Economic analysis of interventions for reducing postpartum hemorrhage
October 3, 2006 Research Team Principal Investigators: Technical Committee Members: Country Investigators: October 3, 2006 Objectives of the Presentation
1) What are the cost-effectiveness ratios of PPH
2) What are the benefit-cost ratios of PPH interventions?
3) What information should we considered in choosing PPH
4) What are the recommended interventions?
October 3, 2006 Methods: Types of Interventions Included October 3, 2006 Methods: Types of Analysis
• Country studies: economic and policy analysis in four
• Global analysis (developing countries): economic
assessment (the focus of this presentation)
October 3, 2006 Methods: Cost
• Incremental cost: additional cost added to the existing system for
• Costs included:
– Logistic costs (wastage, storage and transportation)
• Costs excluded:
– Capital cost (building, equipment, vehicle)
– Cost of side-effects (for both suffer and treatments)
October 3, 2006 Methods: Effectiveness and Benefit
• Effectiveness
• Benefit
– Prevention: treatment cost averted + productivity loss
– Benefit excluded: suffer averted, and averted negative
consequences to family members and relatives
October 3, 2006 Methods: Data and Assumptions
• Distribution of birth delivery by location
• Rate of protection against PPH morbidity and morbidity
• Availability and best possible coverage of intervention
• Wastage, transportation and storage costs
October 3, 2006 Methods: Data Analysis
• Spreadsheet-based tool (Economic Assessment of Post Partum Hemorrhage Interventions (EAPPH))
• The tool consists of three modules: inputs, calculation,
• Results are reported in 18 tables, which are categorized
– PART I: Effectiveness of PPH Interventions– PART II: Cost Associated with PPH Interventions– PART III: Cost-Effectiveness of PPH Interventions– PART IV: Benefits of Interventions– PART V: Cost-Benefits of Interventions
October 3, 2006 Results: Preventive Interventions Table 1. Cost-effectiveness and cost-benefit analysis of preventive interventions Total benefit Total cost of Cost per Benefit/C Ranking intervention ost ratio averted intervention averted ($) October 3, 2006 Results: Curative Interventions Table 2. Cost-effectiveness and cost-benefit analysis of curative interventions Total benefit Total cost of Cost per Benefit/C Ranking intervention ost ratio intervention averted ($) October 3, 2006 Results: Sensitivity Analysis Figure 1. Cost per DALY of preventive interventions with protection rate +/- 5% points of the point estimate r DA e 30 $ p Oxytocin (Uniject) Oxytocin Oxytocin Syntometrine Ergometrine Misoprostol (oral) Misoprostol (monodose) (multidosel) (rectal) Interventions October 3, 2006 Results: Choosing preventive Interventions Table 3. Choosing preventive PPH interventions Efficiency Exclusiveness Total health outcomes October 3, 2006 Results: Choosing Curative Interventions Table 4. Choosing preventive PPH interventions Efficiency Exclusiveness Total health outcomes October 3, 2006 Choosing interventions: Oxy or Miso or Both? Figure 2. The number of PPH case prevented of different interventions (per year) . o f cases ( Oxytocin Misoprostol Oxy+Miso October 3, 2006 3. The health benefit of combined use of oxytocin and misoprostol Misoprostol Health Benefit Oxytocin October 3, 2006 Recommendations
• For prevention of PPH
– Misprostol should be provided where oxytocin is not
• For treatment of PPH:
– Syntometrine/oxytocin monodose (IV drip) or oxytocin in
– Misprostol (either oral or rectal) is recommended for
settings where injectable uterotonics are not available
– Other uterotonics can be considered as 2nd line drugs
– Balloon temponade and anti-shock garment should be
October 3, 2006 Thank You October 3, 2006
O que é a febre? Causas da febre Como medir a TEMPERATURA CORPORAL A temperatura corporal pode termometros de ouvido têm embebido em alcool, antes e mento das instruções de utili-depois da cada utilização. Os zação (rectificação do canal A produção de pirogéneos pode resultar de exposição ex-cessiva ao calor ( excesso de roupa, sobreaquecimento do Paracetamol –
Diagnosed with MGUS May 2003 followed by AL Amyloidosis diagnosis October 2006SCT at BUMC 1/5/2007Achieved partial response Jacqueline Mendels Birn My Amyloidosis My illness started with the discovery in May 2003 of something wrong in my blood during my yearly check-up. My internist Dr. Robert Enelow, first requested a 24 hour urine specimen and then he sent me to the oncologist