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Technical Consultation Meeting Pneumonia Diagnostics Day 1 16 June 2014 Karin Kallander / Kevin Baker / Stefania Rigillo Meeting Agenda Day 1 Time Agenda Item Content Presenter Overview of Malaria Consortium and Pneumonia 8:30-9:30 Welcome


  1. Technical Consultation Meeting Pneumonia Diagnostics Day 1 16 June 2014 Karin Kallander / Kevin Baker / Stefania Rigillo

  2. Meeting Agenda Day 1 Time Agenda Item Content Presenter Overview of Malaria Consortium and Pneumonia 8:30-9:30 Welcome and introduction Karin Kallander Diagnostics Project and introduction of participants Pneumonia management in sick children – the current 9:30 – 10:05 Opening Plenary Wilson Were situation and opportunities 10:05-10:20 Coffee break Presentation on the current landscape on pneumonia 10:20-11:00 Landscape Analysis Update diagnostics as a result of the findings of the work done to Kevin Baker date by Malaria Consortium Discussion on the specifics of respiratory rate measurement 11:00 – 12:30 Respiratory Rate – Session 1 Moderator: Wilson Were and agreement on the gold standard DECISION POINT 12:30-1:30 Lunch break Discussion on appropriate measurement parameters for 1:30 – 3:00 Respiratory Rate – Session 2 Moderator: Shamim Qazi respiratory rate - DECISION POINT 3:00-3:30 Coffee break Role of PO in Clinical Management of Sick Children in Low Jim Black 3:30 – 4:30 Plenary 2 Income Countries Inclusion of PO in IMCI and iCCM – WHO perspective Shamim Qazi Discussion on the specifics of oxygen saturation Pulse Oximetry – Session 1 4:30-6:00 measurement and agreement on the gold standard - Moderator: Debbie Burgess DECISION POINT 6:00-6:15 Wrap up Malaria Consortium

  3. Meeting Agenda Day 2 Agenda for Day 2 of the Technical Consultation ~ 17 June 2014 Time Agenda Item Content Presenter 8:30- Recap of Day One Recap of Day 1 of the Workshop Karin Kallander 9.00 Presenter: David Critical parameters that are needed in 9.00 – Pulse Oximetry – Session Peel considering the use of PO for the diagnosis of 10.30 2 Moderator: Debbie pneumonia - DECISION POINT Burgess 10:30- Coffee break 10:45 10:45- Discussion on diagnostic tools development New developments Udantha Abeyratne 11:45 outside of RR and PO and their evaluation 11.45 – Highlights of meeting outcomes and next Karin Kallander / Wrap-up 12.30 steps planning Kevin Baker 12:30- Lunch break 1:30

  4. Malaria Consortium - Our Mission To improve lives in Africa and Asia through sustainable, evidence-based programmes that combat targeted diseases and promote child and maternal health

  5. What is the Malaria Consortium? A specialist organisation, that implements and improves public health programmes based on evidence. Research Poverty High risk/burden Disease prevention reduction populations NTDs Diagnosis & Treatment Operational Research, Technical assistance Evidence Malaria Resistance Management & Implementation support Child & Maternal Sustainable Existing systems Elimination Health & Nutrition impact Government partners Health Systems Strengthening Monitoring & Evaluation/Surveillance

  6. Where is our expertise? What approaches What diseases? What areas? tools and techniques? Vector Control Community Delivery Malaria Public Health Communications Chemoprevention Research uptake & advocacy Diagnostics NTDs Data Management Case Management M&E & Surveillance Dengue mHealth Clinical quality Pneumonia improvement Capacity building Diarrhoea Resistance Quantitative & Qualitative Management research Malnutrition Costing and economic impact Elimination evaluation

  7. Current research areas Example (not exhaustive) Clinical studies FEAST Uganda Surveillance Serology (Ethiopia) Health Services Colour-coded blisters vs. std packaging Rational use – antibiotics, Pneumonia case mgmt. Barriers to IPTP uptake in Uganda Topics Community Dialogues for NTDs (Mozambique,Ghana) Operational and inSCALE …and Implementation Net Durability research Pneumonia diagnostics Combined longitudinal Beyond Garki

  8. Development of Malaria Consortium • Widened scope to • Began as DFID Malaria • Registered as NGO Communicable diseases, • Established in 5 Resource Centre: NTDs, integrated childhood – Global policy countries illness & health systems. – DFID investment • Combined Technical • Launched large scale strategy support & delivery in Nigeria – Project design and implementation • Launched Asia evaluation 1994 - 2000 2008 - 2009 2003 - 2005 2001 - 2002 2006 - 2007 2010 - 2015 • Grew to 14 Offices in • Expanding NTD work • Initiated country • Testing innovations Africa support • Delivered innovatively to improve delivery programmes • Promoting quality on malaria • Opened offices in • Expanded to other approaches and Uganda & Ghana diseases health system • Grew M&E and integration • Building technical & research capacity M&E leadership

