new paradigm in PMTCT service delivery and end the compartmentalization of services into distinct PMTCT, EID and paediatric HIV subunits . Tingathe CHWs ensured longitudinal care throughout the full PMTCT cascade, starting with diagnosis of the mother at antenatal care (ANC) and ending with final diagnosis and treatment of the infant. This paper provides details on the pilot intervention as well as a current snapshot of our patient cohort. Impact on patient retention, utilization of services and outcomes was evaluated.
The Tingathe-PMTCT pilot programme took place in Area 25 and Kawale, two large peri-urban communities in Lilongwe. The estimated population is 310,000 people, with 15,000 deliveries/year, 2000 HIV-exposed infants delivered/year and 12% adult HIV prevalence . Over 96% of pregnant women attend at least one antenatal visit  and 99% of ANC attendees are tested for HIV [18,19].
All PMTCT clinical care was provided in accordance with MOH and WHO guidelines [20,21]. Figure 2a details all components of the PMTCT cascade available at the intervention sites. HIV testing, counselling and consent were conducted via opt-out testing per MOH guidelines.
At the start of our programme, ART eligibility was defined as WHO Stage 3 or 4 or CD4≤250 cells/mm3 . ART eligibility changed in August 2010 to CD4≤350 cells/mm3 for pregnant or lactating women living with HIV.
For women who did not qualify for ART, single dose nevirapine for the mother and infant and a bottle of zidovudine (AZT) syrup for the infant was dispensed at the first ANC visit. AZT was dispensed beginning at 28 weeks, and mothers returned for monthly refills. A 1-week supply of AZT/lamivudine (3TC) tail was distributed during labour and delivery .
During the intervention period, the national infant feeding guidelines recommended exclusive breastfeeding until 6 months of age followed by gradual weaning [22,23]. Universal ART initiation for HIV-infected infants younger than 1 year of age was the standard of care.
We used three sources for preintervention data. The first was a published report of maternal and infant utilization of PMTCT, EID and paediatric HIV services at five sites (including our two intervention sites) within Lilongwe between 2004 and 2008 . This source contained preintervention comparison data for PMTCT prophylaxis, infant PCRs and ART initiation for HIV-infected infants. For information not included in this report, we used the 2004 Malawi Demographic and Health Survey, which provided national statistics for numbers of women accessing ANC, location of delivery and infant feeding choice after birth . Finally, ANC CD4 log records documented CD4 test dates and whether or not results were returned to pregnant women. Consistent records were not kept at A25. At Kawale, records were available from March to October 2008.
The main focus of this programme was CHW-based patient case management in both the health facility and community (Figure 1). The intervention began at ANC when pregnant women identified as living with HIV were assigned a dedicated CHW and voluntarily enrolled into the programme. CHWs ensured that mother-infant pairs received all necessary PMTCT services. They followed their clients at their homes and at health centres, from initial diagnosis up until confirmation of definitive HIV-uninfected status after cessation of breastfeeding or successful ART initiation for HIV-infected infants. Receipt of PMTCT was recorded only upon confirmation with the mother after delivery to verify that medication had actually been ingested, not just dispensed . Women living with HIV who were identified at labour and delivery or after the birth of the infant were also followed up and provided services but were not included in this cohort.
Criterion for CHW selection included living within the community, completion of primary schooling and ability to read and write in English and Chichewa, ability to ride a bicycle and HIV-infected or affected. Both men and women were recruited. Due to the large volume of applicants, we first conducted group interviews, inviting those who performed well in these for individual interviews. Once selected, CHWs earned a stipend for work-related transportation and food (2.50 USD/day).
A specialized 2-week training, followed by a 2-week on-site orientation, was developed (Figure 2b). Trainees were monitored closely by supervisors and were only allowed to conduct unsupervised patient visits after competency had been verified. CHWs also received half-day quarterly refresher trainings by Baylor paediatricians.
To help free up clinical staff for essential clinical care, specific tasks were shifted to CHWs, including patient registration, nutritional assessments, infant feeding counselling, pill counting and distribution of nutritional supplements. All CHWs were responsible for both health centre-based tasks (40% time) and community work (60% time). CHWs generally followed up to a maximum of 50 mother-infant pairs at one time.
Prior to the programme intervention, consultative meetings were conducted with community leaders. CHWs conducted daily education sessions in the health centres and held ongoing sensitization meetings in the community. The main focus of education was promoting the utilization of PMTCT, EID and paediatric HIV treatment services.
