Journal Article > ResearchFull Text
Disaster Med Public Health Prep. 2016 December 15; Volume 11 (Issue 3); 285-289.; DOI:10.1017/dmp.2016.135
Ali E, Ferir MC, Reid AJ, Gray H, van den Boogaard W, et al.
Disaster Med Public Health Prep. 2016 December 15; Volume 11 (Issue 3); 285-289.; DOI:10.1017/dmp.2016.135
OBJECTIVES
Typhoon Haiyan hit the Philippines in November 2013 and left a trail of destruction. As part of its emergency response, Médecins Sans Frontières distributed materials for reconstructing houses and boats as standardized kits to be shared between households. Community engagement was sought and communities were empowered in deciding how to make the distributions. We aimed to answer, Was this effective and what lessons were learned?
METHODS
A cross-sectional survey using a semi-structured questionnaire was conducted in May 2014 and included all community leaders and 269 households in 22 barangays (community administrative areas).
RESULTS
All houses were affected by the typhoon, of which 182 (68%) were totally damaged. All households reported having received and used the housing material. However, in 238 (88%) house repair was incomplete because the materials provided were insufficient or inappropriate for the required repairs.
CONCLUSION
This experience of emergency mass distribution of reconstruction or repair materials of houses and boats led by the local community was encouraging. The use of "standardized kits" resulted in equity issues, because households were subjected to variable degrees of damage. A possible way out is to follow up the emergency distribution with a needs assessment and a tailored distribution. (Disaster Med Public Health Preparedness. 2017;11:285-289).
Typhoon Haiyan hit the Philippines in November 2013 and left a trail of destruction. As part of its emergency response, Médecins Sans Frontières distributed materials for reconstructing houses and boats as standardized kits to be shared between households. Community engagement was sought and communities were empowered in deciding how to make the distributions. We aimed to answer, Was this effective and what lessons were learned?
METHODS
A cross-sectional survey using a semi-structured questionnaire was conducted in May 2014 and included all community leaders and 269 households in 22 barangays (community administrative areas).
RESULTS
All houses were affected by the typhoon, of which 182 (68%) were totally damaged. All households reported having received and used the housing material. However, in 238 (88%) house repair was incomplete because the materials provided were insufficient or inappropriate for the required repairs.
CONCLUSION
This experience of emergency mass distribution of reconstruction or repair materials of houses and boats led by the local community was encouraging. The use of "standardized kits" resulted in equity issues, because households were subjected to variable degrees of damage. A possible way out is to follow up the emergency distribution with a needs assessment and a tailored distribution. (Disaster Med Public Health Preparedness. 2017;11:285-289).
Journal Article > CommentarySubscription Only
Med J Aust. 2014 May 1; Volume 200 (Issue 9); 512-512.; DOI:10.5694/mja14.00143
Martinez Garcia D, Brown AL
Med J Aust. 2014 May 1; Volume 200 (Issue 9); 512-512.; DOI:10.5694/mja14.00143
Conference Material > Abstract
Thadhani TAF, Phillips EY
Epicentre Scientific Day Paris 2023. 2023 June 8
BACKGROUND
The World Health Organization recommends the use of computer-aided detection (CAD) in conjunction with chest X-rays (CXR) for tuberculosis (TB) screening and triaging in individuals aged 15 and above. This study assessed the feasibility of implementing CAD for TB active case finding (ACF) in Tondo, Manila, Philippines, including a crucial calibration process to determine the appropriate threshold for referring individuals for TB confirmatory testing.
METHODS
We conducted a prospective description of programmatic activities, TB ACF of individuals aged 15 years and above using CAD, and a mixed-methods feasibility and acceptability study in the catchment area of four health centres in Tondo. The calibration process employed an informal mixed methods approach to define, and reactively adjust, a threshold based on the Xpert MTB/Rif positivity rate, Xpert capacity, radiologists' sensitivity and user acceptability. Patients with a CAD score above the defined threshold were directed for sputum collection and Xpert testing.
