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The effect of intramuscular injection technique on injection associated pain; a systematic review and meta-analysis
The effect of intramuscular injection technique on injection associated pain; a systematic review and meta-analysis

Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: JDCR reports personal fees from GSK Pharma, Hologic Diagnostics, Mycovia and Janssen Pharma as well as ownership of shares in GSK Pharma and AstraZeneca Pharma; and is author of the UK and European Guidelines on Pelvic Inflammatory Disease; is a Member of the European Sexually Transmitted Infections Guidelines Editorial Board; is a Member of the National Institute for Health Research Funding Committee (Health Technology Assessment programme); was previously a Member of the National Institute for Health Research HTA Primary Care, Community and Preventative Interventions Panel (2013-2016). He is an NIHR Journals Editor and associate editor of Sexually Transmitted Infections journal. He is an officer of the International Union against Sexually Transmitted Infections (treasurer), and a charity trustee of the Sexually Transmitted Infections Research Foundation. OA and RSH declare no competing interests. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Article Type: Research Article Article History
Abstract

Aim

To review the effect of different intramuscular injection (IMI) techniques on injection associated pain, in adults.

Methods

The review protocol was registered on PROSPERO (CRD42019136097). MEDLINE, EMBASE, British Nursing Index and CINAHL were searched up to June 2020. Included studies were appraised and a meta-analysis, where appropriate, was conducted with a random effects model and test for heterogeneity. Standardised mean difference (SMD) with a 95% confidence interval in reported injection pain (intervention cf. control) was reported.

Results

29 studies were included in the systematic review and 20 studies in the meta-analysis. 13 IMI techniques were identified. 10 studies applied local pressure to the injection site. Of these, applying manual pressure (4 studies, SMD = -0.85[-1.36,-0.33]) and Helfer (rhythmic) tapping (3 studies, SMD = -2.95[-5.51,-0.39]) to the injection site reduced injection pain, whereas the use of a plastic device to apply local pressure to the skin (ShotBlocker) did not significantly reduce pain (2 studies, SMD = -0.51[-1.58,0.56]). Acupressure techniques which mostly involved applying sustained pressure followed by intermittent pressure (tapping) to acupressure points local to the injection site reduced pain (4 studies: SMD = -1.62[-2.80,-0.44]), as did injections to the ventrogluteal site compared to the dorsogluteal site (2 studies, SMD = -0.43[-0.81,-0.06]). There was insufficient evidence on the benefits of the ‘Z track technique’ (2 studies, SMD = -0.20[-0.41,0.01]) and the cold needle technique (2 studies, SMD = -0.73[-1.83,0.37]) on injection pain. The effect of changing the needle after drawing up the injectate on injection pain was conflicting and warming the injectate did not reduce pain. Limitations included considerable heterogeneity, poor reporting of randomisation, and possible bias in outcome measures from unblinding of assessors or participants.

Conclusions

Manual pressure or rhythmic tapping over the injection site and applying local pressure around the injection site reduced IMI pain. However, there was very high unexplained heterogeneity between studies and risk of significant bias within small studies.

Ayinde,Hayward,Ross,and Peña Fernández: The effect of intramuscular injection technique on injection associated pain; a systematic review and meta-analysis

Introduction

Intramuscular injection (IMI) is a common clinical procedure with 16 billion injections administered globally every year [1] in a wide variety of healthcare settings [2]. The widespread use of IMI reflects the range of medications that can be delivered via this route including sedatives, hormonal therapies, vaccines, tumour immunotherapy, immune-suppressants, long-acting antipsychotics, vitamins and antibiotics [3, 4]. The intramuscular route offers a potential advantage by improving drug absorption and bioavailability compared to oral and other parenteral routes [4, 5], and can be used when the tolerability of oral medication is poor [6], and to ensure treatment adherence [4].

Injection site pain is common following IMI [79]. Anxiety and fear associated with pain can reduce the acceptability of treatment to patients [10], and for clinicians the knowledge that a procedure is painful may reduce its use. Given the frequency of IMIs and their importance as a treatment option, IMI site pain is an important issue and a number of pharmacological [7], psychological [11], and procedural (injection technique) interventions [12] have been proposed to reduce injection associated pain. Pharmaceutical interventions, such as injectable or topical anaesthetics can reduce pain [7], but are not always compatible with the medication being injected and may be associated with drug side-effects, allergies and increased cost [13]. Physical and procedural interventions, through the use of an optimal injection technique, have the potential to reduce pain while having little effect on the length or cost of the procedure.

Previous interventional and observational studies have evaluated IMI techniques which reduce pain with many focused on childhood vaccinations. In this younger population pain can be decreased by having the child sit up (or by holding an infant), stroking the skin or applying pressure close to the injection site before and during injection, and performing a rapid intramuscular injection without initial aspiration [14]. A recent systematic review of IMI techniques in adults suggests that IMI to the ventrogluteal site, the Z track, and manual pressure IMI techniques may be effective interventions in reducing IMI associated pain [15]. However, this review restricted the range of electronic databases searched and the language of studies included, and may have missed relevant studies. Given the importance of IMI pain in the management of patients, we provide an extended and updated review of the current evidence on IMI techniques used to reduce pain using a robust search and clear inclusion criteria. The aim of this study was to systematically review the effect of different intramuscular injection techniques on injection pain in adults.

Methods

A systematic review protocol was developed and registered with PROSPERO at the Centre for Reviews and Dissemination, University of York (Registration No. CRD42019136097 http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42019136097).

Eligibility criteria

Studies were considered eligible for review if they met the following inclusion criteria; involved human participants; male or female; aged ≥ 18 years (or the majority of the study population was aged ≥ 18 years); involved IMI of any medicinal or non-medicinal product; specified an injection technique to reduce injection site pain; had a comparator group that also received an IMI of any medicinal or non-medicinal product; and collected data on pain secondary to IMI. There was no restriction on the indication for treatment, the health status of participants, or the healthcare setting. There was also no restriction on the language of publication or the publication date.

