Silman A J
Arthritis and Rheumatism Council, Manchester.
Ann Rheum Dis. 1991 Feb;50(2):95-6. doi: 10.1136/ard.50.2.95.
Mortality data for scleroderma derived from death certificates from England and Wales for the years 1968-1985 were analysed. The overall crude mortalities were 0.9 and 3.8 per million per year in men and women respectively, which are similar to comparable data from the United States. There has been a small but statistically significant increase in mortality of 3% a year over this period, possibly reflecting an underlying increasing trend in incidence. Such analyses are subject to the limitation of the accuracy of death certificates, but in a disease as rare as scleroderma the death rates provide useful data on the trends in occurrence and death from this disease.
对1968年至1985年英格兰和威尔士死亡证明中硬皮病的死亡率数据进行了分析。男性和女性的总体粗死亡率分别为每年每百万人口0.9人和3.8人,这与美国的可比数据相似。在此期间,死亡率每年有小幅但具有统计学意义的3%的上升,这可能反映了发病率潜在的上升趋势。此类分析受到死亡证明准确性的限制,但对于像硬皮病这样罕见的疾病,死亡率提供了有关该疾病发生和死亡趋势的有用数据。