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1.
Arch Cardiovasc Dis ; 109(6-7): 376-83, 2016.
Article in English | MEDLINE | ID: mdl-27020513

ABSTRACT

BACKGROUND: Whereas the coronary artery disease death rate has declined in high-income countries, the incidence of acute coronary syndromes (ACS) is increasing in sub-Saharan Africa, where their management remains a challenge. AIM: To propose a consensus statement to optimize management of ACS in sub-Saharan Africa on the basis of realistic considerations. METHODS: The AFRICARDIO-2 conference (Yamoussoukro, May 2015) reviewed the ongoing features of ACS in 10 sub-Saharan countries (Benin, Burkina-Faso, Congo-Brazzaville, Guinea, Ivory Coast, Mali, Mauritania, Niger, Senegal, Togo), and analysed whether improvements in strategies and policies may be expected using readily available healthcare facilities. RESULTS: The outcome of patients with ACS is affected by clearly identified factors, including: delay to reaching first medical contact, achieving effective hospital transportation, increased time from symptom onset to reperfusion therapy, limited primary emergency facilities (especially in rural areas) and emergency medical service (EMS) prehospital management, and hence limited numbers of patients eligible for myocardial reperfusion (thrombolytic therapy and/or percutaneous coronary intervention [PCI]). With only five catheterization laboratories in the 10 participating countries, PCI rates are very low. However, in recent years, catheterization laboratories have been built in referral cardiology departments in large African towns (Abidjan and Dakar). Improvements in patient care and outcomes should target limited but selected objectives: increasing awareness and recognition of ACS symptoms; education of rural-based healthcare professionals; and developing and managing a network between first-line healthcare facilities in rural areas or small cities, emergency rooms in larger towns, the EMS, hospital-based cardiology departments and catheterization laboratories. CONCLUSION: Faced with the increasing prevalence of ACS in sub-Saharan Africa, healthcare policies should be developed to overcome the multiple shortcomings blunting optimal management. European and/or North American management guidelines should be adapted to African specificities. Our consensus statement aims to optimize patient management on the basis of realistic considerations, given the healthcare facilities, organizations and few cardiology teams that are available.


Subject(s)
Acute Coronary Syndrome/therapy , Cardiac Catheterization , Delivery of Health Care, Integrated/organization & administration , Developing Countries , Health Services Accessibility/organization & administration , Percutaneous Coronary Intervention , Thrombolytic Therapy , Acute Coronary Syndrome/diagnosis , Acute Coronary Syndrome/mortality , Africa South of the Sahara/epidemiology , Cardiac Catheterization/standards , Consensus , Delivery of Health Care, Integrated/standards , Health Services Accessibility/standards , Health Services Needs and Demand/organization & administration , Humans , Incidence , Needs Assessment/organization & administration , Patient Care Team/organization & administration , Percutaneous Coronary Intervention/standards , Prevalence , Thrombolytic Therapy/standards , Time-to-Treatment/organization & administration , Treatment Outcome
2.
Cardiovasc J Afr ; 27(3): 184-187, 2016.
Article in English | MEDLINE | ID: mdl-26815006

ABSTRACT

Acute rheumatic fever (ARF) and rheumatic heart disease (RHD) remain major causes of heart failure, stroke and death among African women and children, despite being preventable and imminently treatable. From 21 to 22 February 2015, the Social Cluster of the Africa Union Commission (AUC) hosted a consultation with RHD experts convened by the Pan-African Society of Cardiology (PASCAR) in Addis Ababa, Ethiopia, to develop a 'roadmap' of key actions that need to be taken by governments to eliminate ARF and eradicate RHD in Africa. Seven priority areas for action were adopted: (1) create prospective disease registers at sentinel sites in affected countries to measure disease burden and track progress towards the reduction of mortality by 25% by the year 2025, (2) ensure an adequate supply of high-quality benzathine penicillin for the primary and secondary prevention of ARF/RHD, (3) improve access to reproductive health services for women with RHD and other non-communicable diseases (NCD), (4) decentralise technical expertise and technology for diagnosing and managing ARF and RHD (including ultrasound of the heart), (5) establish national and regional centres of excellence for essential cardiac surgery for the treatment of affected patients and training of cardiovascular practitioners of the future, (6) initiate national multi-sectoral RHD programmes within NCD control programmes of affected countries, and (7) foster international partnerships with multinational organisations for resource mobilisation, monitoring and evaluation of the programme to end RHD in Africa. This Addis Ababa communiqué has since been endorsed by African Union heads of state, and plans are underway to implement the roadmap in order to end ARF and RHD in Africa in our lifetime.


Subject(s)
Delivery of Health Care, Integrated/organization & administration , Health Priorities/organization & administration , Health Services Needs and Demand/organization & administration , Needs Assessment/organization & administration , Primary Prevention/organization & administration , Rheumatic Fever/prevention & control , Rheumatic Heart Disease/prevention & control , Secondary Prevention/organization & administration , Africa/epidemiology , Anti-Bacterial Agents/supply & distribution , Cardiac Surgical Procedures , Cooperative Behavior , Health Services Accessibility/organization & administration , Humans , International Cooperation , Penicillin G Benzathine/supply & distribution , Registries , Rheumatic Fever/diagnosis , Rheumatic Fever/epidemiology , Rheumatic Heart Disease/diagnosis , Rheumatic Heart Disease/epidemiology
3.
Thromb Res ; 121(3): 413-8, 2007.
Article in English | MEDLINE | ID: mdl-17553552

ABSTRACT

BACKGROUND: Aspirin (ASA) failure to inhibit in vitro platelet function had been termed ASA resistance. The prevalence of this phenomenon as measured with different platelet function tests varies widely among studies. OBJECTIVES: In this study, we propose to determine the prevalence of ASA non-responsiveness in stable coronary artery patients using three different tests. PATIENTS AND METHODS: One hundred ninety-one patients with a stable coronary artery disease and receiving secondary ASA prophylaxis (250 mg/day) were tested. For each patient the ASA-induced platelet inhibition was determined using three different tests: Ivy Bleeding time (BT), collagen/epinephrine closure time (CEPI-CT; PFA-100, Dade-Behring) and urinary 11-dehydrothromboxane B2 (uTxB2) excretion level. The agreement between these tests was evaluated by kappa statistics test. RESULTS: The prevalence of biological ASA resistance was 15.7% (n=30), 20.4% (n=39) and 24.6% (n=47) by BT, PFA-100 and UTxB2, respectively. Only fourteen patients (7.3%) were non-responders for two tests: 6 (3.1%) BT/ PFA-100; 1 (0.5%) BT/UTxB2; 7 (3.7%) PFA-100/UTxB2). A poor agreement was found between these three methods and only 3 patients were resistant with all the tests (1.6%). CONCLUSION: The lack of agreement supposed that different types of aspirin resistance exist. Thus, combination of two tests or more could be a primary solution for a better identification of ASA resistant patients. This hypothesis must be confirmed by a large-scale randomized study with clinically well-defined endpoints.


Subject(s)
Aspirin/pharmacology , Blood Platelets/drug effects , Coronary Artery Disease/blood , Coronary Artery Disease/drug therapy , Platelet Aggregation Inhibitors/pharmacology , Platelet Function Tests/methods , Adult , Aged , Aged, 80 and over , Bleeding Time , Coronary Artery Disease/urine , Drug Evaluation, Preclinical/methods , Drug Resistance , Female , Humans , Male , Middle Aged , Thromboembolism/blood , Thromboembolism/prevention & control , Thromboembolism/urine , Thromboxane B2/analogs & derivatives , Thromboxane B2/urine
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