An individual patient mastercard was used to facilitate patient case management, and a patient register was used to monitor CHW activities. The mother-infant mastercard was opened on programme entry, updated after every visit and key data entered into registers weekly. Information from registers was entered into a Microsoft Access database bimonthly. CHWs were supervised weekly by site supervisors and monthly by the programme coordinator. Supervisors also conducted unscheduled visits with patients to ensure that they were satisfied with the services being provided. CHWs received bi-annual performance evaluations.
Mother-infant pairs exited the programme if they reached one of the following outcomes: (1) maternal death; (2) miscarriage, stillbirth; (3) infant death; (4) transferred/moved outside the catchment area; (5) lost (patient tracing attempted but patient could not be found); (6) despite counselling, patient refused to return for clinical care; (7) infant infected and successfully enrolled into care and started on ART; and (8) infant definitively not infected (weaned and repeat PCR negative).
Data from pregnant women and exposed infants enrolled in the Tingathe-PMTCT programme between March 2009 and March 2011 were analysed. The closing date for follow-up was October 31, 2011. Data were de-identified prior to analysis. Aggregate data were reported as mean with standard deviation or median with interquartile range (IQR) based on normality. For the multivariate logistic regression, all outcomes preventing completion of the PMTCT cascade were grouped together including miscarriage/foetal demise, maternal/infant death, transferred/moved, lost and refused ongoing care. To identify factors that predicted non-completion, unadjusted and adjusted odds ratios and 95% confidence intervals were obtained using binary and multivariate logistic regression, respectively. All covariates, irrespective of the significance of the binary model, were entered into the multivariate model by forward stepwise selection, with entry testing based on the significance of the score statistic and removal testing based on the likelihood-ratio statistic with conditional parameter estimates. Only covariates with a significant score statistic (p<0.05) were retained in the final model. Analyses were performed using IBM SPSS Statistics (version 19; SPSS, Inc., Chicago, IL, USA). The Malawi National Health Sciences Research Committee and the Baylor College of Medicine institutional review board granted ethics approval.
Records from 1688 pregnant women living with HIV were analysed (Table 1). The majority, 92.9%, enrolled during their second or third trimesters and 76.3% were newly diagnosed with HIV. At enrolment, 19.7% were on ART.
CHWs tracked service utilization by each mother-infant pair through the PMTCT cascade (Table 2, Figure 3). Of those mothers not on ART at enrolment, 98% had a CD4 drawn, and 93.6% of these mothers received these results. This compares to 22.5% who received results before the intervention.
Based on CD4 count, 36.8% of mothers met criteria for ART eligibility. Of these, 72.8% were successfully initiated on ART.
Of the 1318 live births, 87.3% received the most ideal combination of either full combination prophylaxis (47.3%) or ART (40%). Prior to the intervention, only 8.8% of mothers received ART.
Prior to delivery, there were 5.7% maternal/foetal deaths/still births, 8.1% transferred/moved. 3.0% lost and 3.4% refused ongoing PMTCT services. There were 1.8% women still recorded as pregnant as of the closing date for data analysis.
DNA PCR testing was performed on 80.7% of the infants. Of the remaining infants, 3.2% were still awaiting their first PCR, and 16.1% exited the programme (as a result of being lost, died, transferred, moved and refused ongoing care) before first PCR. The median age at first PCR was 1.7 months (IQR, 1.5 to 2.5). The overall MTCT transmission rate was 4.1%.
Of the 43 infants found to be HIV-infected, 76.7% were started on ART, with median age at initiation of 4.9 months (IQR, 4.0 to 6.0). This is in contrast to the preintervention period where 34.4% on infected infants were started on ART at a median age of 9.1 months (IQR, 5.4 to 13.8).
Overall, of the initial 1688 women, 1% of mothers died, 4.9% of pregnancies terminated in miscarriages and stillbirths and 3.7% infants died. Furthermore, 16.8% mother-infant pairs moved out of the catchment area, 5.0% were lost, 10.8% refused ongoing care and 16.5% exited the programme after receiving a definitive HIV-negative diagnosis. Of those 182 mothers who refused care, 31.8% refused care during pregnancy, 45.6% refused after delivery but before first PCR and 22.5% refused after the first PCR. There are 672 mother-infant pairs still active in the programme, including 31 mothers who are still pregnant and 641 exposed infants still being breastfed.