Search strategy

Scoping searches were initially carried out to refine the search strategy. Thereafter, the OVID search platform was used to search MEDLINE (1946 to 29th of June 2020) and EMBASE (1974 to 29th of June 2020). The British Nursing Index and Cumulative Index Nursing and Allied Health Literature (CINAHL) were searched via EBSCOhost (1981 to 29th of June 2020). The search terms are shown in S7 Table. Citation searching was carried out on included articles.

Study selection

All identified records were entered into Endnote X7 and duplicates removed. Titles and abstracts, where available, were screened independently by two reviewers (RH and OA) for relevance using the inclusion criteria. Full text articles were sought for all potentially relevant records and the inclusion criteria were applied independently by the same two reviewers. Any disagreement was resolved by discussion or by a third independent reviewer (JR). Foreign language records were included when searching, and titles and abstracts were translated to allow screening. All potentially relevant foreign language studies were translated (full text) for assessment and, if appropriate, data extraction. Reviewers were not blinded to the authors or settings of the studies.

Data extraction

The data extraction form was designed and piloted on three included studies, and finalised following the pilot. Data extraction was performed independently by two reviewers (RH and OA) on all included studies. Disagreements were resolved by discussion and by a third independent reviewer (JR). The following study characteristics were collected; (i) study author; (ii) study design; (iii) country of publication; (iv) number of participants; (v) age range of participants; (vi) gender of participants; and (vii) ethnicity of participants. Specific details of the intramuscular injection technique used in the intervention and comparator groups were collected: (i) clinical setting; (ii) definition/description of the intramuscular injection technique used; (iii) indication for IMI; (iv) substance administered; (v) volume of injection; (vi) needle gauge used; (vii) needle length used; (viii) intramuscular site of injection; (ix) presence of co-morbidities; (x) frequency of injection and; (xi) length of follow up. Data on the outcome measure (pain secondary to IMI) including: (i) definition/description of pain measurement tool used (ii) timing of pain assessment (iii) information on who completed the pain assessment (iv) severity of pain (v) duration of pain (vi) summary statistics, and test statistics.

Risk of bias

Risk of bias assessment was included within the data extraction form and was independently assessed by two reviewers (RH and OA). The risk of bias of randomised controlled trials (RCTs) was assessed with the Cochrane Collaboration’s tool for assessing risk of bias of RCTs [16], for quasi-experimental studies this was performed with the non-randomised studies on interventions (ROBINS-1) tool [17], and for systematic reviews this was assessed with the risk of bias in systematic reviews (ROBIS) tool [18].

Meta-analysis

Meta-analysis was performed for the primary outcome when appropriate and possible. Studies using either parallel or crossover designs were combined in the meta-analysis. Results from both periods of crossover studies were used unless there was reason to believe carryover of effects from one period to another posed a serious problem. IMI pain was considered as a continuous outcome, and in studies with multiple intervention or comparator (control) arms, the interventions (Raddadi et al. [19]) or control (Çelik and Korshid [20]) arms were combined and pooled means and standard deviations were estimated. Standardised mean differences (SMD) were used to estimate the outcome, since pain was measured with a variety of scales between studies. In studies where pain was measured with multiple instruments, preference was given to measures from the ‘visual analogue scale’ (VAS), then the ‘numerical rating scale’ (NRS) and the ‘verbal rating scale’ (VRS) in that order. In studies where pain was measured at different time points post injection (Kanika and Rani [21]; Khanra et al. [22]), the outcome measure at the earliest reported time was used in the meta-analysis. Studies with no discernible control arm were excluded from the meta-analyses.

Statistical details

In studies with crossover design, within-study comparisons were based on paired t-tests. Correlations (rho) between repeat outcomes on the same patient were estimated when possible from P-values, paired t-statistic or from any relevant summary data. When correlations could not be estimated, they were imputed for each outcome using the lowest (positive) estimate among other studies in the meta-analysis [23, 24]. Sensitivity analyses were undertaken to investigate the robustness of results to imputed quantities.

For parallel arm studies the SMD was calculated as the difference in mean outcome between groups divided by the standard deviation of outcome among participants, and for cross-over studies the SMD was calculated as the mean of the within patient difference between the intervention and comparator injection pain outcome, divided by the between patient standard deviation of the outcome. An approximate variance for the SMD for crossover studies was taken as, 2(1rho) [25] where rho is the estimated or imputed correlation between repeated outcome measurements. Not all studies reported the same outcome measures (e.g., means, standard deviations), therefore some of the effect sizes were calculated with transformed data. An SMD of zero means that the intervention and the comparator have equivalent effects on IMI pain, and SMDs lower than zero indicate that the intervention was more beneficial than the comparator.

Heterogeneity and subgroup analyses

Clinical heterogeneity was examined prior to performing a meta-analysis but did not preclude the combination of results. Studies were also found to be methodologically heterogeneous and thus random-effects analyses with the DerSimonian-Laird method were undertaken in preference to fixed effect analyses in order to encompass residual variation between studies into the confidence interval for a pooled effect. Sensitivity analyses were undertaken to investigate the impact of this preference on the estimate. I2 was used as an indicator of heterogeneity, I2 value of 0% indicates an absence of dispersion, and larger values show increasing levels of heterogeneity [26]. Random effects meta-regression was used to compare subgroups where appropriate. The following subgroup analyses were specified a priori and were carried out:

    The intervention effect where IMI techniques have similar operating procedures

    The effect of experimental design (RCT vs Quasi-experimental studies) on the pooled estimate

Reporting bias

Funnel plots were used to assess the risk of reporting bias (small study and/or publication bias). Contour enhanced funnel plots and Egger’s meta-regression test for funnel plot asymmetry were conducted.

Sensitivity analyses

The following sensitivity analyses were carried out to assess the robustness of our findings:

    Fixed effect meta-analyses (which do not incorporate heterogeneity between studies)

    Analyses that ignore crossover design of studies

    Exclusion of small studies from the meta-analysis of interventions using local pressure techniques—parallel studies with study size ≤ 100 and cross over studies with studies size ≤ 50 were excluded.