RESULTS
The initial threshold, set at 25, resulted in a 35% referral rate for Xpert testing, which was subsequently increased to 28 (34% referral) to align with Xpert system capacity. 4,853 patients were included, with 13% testing positive on the symptom screening. The Xpert positivity rate was 5% among individuals screened, 13% among individuals tested, and 15% among individuals with a CAD score of 28 or higher. Users found CAD4TB® both feasible and acceptable, provided there were dedicated human resources with technical capacity for CAD implementation and the project design accounted for CAD limitations. The use of CAD increased screening capacity and supported decision-making.
CONCLUSION
The ACF conducted in Tondo revealed a remarkably high positivity rate among the screened individuals. CAD enables the rapid screening of patients in the community with reduced turnaround times. If the implementation accounts for the limitations identified, CAD can be a powerful tool for TB screening.
KEY MESSAGE
CAD4TB® implementation in Tondo, Manila, was assessed for TB screening feasibility. Promising results indicate increased capacity and support for decision-making, emphasizing potential as a powerful tool.
This abstract is not to be quoted for publication.
The World Health Organization recommends the use of computer-aided detection (CAD) in conjunction with chest X-rays (CXR) for tuberculosis (TB) screening and triaging in individuals aged 15 and above. This study assessed the feasibility of implementing CAD for TB active case finding (ACF) in Tondo, Manila, Philippines, including a crucial calibration process to determine the appropriate threshold for referring individuals for TB confirmatory testing.
METHODS
We conducted a prospective description of programmatic activities, TB ACF of individuals aged 15 years and above using CAD, and a mixed-methods feasibility and acceptability study in the catchment area of four health centres in Tondo. The calibration process employed an informal mixed methods approach to define, and reactively adjust, a threshold based on the Xpert MTB/Rif positivity rate, Xpert capacity, radiologists' sensitivity and user acceptability. Patients with a CAD score above the defined threshold were directed for sputum collection and Xpert testing.
RESULTS
The initial threshold, set at 25, resulted in a 35% referral rate for Xpert testing, which was subsequently increased to 28 (34% referral) to align with Xpert system capacity. 4,853 patients were included, with 13% testing positive on the symptom screening. The Xpert positivity rate was 5% among individuals screened, 13% among individuals tested, and 15% among individuals with a CAD score of 28 or higher. Users found CAD4TB® both feasible and acceptable, provided there were dedicated human resources with technical capacity for CAD implementation and the project design accounted for CAD limitations. The use of CAD increased screening capacity and supported decision-making.
CONCLUSION
The ACF conducted in Tondo revealed a remarkably high positivity rate among the screened individuals. CAD enables the rapid screening of patients in the community with reduced turnaround times. If the implementation accounts for the limitations identified, CAD can be a powerful tool for TB screening.
KEY MESSAGE
CAD4TB® implementation in Tondo, Manila, was assessed for TB screening feasibility. Promising results indicate increased capacity and support for decision-making, emphasizing potential as a powerful tool.
This abstract is not to be quoted for publication.
Journal Article > ResearchFull Text
Lancet. 2011 April 19; Volume 377 (Issue 9776); DOI:10.1016/S0140-6736(11)60438-8
Boehme CC, Nicol MP, Nabeta P, Michael JS, Gotuzzo E, et al.