In bivariate analysis, maternal age of at least 20 years, along with being ART-eligible but not on ART, were associated with failure to complete the PMTCT cascade, whereas enrolment later in pregnancy and having a partner who was not involved (partner dead or separated from mother) were associated with a higher rate of successful completion of the cascade (Table 3). On multivariate analyses, two variables predicted failure to complete the PMTCT cascade, namely, being ART-eligible but not receiving therapy (odds ratio (OR), 1.69; 95% confidence interval (CI), 1.18 to 2.42) and having a partner who was involved but not disclosed to (unaware of the maternal HIV status; OR, 1.54; 95% CI, 1.06 to 2.23). On the other hand, the strongest predictors of successful completion of the PMTCT cascade were enrolment in the third trimester (OR, 0.37; 95% CI, 0.24 to 0.58), having newly diagnosed HIV infection (OR, 0.50; 95% CI, 0.33 to 0.75) and having a partner who was not involved (OR, 0.43; 95% CI, 0.24 to 0.78).
Ensuring a continuum of care between services in the PMTCT cascade is essential if the goal of ending new paediatric HIV infection is to be reached. Our results demonstrate that coordinated, longitudinal care of mother-infant pairs is possible in high-burden, resource-limited countries like Malawi. In this intervention, dedicated CHWs functioning as case coordinators created a bridge between disparate clinical services and improved retention and service utilization at virtually every step within the PMTCT cascade.
Key areas of improvement for mothers included receiving CD4 counts, being started appropriately on ART if eligible and receiving proper combination prophylaxis if not eligible for ART. Prior to our intervention, over 90% of women only received single dose nevirapine, reflecting the slow adoption of the 2006 WHO recommendations [20,21]. In our cohort, the majority of mother-infant pairs received the recommended regimen of either combination prophylaxis or ART, resulting in a significant reduction in HIV transmission at first PCR. Enrolment of exposed infants into care, measurement and receipt of DNA PCR results and, finally, initiation of ART for infected infants also improved dramatically.
Our results show marked improvement in retention compared, not only to preintervention data from Malawi but also to reports from other countries within the region. WHO estimates that in sub-Saharan Africa, only half of women living with HIV receive any PMTCT intervention, 43% of HIV-exposed infants receive ARV prophylaxis and a mere 6% to 15% of HIV-exposed infants receive an HIV test [24,25].
The small percentage of infants receiving HIV testing is an especially important issue . Improving the continuum of care within the PMTCT cascade is not only critical for preventing HIV in exposed infants but also for reducing mortality in those infants who become infected. The CHER study demonstrated that HIV-infected infants suffer from rapid immunologic deterioration, disease progression and high mortality without early ART initiation . By linking mothers to infants, our CHWs were able to significantly improve DNA PCR testing and entry into care and thereby improve the rate of prompt ART initiation in infected infants.
CHW case management improved not only programme implementation but monitoring as well. Several studies have documented that data collected and reported within national PMTCT programs are often inaccurate and incomplete [28,29]. Some have suggested routine HIV testing of infants at immunization clinics and inpatient facilities as a means for improving PMTCT monitoring . While such testing is important and will provide reliable measures for programme evaluation, the opportunities for effective interventions have largely been missed by the time testing takes place. CHW case management, by contrast, facilitates both service delivery and programme monitoring.
Though our results demonstrate a marked improvement over preintervention data, we have not yet achieved the desired goal of greater than 90% delivery at each step of the cascade for PMTCT to be optimally effective . Reasons for attrition included refusal to continue follow-up, movement from the area and loss to follow up, such that close to a third of the cohort did not complete the programme.
The population we serve is highly mobile, as demonstrated by the 16.8% of patients who moved outside the catchment area. Many mothers within our programme returned to their home villages for additional support. Though our CHWs were often aware of the move and were able to keep in touch with some of their clients, for most, they had no means to document whether or not mothers successfully entered care in their new location. A national medical ID system would assist with this type of tracking . Within the programme, we are developing improved predelivery counselling to identify those mothers planning to return to home villages, exploring strategies with maternal support groups organized by home villages, and cell-phone text messaging to track clients if they move outside our direct service areas.
We are conducting qualitative studies to further evaluate reasons for and possible strategies to mitigate refusal of CHW follow-up. Refusals occur throughout the cascade. Couples counselling and testing with enhanced disclosure support may help reduce refusal during pregnancy. Characterizing and addressing misconceptions about testing results and the likelihood of infection may reduce the number of mothers refusing to get their children tested. Stressing the importance of follow-up testing after weaning may reduce the number of patients who default after a negative first PCR. Malawi's increasing emphasis on family-centred HIV care may also encourage partners to attend clinic together, possibly improving communication and retention in care .
