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Assessing pain in non-intubated critically ill patients unable to self report: an adaptation of the Behavioral Pain Scale.

机译:评估无法自我报告的非插管危重患者的疼痛:行为疼痛量表的改编。

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PURPOSE: To validate an adaptation of the Behavioral Pain Scale (BPS) for its use in non-intubated intensive care unit (ICU) patients unable to self-report their pain because of the occurrence of delirium. The "vocalization" domain was inserted to construct the BPS-non intubated (BPS-NI) scale, ranging from 3 (no pain) to 12 (most pain). DESIGN: Prospective psychometric study in a medical-surgical ICU. METHODS: The same physician and one bedside nurse rated pain in non-intubated patients unable to self-report their pain during four conditions: before and after a catheter dressing change (non-nociceptive procedure) and before and after turning the patient (nociceptive procedure). Delirium was assessed by the Confusion Assessment Method for the ICU (CAM-ICU). RESULTS: A total of 120 paired evaluations were performed in 30 consecutive adult patients, 84% with delirium (CAM-ICU positive). BPS-NI scores were higher during painful procedures than at rest [6.0 (5.0-8.0) vs. 3.0 (3.0-3.8); P < 0.001], while no changes in BPS-NI scores were found during non-nociceptive procedures (discriminative validity). The BPS-NI had good internal consistency (standardized Cronbach alpha = 0.79), and each domain reflected the pain expression factor in a balanced way (coefficients between 0.57 and 0.59). The BPS-NI had a good inter-rater reliability (weighted kappa coefficient = 0.89 for the four conditions and 0.82 during nociceptive procedures) and a good responsiveness, with an effect size ranging from 1.5 to 3.6. CONCLUSIONS: Pain during procedures is perceived even in non-intubated ICU patients with delirium. In those patients, pain level can be assessed with the BPS-NI scale since this instrument exhibited good psychometric properties. Electronic supplementary material The online version of this article (doi:10.1007/s00134-009-1590-5) contains supplementary material, which is available to authorized users.
机译:目的:验证行为疼痛量表(BPS)的适应性,以用于因发生del妄而无法自我报告疼痛的非插管重症监护病房(ICU)患者。插入“发声”域以构建BPS非插管(BPS-NI)量表,范围从3(无痛苦)到12(最痛苦)。设计:外科ICU中的前瞻性心理测量研究。方法:同一位医生和一名床边护士对以下四种情况下无法自我报告疼痛的非插管患者的疼痛进行了评分:四种情况:导管敷料更换前后(非伤害性过程)和翻身前后(伤害性过程) )。 r妄通过ICU的混淆评估方法(CAM-ICU)进行评估。结果:30例成年患者中共进行了120次配对评估,其中84%的患者有ir妄(CAM-ICU阳性)。疼痛过程中的BPS-NI评分高于休息时[6.0(5.0-8.0)对3.0(3.0-3.8); P <0.001],而在非伤害性手术过程中未发现BPS-NI得分有变化(判别效度)。 BPS-NI具有良好的内部一致性(标准化Cronbach alpha = 0.79),并且每个域以平衡的方式反映疼痛表达因子(系数介于0.57和0.59之间)。 BPS-NI具有良好的评估者间可靠性(四种情况下的加权kappa系数= 0.89,伤害过程中的kappa系数= 0.82)和良好的响应能力,效果范围为1.5至3.6。结论:即使在未插管的ICU del妄患者中,也可感觉到手术过程中的疼痛。在那些患者中,可以使用BPS-NI量表评估疼痛程度,因为该仪器具有良好的心理测量特性。电子补充材料本文的在线版本(doi:10.1007 / s00134-009-1590-5)包含补充材料,授权用户可以使用。

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