Lancet. 2011 April 19; Volume 377 (Issue 9776); DOI:10.1016/S0140-6736(11)60438-8
BACKGROUND: The Xpert MTB/RIF test (Cepheid, Sunnyvale, CA, USA) can detect tuberculosis and its multidrug-resistant form with very high sensitivity and specificity in controlled studies, but no performance data exist from district and subdistrict health facilities in tuberculosis-endemic countries. We aimed to assess operational feasibility, accuracy, and effectiveness of implementation in such settings. METHODS: We assessed adults (≥18 years) with suspected tuberculosis or multidrug-resistant tuberculosis consecutively presenting with cough lasting at least 2 weeks to urban health centres in South Africa, Peru, and India, drug-resistance screening facilities in Azerbaijan and the Philippines, and an emergency room in Uganda. Patients were excluded from the main analyses if their second sputum sample was collected more than 1 week after the first sample, or if no valid reference standard or MTB/RIF test was available. We compared one-off direct MTB/RIF testing in nine microscopy laboratories adjacent to study sites with 2-3 sputum smears and 1-3 cultures, dependent on site, and drug-susceptibility testing. We assessed indicators of robustness including indeterminate rate and between-site performance, and compared time to detection, reporting, and treatment, and patient dropouts for the techniques used. FINDINGS: We enrolled 6648 participants between Aug 11, 2009, and June 26, 2010. One-off MTB/RIF testing detected 933 (90·3%) of 1033 culture-confirmed cases of tuberculosis, compared with 699 (67·1%) of 1041 for microscopy. MTB/RIF test sensitivity was 76·9% in smear-negative, culture-positive patients (296 of 385 samples), and 99·0% specific (2846 of 2876 non-tuberculosis samples). MTB/RIF test sensitivity for rifampicin resistance was 94·4% (236 of 250) and specificity was 98·3% (796 of 810). Unlike microscopy, MTB/RIF test sensitivity was not significantly lower in patients with HIV co-infection. Median time to detection of tuberculosis for the MTB/RIF test was 0 days (IQR 0-1), compared with 1 day (0-1) for microscopy, 30 days (23-43) for solid culture, and 16 days (13-21) for liquid culture. Median time to detection of resistance was 20 days (10-26) for line-probe assay and 106 days (30-124) for conventional drug-susceptibility testing. Use of the MTB/RIF test reduced median time to treatment for smear-negative tuberculosis from 56 days (39-81) to 5 days (2-8). The indeterminate rate of MTB/RIF testing was 2·4% (126 of 5321 samples) compared with 4·6% (441 of 9690) for cultures. INTERPRETATION: The MTB/RIF test can effectively be used in low-resource settings to simplify patients' access to early and accurate diagnosis, thereby potentially decreasing morbidity associated with diagnostic delay, dropout and mistreatment. FUNDING: Foundation for Innovative New Diagnostics, Bill & Melinda Gates Foundation, European and Developing Countries Clinical Trials Partnership (TA2007.40200.009), Wellcome Trust (085251/B/08/Z), and UK Department for International Development.
Journal Article > Meta-AnalysisFull Text
PLOS Med. 2012 August 28; Volume 9 (Issue 8); DOI:10.1371/journal.pmed.1001300
Ahuja SD, Ashkin D, Avendano M, Banerjee R, Bayona J, et al.
PLOS Med. 2012 August 28; Volume 9 (Issue 8); DOI:10.1371/journal.pmed.1001300
Treatment of multidrug resistant tuberculosis (MDR-TB) is lengthy, toxic, expensive, and has generally poor outcomes. We undertook an individual patient data meta-analysis to assess the impact on outcomes of the type, number, and duration of drugs used to treat MDR-TB.
Journal Article > Meta-AnalysisFull Text
PLOS One. 2012 August 30; Volume 7 (Issue 8); DOI:10.1371/journal.pone.0043953
Ford NP, Hargreaves S, Shanks L
PLOS One. 2012 August 30; Volume 7 (Issue 8); DOI:10.1371/journal.pone.0043953
Sepsis is one of the leading causes of childhood mortality, yet controversy surrounds the current treatment approach. We conducted a systematic review to assess the evidence base for fluid resuscitation in the treatment of children with shock due to sepsis or severe infection.
Journal Article > ResearchFull Text
Public Health Nutr. 2023 February 3; Volume 26 (Issue 4); 803-819.; DOI:10.1017/S136898002300023X
Khara T, Myatt M, Sadler K, Bahwere P, Berkley JA, et al.
Public Health Nutr. 2023 February 3; Volume 26 (Issue 4); 803-819.; DOI:10.1017/S136898002300023X
OBJECTIVE
To understand which anthropometric diagnostic criteria best discriminate higher from lower risk of death in children and explore programme implications.
DESIGN
A multiple cohort individual data meta-analysis of mortality risk (within 6 months of measurement) by anthropometric case definitions. Sensitivity, specificity, informedness and inclusivity in predicting mortality, face validity and compatibility with current standards and practice were assessed and operational consequences were modelled.