Male involvement has been touted as a possible way to engage more women in PMTCT services. Our findings (Table 3) suggest that women without any partner involvement were most likely to complete the cascade, whereas those women with involved but undisclosed partners were least likely. These findings not only reemphasize the importance of partner disclosure but also highlight the potentially obstructive role that partners may play in accessing services, as observed in other studies , or the value of women's independence to make their own decisions.
There are several limitations to our study. The first is a lack of directly comparable preintervention data. Our prior referenced study was from the same area and immediately preceded our intervention, retrospectively analysing all available records over a 4-year period . By contrast, the present study only followed up patients enrolled in the Tingathe programme, which may have introduced measurement bias and favourably skewed outcomes. On the other hand, the prior study had a much longer follow-up period and also included infant testing data from the inpatient ward at Kamuzu Central Hospital and the attached Baylor Centre of Excellence, which may have inflated the infant follow-up results. Many of these infants likely fell out of the PMTCT cascade, but reentered when ill and were identified on admission at Kamuzu Central Hospital or the Baylor Centre of Excellence. Despite these qualifications, this report provided the most direct preintervention data with which to compare our results. Moving forward, the data presented here provides a good baseline for similarly designed prospective programmatic studies.
Our second limitation was that we did not measure ANC attendance or HIV testing at ANC. As prior studies had already demonstrated both were over 95% [17–19] in our setting, we did not independently assess this. This limits the external validity of our study, as ANC attendance and HIV testing rates are not as robust in many comparable settings.
Third, we noted that some women were lost between HIV testing and referral to our CHWs. To address this issue, HIV testing at ANC was largely shifted to our CHWs, so that registration could be made immediately upon diagnosis. We do not have good data on how many women may have refused services between HIV testing and enrolment into our programme. To address this issue, we have developed an enrolment register that we are now piloting at our sites. This, combined with improved documentation of testing within ANC, will provide us with solid data on this critical service point in the future .
Finally, this programme was not implemented as part of a controlled trial, and there were other providers of services at various time points during the intervention. These providers may also have contributed to the overall improved outcomes observed.
Changes being made in the Malawi PMTCT guidelines provide both new opportunities and challenges for effective service delivery. In 2011, Malawi adopted an approach for PMTCT referred to as Option B+, where pregnant and lactating women living with HIV will automatically be started on ART for life . This welcome approach simplifies the maternal assessment, obviating the need for CD4 measurements. However, the efficacy of this simplified approach will be compromised unless efforts are made to link newly identified women to ART services and to ensure identification, enrolment into care and testing of exposed infants. This is especially true as infant feeding guidelines now recommend breastfeeding for all children, including HIV-exposed infants, through the second year of life . Furthermore, we need to ensure that pregnant women present earlier to care, as a significant portion of women in our study presented late. We also need to prevent women from refusing care and dropping out, for whatever reason. Ensuring continued clinical care and follow-up testing after weaning through this extended period will be a considerable challenge that may be facilitated by CHW case management.
We believe the Tingathe-PMTCT programme has defined a new paradigm for PMTCT service delivery. We attempted to break down the compartmentalization and resulting loss to follow-up between PMTCT, EID and paediatric HIV services. We believe that with further refinement, CHWs can help establish a system in which mothers and infants are effectively followed up and linked throughout the full PMTCT cascade. Establishing such systems that ensure continuity of care will be critical if the goal of ending new paediatric infections is to be reached.
We thank the Malawi Ministry of Health for their partnership in this endeavour. We thank the Baylor College of Medicine Children's Foundation Malawi data team, clinicians and nurses who participated in data collection, organization and cleaning. We are grateful to all the HIV-infected women and children who enrolled in our programme, and the CHWs and clinicians who helped care for them. Special thanks to Elaine Abrams for her editorial support. This publication was made possible by support from USAID. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of USAID. This paper was presented in part as a poster at the International AIDS Society Conference in Rome, July 2011 Abstract #TUPE291.
The authors declare that they have no competing interests.
MHK and SA conceived and designed the study, helped analyze the data, interpreted findings and wrote the manuscript. WCB, AB and DN assisted with the study in the field, contributed to data management and reviewed the manuscript. GP revised it critically and participated in statistical analysis and interpretation. MCH, PNK, FC, TPG, EYC, GSC and MWK revised it critically for important intellectual content. All authors have read and approved the final manuscript.
3TC, lamivudine; ANC, antenatal care; ART, antiretroviral therapy; AZT, zidovudine; CHWs, community health workers; CI, confidence interval; EID, early infant diagnosis; IQR, interquartile range; OR, odds ratio; PMTCT, prevention of mother to child transmission of HIV.
