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Acute Pain | Chronic Pain | General

Vapocoolant sprays for cannulation pain

Clinical bottom line

Four trials (741 participants) say that coolant spray works. Another four (529 participants) say it doesn't. We have insufficient information on which to base a solid judgement on sprays themselves, or how they compare with other methods..


Reference


A Moore et al. Minimising intravenous cannulation pain - a cool solution at last? BMJ 200X XX:XXX-XXX.


Systematic review

A brief systematic review of vapocoolant sprays for cannulation pain carried out in November 2008.

Results

Eight randomised trials of coolant sprays with a placebo or no-treatment control give a mixed message (Table 1). Four trials (741 participants) say that coolant spray works. Another four (529 participants) say it doesn't. It isn't easy to explain why sometimes it does, and sometimes it doesn't. As the table demonstrates, success or failure was independent of trial quality, numbers, adults or children, needle size, type of coolant, or placebo or no-treatment control.

Table 1: Randomised trials of vapocoolant sprays for cannulation pain

Reference
Participants
Design
Intervention spray
Control
Main outcome
Result
(with SD or 95% CI)
Comment
Significant benefit of vapocoolant over placebo/no treatment
Hijazi et al, 2008 Adult emergency department patients requiring IV cannulation
Needle size 18/20 gauge
Randomised, double blind
QS=5/5
N=201
Vapocoolant Mineral water at room temperature Pain immediately after cannulation, self-reported
100 mm VAS
Cannulation pain:
Placebo 36 mm (IQR 19 to 51)
Vapocoolant 12 mm (5 to 40)
No or mild pain (30 mm):
Placebo 33/103
Vapocoolant 59/98
No difference in rate of successful cannulation
Farion et al, 2008 Children aged 6-12 years requiring IV cannulation
Needle size 24 gauge
Randomised, double blind,
QS=5/5
N=80
Vapocoolant with pentafluoropropane and tetrafluoroethan at room tempterature Saline spray at room temperature Pain immediately after cannulation, self-reported by children
100 mm VAS
Mean pain score:
Placebo 56 mm
Vapocoolant 37 mm
No/minimal pain (<40 mm on 100 mm VAS)
Placebo 13/40
Vapocoolant 20/40
Vapocoolant had fewer with severe pain >70 mm
Successful cannulation on first attempt:
Vapocolant 34/40
Placebo 25/40
Robinson et al, 2007 Emergency department patients requiring cannulation
Needle size 16-21 gauge
Randomised, open
QS=3/5
N=300
Ethyl chloride No anaesthesia
Entonox
Intrademal lidocaine
Pain immediately after cannulation, self-reported
100 mm VAS
Mean pain scores:
No treatment 20 mm (15 to 25)
Ethyl chloride 11 mm (7 to 15)
Lignocaine 1 mm (0 to 6 mm)
Entonox 13 mm (8 to 18 mm)
Ethyl chloride and lignocaine appeared to reduce those with more severe pain
Selby & Bowles, 1995 Women needing IV cannula for general anaesthetic
Needle size 20 gauge
Randomised, open
QS=1/5
N=160
Ethyl chloride No analgesia
EMLA cream
Intrademal lidocaine
Pain immediately after cannulation, self-reported
100 mm VAS
Mean pain scores:
No treatment 24 mm (IQR 12 to 48)
Ethyl chloride 4 mm (0 to 21)
EMLA 17 mm (6 to 26)
Lignocaine 1 mm (0 - 11)
Ethyl chloride and lignocaine better than no treatment, but lignocaine associated with slighly higher number of failed first cannulations
No significant benefit of vapocoolant over placebo/no treatment
Hartstein & Barry, 2008 Adult emergency department patients requiring IV cannulation
Needle size 18/22 gauge
Randomised, open
QS=3/5
N=92
Coolant No coolant Pain immediately after cannulation, self-reported
100 mm VAS
Mean pain scores:
Coolant 27 mm (20 to 34)
No treatment 28 mm (20 to 36)
No or minimal pain (<40 mm):
Coolant 30/48
Control 32/45
Distribution of pain scores highly skewed
Costell et al, 2006 Children aged 9-18 years requiring IV cannulation or venepuncture
Needle size 22 gauge
Randomised, double blind,
QS=5/5
N=127
Ethyl vinyl chloride Isopropyl alcohol spray
No spray
Pain immediately after cannulation, self-reported
100 mm VAS
Ethyl vinyl choloride 34 26 mm
Isopropyl alcohol 33 25 mm
No treatment 31 25 mm
No difference in ease of cannulation or percent of successful first attempts (about 80%)
Ramsook et al, 2001 Children aged 3-18 years requiring IV cannulation
Needle size 22 gauge
Randomised, double blind,
QS=4/5
N=222
Ethyl chloride Isporpopyl alcohol spray Pain immediately after cannulation, self-reported
Faces pain scale
No difference for any age group. Median pain scores (0-10 scale) varied between 6/10 for younger to 2 or 3/10 for older children No difference in success rate
Crecelius et al, 1999 Adults scheduled for dental surgery with IV cannulation
Needle size 20/22 gauge
Randomised, open
QS=1/5
N=88
Ethyl chloride Distilled water spray (room temperature) Pain immediately after cannulation, self-reported
100 mm VAS
Ethyl chloriode 13 18 mm
Placebo 18 20 mm
No major differences in any measures of pain or anxiety

