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[一种测量量表的验证:法国药物不良反应可预防性量表示例]

[Validation of a measurement scale: example of a French Adverse Drug Reactions Preventability Scale].

作者信息

Olivier Pascale, Caron Jacques, Haramburu Françoise, Imbs Jean-Louis, Jonville-Béra Annie-Pierre, Lagier Georges, Sgro Catherine, Vial Thierry, Montastruc Jean-Louis, Lapeyr-Mestre Maryse

机构信息

Service de Pharmacologie Clinique, Centre Midi-Pyrénées de Pharmacovigilance, de Pharmacoépidémiologie et d'Informations sur le Medicament; Inserm U657, Faculté de Médecine, Toulouse, France.

出版信息

Therapie. 2005 Jan-Feb;60(1):39-45. doi: 10.2515/therapie:2005005.

Abstract

Adverse drug reactions (ADRs) have been recognised as an important cause of hospital admission. Most of these drug-related admissions were expected ADRs and, thus, partly preventable. However, as far as we know, the assessment of the preventability of ADRs was addressed in only two studies performed in France. In contrast, several other studies have been performed, mainly in the USA, and using different methods of assessing preventability. None of these methods were clearly evaluated with regard to reproducibility, validity or relevance. The purpose of this study was to initiate the validation of a French preventability scale. Here, we propose the first two phases of validation: the content validity and reliability of the scale. A working group of pharmacovigilance experts has been specifically established for this purpose. The content validity was assessed by collecting items representative of preventability. The choice and the formulation of items and a proposal of a score (global and for each item) were adopted after the consensus of the experts. A definitive version of the ADR preventability scale was used for the assessment of reliability. During the second phase, experts independently tested the new scale from observations of ADRs (49 central nervous system haemorrhages with antivitamine K). The concordance of the experts' judgements was calculated using two statistical methods (Kappa statistic and correlation coefficient). The content validity phase was performed during several workshops where experts discussed the choice and formulation of the best items. We decided to construct a scale with a small number of items, allowing a rapid evaluation of the preventability of ADRs. On the basis of a global score, four categories of preventability of ADRs ("preventable", "potentially preventable", "unclassable", "not preventable" ADRs) were proposed. The agreement of experts regarding the global score was low, with a poor correlation coefficient value (coefficient interclass = 0.491). Classification of ADRs in the four categories by the experts showed discrepancies (Kappa = 0.1136). The preventability assessment using this scale was feasible, although poor concordance between the judges has raised some questions. Several experts found use of this scale difficult in terms of a clear understanding of the items, and found that two of them were redundant. We have oversimplified some items and revision of their formulation will be necessary. Moreover, most of ADR notifications were poorly documented, resulting in a frequent choice of an "unevaluable" item. This represented an important bias in the calculation of the global score. This experience suggests the need for further studies to improve this French ADR preventability scale and validate it in differing circumstances, in order to provide a useful tool to enhance the rational use of drugs.

摘要

药物不良反应(ADR)已被公认为住院的一个重要原因。这些与药物相关的住院情况大多是预期的药物不良反应,因此部分是可预防的。然而,据我们所知,仅在法国进行的两项研究中涉及了对药物不良反应可预防性的评估。相比之下,其他几项研究主要在美国进行,采用了不同的可预防性评估方法。这些方法在可重复性、有效性或相关性方面均未得到明确评估。本研究的目的是启动对法国可预防性量表的验证。在此,我们提出验证的前两个阶段:量表的内容效度和信度。为此专门成立了一个药物警戒专家工作组。通过收集代表可预防性的项目来评估内容效度。在专家达成共识后,采用了项目的选择和表述以及评分建议(整体评分和每个项目的评分)。使用ADR可预防性量表的最终版本来评估信度。在第二阶段,专家们根据ADR的观察结果(49例使用抗维生素K导致的中枢神经系统出血)独立测试了新量表。使用两种统计方法(卡方统计量和相关系数)计算专家判断的一致性。内容效度阶段在几个研讨会上进行,专家们讨论了最佳项目的选择和表述。我们决定构建一个项目数量较少的量表,以便快速评估ADR的可预防性。基于整体评分,提出了ADR可预防性的四类(“可预防”、“潜在可预防”、“无法分类”、“不可预防”的ADR)。专家们对整体评分的一致性较低,相关系数值较差(组内系数 = 0.491)。专家们将ADR分为四类时存在差异(卡方 = 0.1136)。使用该量表进行可预防性评估是可行的,尽管评判者之间的一致性较差引发了一些问题。几位专家发现,就对项目的清晰理解而言,使用该量表很困难,并且发现其中两个项目是多余的。我们对一些项目进行了过度简化,因此有必要对其表述进行修订。此外,大多数ADR报告记录不充分,导致经常选择“无法评估”的项目。这在整体评分的计算中是一个重要偏差。这一经验表明,需要进一步开展研究以改进这个法国ADR可预防性量表,并在不同情况下对其进行验证,以便提供一个有助于促进合理用药的有用工具。

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