SETTING
Community-based cohort studies in twelve low-income countries between 1977 and 2013 in settings where treatment of wasting was not widespread.
PARTICIPANTS
Children aged 6 to 59 months.
RESULTS
Of the twelve anthropometric case definitions examined, four (weight-for-age Z-score (WAZ) <−2), (mid-upper arm circumference (MUAC) <125 mm), (MUAC < 115 mm or WAZ < −3) and (WAZ < −3) had the highest informedness in predicting mortality. A combined case definition (MUAC < 115 mm or WAZ < −3) was better at predicting deaths associated with weight-for-height Z-score <−3 and concurrent wasting and stunting (WaSt) than the single WAZ < −3 case definition. After the assessment of all criteria, the combined case definition performed best. The simulated workload for programmes admitting based on MUAC < 115 mm or WAZ < −3, when adjusted with a proxy for required intensity and/or duration of treatment, was 1·87 times larger than programmes admitting on MUAC < 115 mm alone.
CONCLUSIONS
A combined case definition detects nearly all deaths associated with severe anthropometric deficits suggesting that therapeutic feeding programmes may achieve higher impact (prevent mortality and improve coverage) by using it. There remain operational questions to examine further before wide-scale adoption can be recommended.
To understand which anthropometric diagnostic criteria best discriminate higher from lower risk of death in children and explore programme implications.
DESIGN
A multiple cohort individual data meta-analysis of mortality risk (within 6 months of measurement) by anthropometric case definitions. Sensitivity, specificity, informedness and inclusivity in predicting mortality, face validity and compatibility with current standards and practice were assessed and operational consequences were modelled.
SETTING
Community-based cohort studies in twelve low-income countries between 1977 and 2013 in settings where treatment of wasting was not widespread.
PARTICIPANTS
Children aged 6 to 59 months.
RESULTS
Of the twelve anthropometric case definitions examined, four (weight-for-age Z-score (WAZ) <−2), (mid-upper arm circumference (MUAC) <125 mm), (MUAC < 115 mm or WAZ < −3) and (WAZ < −3) had the highest informedness in predicting mortality. A combined case definition (MUAC < 115 mm or WAZ < −3) was better at predicting deaths associated with weight-for-height Z-score <−3 and concurrent wasting and stunting (WaSt) than the single WAZ < −3 case definition. After the assessment of all criteria, the combined case definition performed best. The simulated workload for programmes admitting based on MUAC < 115 mm or WAZ < −3, when adjusted with a proxy for required intensity and/or duration of treatment, was 1·87 times larger than programmes admitting on MUAC < 115 mm alone.
CONCLUSIONS
A combined case definition detects nearly all deaths associated with severe anthropometric deficits suggesting that therapeutic feeding programmes may achieve higher impact (prevent mortality and improve coverage) by using it. There remain operational questions to examine further before wide-scale adoption can be recommended.
Protocol > Research Study
BMJ Open. 2021 January 25; Volume 11 (Issue 1); e045826.; DOI:10.1136/bmjopen-2020-045826
Chandna A, Aderie EM, Ahmad R, Arguni E, Ashley EA, et al.
BMJ Open. 2021 January 25; Volume 11 (Issue 1); e045826.; DOI:10.1136/bmjopen-2020-045826
INTRODUCTION
In rural and difficult-to-access settings, early and accurate recognition of febrile children at risk of progressing to serious illness could contribute to improved patient outcomes and better resource allocation. This study aims to develop a prognostic clinical prediction tool to assist community healthcare providers identify febrile children who might benefit from referral or admission for facility-based medical care.
METHODS AND ANALYSIS
This prospective observational study will recruit at least 4900 paediatric inpatients and outpatients under the age of 5 years presenting with an acute febrile illness to seven hospitals in six countries across Asia. A venous blood sample and nasopharyngeal swab is collected from each participant and detailed clinical data recorded at presentation, and each day for the first 48 hours of admission for inpatients. Multianalyte assays are performed at reference laboratories to measure a panel of host biomarkers, as well as targeted aetiological investigations for common bacterial and viral pathogens. Clinical outcome is ascertained on day 2 and day 28.Presenting syndromes, clinical outcomes and aetiology of acute febrile illness will be described and compared across sites. Following the latest guidance in prediction model building, a prognostic clinical prediction model, combining simple clinical features and measurements of host biomarkers, will be derived and geographically externally validated. The performance of the model will be evaluated in specific presenting clinical syndromes and fever aetiologies.