 

In trials of analgesics, the ability to discern analgesic effect usually depends on having enough pain there to measure it. Typically this means pain being of at least moderate intensity (usually at least 30 mm on a 100 mm visual analogue scale). That doesn't help here. With these trials, significance was not determined by whether placebo pain score was above or below 30 mm.

Bigger needles cause more pain, especially those of 16-gauge or bigger in adults. Despite needle size being generally 18-gauge or smaller in the eight trials, significant amounts of moderate or severe pain still occurred with needles smaller than 16-gauge. Cannulation pain scores with placebo ranged from 18% to 56% of maximum on average. A small number of patients with lots of pain drives up average pain scores.

Comment

We have been here before, faced with trials of modest group size, sometimes quite well done, but with results which point in different directions. In his thoughtful explanation about why most published research findings are false, Ioannides calculated that meta-analyses of small inconclusive studies were three times more likely to be false than true. The situation with coolant sprays is not quite that bad, but we have insufficient information on which to base a solid judgement on sprays themselves, or how they compare with other methods.

References
  1. Hijazi R, Taylor D, Richardson J. Topical alkane vapocoolant spray reduces intravenous cannulation pain in emergency department patients: a randomised, double-blind, placebo-controlled trial. BMJ 2008;XX:XXX-XXX.
  2. Farion KJ, Splinter KL, Newhook K, Gaboury I, Splinter WM. The effect of vapocoolant spray on pain due to intravenous cannulation in children: a randomized controlled trial. CMAJ 2008;179:31-6.
  3. Robinson PA, Carr S, Pearson S, Frampton C. Lignocaine is a better analgesic than either ethyl chloride or nitrous oxide for peripheral intravenous cannulation. Emerg Med Australas 2007;19:427-32.
  4. Selby IR, Bowles BJ. Analgesia for venous cannulation: a comparison of EMLA (5 minutes application), lignocaine, ethyl chloride, and nothing. J R Soc Med 1995;88:264-7.
  5. Hartstein BH, Barry JD. Mitigation of pain during intravenous catheter placement using a topical skin coolant in the emergency department. Emerg Med J 2008;25:257-61.
  6. Costello M, Ramundo M, Christopher NC, Powell KR. Ethyl vinyl chloride vapocoolant spray fails to decrease pain associated with intravenous cannulation in children. Clin Pediatr (Phila) 2006;45:628-32.
  7. Ramsook C, Kozinetz CA, Moro-Sutherland D. Efficacy of ethyl chloride as a local anesthetic for venipuncture and intravenous cannula insertion in a pediatric emergency department. Pediatr Emerg Care 2001;17:341-3.
  8. Crecelius C, Rouhfar L, Beirne OR. Venous cannulation and topical ethyl chloride in patients receiving nitrous oxide. Anesth Prog 1999;46:100-3.