The programme was financially supported by the Clinton HIV-AIDS Initiative (CHAI), Bristol-Myers Squibb Foundation, Abbott Fund, Texas Children's Hospital and United States Agency For International Development (USAID).
|1.||UNAIDSCountdown to zero: global plan towards the elimination of new HIV infections among children by 2015 and keeping their mothers alive, 2011–2015Year: 2011GenevaUNAIDS|
|2.||Mofenson LM. Successes and challenges in the perinatal HIV-1 epidemic in the United States as illustrated by the HIV-1 serosurvey of childbearing womenArch Pediatr Adolesc MedYear: 20041584422515123471|
|3.||European Collaborative StudyMother-to-child transmission of HIV in the era of highly active antiretroviral therapyClin Infect DisYear: 20054034586515668871|
|4.||WHOAntiretroviral drugs for treating pregnant women and preventing HIV infection in infants: recommendations for a public health approachYear: 2010GenevaWHO|
|5.||Ahoua L,Ayikoru H,Gnauck K,Odaru G,Odar E,Ondoa-Onama C,et al. Evaluation of a 5-year programme to prevent mother-to-child transmission of HIV infection in Northern UgandaJ Trop PediatrYear: 2010561435219602489|
|6.||Stringer EM,Ekouevi DK,Coetzee D,Tih PM,Creek TL,Stinson K,et al. PEARL Study Team. Coverage of nevirapine-based services to prevent mother-to-child HIV transmission in 4 African countriesJAMAYear: 2010304329330220639563|
|7.||Mirkuzie AH,Hinderaker SG,Sisay MM,Moland KM,Mørkve O. Current status of medication adherence and infant follow up in the prevention of mother to child HIV transmission programme in Addis Ababa: a cohort studyJ Int AIDS SocYear: 2011145022017821|
|8.||Manzi M,Zachariah R,Teck R,Buhendwa L,Kazima J,Bakali E,et al. High acceptability of voluntary counselling and HIV-testing but unacceptable loss to follow up in a prevention of mother-to-child HIV transmission program in rural Malawi: scaling up requires a new way of actingTrop Med Int HealthYear: 20051012425016359404|
|9.||Ciaranello A,Park J,Ramirez-Avila L,Freedberg K,Walensky R,Leroy V. Early infant HIV-1 diagnosis programs in resource-limited settings: opportunities for improved outcomes and more cost-effective interventionsBMC MedYear: 201195921599888|
|10.||Barker PM,Mphatswe W,Rollins N. Antiretroviral drugs in the cupboard are not enough: the impact of health Systems’ performance on mother-to-child transmission of HIVJ Acquir Immune Defic SyndrYear: 2010562e45821084998|
|11.||Zachariah R,Ford N,Philips M,Lynch S,Massaquoi M,Janssens V,et al. Task shifting in HIV/AIDS: opportunities, challenges and proposed actions for sub-Saharan AfricaTrans R Soc Trop Med HygYear: 200910365495818992905|
|12.||McCollum ED,Preidis GA,Kabue MM,Singogo EB,Mwansambo C,Kazembe PN,et al. Task shifting routine inpatient pediatric HIV testing improves program outcomes in urban Malawi: a retrospective observational studyPLoS OneYear: 201053e962620224782|
|13.||Lehmann U,Van Damme W,Barten F,Sanders D. Task shifting: the answer to the human resources crisis in Africa?Hum Resour HealthYear: 200974919545398|
|14.||Callaghan M,Ford N,Schneider H. A systematic review of task-shifting for HIV treatment and care in AfricaHum Resour HealthYear: 20108820356363|
|15.||Haines A,Sanders D,Lehmann U,Rowe AK,Lawn JE,Jan S,et al. Achieving child survival goals: potential contribution of community health workersLancetYear: 2007369957921213117586307|
|16.||Lilongwe District Health OfficeSemi-permanent dataYear: 2008LilongweLilongwe District Health Office|
|17.||National Statistical Office (Malawi) and ORC MacroMalawi Demographic and Health Survey 2004Year: 2005CalvertonNSO and ORC Macro|
|18.||Moses A,Zimba C,Kamanga E,Nkhoma J,Maida A,Martinson F,et al. UNC Project Call to Action Program. Prevention of mother-to-child transmission: program changes and the effect on uptake of the HIVNET 012 regimen in MalawiAIDSYear: 200822183718090395|
|19.||Braun M,Kabue MM,McCollum ED,Ahmed S,Kim M,Aertker L,et al. Inadequate coordination of maternal and infant HIV services detrimentally affects early infant diagnosis outcomes in Lilongwe, MalawiJ Acquir Immune Defic SyndrYear: 2011565e122821224736|
|20.||WHOAntiretroviral drugs for treating pregnant women and preventing HIV infection in infants: recommendations for a public health approachYear: 2006GenevaWHO|