    Inclusion of the Najafidolatbad et al. [27] study into the Z track meta-analysis. This study did not have a control arm as a comparator but rather compared two interventions.

    Analyses that ignore the L14 pressure point (other acupressure studies were conducted with the UB/BL32 or UB31 pressure point) intervention arm in the Raddadi et al. [19] study.

Statistical analyses were performed with Stata 15 for windows, and a two tailed P<0.05 was considered statistically significant.

Results

Database searches identified 604 potential articles. Duplicates were removed and two reviewers screened 397 articles independently. 355 records were excluded including 5 studies where full texts were not available. 42 articles and a further 13 studies identified from citation searches were independently assessed for eligibility against the pre-specified inclusion criteria by the same two independent reviewers. Any disagreements were resolved by discussion. 29 studies met the inclusion criteria and were included in the qualitative analysis and 20 studies were included in the quantitative analysis. The PRISMA flow diagram in Fig 1 shows the study selection process.

PRISMA flow diagram for the systematic review of intramuscular injection technique and the effect on pain.
Fig 1

PRISMA flow diagram for the systematic review of intramuscular injection technique and the effect on pain.

Characteristics of included studies

Table 1 summarises the characteristics of the included studies. 29 studies, with a total of 2442 participants, comprising 13 randomised controlled trials (RCTs), 15 quasi-experimental studies and 1 systematic review/meta-analysis were included in this descriptive analysis. The sample size of the experimental studies ranged from n = 25 to n = 242. Where gender distribution was reported, the study participants were mostly women (1431/2186). The clinical setting for the studies varied, with 14 of the 28 (50%) experimental studies conducted with hospital inpatients. Thirteen (manual pressure, Helfer skin tap, ShotBlocker, post injection massage, Z track, acupressure, two-needle technique, altering injection speed, cold needle, application of ice to the injection site, airlock technique, gluteal injection site and altering the temperature of the injectate) different IMI techniques to reduce injection pain were evaluated within the included studies. In studies reporting ‘standard technique’ as the control, the definition of ‘standard’ varied considerably and included insertion of the injecting needle at 900 to the skin [20], aspiration prior to injection [20], a two needle technique (changing the needle between drawing up material and injecting it) [28] and the airlock technique (including a small quantity of air in the syringe) [2931]. However, in other studies, aspiration [29, 30, 32], the airlock technique [32, 33], and 90o needle insertion [3236] were used as part of the intervention. 27/28 of the experimental studies used a quantitative scale as their outcome assessment measure—a visual analogue scale was the most common (19/28), followed by a numerical rating scale (5/28). One study [37] used a 4-point Likert scale, utilising the descriptors “None, Mild, Moderate, or Severe”.

Table 1
Characteristics of included studies.
Study (Year of publication)DesignCountrySample SizeGenderAge Range* (years)PopulationIntervention to reduce painComparatorPain Measurement ToolTiming of pain assessment
Barnhill et al. [34] 1996Quasi-experimentalUSA93M32 F61>18CommunityManual pressureNo pressureVisual Analogue ScaleImmediately after injection
Chung et al. [38] 2002Quasi-experimentalHong Kong74M33 F4118–42CommunityManual pressureStandard techniqueVerbal Rating ScaleAfter each injection
Zore and Dias [39] 2014Quasi-experimental (crossover design)India50M20 F3015–55Hospital outpatientManual pressure & progressive muscle relaxation therapyStandard protocol (undefined)Numerical Rating Scale and Behavioural ObservationFollowing injection
Öztürk et al. [28] 2016Quasi-experimentalTurkey123M13 F11018–30Hospital outpatientManual pressureStandard techniqueNumerical Rating ScaleImmediately after injection
Shah and Narayan [13] 2016Quasi-experimental (crossover design)India82M39 F4320–60Hospital inpatientHelfer Skin TapStandard techniqueSimple descriptive pain intensity and Visual Analogue ScaleDuring injection
Hassnein and Soliman [40] 2016Quasi- experimental (crossover design)Egypt100M38 F6220–60Hospital inpatientHelfer Skin TapStandard techniqueUniversal Pain Assessment ToolWithin 1 min of injection
Khanra et al. [22] 2018RCTIndia60M29 F3120–60Hospital inpatientHelfer Skin TapStandard techniqueNumerical Rating Scale8AM and 8PM of the 1st + 2nd day following injection
Çelik and Korshid [20] 2015RCTTurkey180M75 F10518–80Hospital outpatientShotblocker1. Standard technique (no Shotblocker)Visual Analogue ScaleAfter injection
2. Placebo control (smooth aspect Shotblocker)
Emel et al. [35] 2017RCTTurkey242M42 F20018–31CommunityShotBlockerNo ShotBlockerVisual Analogue ScaleImmediately after injection
Kanika and Rani [21] 2011Quasi-experimental (crossover design)India30M14 F1618–59Hospital inpatientMassage after injectionNo massage after injectionVisual Analogue Scale and Verbal Rating Scale<5 mins 30 mins 1 hour
Keen et al. [37] 1986Quasi-experimentalUSA50M37 F1321–57Hospital inpatientZ track techniqueStandard technique4-point Likert ScaleImmediately after injection and 12 hours after
Najafidolatabad et al. [27] 2010RCTIran90M0 F9018–60Hospital inpatientProne position and Z trackProne position and air lock techniqueVisual Analogue ScaleUnclear
Kara and Güneş [32] 2016RCT (crossover design)Turkey86M29 F46 (11 lost to follow up)Mean 46.4 (SD 15.2)Hospital inpatient1.Prone position one foot internally rotatedProne position toes pointed downVisual Analogue ScaleUnclear
2. Z track technique
Yilmaz et al. [36] 2016RCTTurkey66M34 F26 (6 excluded)18–65Hospital inpatientZ track techniqueStandard techniqueVisual Analogue ScaleDuring injection
Alavi [41] 2007Quasi-experimental (crossover design)Iran64M32 F3215–59Hospital outpatientPressure to acupressure point UB31Standard Protocol (WHO guidelines)Visual Analogue ScaleNot stated
Suhrabi and Taghinejad [42] 2014Quasi-experimentalIran150M0 F15015–55Hospital inpatientPressure to acupressure point UB32Standard techniqueVisual Analogue ScaleNot stated
Raddadi et al. [19] 2017RCTIran90M0 F9016–65Emergency Department1. Pressure to acupressure point BL32Standard Protocol (WHO guidelines)Visual Analogue ScaleImmediately after injection
2. Pressure and pinching to acupressure point L14
Najafi et al. [43] 2018Quasi-experimental (crossover design)Iran48M0 F4817–39Hospital inpatient1. Pressure to acupressure point UB32Standard techniqueVisual Analogue ScaleImmediately after injection
2. Pressure to sham acupressure point
Rock [44] 2000Quasi-experimentalAustralia70Not statedNot statedHospital outpatientTwo-needle techniqueOne-needle techniqueVisual Analogue ScaleNot stated
Aǧaç and Güneş 2011 [29]RCTTurkey100M65 F3518–54Hospital inpatientTwo-needle techniqueOne-needle techniqueNumerical Rating ScaleImmediately after each injection
Ozdemir et al. [45] 2013Quasi-experimental (crossover design)Turkey25M15 F1018–80Hospital inpatient30 second injection10 second injectionVisual Analogue ScaleImmediately after injection + every 5 mins for the first 35 mins
Tuǧrul and Khorshid [46] 2014Quasi-experimental (crossover design)Turkey60M29 F3118–62Hospital outpatientInjection speed 5seconds/mLInjection speed 10seconds/mLVisual Analogue ScaleImmediately after injection
Bartell et al [47] 2008RCT (Factorial design)USA80Not available (majority female)Mean 26.7 (SD 0.99)CommunityCold needle (-20°C)Room temperature needleVisual Analogue ScaleImmediately after each injection and 2 to 4 days later
Thomas et al. [48] 2019RCT (crossover design)India100Not stated (5 lost to follow up)13–45Hospital inpatientCold needle (0–2°C)Room temperature needleNumerical Rating ScaleDuring Injection
Güneş et al. [31] 2013Quasi-experimental (crossover design)Turkey70M32 F3851.5 (SD 12.4)Hospital inpatientRight ventrogluteal site, patients positioned lateral with uppermost extremities in flexion (injections with airlock technique)Left dorsogluteal site, patients placed in prone position with extremities internally rotated (injections with airlock technique)Visual Analogue ScaleImmediately after each injection
Yilmaz et al. [30] 2016RCTTurkey60M25 F35>18 yearsHospital inpatientInjection to the ventrogluteal site with or without the airlock techniqueInjection to the dorsogluteal site with or without the airlock techniqueVisual Analogue ScaleImmediately after each injection
Maiden et al. [49] 2003RCTAustralia150M92 F5816–91Emergency Department 1. Rubbed vaccine (~27°C)Cold Vaccine (~19°C)McGill Present Pain Intensity Questionnaire5 mins

