Quality assessment No of patients Effect. Topical. Other considerations. serious 9 none 14/83 (16.9%)

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Author(s): VS/AT Date: 2015-07-23 Question: Should topical anesthetics vs placebo/control be used for reducing vaccine injection pain in children 0-12 years? 1,2,3,4 Settings: clinics, schools Bibliography: Abuelkeir 2014, Achema 2011 (2), Basiri-Moghadam 2014, Cassidy 2001, Cohen 1999 (2), Cohen 2006 (3,4), Cohen Reis 1997 (2), Dilli 2009 (2), Gupta 2013 (1), Halperin 2000, Halperin 2002, Kumar 2014, O'Brien 2004 (2004 thesis), Taddio 1994, Uhari 1993 Quality assessment No of patients Effect Quality Importance No of studies Design Risk of bias Inconsistency Indirectness Imprecision Other considerations Topical Relative Placebo/control anesthetics (95% CI) Absolute Pain 5 (measured with: validated tools (Faces Pain Scale 0-6); Better indicated by lower values) 7 serious 8 none 138 131 - SMD 0.29 lower (0.64 lower to 0.05 5 VERY Pain (yes/no) (assessed with: validated tool (Faces Pain Scale, yes/no)) serious 9 none 14/83 (16.9%) 33/76 (43.4%) RR 0.39 (0.23 to 0.67) 265 fewer per 1000 (from 143 fewer to 334 fewer) Fear (measured with: validated tool; Better indicated by lower values) serious 8 none 34 34 - SMD 0.04 higher (0.29 lower to 0.37 VERY Distress Pre-procedure (measured with: validated tool (Child Facial Coding System 0-19, Children's Hospital of Eastern Ontario Pain Scale 4-13) by researcher; Better indicated by lower values) serious 8 none 81 71 - MD 0.22 lower (0.54 lower to

0.1 Distress Pre-procedure + Acute 10 (measured with: validated tool (Modified Behavioural Pain Scale 0-10) by researcher; Better indicated by lower values) 11 serious 12 serious 8 none 42 42 - SMD 0.14 higher (0.29 lower to 0.56 10 VERY Distress Acute 13,14,15 (measured with: validated tools (Modified Behavioural Pain Scale 0-10, Visual Analog Scale 0-10, Child Facial Coding System 0-19, Children's Hospital of Eastern Ontario Pain Scale 4-13, Neonatal Infant Pain Scale 0-7, Modified Facial Coding Score 0-6, Neonatal Facial Coding System 0-10, Pain Assessment in Advanced Dimentia modified 0-10) by researcher, clinician, parent; Better indicated by lower values) 1,16 17 none 714 710 14 - SMD 0.91 lower (1.36 to 0.47 lower) 13,14,15 Distress Acute (yes/no) (assessed with: validated tool (Neonatal Infant Pain Scale 0-7) by researcher) serious 8 none 1/7 (14.3%) 7/7 (100%) RR 0.20 (0.05 to 0.86) 800 fewer per 1000 (from 140 fewer to 950 fewer) Distress Acute + Reco (measured with: validated tool (Cry duration) by researcher; Better indicated by lower values) 5 randomised serious 8 none 273 273 - SMD 0.68 lower (1.24 to 0.13 lower) Distress Acute + Reco (yes/no) (assessed with: validated tool (Cry, yes/no) by researcher) serious 9 none 115/168 (68.5%) 138/168 (82.1%) RR 0.84 (0.75 to 0.93) 131 fewer per 1000 (from 57 fewer to 205 fewer) Distress Reco (measured with: validated tools (Modified Facial Coding Score 0-6, Modified Behavioural Pain Scale 0-10) by researcher; Better indicated by lower

values) serious 18 risk of bias serious 8 none 105 105 - SMD 2.15 lower (4.68 lower to 0.37 Distress Pre-procedure + Acute +Reco 19 (measured with: validated tool (Child-Adult Medical Procedure Interaction Scale-Revised) by researcher; Better indicated by lower values) serious 8 none 34 34 - SMD 0.19 higher (0.14 lower to 0.52 19 VERY Distress Acute (observer report for child) (measured with: validated tools (Visual Analog Scale 0-10, Faces Pain Scale 0-6) by parent/nurse ; Better indicated by lower values) serious 20 serious 9 none 21 21 - SMD 1.13 lower (1.78 to 0.47 lower) Safety (skin reactions) (assessed with: observation of site for pallor, erythema (yes/no) by researcher) serious 9 none 51/80 (63.8%) 11/79 (13.9%) RR 3.09 (0.51 to 18.59) 291 more per 1000 (from 68 fewer to 1000 Safety, Pallor 21 (assessed with: observation of site for pallor (yes/no) by researcher) 6 randomised none 187/442 (42.3%) 78/439 (17.8%) RR 2.59 (1.56 to 4.29) 21 283 more per 1000 (from 99 more to 585 Safety, Erythema 21 (assessed with: observation of site of erythema (yes/no) by researcher) 5 randomised none 129/442 87/439 RR 1.42 (0.99 to 83 more per 1000 (from 2