|21.||Malawi Ministry of HealthPrevention of mother to child transmission of HIV and paediatric HIV care guidelinesYear: 20082nd edLilongweMalawi Ministry of Health|
|22.||WHOHIV and infant feeding: new evidence and programmatic experience: report of a technical consultation held on behalf of the Inter-agency Task Team (IATT) on Prevention of HIV Infections in Pregnant Women, Mothers and their InfantsYear: 2006GenevaWHO|
|23.||Malawi Ministry of HealthInfant and young child nutrition policy and guidelinesYear: 2005LilongweMalawi Ministry of Health|
|24.||WHOTowards universal access: scaling up priority HIV/AIDS interventions in the health sector: progress reportYear: 2010GenevaWHO|
|25.||UNICEFChildren and AIDS fifth stocktaking report, 2010Year: 2010New YorkUNICEF|
|26.||Kellerman S,Essajee S. HIV testing for children in resource-limited settings: what are we waiting for?PLoS MedYear: 201077e100028520652012|
|27.||Violari A,Cotton MF,Gibb DM,Babiker AG,Steyn J,Madhi SA,et al. CHER Study Team. Early antiretroviral therapy and mortality among HIV-infected infantsN Engl J MedYear: 200835922334419020325|
|28.||Mate KS,Bennett B,Mphatswe W,Barker P,Rollins N. Challenges for routine health system data management in a large public programme to prevent mother-to-child HIV transmission in South AfricaPLoS OneYear: 200945e548319434234|
|29.||Stringer EM,Chi BH,Chintu N,Creek TL,Ekouevi DK,Coetzee D,et al. Monitoring effectiveness of programmes to prevent mother-to-child HIV transmission in lower-income countriesBull World Health OrganYear: 2008861576218235891|
|30.||Rollins N,Mzolo S,Moodley T,Esterhuizen T,van Rooyen H. Universal HIV testing of infants at immunization clinics: an acceptable and feasible approach for early infant diagnosis in high HIV prevalence settingsAIDSYear: 2009231851719491653|
|31.||Malawi Ministry of HealthClinical management of HIV in children and adults, Malawi integrated guidelines for providing HIV services in: antenatal care, maternity care, under 5 clinics, family planning clinics, exposed infant/pre-ART clinics, ART clinicsYear: 2011Month: 7 1st edLilongweMalawi Ministry of Health|
|32.||Bwirire LD,Fitzgerald M,Zachariah R,Chikafa V,Massaquoi M,Moens M,et al. Reasons for loss to follow-up among mothers registered in a prevention-of-mother-to-child transmission program in rural MalawiTrans R Soc Trop Med HygYear: 200810212119520018485431|
|33.||Schouten EJ,Jahn A,Midiani D,Makombe SD,Mnthambala A,Chirwa Z,et al. Prevention of mother-to-child transmission of HIV and the health-related Millennium Development Goals: time for a public health approachLancetYear: 20113789787282421763940|
Characteristics of mothers at programme enrolment
|Median maternal age, years (IQR)||27.0 (23.8 to 30.8)|
|Trimester of pregnancy, n (%)|
|First (0 to 13 weeks)||107 (6.3)|
|Second (14 to 26)||1025 (60.7)|
|Third (27 to 40)||543 (32.2)|
|HIV status at enrolment, n (%)|
|Already known to be HIV-infected||400 (23.7)|
|Newly diagnosed as HIV-infected||1288 (76.3)|
|ART eligibility by CD4 counta, n (%)|
|On ART||333 (19.7)|
|ART eligible||499 (29.6)|
|Does not meet ART criterion||777 (46)|
|ART eligibility was not determined||79 (4.7)|
|WHO stage at programme registration, n (%)|
|Stage 1/2||30 (1.7)|
|Stage 3||11 (0.7)|
|Stage 4||8 (0.5)|
|Not done||1639 (97.1)|
|CD4 cells/mm3 for women not on ARTb||1355|
|<200, n (%)||204 (15.1)|
|200 to 349, n (%)||336 (24.8)|
|350 to 499, n (%)||353 (26.0)|
|≥500, n (%)||375 (27.7)|
|CD4 taken but unknown resultc||60 (4.4)|
|CD4 not taken||27 (2.0)|
|Partner disclosure status, n (%)d|
|Partner involved and disclosed||423 (25.1)|
|Partner involved but not disclosed||1158 (68.6)|
|Partner not involved||106 (6.3)|
|Missing data||1 (<0.0)|
aDefinition of ART eligibility changed in August 2010 from CD4≤250 cells/mm3 to CD4≤ 350 cells/mm3 for HIV-infected pregnant women;
bCD4 routinely performed only on women not already on ART at registration;
cthe majority of these were CD4 samples that were clotted or otherwise could not be processed by the laboratory facility;
dpartner disclosed defined as partner having knowledge of maternal HIV status. Partner non-involved defined as a partner who is dead or is otherwise separated from the mother.
