Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Peterson et al. 2014 USA | Adult ongoing LP for any clinical indication. In an emergency department (ED) setting. Randomization to the US group or the palpation landmarks group (PL). The US group: the right space was priory localized with the standard US procedure then the usual LP procedure. | Prospective randomized controlled trial | Number of needle reinsertion | No significant difference (3 in the US group vs 5 in the PL group) | The major weakness of this study is the training time of operator. An independent investigator trained them at the time of enrolment immediately prior to do the procedure. This would underestimate the results. No blinding. Convenience sample. |
Success of LP (return of a non traumatic CSF) | No significant difference (78% in the US group vs 76% in the PL group) | ||||
Pain measured on a VAS | No significant difference (1.1 in the US group vs 3.0 in the PL group | ||||
Patient satisfaction (5 point likert scale) | No significant difference (5 vs 5) | ||||
Median time of procedure | No significant difference (1.6 min in the US group vs 2.0 min in the PL group) | ||||
Mofidi et al. 2013 Iran | Adults >18 years old <60, who needed an LP. Exclusion: cerebral lesion, local infection, pregnant women, coagulopathy, previous spinal surgery. In an emergency department setting. Patients were randomized to PL group or to US group. | Prospective randomized clinical trial | Number of attempts | Reduced number of attemps (1 in the US group vs 2 in the PL group, p=-0.047) | No blinding of patients nor LP operator. This could overestimate the results. |
Number of traumatic LP | Reduced number of traumatic tap (5 in the US group vs 18 in the PL group, p=0.024) | ||||
Pain score with a numerical 0 to 10 scale | In the US guided LP, the pain score was significantly lower (4.4 vs 7.4). | ||||
Procedure time | Time (minutes) was significantly lower in the US group 3.3 vs 6.4 min | ||||
Shaikh et al. 2013 Canada | Inclusion criteria for randomized control trial: - Randomization - Comparing US marking vs palpation procedure Reported at least one primary outcomes, Clinical trial, observation study and diagnostic studies were included. 14 trials were included, 5 for lumbar puncture, 674 patients in the US group and 660 in the PL group. | Systematic review and meta-analysis | Failed procedure | Reduced failed procedure, 6 in the US group vs 44 in the PL group (RR 0,21 [CI 95% 0.10-0.43]), NNT 16 to reduce one failure | Search strategy seems to be not enough sensible; the grey literature was not searched. 7 studies were done in an anaesthesia settings. |
Traumatic procedure | Reduced traumatic procedure (RR 0.27 [CI 95% 0.11-0.67]) | ||||
Number of needle reinsertion | Reduced number of reinsertion needle by a mean of -0.44 (-0.64 to -0.24) | ||||
Number of needle redirection | Reduced number of redirection by a mean of -1.00 per procedure (-1.24 to -0.75, p<0.001) | ||||
Time of the procedure | Time of the procedure could not be evaluated due to heterogeneity. | ||||
Nomura et al. 2007 USA | Adults >18 years old, who needed a LP; In an (ED) setting. All patients had a prior ultrasound to localize the right space and marked with an ultraviolet (UV) ink in a separate room, the LP operator then localized the right space by placing an UV ink by palpation landmarks. Randomization occurred after. A different investigator showed the mark to use based on the randomization results to the LP operator who was blinded to the origin of the mark. | Randomized controlled double-blind study | Number of attempts | No significant difference in number of attempts (2 vs 2) | Subgroup analysis very interesting but probably lacks power due to a small sample size. For the US procedure, the localization of the right angle was not included in the procedure. |
Presence of a traumatic tap | No significant difference (RR=1.04 [CI 95% 0.83-1.31]) | ||||
Success or failure of procedure | Increased success rate for US (RR 1.32 [CI 95% 1.01-1.72]), 1 failed in the US and 6 in the PL procedure | ||||
Length of operation | No significant difference (15 min in the US group vs 10.5 in the PL group) | ||||
Evaluation of the procedure (ease by the LP operator on a 10 cm VAS scale) | No significant difference (3 in the US group vs 5.2 in the PL group) | ||||
Subgroup analysis for obese patients with a BMI >30 | Ease of procedure significantly better (2.7 cm for US vs 6.9 cm for PL), Others results had no significant difference but a trend toward US procedure |