Seawoods Hospital, Navi Mumbai, Maharashtra, India.
Int J Evid Based Healthc. 2013 Dec;11(4):285-90. doi: 10.1111/1744-1609.12048.
The craniocervical flexion test (CCFT) is generally undertaken using a pressure biofeedback unit. However, the high costs of the device limits its availability in poorly resourced healthcare settings. The use of alternate measures such as the aneroid sphygmomanometer to undertake CCFT need to be investigated.
The objective of this study was to establish the concurrent validity, intra- and inter-rater reliability of the aneroid sphygmomanometer using a paediatric size cuff for CCFT in asymptomatic adults.
This cross-sectional observational study involved 300 asymptomatic participants randomly allocated to either validity (n = 100), intra-rater (n = 100) or inter-rater (n = 100) testing. Participants were asked to perform CCFT to assess craniocervical flexors performance using the pressure biofeedback unit and the aneroid sphygmomanometer with a paediatric cuff. Inter-rater reliability test was performed by two different raters on the same day with rest of 30 min between tests. An independent observer checked and recorded the pressures noted on the pressure dial thus ensuring blinded outcome measurement. Correlation between the two instruments was determined by computing the stability coefficient (Pearson product moment correlation) and associated P-values for statistical significance. Intra-class correlation coefficients and its 95% confidence intervals (CIs) were calculated to determine the intra- and inter-rater reliability.
The concurrent validity of aneroid sphygmomanometer as per Pearson's product moment correlation was r = 0.856 for activation score. The intra-class correlation coefficients for intra-rater reliability was 0.92 (95% CI 0.89-0.94), and inter-rater reliability was 0.87 (95% CI 0.80-0.91).
This study has confirmed high concurrent validity, intra- and inter-rater reliability of the aneroid sphygmomanometer using a paediatric cuff for CCFT in asymptomatic adults. Its use in people with neck pain warrants investigation.
颈椎屈伸试验(CCFT)通常使用压力生物反馈装置进行。然而,该设备的高成本限制了其在资源匮乏的医疗环境中的可用性。因此需要研究使用替代措施,如无液血压计,来进行 CCFT。
本研究旨在确定使用小儿尺寸袖带的无液血压计在无症状成年人中进行 CCFT 的同时效度、内部和外部测试者间可靠性。
这是一项横断面观察性研究,纳入 300 名无症状参与者,随机分为有效性测试组(n = 100)、内部测试者组(n = 100)或外部测试者组(n = 100)。要求参与者使用压力生物反馈装置和带小儿袖带的无液血压计进行 CCFT,以评估颈椎屈肌的表现。外部测试者间可靠性测试由两名不同的测试者在同一天进行,两次测试之间休息 30 分钟。一名独立观察员检查并记录压力计上记录的压力,从而确保盲法测量结果。通过计算稳定性系数(皮尔逊积矩相关系数)和相关 P 值来确定两种仪器之间的相关性,以确定统计显著性。计算了内-组间相关系数及其 95%置信区间(CI),以确定内部和外部测试者间的可靠性。
根据皮尔逊积矩相关系数,无液血压计的同期效度为激活评分 r = 0.856。内部测试者间可靠性的组内相关系数为 0.92(95%CI 0.89-0.94),外部测试者间可靠性为 0.87(95%CI 0.80-0.91)。
本研究证实了在无症状成年人中,使用小儿袖带的无液血压计进行 CCFT 具有高度的同期效度、内部和外部测试者间可靠性。其在颈痛患者中的应用值得进一步研究。