Abbreviations: IQR, interquartile range; ART, antiretroviral therapy.
Steps of the PMTCT cascade completed by mother-infant pairs: preintervention data and programme intervention results
|STEP in PMTCT Cascade||Description||Preintervention data||Programme intervention result|
|ACCESS Antenatal Care||Pregnant women accessing antenatal care||96.4% [Ref. 17]a||NA|
|TEST for HIV infection and ENROLL into care||Number of women tested for HIV||99% [Ref. 19]b||NA|
|HIV-infected pregnant women, n||1688|
|DETERMINE ART eligibility||ART status, n/N (%)|
|on ART||Unknown||333/1688 (19.7)|
|Not on ART||Unknown||1355/1688 (80.3)|
|Needed CD4 testing||1355|
|Mom received CD4 testing, n/N (%)||91.3%b,c||1328/1355 (98)|
|CD4 results returned to health centre from laboratory, n/N (%)||Unknown||1268/1328 (95.5)|
|Mom received CD4 results, n/N (%)||22.5%b,c||1243/1328 (93.6)|
|INITIATE ART/PMTCT prophylaxis||ART eligible by CD4 count, n/N (%)d||499/1688 (29.6)|
|Started on ART, n/N (%)||Unknown||363/499 (72.8)|
|Number of live births to date, n||1318|
|Mom received PMTCT prophylaxis or ART n/N (%)||1264/1318 (95.9)|
|Nevirapine only||90.6% [Ref. 19]b (meds distributed at ANC only)||39/1318 (2.9)|
|Nevirapine and AZT only||Not applicablee||75/1318 (5.7)|
|Full combination prophylaxis (sdNVP, AZT and Combivir)||Not applicablee||624/1318 (47.3)|
|Antiretroviral therapy for mothers health||8.8% [Ref. 19]b||526/1318 (40.0)|
|Unknown/missing data||Not applicable||1/1318 (0.1)|
|FOLLOW UP||Place of delivery, n/N (%)|
|Hospital/health centre||57.2% [Ref. 17]a||1273/1318 (96.6)|
|Home||29.4% [Ref. 17]a||36/1318 (2.7)|
|Traditional birth attendant||12.1% [Ref. 17]a||2/1318 (0.2)|
|Other/unknown/missing data||1.2% [Ref. 17]a||7/1318 (0.5)|
|ACCESS Postnatal Care||Infant received PMTCT prophylaxis, n/N (%)||1285/1318 (97.5)|
|Nevirapine only||47.2% [Ref. 19]b||89/1318 (6.8)|
|Neviparine and zidovudine||Not applicablee||1193/1318 (90.5)|
|AZT syrup only||Not applicablee||3/1318 (0.2)|
|None||Not applicable||22/1318 (1.7)|
|Unknown/missing data||52.8% [Ref. 19]b||11/1318 (0.8)|
|Infant feeding choice after birth, n/N (%)|
|Exclusive breastfeeding||75.2% [Ref. 17]a||1249/1318 (94.8)|
|Replacement feeding||1.6% [Ref. 17]a||20/1318 (1.5)|
|Mixed feeding||23.3% [Ref. 17]a||2/1318 (0.2)|
|Unknown/missing data||47/1318 (3.5)|
|TEST for HIV infection and ENROLL into care||Infant received PCR test and CPT, n/N (%)f||53.6% [Ref. 19]b||1064/1318 (80.7)|
|Number (%) tested at ≤2months of age||Unknown||680/1064 (63.9)|
|Number (%) tested at ≤3months of age||Unknown||904/1064 (85)|
|Median infant age at first HIV DNA PCR, months (IQR)||3 (0.5 to 8.6) [Ref. 19]b||1.7 (1.5 to 2.5)|
|DETERMINE HIV status of infant||First DNA PCR test result returned from lab||53.6% [Ref. 19]b||1047/1064 (98.2)|
|First DNA PCR test results given to the caregiver||Unknown||1024/1064 (96.2)|
|Median time from first DNA PCR test to results given to caregiver, days (IQR)||Unknown||47.5 (29.0 to 63.0)|
|First DNA PCR result negative||86.2%||1004/1047 (95.9)|
|First DNA PCR result positive||13.8% [Ref. 19]b||43/1047 (4.1)|
|INITIATE ART||Enrolled in ART clinic||29.5% [Ref. 19]b||36/43 (83.7)|
|Infected children started on ART||34.4% [Ref. 19]b||33/43 (76.7)|