24hrs

48 hrs
2. Warmed vaccine (~29°C)
Farhadi and Esmailzaseh [50] 2011RCTIran60M30 F3015–50Hospital outpatientIce applied to skin prior to injectionStandard techniqueVisual Analogue ScaleImmediately after injection
Study (Year of publication)DesignCountryP(population) I (intervention) C(comparator) O (outcome) S (study)Number of included studiesStudy typesSearch periodAgeIMI interventions identified
Şanlialp et al. [15] 2019Systematic review & meta-analysisTurkeyP- Adults (≥ 18 years) administered IM I in any setting I- physical procedural interventions used during IMI C- any physical procedural IMI technique O- pain scale measures S- RCTS and quasi-experimental studies159 RCTs 6 Quasi-experimental studiesTill November 2017Adult1. Manual pressure
2. ShotBlocker
3. Z track technique
4. Airlock technique
5. Post injection massage of injection site
6. Injection speed
7. Two-needle technique
8. Acupressure
9. Gluteal injection site

*where age range not available mean and standard deviation (SD) provided

† technique used in addition to comparator.

ⱡ- Warmed vaccine- vaccine warmed in a 37°C warming cupboard for 5 minutes; rubbed vaccine- vaccine rubbed for 1 minute between nurse’ hand.

Risk of bias assessment

Studies included in this review were of variable methodological quality. The reporting of sequence generation and allocation concealment were often unclear in the included RCTs. Pain is a subjective measure and blinding of participants was reported in 4/13 (31%) of RCTs (Fig 2). The overall risk of bias for the quasi-experimental studies was low or moderate, with a moderate risk of bias associated with unblinding in the ‘measurement of the outcome’ domain for majority (9/15 [60%]) of the studies (Table 2). For the included systematic review and meta-analysis, the overall risk of bias was low, but the risk of bias in the ‘study eligibility criteria’ domain was high (Table 2).

Risk of bias assessment for included randomised controlled trials.
Fig 2

Risk of bias assessment for included randomised controlled trials.

Red–high risk of bias, yellow–unclear, green–low risk of bias.

Table 2
Risk of bias for included quasi-experimental studies and systematic review.
Study (author and publication year)Bias due to confoundingBias in selection of participantsBias in classification of interventionBias due to deviations from intended interventionsBias due to missing dataBias in measurement of outcomesBias in selection of the reported resultOverall bias
Manual pressure
Barnhill et al. [34] 1996ModerateLowLowLowModerateModerateLowModerate
Chung et al. [38] 2002ModerateLowLowLowLowModerateLowModerate
Zore and Dias [39] 2014LowNILowLowModerateModerateLowModerate
Öztürk et al. [28] 2016LowLowLowLowLowLowLowLow
Helfer skin tap
Shah and Narayan [51] 2016LowLowLowLowLowModerateLowModerate
Hassnein and Soliman [40] 2016LowLowLowLowLowLowLowLow
Massage after injection
Kanika et al. [21] 2011LowLowLowLowLowModerateLowModerate
Z track
Keen [37] 1986ModerateLowLowLowLowLowLowModerate
Acupressure
Alavi [41] 2007LowLowlowLowLowLowLowLow
Suhrabi and Taghinejad [42] 2014LowNILowLowLowModerateLowModerate
Najafi et al. [43] 2018LowLowLowLowLowLowLowLow
Two-needle technique
Rock [44] 2000LowLowLowLowNIModerateLowModerate
Injection speed
Ozdemir et al. [45] 2013LowLowLowLowLowLowLowLow
Tuǧrul and Khorshid [35] 2014LowLowLowLowLowModerateLowModerate
Gluteal injection site
Güneş et al. [31] 2013LowLowLowLowLowModerateLowModerate
Systematic review
Study (author and publication year)Bias from study eligibility criteriaBias in identification and selection of studiesBias in data collection and appraisalBias in synthesis and findingsOverall bias
Şanlialp et al. [15] 2019HighLowLowLowLow

NI- No information.