  9. Where we work

  10. Income by Country FY ending March 2014 Other, 4% Asia, 6% Multi wide Africa, 4% Mozambique, 6% Nigeria, 40% South Sudan, 6% Uganda, 33%

  11. Total Income by Donor FY 2006 -2014F £m 40 £m 35 Other 30 Irish Aid UNITAID 25 UNOCHA UNICEF 20 Comic Relief BMGF 15 GF CIDA 10 USAID DFID 5 0 2006 2007 2008 2009 2010 2011 2012 2013 2014F

  12. Why pneumonia diagnostics? 15,470 CHW prescriptions in Midwest Uganda ACTs Amoxicillin ORS

  13. Project Overview Title: Use of improved tools for measuring respiratory rate and oxygen saturation among community health workers: Sub- Saharan Africa and Southeast Asia Goal: To identify the most accurate, acceptable, scalable and user-friendly respiratory rate timers and pulse oximeters for diagnosis of pneumonia symptoms by CHWs and FLHFWs in four low-income countries – Cambodia, Ethiopia, South Sudan and Uganda. Timescales: November 2013 – June 2015 (6 Research Stages)

  14. Project Objectives - Obj 1: To systematically review the landscape for existing RR mobile phone apps, automated RR timing tools and POx devices appropriate for low resource settings. - Obj 2: To identify, using pre-defined criteria, the most promising and appropriate devices for field-testing in Sub-Saharan Africa and South-East Asia. - Obj 3: To establish the accuracy of the RR timing/classification device to diagnose symptoms of pneumonia and the POx devices to measure oxygen saturation, respectively, when used by CHWs and first level health workers in Sub-Saharan Africa and South-East Asia - Obj 4: To explore the acceptability and usability of existing RR mobile phone apps, automated RR timing tools and POx devices as perceived by caregivers, CHWs and FLHFWs.

  15. Pneumonia Diagnostics Project Workflow Device Evaluation Field Testing Device Selection Landscape Landscape Analysis Reports X 2 Stage 4: Select 3 Stage 3: Evaluation Pile sorting devices Stage 1 Accuracy Stage 1 Report Research Evaluation Research Report Stage 5 : Field Test FINAL Field Report Testing REPORT Dissemination Stage 6: Caregiver 12 Devices 6 Devices TPP Process meetings Caregiver Perceptions selected Interviews Report Stage 2 Stage 2 Research Research Report Scientific Advisory Committee

  16. Project Timescales 11/13-1/14 2/14-4/14 5/14-7/14 8/14-10/14 11/14-01/15 2/15-4/15 Landscape Analysis Stage 1 – FGDs Stage 2 – Pile sorting Advisory Committee/Technical Consultation Stage 3 – Evaluation Stage 4 – Pile sorting Stage 5 Field Evaluation Stage 6 Parents Interviews Dissemination

  17. Technical Consultation Meeting Objectives • To facilitate discussion and agreement on the ‘gold standard’ measures for respiratory rate and pulse oximetry • To facilitate discussion and agreement on appropriate accuracy measurements for both RR and pulse Oximetry

  18. Landscape Analysis Update Kevin Baker

  19. Landscape Analysis • Based on initial landscape review done by PATH on over 150 possible RR timers • Stage 1: Consultant engaged to update this work based on a defined set of criteria (Availability/suitability/usable/affordable) • Consultant also included 30 PO devices as this was not included originally • Objective was to help facilitate the creation of a shortlist of devices for field testing • Analysis conducted using desk research and phone interviews

  20. Landscape Analysis - findings Possible RR Devices 158 Possible PO Devices 30 TOTAL 188 Study Eligibility Criteria: 1. Availability 88 2. Suitability 32 3. Usability 10 4. Affordability 45 Possible devices available 13 for field testing

  21. Landscape Analysis - learnings • Complete product specifications very difficult to obtain • Many devices are not suitable for our target audience – children under 5 • More analysis needed from a technical perspective • Some devices fall outside initial proposal scope – measurement of cough sounds/breathe/joint PO and RR devices

  22. Critical parameters needed in considering the use of PO for the diagnosis of pneumonia Presenter: David Peel Moderator: Debbie Burgess

  23. Sensor Performance • Cost: 2 to 5 years costing • Lifetime ≥ 1 year • Guarantee conditions and duration • Ease of use on neonates and children • Reproducibility with different sensors • Testing on nurse before use

  24. Pulse Oximeter Performance • Cost – total cost for 2 or 5 years • Lifetime – failure rate • Guarantee conditions and duration • Display, size of numbers, colour coding • Alarms with adjustable limits • Ease of use by nurses • Reproducibility – evaluation on patients needed • Independent testing of function • Testing on nurse before use

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