1 Amil Critical Care Group, Hospital Paulistano, São Paulo, Brazil.
2 Respiratory Intensive Care Unit, Pulmonary Division, Heart Institute, Hospital das Clínicas, University of São Paulo, São Paulo, Brazil; and.
Ann Am Thorac Soc. 2016 Oct;13(10):1775-1783. doi: 10.1513/AnnalsATS.201603-154OC.
Pressure ulcers are preventable events. Critically ill patients are particularly vulnerable. The Braden scale has been used to identify hospitalized patients at high risk for the development of pressure ulcers; however, this predictive tool has not been adequately validated for critically ill patients.
We aimed to validate and improve the Braden scale for critically ill patients by adding clinical variables to the original scale.
We conducted a cohort study in 12 intensive care units (ICUs) within a network of hospitals in Brazil during 2013. We excluded patients who stayed less than 48 hours, patients with one or more pressure ulcers at admission, and those who developed a pressure ulcer within the first 48 hours. We evaluated the Braden scale and clinical variables through a competing risk analysis. Discrimination and calibration were evaluated using the Concordance index (C-index) and a calibration plot, respectively. We used bootstrapping to assess internal validation.
Our primary outcome was incident pressure ulcer within 30 days of ICU admission. We analyzed 9,605 patients and observed 157 pressure ulcers (rate of 3.33 pressure ulcers/1,000 patient-days). The majority of pressure ulcers were detected at stage I or II (28.7 and 66.2%, respectively). The Braden scale had good discrimination (C-index, 0.753; 95% confidence interval, 0.712-0.795), although its performance decreased for the most severely ill patients. We derived a modified predictive tool by adding eight clinical variables to the Braden scale: age, sex, diabetes mellitus, hematological malignancy, peripheral artery disease, hypotension at ICU admission, and need for mechanical ventilation or renal replacement therapy in the first 24 hours after ICU admission. The derived score had better discrimination and calibration than the original Braden scale. The best score cutoff was at least 6 points, with a sensitivity of 87% and a specificity of 71%.
The original Braden scale measured at ICU admission is a valuable tool for pressure ulcer prediction, although it is not accurate for severely ill patients. To overcome the limitations of the original scale, we derived a modified score with better performance, which may identify high-risk ICU patients and support target interventions. External validation of the proposed clinical prediction score is needed.
压疮是可预防的事件。危重症患者尤其容易发生。Braden 量表已用于识别有发生压疮风险的住院患者;然而,该预测工具尚未充分验证应用于危重症患者。
通过向原始量表中添加临床变量,对用于危重症患者的 Braden 量表进行验证和改进。
我们于 2013 年在巴西一家医院网络的 12 个重症监护病房(ICU)内开展了一项队列研究。我们排除了入住时间少于 48 小时、入院时已有一处或多处压疮以及入住后 48 小时内发生压疮的患者。我们通过竞争风险分析评估 Braden 量表和临床变量。分别通过一致性指数(C 指数)和校准图评估区分度和校准度。我们使用自举法评估内部验证。
我们的主要结局为 ICU 入住后 30 天内发生的新发压疮。我们分析了 9605 例患者,观察到 157 例压疮(压疮发生率为 3.33/1000 患者日)。大多数压疮处于 I 期或 II 期(分别为 28.7%和 66.2%)。Braden 量表具有良好的区分度(C 指数为 0.753;95%置信区间为 0.712-0.795),但对于病情最严重的患者,其性能有所下降。我们通过向 Braden 量表中添加 8 个临床变量,得出了一个改良的预测工具:年龄、性别、糖尿病、血液恶性肿瘤、外周动脉疾病、入 ICU 时低血压以及 ICU 入科后 24 小时内需要机械通气或肾脏替代治疗。得出的评分具有比原始 Braden 量表更好的区分度和校准度。最佳评分截点为至少 6 分,灵敏度为 87%,特异性为 71%。
入 ICU 时测量的原始 Braden 量表是压疮预测的有价值工具,尽管对于重症患者不太准确。为了克服原始量表的局限性,我们得出了一个改良的评分,性能更好,可识别高危 ICU 患者并支持针对性干预。需要对提出的临床预测评分进行外部验证。