IMI techniques reporting significant reduction in injection pain

In Table 3, we report the mean pain scores for IMI interventions and their respective comparators. Manual pressure (4 studies), Helfer skin tap (3 studies), post injection massage (1 study), acupressure to UB31/UB32/BL32 acupoint (4 studies), airlock technique (1 study), and application of ice to the injection site (1 study) IMI techniques were found to be potentially beneficial in reducing injection pain compared to their respective comparators.

Table 3
Pain scores following interventions to reduce intramuscular injection pain.
Study (Year of publication)Indication for IM injectionSubstance injectedSite of injectionPain Measurement ToolPain descriptorsMean score interventionMean score comparatorStatistical Significance
Manual Pressure
Barnhill et al. [34] 1996VaccinationImmunoglobulinGlutealVisual Analogue Scale100mm “no pain” to “pain as bad as it could be”13.6*21.5*p = 0.03
Chung et al. [38] 2002VaccinationHepatitis A/B vaccineDeltoidVerbal rating Scale (Cantonese)0 to101.77 (SD1.49)2.86 (SD 1.58)p<0.0001
Zore and Dias [39] 2014InfectionBenzathine penicillinNot statedNumerical Rating Scale and behavioural observationNot statedNot statedNot statedP<0.05
Öztürk et al. [28] 2016VaccinationHepatitis A/B vaccineDeltoidNumerical Rating Scale0 to103.17 (SD 1.95)4.0 (SD 2.20)p = 0.002
Helfer Skin Tap
Shah and Narayanan [13] 2016Pain relief (post orthopaedic surgery)DiclofenacVentroglutealVisual Analogue ScaleNot statedNot stated1.41 (SD 0.51)¤<0.001
Hassnein and Soliman [40] 2016Pain reliefAnalgesic or vitaminDorsoglutealUniversal Pain Assessment Tool (Verbal description [VDS], Wong Baker face grimace [WFGS] and activity tolerance scales [ATS])VDS (0 to 10)-“no pain”(0), to “worst pain”(9 to10) WFGS-“alert smiling” (0) to “eyes closed” (9 to 10) ATS- “no pain” (0), “bed rest required” (9 to 10)Not statedNot statedVDS, p = 0.002
WFGS, p = 0.002
ATS, p = 0.003
Khanra et al. [22] 2018Pain relief (post-operative patients)AnalgesicDorsoglutealNumerical Rating ScaleNot stated1st day 8 am; 1.97(0.4)1st day 8 am; 4.7(0.82)1st day 8 am; p<0.001
1st day 8pm; 0.73 (0.5)1st day 8pm; 4.03 (0.79)1st day 8pm; p<0.001
2nd day 8 am; 1.37(0.55)2nd day 8 am; 4.90(0.65)2nd day 8 am; p<0.001
2nd day 8 pm 0.40 (0.57)2nd day 8 pm 4.30 (0.90)2nd day 8 pm; p<0.001
ShotBlocker
Çelik and Khorshid [20] 2015Pain reliefDiclofenacVentroglutealVisual Analogue Scale0 “no pain” to 100 “worst pain”7.85 (SD 7.03)26.7 (SD 20.3)-comparator 20.3 (SD 14.4)-placebop<0.001 for intervention vs placebo vs comparator
Emel et al. [35] 2017VaccinationHepatitis B vaccineDeltoidVisual Analogue ScaleNot stated33.8 (SD 26.1)33.0 (SD 23.9)p = 0.796
Massage after injection
Kanika and Rani [21] 2011Pain reliefDiclofenac and/or vitamin KGlutealVisual Analogue Scale (VAS) Verbal rating Scale (VRS)VAS; 0 to 10 VRS; 0 “no pain” to 5 “worst possible”VAS (<5mins); 2.02VAS (<5mins); 2.9VAS at 5mins, 30 mins and 1 hour P<0.05
VAS (30mins); 1.13VAS (30mins); 1.82
VRS at 5mins, 30 mins and 1 hour P<0.05
VAS (1 hour); 0.3VAS (1 hour); 0.98
VRS (<5mins); 2.02VRS (<5mins); 2.57
VRS (30mins); 0.93VRS (30mins); 1.43
VRS (1 hour); 0.13VRS (1 hour); 0.62
Z track technique
Keen et al. [37] 1986Pain reliefMeperidine hydrochloride alone or combined with promethazine hydrochlorideVentrogluteal4-point Likert ScaleNone, mild, moderate, severeNot statedNot statedThe incidence and severity of discomfort were significantly lower in the intervention compared to the comparator group at selected time intervals and not all time intervals.
Najafidolatabad et al. [27] 2010Pain reliefTramadolNot statedVisual Analogue Scale0-10cm4.56 (SD 1.66)2.84 (SD 1.24)p<0.05 (air lock technique superior to z track)
Kara and Güneş [32] 2016Pain relief (surgery associated pain)DiclofenacDorsoglutealVisual Analogue Scale0-100mm 0 “no pain” to 100 “extreme pain’Foot internally rotated, 0.95 (SD 0.91) Z track, 1.25 (SD 1.44)Toes pointing down 1.49 (SD 1.28)p = 0.009 for comparison of foot internally rotated vs Z track vs toes pointing down
Yilmaz et al. [36] 2016Pain reliefDiclofenacGlutealVisual Analogue Scale0 “no pain to 100 “most intense pain"28.3 (SD 23.0)36.4 (SD 32.5)p = 0.336
Pressure to acupressure point
Alavi [41] 2007InfectionPenicillin G procaineDorsoglutealVisual Analogue Scale0 to 103 (SD 2)5 (SD 2)p<0.001
Suhrabi and Taghinejad [42] 2014InfectionPenicillinGlutealVisual Analogue Scale0 “no pain” to 10 “most severe pain”2.34 (SD 1.47)7.12 (SD 1.88)P<0.001
Raddadi et al. [19] 2017InfectionProcaine PenicillinDorsoglutealVisual Analogue Scale0 “no pain” to 10 “severest pain”BL32 acupoint, 1.76 (SD 2.45)2.76 (SD 1.80)p = 0.006 for comparator vs BL32
