हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।
ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं
Richard R Love and Sheikh I Ahamed
The majority of global deaths are characterized by misery and limited palliation and occur in low- and middleincome countries (LMICs). Strategies for addressing the growing challenges of end-of-life palliative care, particularly those concerned with physical aspects of care, have been defined based on high-income country models of health care services and research. In LMICs, access to adequate quality primary care practitioners and oncologists is limited, and calls for training these specialists and palliative care physician specialists, even if heeded, cannot be expected to meet the growing palliative care population needs.
An applicable general framework for addressing this patient-centred abyss however, is now apparent, grounded in emerging favourable data about three components: new kinds of health paraprofessionals; information technology (IT) tools; and innovative health system approaches.
Routinizing palliative care can allow development of paraprofessional palliative care specialists. IT tools of importance include cell phone-based symptom questionnaires; internet facilitated virtual caregiver-patient visits and sharing of personal patient and family educational materials, and automated decision-making algorithms for symptom management. Health system approaches with these foregoing operational efficiencies and improved productivity can allow more and higher-quality care for more patients in need.
New local approaches are needed to address the right questions about public health palliative care.