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利用同胞生存数据测量成人死亡率:一种新的分析方法及 1974-2006 年 44 个国家的新结果。

Measuring adult mortality using sibling survival: a new analytical method and new results for 44 countries, 1974-2006.

机构信息

Institute for Health Metrics and Evaluation, University of Washington, Seattle, Washington, United States of America.

出版信息

PLoS Med. 2010 Apr 13;7(4):e1000260. doi: 10.1371/journal.pmed.1000260.


DOI:10.1371/journal.pmed.1000260
PMID:20405004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2854132/
Abstract

BACKGROUND: For several decades, global public health efforts have focused on the development and application of disease control programs to improve child survival in developing populations. The need to reliably monitor the impact of such intervention programs in countries has led to significant advances in demographic methods and data sources, particularly with large-scale, cross-national survey programs such as the Demographic and Health Surveys (DHS). Although no comparable effort has been undertaken for adult mortality, the availability of large datasets with information on adult survival from censuses and household surveys offers an important opportunity to dramatically improve our knowledge about levels and trends in adult mortality in countries without good vital registration. To date, attempts to measure adult mortality from questions in censuses and surveys have generally led to implausibly low levels of adult mortality owing to biases inherent in survey data such as survival and recall bias. Recent methodological developments and the increasing availability of large surveys with information on sibling survival suggest that it may well be timely to reassess the pessimism that has prevailed around the use of sibling histories to measure adult mortality. METHODS AND FINDINGS: We present the Corrected Sibling Survival (CSS) method, which addresses both the survival and recall biases that have plagued the use of survey data to estimate adult mortality. Using logistic regression, our method directly estimates the probability of dying in a given country, by age, sex, and time period from sibling history data. The logistic regression framework borrows strength across surveys and time periods for the estimation of the age patterns of mortality, and facilitates the implementation of solutions for the underrepresentation of high-mortality families and recall bias. We apply the method to generate estimates of and trends in adult mortality, using the summary measure (45)q(15)-the probability of a 15-y old dying before his or her 60th birthday-for 44 countries with DHS sibling survival data. Our findings suggest that levels of adult mortality prevailing in many developing countries are substantially higher than previously suggested by other analyses of sibling history data. Generally, our estimates show the risk of adult death between ages 15 and 60 y to be about 20%-35% for females and 25%-45% for males in sub-Saharan African populations largely unaffected by HIV. In countries of Southern Africa, where the HIV epidemic has been most pronounced, as many as eight out of ten men alive at age 15 y will be dead by age 60, as will six out of ten women. Adult mortality levels in populations of Asia and Latin America are generally lower than in Africa, particularly for women. The exceptions are Haiti and Cambodia, where mortality risks are comparable to many countries in Africa. In all other countries with data, the probability of dying between ages 15 and 60 y was typically around 10% for women and 20% for men, not much higher than the levels prevailing in several more developed countries. CONCLUSIONS: Our results represent an expansion of direct knowledge of levels and trends in adult mortality in the developing world. The CSS method provides grounds for renewed optimism in collecting sibling survival data. We suggest that all nationally representative survey programs with adequate sample size ought to implement this critical module for tracking adult mortality in order to more reliably understand the levels and patterns of adult mortality, and how they are changing. Please see later in the article for the Editors' Summary.

摘要

背景:几十年来,全球公共卫生工作的重点一直是制定和应用疾病控制方案,以提高发展中国家儿童的生存率。为了在各国可靠地监测此类干预方案的影响,人口学方法和数据源取得了重大进展,特别是在具有大规模跨国调查方案(如人口与健康调查)的情况下。尽管在成人死亡率方面没有进行类似的努力,但拥有大量包含人口普查和家庭调查中成人生存信息的数据集,为我们提供了一个重要的机会,可以大大提高我们对没有良好生命登记制度的国家成人死亡率水平和趋势的了解。迄今为止,人们试图通过人口普查和调查中的问题来衡量成人死亡率,但由于调查数据中存在生存和回忆偏差等固有偏差,通常导致成人死亡率低得令人难以置信。最近的方法发展和越来越多的包含有关兄弟姐妹生存信息的大型调查表明,重新评估过去对使用兄弟姐妹史来衡量成人死亡率的悲观态度可能是适时的。

方法和发现:我们提出了校正的兄弟姐妹生存(CSS)方法,该方法解决了困扰使用调查数据估计成人死亡率的生存和回忆偏差问题。我们的方法通过逻辑回归,直接从兄弟姐妹史数据估计给定国家、性别和时期的死亡概率。逻辑回归框架通过调查和时期的强度来估计死亡率的年龄模式,并为解决高死亡率家庭代表性不足和回忆偏差问题提供便利。我们使用来自 DHS 兄弟姐妹生存数据的 44 个国家的综合指标(45)q(15)-15 岁者在 60 岁生日前死亡的概率,生成了成人死亡率的估计值和趋势。我们的研究结果表明,许多发展中国家普遍存在的成人死亡率水平远远高于之前其他分析兄弟姐妹史数据所表明的水平。一般来说,我们的估计表明,在撒哈拉以南非洲人口中,女性在 15 至 60 岁之间的成人死亡风险约为 20%-35%,男性为 25%-45%。在南部非洲国家,艾滋病毒流行最为严重,多达十分之八的 15 岁男性将在 60 岁之前死亡,十分之六的女性也将如此。亚洲和拉丁美洲人口的成人死亡率水平普遍低于非洲,女性尤其如此。海地和柬埔寨是例外,其死亡率风险与非洲的许多国家相当。在所有其他有数据的国家,女性的 15 至 60 岁之间的死亡风险通常约为 10%,男性为 20%,与一些更发达国家的水平相差不大。

结论:我们的研究结果代表了对发展中国家成人死亡率水平和趋势的直接知识的扩展。CSS 方法为收集兄弟姐妹生存数据提供了新的乐观依据。我们建议,所有具有足够样本量的具有代表性的国家调查方案都应该实施这一关键模块,以跟踪成人死亡率,以便更可靠地了解成人死亡率的水平和模式,以及它们是如何变化的。请在文章后面查看编辑总结。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/05ca15945c6c/pmed.1000260.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/e15c151848c6/pmed.1000260.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/47727b56b2af/pmed.1000260.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/f578ff671da0/pmed.1000260.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/d994d4fa0477/pmed.1000260.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/be8e74a3d65e/pmed.1000260.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/e6b0c6adc573/pmed.1000260.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/92188d63ddec/pmed.1000260.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/04f88f190d97/pmed.1000260.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/b58230a71ceb/pmed.1000260.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/1f84dc6b23d5/pmed.1000260.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/05ca15945c6c/pmed.1000260.g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/e15c151848c6/pmed.1000260.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/47727b56b2af/pmed.1000260.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/f578ff671da0/pmed.1000260.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/d994d4fa0477/pmed.1000260.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/be8e74a3d65e/pmed.1000260.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/e6b0c6adc573/pmed.1000260.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/92188d63ddec/pmed.1000260.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/04f88f190d97/pmed.1000260.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/b58230a71ceb/pmed.1000260.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/1f84dc6b23d5/pmed.1000260.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7302/2854132/05ca15945c6c/pmed.1000260.g011.jpg

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