L14 acupoint, 2.33 (SD 1.80) Ŧ
p = 0.051 for comparator vs L14
p = 0.030 BL32 vs L14
Najafi et al. [43] 2018Pre-eclampsia/ EclampsiaMagnesium sulphateDorsoglutealVisual Analogue Scale0 “no pain” to 10 “worst imaginable pain”Intervention, 1.94 (SD 1.27)7.22 (2.08)p<0.001 for Intervention vs Comparator; Intervention vs Sham; and Sham vs comparator
Sham intervention, 4.75 (SD 2.08)
Two-needle technique
Rock [44] 2000Mental HealthNeuroleptic medicationDorsoglutealVisual Analogue Scale0 to 100Not statedNot statedp = 0.895
Aǧaç and Güneş [29] 2011Pain relief (secondary to a traffic accident)DiclofenacDorsoglutealNumerical Rating Scale0 “no pain” to 10 “worst imaginable pain”5.53 (SD 1.64)6.43 (SD 1.35)p<0.001
Variable injection speed
Ozdemir et al. [45] 2013Dermatological conditionMethylprednisoloneDorsoglutealVisual Analogue Scale0 “no pain” to 10 “unbeareable pain”3.4 (SD 1.6);0 min4.1 (SD 2.1); 0 minp = 0.016; 0 min
3.1 (SD 1.5); 5 min3.6 (SD 1.9); 5 minp = 0.136; 5 min
2.2 (SD 1.4); 10 min3.0 (SD 1.7); 10 minp = 0.036;10 min
1.2 (SD 1.2); 15min2.2 (SD 1.6); 15minp = 0.004; 15min
0.5 (SD 0.8); 20 min1.5 (SD 1.5); 20 minp = 0.008;20 min
0.1 (SD 0.4); 25 min0.7 (SD 1.1); 25 minp = 0.013; 25 min
0.1 (SD 0.4); 30 min0.2 (SD 0.5); 30 minp = 0.265; 30 min
0.0 (SD 0.0); 35 min0.1 (SD 0.2); 35 minp = 0.327; 35 min
Tuǧrul and Khorshid [46] 2014InfectionPenicillin GVentro/dorsoglutealVisual Analogue Scale0 “no pain” to 10 “excruciating pain”43.8 (SD 22.2); VG 45.8 (SD 20.3); DG48.6 (SD 24.5); VG 49.6 (24.5); DGp = 0.230 for; VG
p = 0.067 for DG
Cold needle technique
Bartell et al. [47] 2008Vaccinationinfluenza vaccination salineDeltoidVisual Analogue Scale10 cm ‘‘no pain” to ‘‘most painful injection ever.”32.2 (SE 3.2); Flu vaccine 25.2 (SE 3.0); Saline36 (SE 3.8); Flu vaccine 23.7 23.7(SE 3.2); Salinep = 0.450 for cold needle vs room temperature needle with Flu vaccine
p = 0.733 for cold needle vs room temperature needle with Saline
Thomas et al. [48] 2019InfectionPenicillin benzathineNot statedNumerical Rating Scale0 “no pain” to 10 “worst imaginable pain”3.37 (SD 1.75)5.58 (1.68)P = 0.001
Gluteal injection site (VG vs DG)
Güneş et al. [31]Pain relief (patients with spinal disc herniation)DiclofenacVentro/dorsoglutealVisual Analogue Scale0 “no pain” to 10 “worst imaginable pain”1.24 (1.18)1.89 (1.49)p = 0.019
Yilmaz et al. [30] 2016Pain reliefDiclofenacGlutealVisual Analogue Scale0 “no pain” to 10 “worst imaginable pain”2.53 (SD 2.52); air lock-VG3.30 (SD 2.70); air lock-DGp = 0.197; VG vs DG
2.99 (SD 2.86); without airlock-VG3.16 (SD 2.74); without airlock-DGp = 0.519; VG vs DG
Other Techniques
Maiden et al. [49] 2003VaccinationDiphtheria/tetanusDeltoidMcGill Present Pain Intensity Questionnaire0 “no pain” to 5 “excruciating pain”Median 1.0 (IQR 1.0–2.0)-Warmed vaccineMedian 1.0 (IQR 1.0–2.0)- cold vaccinep = 0.630 for warmed vs rubbed vs cold vaccine
Median 1.0 (IQR 1.0–2.0)- Rubbed vaccine
Farhadi and Esmailzaseh [50] 2011InfectionBenzathine penicillinDorsoglutealVisual Analogue Scale0 to 104.47 (1.42)7.39 (1.55)p< 0.001
Systematic review and meta-analysis
Study (Year of publication)Risk of bias of reviewed studiesInter-study heterogeneityPooled outcomeAuthor’s conclusions on IMI techniques and injection pain
Şanlialp et al. [15] 2019Allocation concealment was unclear and risk from blinding of participant and personnel was unclear or high in RCTs. For quasi-experimental studies, half of the studies reliably measured the outcome.Significant inter-study heterogeneitystandardised mean difference in pain scores (95%CI) for all intervention techniques vs comparator 0.595(0.417 to 0.773; p = 0.001).No evidence for a single IMI technique, however, the VG site, Z track technique, and manual pressure were most effective in reducing IMI pain. Other effective methods were the two‐needle technique, post-injection massage, and the ShotBlocker.
Subgroup analysis by IM intervention vs comparator
SMD manual pressure, 3 studies 0.557 (0.372 to 0.741, p = 0.001)
SMD Z track, 3 studies 0.587 (0.044 to 1.130, p = 0.001)
SMD ShotBlocker 1.021 (0.468 to 1.574, p = 0.001)
SMD Two needle technique 0.744 (0.335 to 1.154, p = 0.001)
SMD Acupressure 0.403(-0.123 to 0.929, p = 0.133)
SMD Airlock technique 0.295 (-0.391 to 0.981, p = 0.400)
SMD Injection speed 0.352 (0.073 to 0.777, p = 0.105)
Subgroup analysis by injection site
SMD deltoid, 2 studies 0.545 (0.032 to 1.059, p = 0.037)
SMD dorsogluteal, 7 studies 0.493 (0.208 to 0.778, p = 0.001)
SMD ventrogluteal 3 studies 0.791 (0.355 to 1.227, p<0.001)
SMD DG&VG, 3 studies 0.701 (0.243 to 1.158; p = 0.003)

