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[利用精神病病例登记册进行的精神分裂症研究]

[Schizophrenia research using psychiatric case registries].

作者信息

Häfner H, an der Heiden W

出版信息

Fortschr Neurol Psychiatr. 1985 Aug;53(8):273-90. doi: 10.1055/s-2007-1001973.

Abstract

Almost 60 years after the establishment of the National Register of Psychoses in Norway psychiatric case registers have become an indispensable instrument of psychiatric research. By enabling a consecutive, person-related registration of contacts with the health care services of a geographically circumscribed region over long periods they have opened up new perspectives for epidemiological and followup studies and the evaluation of the care provided for schizophrenics. The severity of the illness and the fact that it frequently takes a long-term course are highly likely to lead to contacts with psychiatric services in areas with well-developed service structures. In this way case registers permit relatively reliable estimates of the treatment prevalence and first contacts, providing indicators of the true incidence. In the Federal Republic of Germany, however, as the only country in the world, cumulative psychiatric case registers have become illegal. An examination of long-term ecological, social and individual distribution processes among persons fallen ill with schizophrenia shows that the uneven distribution becomes effective even prior to the first onset. This is reflected in the marriage rates--the more so among males than females--, in the choice of occupation and the social chances of the schizophrenics to-be. In contrast, there is no reliable evidence for an increased risk of falling ill with schizophrenia after exposure to severe stress over a longer period of time. The age at first onset is some 10 years lower for males than females. Neither for this finding nor for the deviating birth season distribution, exhibited by approximately 10% of the schizophrenics, has any conclusive explanation been found. Even after the successful combat against tuberculosis falling ill with schizophrenia clearly reduces further life expectancy. The linkage of data from psychiatric case registers with twin, adoption and birth registers confirms the assumption that the probability of falling ill with schizophrenia is increased by genetic factors, thus refuting the alternative hypothesis of an environment-related transmission of the illness. Case registers are an indispensable means for the evaluation and cost analysis of the care provided for schizophrenics, above all in the establishment of new programmes of community-based complementary care for the chronically ill. Furthermore, they provide a solid basis for methodological studies on questions such as the stability of or transitions in the diagnosis over time.

摘要

在挪威建立国家精神病登记册近60年后,精神病病例登记册已成为精神病学研究不可或缺的工具。通过对一个地理区域内的医疗服务机构进行长期、连续且与个人相关的接触登记,它们为流行病学和随访研究以及对精神分裂症患者所接受护理的评估开辟了新的视角。疾病的严重性以及其通常具有的长期病程很可能导致在服务结构完善地区的精神病服务机构进行接触。通过这种方式,病例登记册能够对治疗患病率和首次接触情况进行相对可靠的估计,提供真实发病率的指标。然而,在德意志联邦共和国,作为世界上唯一的国家,累积精神病病例登记册已属非法。对精神分裂症患者的长期生态、社会和个体分布过程进行的研究表明,这种不均衡分布甚至在首次发病之前就已产生影响。这体现在结婚率上——男性比女性更为明显——以及职业选择和未来精神分裂症患者的社会机会方面。相比之下,没有可靠证据表明在长期遭受严重压力后患精神分裂症的风险会增加。男性的首次发病年龄比女性约低10岁。对于这一发现以及约10%的精神分裂症患者所呈现的偏离出生季节分布情况,均未找到确凿的解释。即使在成功抗击结核病之后,患精神分裂症仍会明显缩短预期寿命。将精神病病例登记册的数据与双胞胎、收养和出生登记册的数据相联系,证实了以下假设:遗传因素会增加患精神分裂症的概率,从而反驳了疾病与环境相关传播的另一种假设。病例登记册是评估精神分裂症患者所接受护理并进行成本分析的不可或缺的手段,尤其是在为慢性病患者建立新的社区补充护理计划时。此外,它们为诸如诊断随时间的稳定性或转变等问题的方法学研究提供了坚实的基础。

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