The Comparison of the Minimum Data Set for Elderly Health in Selected Countries

نویسندگان

  • Farahnaz Sadoughi
  • Mehraban Shahi
  • Maryam Ahmadi
  • Nasrin Davaridolatabadi
چکیده

INTRODUCTION Ongoing increase in the elderly population in many developed countries has drawn attention to health of this age group. Recording adequate and relevant data for the elderly is considered as the basis for future planning for this segment of society. So this study was conducted to compare minimum data about elderly health in selected countries. METHODS This review study was conducted through Internet and library studies. Key words were extracted from search engines and data bases including Google, Yahoo, Google Scholar, PubMed, ProQuest and Iranian National Medical Digital Library. Inclusion criteria included English language with no time limits. All articles, research projects, theses, guidelines and progress reports were retrieved from the United States, Sweden, Japan and Iran and reviewed. Also, websites of organizations responsible for elderly health in selected countries were visited and their documents were reviewed. Results from this search were provided narratively and finally were presented within comparison tables. FINDINGS The findings of this study showed that elderly data in the selected countries are collected around four axis including minimum demographic data, medical histories, health assessment and financial data of elderly health. DISCUSSION AND CONCLUSION Given the importance of the minimum data set of elderly health for future planning, the use of experiences of leading countries in elderly health seems necessary; however, localization of it according to the country's needs is inevitable.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

National Minimum Data Set for Antimicrobial Resistance Management: Toward Global Surveillance System

Background: Success of infection treatment depends on the availability of accurate, reliable, and comprehensive data, information, and knowledge at the point of therapeutic decision-making. The identification of a national minimum data set will support the development and implementation of an effective surveillance system. The goal of this study was to develop a national antimicrobial resistanc...

متن کامل

Reporting Adverse Drug Reactions With Emphasis on the Designing National Minimum Data Set

Objective: One of the most common causes of death is the adverse drug reactions. The volume and dispersion of information is one of the problems of information systems for registering unwanted adverse drug reactions. This study aims to design a National Minimum Dataset (NMDS) for reporting the unwanted adverse drug reactions. Methods: This descriptive-comparative study was conducted in Mashhad...

متن کامل

مدیریت ناهنجاری مادرزادی در ایران : طراحی مجموعه حداقل داده‌های ملی

 Introduction: Congenital anomalies are the leading causes of infant death at birth and during infancy, and are considered as significant and costly health problems. Therefore, a national registry of congenital anomalies is needed to calculate health indexes because collecting and reporting birth anomalies facilitate assessment, and health planning. Consequently, this study aimed to determine t...

متن کامل

A Minimum Data Set of Educational Self-care Software for Patients with Cirrhosis

Introduction: Liver cirrhosis has grown significantly in Asian countries over the last few years. However, there is no tool for collecting liver cirrhosis data. The purpose of this study was to design a minimum data set for the self-care education of liver cirrhosis. Methods: This descriptive study was conducted in the first half of 2018 in cooperation with 16 liver specialists of Rasool Akram ...

متن کامل

A Minimum Data Set of Educational Self-care Software for Patients with Cirrhosis

Introduction: Liver cirrhosis has grown significantly in Asian countries over the last few years. However, there is no tool for collecting liver cirrhosis data. The purpose of this study was to design a minimum data set for the self-care education of liver cirrhosis. Methods: This descriptive study was conducted in the first half of 2018 in cooperation with 16 liver specialists of Rasool Akram ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 23  شماره 

صفحات  -

تاریخ انتشار 2015