Thanou Aikaterini, Chakravarty Eliza, James Judith A, Merrill Joan T
Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Department of Internal Medicine, Section of Rheumatology, University of Oklahoma Health Science Center and Clinical Pharmacology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Department of Internal Medicine, Section of Rheumatology, University of Oklahoma Health Science Center and Clinical Pharmacology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA. Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Department of Internal Medicine, Section of Rheumatology, University of Oklahoma Health Science Center and Clinical Pharmacology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Rheumatology (Oxford). 2014 Dec;53(12):2175-81. doi: 10.1093/rheumatology/keu153. Epub 2014 Apr 11.
Accurate assessment of lupus flares is critical but problematic in clinical trials. This study examined the impact of modifications to the classic Safety of Estrogens in Lupus Erythematosus National Assessment (SELENA)-SLEDAI flare index (cSFI).
Ninety-one SLE patient records were evaluated at two visits at which the SLEDAI and BILAG had been scored prospectively. The cSFI was compared with an experimental version (eSFI) that eliminated medication criteria and separated the mild/moderate flare category into its components by clinical judgement based on records. The revised SFI (SFI-R) and some physician's global assessments (PGAs) were also scored using chart notes.
eSFI-rated moderate flares had higher PGA and BILAG scores than those rated as mild. When medication criteria were excluded, 42 of 55 cSFI severe flares and 15 of 49 mild/moderate flares were downgraded in severity. Comparing flares that remained severe with those that were downgraded, disease activity was higher by PGA (P < 0.001), SLEDAI (P < 0.001), BILAG (P < 0.001), number of active BILAG organs (P < 0.04) and flaring SFI-R organs (P < 0.01). PGA (P < 0.001) and the number of SFI-R domains flaring (P < 0.001) were higher in mild/moderate eSFI flares than in those that were downgraded. Twenty-one of 83 (25%) medication changes occurred with no flare. Forty-six of 52 (88%) medication changes defining severe flare by cSFI involved patients rated by physicians with no, mild or moderate flares.
A deconstructed flare index improves the discrimination of mild from moderate flares and selects more ill patients with true clinical worsening for each category of flare.
在临床试验中,准确评估狼疮病情发作至关重要但也存在问题。本研究考察了对经典的狼疮性红斑全国评估(SELENA)-系统性红斑狼疮疾病活动指数(SLEDAI)病情发作指数(cSFI)进行修改的影响。
对91例系统性红斑狼疮患者的记录在两次就诊时进行评估,这两次就诊时已前瞻性地对SLEDAI和不列颠狼疮评估组指数(BILAG)进行了评分。将cSFI与一个实验版本(eSFI)进行比较,该实验版本消除了用药标准,并根据记录通过临床判断将轻度/中度病情发作类别细分为各个组成部分。还使用病历记录对修订后的病情发作指数(SFI-R)和一些医生整体评估(PGA)进行评分。
eSFI评定为中度病情发作的患者,其PGA和BILAG评分高于评定为轻度的患者。当排除用药标准时,55例cSFI重度病情发作中的42例以及49例轻度/中度病情发作中的15例病情严重程度被下调。将仍为重度的病情发作与病情严重程度被下调的发作进行比较,疾病活动度在PGA(P<0.001)、SLEDAI(P<0.001)、BILAG(P<0.001)、活跃的BILAG器官数量(P<0.04)和病情发作的SFI-R器官数量(P<0.01)方面更高。轻度/中度eSFI病情发作的PGA(P<0.001)和SFI-R发作域数量(P<0.001)高于病情严重程度被下调的发作。83次用药变化中有21次(25%)发生时无病情发作。cSFI定义为重度病情发作的52次用药变化中有46次(88%)涉及医生评定为无、轻度或中度病情发作的患者。
一个解构的病情发作指数提高了对轻度与中度病情发作的区分能力,并为每个病情发作类别挑选出更多临床状况真正恶化的病情较重患者。