While many countries struggle with the consequences and problems of communicable diseases, chronic noncommunicable diseases are on the rise. In addition to being a major cause of death, many surviving stroke patients are disabled and need help in activities of daily living, which must be provided by family members, the health system, or other social institutions.
Lack of data on stroke from many countries hampers efficient coordination of stroke prevention, treatment, and rehabilitation. Due to future demographic changes, strategies to reduce future stroke burden and ensure adequate health resources are urgently needed. WHO STEPS stroke surveillance provides the framework for data collection and comparisons between and within populations.
TELAH TERBIT GUIDELINES EDISI KE-3...!!!
A patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified out ...
Penderita Stroke Akan Didata
SEMARANG. KOMPAS - Mulai tahun 2013, penderita stroke akan didata melalui seluruh rumah sakit di Indonesia. Pendataan dibutuhkan untuk mendapatkan angka penderita stroke ...
20 items in the Registration Data Set
The minimum amount of trial information that must appear in a register in order for a given trial to be considered fully registered.
1. Primary Registry and T ...
INDONESIA AKAN MELAKUKAN "JAMU REGISTRY"
Integrasi pelayanan kesehatan tradisional dalam pelayanan kesehatan formal merupakan suatu program pemerintah utamanya ...