Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
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Chale S. Singer AJ. Marchini S. McBride MJ. Kennedy D 10/06 USA | 55 patients presenting to a university-based ED > 8 y/o with finger lacerations. Pts were randomized to digital or local anesthesia w/LET. Pts were then assessed for quality of anesthesia s/p repair. | Single-center, prospective, randomized, clinical-trial design | Pain of needle insertion, anesthetic injection, and suturing. Secondary outcomes included patient satisfaction, time until anesthetic onset, and the presence of wound infection and persistent numbness. | Based on a validated visual analog scale, there was no between-group differences in pain of needle insertion, anesthetic infiltration, or suturing. | -Study size of 55 -Not double-blinded, practitioner and patient knew which arm of the study they were in. -No LET administered to digital block (even if it would provide a placebo effect) -VAS is a subjective form of data collection -1% Lidocaine was neither warmed, buffered, nor had any epi -Topical anesthesia for local group only administered for 15 mins -One study site |
Robson AK. Bloom PA. 11/1990 UK | 62 patients presenting to the Accident Department of the Bristol Royal Infirmary > 16 y/o w/finger lacerations not involving deep structures or under the influence of drugs/ETOH. Pts were randomized into a group receiving a digital block, the other local infiltration. Pts were then assessed for quality of anesthesia after repair was performed | A single-center, prospective, randomized trial | Primary outcomes included pain of administiring the anesthetic and pain of suturing posed to both physician and patient in the form of a questionaire | In each of the 4 q's posed by the questionairre, digital block was more effective than local infiltration | -study size of 62 -Not double-blinded, both practioner and patient knew which arm of the study they were in -only data presented is "p" values, so it is impossible to determine the clinical significance of the study -VAS used in questionnaire is a subjective form of data acquisition -2% lignocaine (lidocaine) was neither warmed, buffered, nor contained epi -One study site |