López-López Candelas, Robleda-Font Gemma, Sánchez-Sánchez María Del Mar, Sarabia-Cobo Carmen María, Latorre-Marco Ignacio, Solís-Muñoz Montserrat, Pérez-Pérez Teresa, Martín-Arriscado Arroba Cristina, Schnakers Caroline, Roldan-Merino Juan
Hospital Universitario 12 de Octubre, 28041 Madrid, Madrid, Spain.
Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), 28041 Madrid, Madrid, Spain.
Nurs Rep. 2025 Jul 30;15(8):278. doi: 10.3390/nursrep15080278.
: Pain assessment scales provide a clear clinical benefit in patients who are unable to self-report. The Nociception Coma Scale-Revised-adapted for Intubated patients (NCS-R-I) was developed to assess pain in patients with acquired brain injury who are unable to self-report. However, this instrument has not yet been translated and validated for use in Spain. The objective was to translate the Nociception Coma Scale-Revised-adapted for Intubated patients (NCS-R-I) into Spanish and to assess the reliability and validity of the Spanish version in patients with brain injury. : This study was carried out in two phases. First, the scale was translated into Spanish. Next, a psychometric analysis was performed to determine the reliability and validity of the Spanish version of the NCS-R-I in 207 critically ill patients with acquired brain injury and disorders of consciousness. Two blinded observers administered the scale at three time points: 5 min before, during, and 15 min after a series of nociceptive and non-nociceptive procedures. : The internal consistency of the NCS-R-I was acceptable (ordinal alpha = 0.60-0.90). Interobserver agreement was good (kappa = 0.80; intraclass correlation coefficient = 0.90). In terms of discriminant validity, the AUC was 0.952 (95% CI: 0.931-0.973). NCS-R-I scores increased significantly during performance of nociceptive procedures compared to scores obtained before and after these procedures, confirming the scale's sensitivity to change. Similarly, during the performance of nociceptive procedures, scores on the NCS-R-I were significantly higher ( < 0.001) than those observed during non-nociceptive procedures. : The results of this study demonstrate that the NCS-R-I is a valid, reliable tool for the assessment of pain in patients with acquired brain injury who are unable to self-report.
疼痛评估量表对无法自我报告的患者具有明确的临床益处。为插管患者修订的伤害感受性昏迷量表(NCS-R-I)旨在评估无法自我报告的获得性脑损伤患者的疼痛情况。然而,该工具尚未在西班牙进行翻译和验证。目的是将为插管患者修订的伤害感受性昏迷量表(NCS-R-I)翻译成西班牙语,并评估其在脑损伤患者中的可靠性和有效性。 :本研究分两个阶段进行。首先,将该量表翻译成西班牙语。接下来,进行了心理测量分析,以确定西班牙语版NCS-R-I在207例患有获得性脑损伤和意识障碍的重症患者中的可靠性和有效性。两名盲法观察者在三个时间点使用该量表:一系列伤害性和非伤害性操作前5分钟、操作期间和操作后15分钟。 :NCS-R-I的内部一致性可接受(序数阿尔法系数=0.60-0.90)。观察者间一致性良好(kappa=0.80;组内相关系数=0.90)。在区分效度方面,曲线下面积为0.952(95%可信区间:0.931-0.973)。与这些操作之前和之后获得的分数相比,在进行伤害性操作期间,NCS-R-I分数显著增加,证实了该量表对变化的敏感性。同样,在进行伤害性操作期间,NCS-R-I的分数显著高于(<0.001)非伤害性操作期间观察到的分数。 :本研究结果表明,NCS-R-I是评估无法自我报告的获得性脑损伤患者疼痛的有效、可靠工具。