Barnsley L, Lord S, Wallis B, Bogduk N
Cervical Spine Research Unit, University of Newcastle, Callaghan, Australia.
Clin J Pain. 1993 Jun;9(2):124-30. doi: 10.1097/00002508-199306000-00007.
To determine the false-positive rate of anesthetic blocks of the medial branches of the cervical dorsal rami in the diagnosis of cervical zygapophysial joint pain.
Comparison between single diagnostic blocks, and a criterion standard of double-blind, controlled, differential anesthetic blocks.
Tertiary referral center.
The first 55 consecutive patients with neck pain for > 3 months after and attributable to a motor vehicle accident, and who had completed a second diagnostic block after an initial positive response. A total of 60 joints was studied, with five patients providing two joints each. The mean age was 41 years; 61% were female.
Each patient had been investigated with radiologically controlled blocks of the medial branches of the cervical dorsal rami to anesthetize the target cervical zygapophysial joint. The initial block was performed using either 0.5% bupivacaine or 2% lignocaine, randomly selected. The duration of pain relief was assessed in a double-blind fashion. The procedure was repeated with the complementary anesthetic. Only patients experiencing a longer period of pain relief from bupivacaine were considered to have true-positive responses.
The second block failed to relieve pain in two of the tested joints. In a further 14 joints, the control blocks relieved pain, but the patient failed to correctly discriminate the longer acting anesthetic. The remaining 44 joints met the criteria for true-positive responses. The false-positive rate of single blocks was 16 of 60 or 27% (95% confidence interval 15%, 38%).
Uncontrolled diagnostic blocks are compromised by a significant false-positive rate that seriously detracts from the specificity of the test.
确定颈背神经内侧支麻醉阻滞在诊断颈椎小关节疼痛中的假阳性率。
单诊断性阻滞与双盲、对照、鉴别性麻醉阻滞标准之间的比较。
三级转诊中心。
连续55例颈部疼痛超过3个月且由机动车事故引起的患者,这些患者在初次阳性反应后完成了第二次诊断性阻滞。共研究60个关节,5例患者每人提供两个关节。平均年龄41岁;61%为女性。
对每位患者进行放射学引导下的颈背神经内侧支阻滞,以麻醉目标颈椎小关节。初次阻滞随机使用0.5%布比卡因或2%利多卡因。以双盲方式评估疼痛缓解持续时间。用补充麻醉剂重复该操作。只有从布比卡因获得更长时间疼痛缓解的患者才被视为真阳性反应。
第二次阻滞在两个测试关节中未能缓解疼痛。在另外14个关节中,对照阻滞缓解了疼痛,但患者未能正确区分作用时间更长的麻醉剂。其余44个关节符合真阳性反应标准。单次阻滞的假阳性率为60个中有16个,即27%(95%置信区间15%,38%)。
未控制的诊断性阻滞存在显著的假阳性率,严重降低了该测试的特异性。