*-Adjusted mean.

¤- Mean difference and standard deviation of mean difference comparator vs intervention.

†- Technique used in addition to comparator.

Ŧ- Two interventions; acupressure to acupoint BL32 or acupoint L14.

VG-Ventrogluteal; DG-dorsogluteal.

SE—Standard error; IQR—Interquartile range.

ⱡ- Warmed vaccine- vaccine warmed in a 37°C warming cupboard for 5 minutes; rubbed vaccine- vaccine rubbed for 1 minute between nurse’ handswp.

All four quasi-experimental studies that employed the application of manual pressure to the injection site reported a significant reduction in injection pain [28, 34, 38, 39]. Three of these studies applied pressure for 10 seconds prior to giving a vaccination to the deltoid muscle in healthy volunteers [28, 34, 38], and in the fourth study, participants received benzathine penicillin injection into the gluteal muscle [39].

The Helfer skin tap (rhythmic tapping over the skin at the site of injection to relax the muscle before and during the injection) injection technique also reduced injection pain. These studies included one RCT [22] and two quasi-experimental studies [40, 51] involving inpatients who received injections into the gluteal muscle. Post injection massage reduced injection pain compared to the control group, in a quasi-experimental study of hospital inpatients receiving gluteal injections of an analgesic or vitamin K [21].

The acupressure IMI technique involved applying manual pressure for 1 minute to the acupoint UB31/BL32 located in the inner upper quadrant of the dorsogluteal muscle, followed by rhythmic application of pressure with the thumb three times to the acupoints. This was found to be beneficial in reducing injection associated pain in a cohort of hospital inpatients who received antibiotic injections [19, 41, 42] or magnesium sulphate [43].

Najafidolatabad et al [27] compared two different interventions to reduce IMI in a RCT of hospital inpatients receiving analgesic injections at the gluteal site. The Z track technique involved pulling the overlying skin and subcutaneous tissues approximately 2.5 cm laterally, holding the skin taut with the non-dominant hand, and then injecting the medication. The second intervention was the air lock technique in which additional air is drawn up into the syringe after the injectate. The air is then injected into the participant along with the injectate. Injection site pain was reported to be significantly lower with the use of the air lock technique compared to the Z track technique.

Application of ice on the injection site for 30 seconds prior to injection significantly reduced injection pain in a RCT of outpatients receiving IM benzathine penicillin [50].

IMI techniques with reported non-significant reduction in injection pain

The Z track technique (3 studies), altering the temperature of injectate (1 study), and acupressure to L14 acupoint (1 study) did not significantly affect injection pain (Table 3).

Yimaz et al. [36] found that the Z track technique did not confer a significant advantage over the standard IMI technique in reducing injection pain, although Z track reduced drug leakage. Kara and Güneş [32] compared three different techniques with patients in the prone position; (1) ‘toes pointing down’ only (2) ‘internally rotated foot’ only and (3) ‘toes pointing down’ combined with the Z track technique. Injection pain was reduced in the ‘toes pointing down’ combined with Z track group compared to the ‘toes pointing down’ only group (mean VAS 1.25 vs 1.49 respectively). However, injections with the ‘toes pointing down’ combined with Z track were more painful when compared to injections with ‘internally rotated feet ‘only (mean VAS 1.25 vs 0.95). Keen et al. [37], also investigated the effect of Z track technique on injection pain in participants and measured the intensity of discomfort (burning, stinging, aching, being sore or hurting when touched or moving the leg) with a 4-point Likert scale. The severity of discomfort (immediately after injection and 3 to 5 hours after initial injection) was similar for both the Z track technique and the standard technique arms, although the Z track was effective at reducing the incidence of selected descriptors of discomfort at other selected time intervals. All three studies involved hospital inpatients receiving IM analgesic injections.

Maiden et al. [49] investigated the influence of the injectate temperature on IMI pain using combined adult diphtheria and tetanus vaccine. “Cold” vaccine with no deliberate warming (mean temperature 19.1°C), “rubbed” vaccine which was rubbed for 1 minute between the nurses’ hands (mean temperature 26.9°C), and “warmed” vaccine which was placed in a warming cupboard for 5 minutes (mean temperature 28.9°C) were injected into the deltoid muscle. Across all time points measured, post injection pain was similar regardless of the temperature of vaccine injected (Table 3).

Raddadi et al. [19] investigated the effect of applying acupressure to acupoint L14 (a region between the thumb and index finger) on injection pain. Acupressure to the L14 acupoint did not significantly reduce injection pain when compared to a control group who did not receive acupressure (mean VAS 2.33 vs 2.76), and injection pain was significantly higher in those randomised to the L14 acupoint compared to the BL32 acupoint (local to the gluteal injection site)—mean VAS 2.33 vs 1.76.