ETHICS AND DISSEMINATION
The study has received approval from all relevant international, national and institutional ethics committees. Written informed consent is provided by the caretaker of all participants. Results will be shared with local and national stakeholders, and disseminated via peer-reviewed open-access journals and scientific meetings.
TRIAL REGISTRATION NUMBER NCT04285021.
In rural and difficult-to-access settings, early and accurate recognition of febrile children at risk of progressing to serious illness could contribute to improved patient outcomes and better resource allocation. This study aims to develop a prognostic clinical prediction tool to assist community healthcare providers identify febrile children who might benefit from referral or admission for facility-based medical care.
METHODS AND ANALYSIS
This prospective observational study will recruit at least 4900 paediatric inpatients and outpatients under the age of 5 years presenting with an acute febrile illness to seven hospitals in six countries across Asia. A venous blood sample and nasopharyngeal swab is collected from each participant and detailed clinical data recorded at presentation, and each day for the first 48 hours of admission for inpatients. Multianalyte assays are performed at reference laboratories to measure a panel of host biomarkers, as well as targeted aetiological investigations for common bacterial and viral pathogens. Clinical outcome is ascertained on day 2 and day 28.Presenting syndromes, clinical outcomes and aetiology of acute febrile illness will be described and compared across sites. Following the latest guidance in prediction model building, a prognostic clinical prediction model, combining simple clinical features and measurements of host biomarkers, will be derived and geographically externally validated. The performance of the model will be evaluated in specific presenting clinical syndromes and fever aetiologies.
ETHICS AND DISSEMINATION
The study has received approval from all relevant international, national and institutional ethics committees. Written informed consent is provided by the caretaker of all participants. Results will be shared with local and national stakeholders, and disseminated via peer-reviewed open-access journals and scientific meetings.
TRIAL REGISTRATION NUMBER NCT04285021.
Conference Material > Video (talk)
Hossain FN
MSF Scientific Days Asia 2021. 2021 August 26
Journal Article > ResearchFull Text
PLOS Glob Public Health. 2022 December 7; Volume 2 (Issue 12); e0001337.; DOI:10.1371/journal.pgph.0001337
Sweeney S, Berry C, Kazounis E, Motta I, Vassall A, et al.
PLOS Glob Public Health. 2022 December 7; Volume 2 (Issue 12); e0001337.; DOI:10.1371/journal.pgph.0001337
Current options for treating tuberculosis (TB) that is resistant to rifampicin (RR-TB) are few, and regimens are often long and poorly tolerated. Following recent evidence from the TB-PRACTECAL trial countries are considering programmatic uptake of 6-month, all-oral treatment regimens. We used a Markov model to estimate the incremental cost-effectiveness of three regimens containing bedaquiline, pretomanid and linezolid (BPaL) with and without moxifloxacin (BPaLM) or clofazimine (BPaLC) compared with the current mix of long and short standard of care (SOC) regimens to treat RR-TB from the provider perspective in India, Georgia, Philippines, and South Africa. We estimated total costs (2019 USD) and disability-adjusted life years (DALYs) over a 20-year time horizon. Costs and DALYs were discounted at 3% in the base case. Parameter uncertainty was tested with univariate and probabilistic sensitivity analysis. We found that all three regimens would improve health outcomes and reduce costs compared with the current programmatic mix of long and short SOC regimens in all four countries. BPaL was the most cost-saving regimen in all countries, saving $112-$1,173 per person. BPaLM was the preferred regimen at a willingness to pay per DALY of 0.5 GDP per capita in all settings. Our findings indicate BPaL-based regimens are likely to be cost-saving and more effective than the current standard of care in a range of settings. Countries should consider programmatic uptake of BPaL-based regimens.