(29.2%) (19.8%) 2.03) 21 fewer to 204 Safety (immunogenicity) 22 (assessed with: validated tools (protective antibody titre)) none - - - - Parent Preference 23 (measured with: validated tool (Visual Analog Scale 0-10 or yes/no) questionnaire about future use; Better indicated by lower values) serious 24 serious 25 none 21 21 - SMD 0.26 lower (0.87 lower to 0.35 Parent Use of Intervention 26,27 (assessed with: visual inspection of application site by researcher) serious 9 none - - - - Procedure Outcomes, Parent Fear, Vaccine Compliance, Memory, Preference, Satisfaction (assessed with: no data were identified for these important outcomes) 0 No evidence available none - - - - Parent Fear Acute (measured with: validated tool (Visual Analog Scale 0-10); Better indicated by lower values) serious 24 serious 8 none 21 21 - SMD 0.50 lower (1.11 lower to 0.12 1 In study by Cohen (1999), a cross-over design was used whereby children received 3 treatments (video distraction, topical anesthesia, or no treatment). Cohen 1999 (2) compares topical anesthesia to no treatment. 2 In study by Cassidy (2001) and Taddio (1994), parents applied the topical anesthetic at home prior to coming to the clinic. In study by Taddio (1994), 91% of parents reported it was easy to apply the cream. 3 In 9 included studies, vaccines were administered intramuscularly; in 2 studies, they were administered subcutaneously; in 2 studies both intramuscular and subcutaneous vaccines were given; and in 1 study both intramuscular and intradermal vaccines were given. 4 In 5 of the 14 included studies (Achema 2011, Basiri-Moghadam 2014, Cohen 1999, 2006, Dill 2009), there was a no treatment control group; in 1 study (Kumar 2014) there was a water spray control group; the remaining 8 studies included a placebo control group. 5 In study by Cohen 1999, there was a high risk of bias due to lack of blinding, co-intervention and vaccination of children in groups. Removal of the data from this study alters the

meta-analytic result: SMD -0.47 (95% Confidence Interval -0.73, -0.21). 6 In one study (Cohen 1999), there was no blinding and there was co-intervention bias - more distraction delivered in the comparison (no treatment control) group. In study by Cohen Reis (1997), immunizers and outcome assessors were not blinded. 7 Heterogeneity can be explained by differences in study design and quality (blinding vs. no blinded) and environmental factors (setting of vaccination - school vs clinic; time delay for topical anesthetic deli; vaccination in groups vs independent; behaviours of immunizers) 8 Confidence interval crosses the line of nonsignificance and the sample size was below the recommended optimum information size (OIS) of 400 for an effect size of 0.2 9 Sample size was below the recommended optimum information size (OIS) of 400 for an effect size of 0.2 10 The sample size/group was assumed to be equal 11 In study by Cohen 2006 (3,4), analysis (3) compared the intervention (topical anesthesia) to control (no treatment) at 12 months, and analysis (4) compared the intervention (topical anesthesia) to control (no treatment at 18 months). The data are considered independent due to the loss of 50% of the study sample. 12 Not truly random; immunizer, parent not blinded; outcome assessor blinded 13 In study by Cassidy (2001), a sample size of 83 was used for the intervention (topical anesthetic) group and 78 for the control (placebo) group 14 In study by Uhari (1993), 71% of parents reported they hoped the study intervention would be used on the next occasion. For the remainder, reasons for not using the intervention include; inconvenience and discomfort caused by removal of the occlusive dressing. 15 In study by Abuelkheir 2014, 8/216 participants were 4-6 years; the remainder were 2-24 months 16 In one study by Achema 2011, there was no blinding 17 Heterogeneity can be explained by differences in age (6 weeks to 15 years), setting (school, hospital, clinic) and variability in assessment techniques. 18 Unexplained heterogeneity 19 Scores not standardized 20 Immunizers not blinded; outcome assessors not blinded 21 Analysis includes data from Taddio (1992) in adults 22 In 3 included studies including 445 infants and children (Halperin 2000, 2002, O'Brien 2004), none demonstrated an effect on antibody titre levels in the topical anesthetic group compared to placebo. The vaccines studied included Measles-Mumps-Rubella, Diphtheria-Tetanus-acellular Pertussis-inactivated Poliovirus-Haemophilus influenza type b, and Hepatitis B. Separately, a controlled trial by Dohlwitz (1998) reported no effect on Bacillus-Calmette-Guerin in 388 children. 23 In study by Uhari (1993), 106/155 (70%) of parents reported that they preferred the cream be used on the next occasion. In study by Taddio (1994), 84/96 (88%) of parents reported that they could fit the application of the cream in their schedules and 87 (91%) reported that the cream was not difficult to apply. Separately, in study by Cohen Reis (1997) investigating topical anesthetics + distraction vs vapocoolant + distraction vs distraction alone, parents reported they were willing to pay $11.90 for topical anesthetics for future injections. 24 Immunizer not blinded; outcome assessors not blinded 25 Small sample size 26 In study by Taddio (1994), 96/100 (96%) of parents applied the topical anesthetic cream correctly (i.e., adequate quantity of cream, duration of cream application, and occlusion of cream on skin with dressing). In study by Cassidy (2001), 154/161 (96%) of parents applied the topical anesthetic patch correctly (i.e., correct patch application location, duration of patch application, and adherence of patch on skin). 27 In study by Abuelkheir (2014), the mean waiting time before vaccine injection was 57 minutes (SD = 16.7). Separately, Taddio (2012) reported a mean waiting time of 41.6 minutes (SD = 28.7).