|Median age at ART initiation months (IQR)||9.1 (5.4 to 13.8) [Ref. 19]b||4.9 (4.0 to 6.0)|
|FOLLOW UP||Mother-infant pairs still being followed in programme intervention||672|
aMalawi countrywide data;
bpreintervention data from intervention sites;
cdata from Kawale site CD4 logbooks, March to October 2008;
ddefinition of ART eligibility changed in August 2010 from CD4≤250 cells/mm3 to CD4≤350 cells/mm3 for HIV-infected pregnant women;
eonly maternal ART and nevirapine for mother and infant were available during the preintervention period;
fof the 1318 live births, 212 were discharged from the programme due to death, moving to another location or refusing ongoing care prior to receiving their first PCR; 42 infants are still active in the programme and awaiting their first PCR.
Abbreviations: ART, antiretroviral therapy; sd-NVP, single dose nevirapine; AZT, zidovudine; PCR, polymerase chain reaction; CPT, cotrimoxazole prophylaxis, IQR, interquartile range.
Maternal characteristics at programme enrolment associated with failure to complete PMTCT cascadea
|n/N (%) (n=1688)||OR of failure (95% CI)||p-value||AOR of failure (95% CI)b||p-value|
|Maternal age, n (%)|
|Maternal age<20||35/110 (31.8)||1.00|
|20+||673/1578 (42.6)||1.59 (1.05 to 2.41)||0.027||–||0.056|
|Trimester of pregnancy, n (%)|
|Second||480/1025 (46.8)||0.74 (0.50 to 1.11)||0.147||0.79 (0.52 to 1.19)||0.260|
|Third||164/543 (30.2)||0.37 (0.24 to 0.56)||<0.001||0.37 (0.24 to 0.58)||<0.001|
|HIV status at enrolment, n (%)|
|Already known to be HIV-infected||178/400 (44.5)||1.00||1.00|
|Newly diagnosed as HIV-infected||530/1288 (41.1)||0.87 (0.70 to 1.09)||0.236||0.50 (0.33 to 0.75)||<0.001|
|ART eligibility at enrolment, n (%)|
|On ART||134/333 (40.2)||1.00||1.00|
|Eligible but not on ART||244/499 (48.9)||1.42 (1.07 to 1.88)||0.014||1.69 (1.18 to 2.42)||0.004|
|Not eligible||284/777 (36.6)||0.86 (0.66 to 1.11)||0.245||1.09 (0.77 to 1.54)||0.632|
|Partner disclosure status at enrolment, n (%)c|
|Partner involved and disclosed||177/423 (41.8)||1.00||1.00|
|Partner involved, not disclosed||510/1158 (44.0)||1.09 (0.87 to 1.37)||0.435||1.54 (1.06 to 2.23)||0.024|
|Partner not involved||21/106 (19.8)||0.34 (0.12 to 0.58)||<0.001||0.43 (0.24 to 0.78)||0.005|
aFailure to complete PMTCT cascade defined as maternal death, miscarriage, abortion, infant death, transferred out, moved, lost or refusal of ongoing care prior to the infant's final HIV-negative diagnosis or if found to be HIV-infected-initiatied on ART;
ball five covariates were tested for entry into the multivariate model, and all covariates except maternal age were retained in the final equation, based on the significance (p-value) of the Wald score;
cpartner disclosed defined as partner having knowledge of maternal HIV status. Partner non-involved defined as a partner who has died or is otherwise separated from the mother.
Abbreviations: OR, odds ratio; CI, confidence interval; ART, antiretroviral therapy.
Keywords: prevention of mother to child transmission (PMTCT), early infant diagnosis (EID), paediatric HIV, HIV, task shifting, community engagement, community health workers, retention, loss to follow up.
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