IMI techniques with inconsistent effects on injection pain

The evidence supporting the benefits of IMI techniques such as ‘ShotBlocker’ (2 studies), two-needle technique (2 studies), injection speed (2 studies), altering the temperature of the injecting needle (2 studies) and using the ventrogluteal or dorsogluteal sites for injection (2 studies), were inconsistent across studies (Table 3).

Çelik and Khorshid [20] reported a significant reduction in post injection pain with the use of the ‘ShotBlocker’ device (a plastic device used to apply local pressure to the skin) as an intervention in hospital inpatients who received an analgesic injection into the gluteal muscle (mean VAS 7.85 vs 20.3 vs 26.7, intervention vs placebo control vs non-placebo control respectively). However, a larger study (n = 242) by Emel et al. [35] did not find post injection pain to be reduced with use of a ‘ShotBlocker’ (mean VAS 33.8 vs 33.0, ‘ShotBlocker’ vs ‘No ShotBlocker’), although in this study patients received a smaller volume injection to the deltoid muscle. Both Çelik’s and Emel’s studies were RCTs.

Aǧaç and Güneş [29] found that a two-needle technique produced less pain compared to a one needle technique (mean VAS 5.53 vs 6.43) in an RCT involving a cohort of road traffic accident trauma patients. Those receiving the two-needle technique had the needle changed after drawing up the injectate and prior to the injection of the analgesic. In contrast, Rock [44] did not find a significant (p = 0.895) reduction in injection site pain when the two-needle technique was compared to a one-needle technique in quasi-experimental study of psychiatric out-patients receiving IMI of neuroleptics. Aǧaç and Güneş [29] and Rock [44] used the airlock and Z track injection technique respectively in both the intervention and control groups.

Slow injection (30 seconds) was found to be beneficial in reducing injection pain following injection of 1ml methylprednisolone at the gluteal site compared to a fast injection (10 seconds) [45]. In contrast, Tuǧrul and Khorshid [46] found that injection pain following IM injection of 800,000IU penicillin diluted with 2ml of sterile injectable water at a speed of 1ml/5s (fast injection) was similar to that of an injection speed of 1ml/10s regardless of whether the injection site was dorsogluteal or ventrogluteal.

In a RCT with factorial design study, Bartell et al. [47] randomised patients to receive influenza vaccination with either a cold (-20°C) or room temperature needle. The same participants were then randomised a second time to receive a saline injection with either a cold or room temperature needle. The mean pain score did not differ significantly between the two groups, regardless of the substance injected. However, in another RCT, IMI with a cold needle (-2 to 0°C) was associated with significantly reduced injection pain compared to injections with room temperature needles. This was a study with hospital outpatients with rheumatic heart disease receiving IMI of benzathine penicillin [48].

Participants in Yilmaz et al. [30] were randomised to receive analgesic injections into either dorsogluteal or ventrogluteal site, injections to the randomised injection sites being administered with and without the use of the airlock injection technique. The reported pain was similar at both injection sites regardless of the use of the airlock injection technique. This finding is in contrast with an earlier study by Güneş et al. [31] where injections to the right ventrogluteal muscle were associated with lower IMI pain compared to the left dorsogluteal muscle in patients receiving analgesic injections with the airlock injection technique.

Meta-analyses of studies

Meta-analyses of the studies using local pressure (manual pressure, Helfer skin tap, ShotBlocker, and post injection massage), acupressure, Z track IMI techniques, cold needle technique and the choice of gluteal muscle injection site were performed (Figs 37). Application of local pressure to the injection site (10 studies, SMD = -1.44 [95% CI -1.99,-0.89]) or to specific acupressure points—acupressure (4 studies, SMD = -1.62 [95% CI -2.80,-0.44]) were effective in reducing injection site pain (Figs 3 and 5). Although the direction of effect for most of the studies in these meta-analyses was consistent, there was considerable heterogeneity between the studies (I2 = 95% [92,97] and 96%[92,98] for local pressure to injection site and acupressure respectively). For gluteal injections administered with the airlock technique, use of the ventrogluteal injection site conferred some benefit on injection pain (2 studies, SMD = -0.43 [-0.81,-0.06]), and between study heterogeneity was low (I2 = 0%)—Fig 7. Both the Z track and cold needle IMI techniques reduced injection pain but did not reach statistical significance. For the Z track technique (2 studies, SMD = -0.20 [95% CI -0.41,0.01]), heterogeneity was low between studies (I2 = 0%)—Fig 4. However, for the cold needle technique (2 studies, SMD = -0.73 [95%CI -1.83,0.37]) heterogeneity was high between studies (I2 = 92% [72,98])—Fig 6.

Effect on pain of techniques applying local pressure to the IMI site.
Fig 3

Effect on pain of techniques applying local pressure to the IMI site.

*-Placebo control and non-placebo control arms combined.

Effect of Z track IMI technique on injection pain.
Fig 4

Effect of Z track IMI technique on injection pain.

Effect of acupressure IMI technique on injection pain.
Fig 5

Effect of acupressure IMI technique on injection pain.

*Combined estimates from acupressure to BL32 and L14 pressure points.

Effect of cold needle IMI technique on injection pain.
Fig 6

Effect of cold needle IMI technique on injection pain.

Effect of gluteal injection site on injection pain.
Fig 7

Effect of gluteal injection site on injection pain.

Intervention is ventrogluteal (VG) injection site and comparator is the dorsogluteal (DG) injection site. *- results of injection to either VG or DG site with airlock IMI technique.

Studies investigating the application of local pressure

Sub-group analyses to explore heterogeneity, and identify the effects of closely related IMI techniques and the type of study design on the pooled estimate were performed for studies investigating the application of local pressure.

A meta-regression on the differences between the type of pressure application and the effect size was not feasible owing to the relatively large number (four) of different techniques. However, as shown in Table 4, the pooled estimate for the ShotBlocker technique failed to reach statistical significance (2 studies, SMD = -0.51 [-1.58,0.56]). Application of manual pressure (4 studies; SMD = -0.85[-1.36,-0.33]) and Helfer skin tap (3 studies, SMD = -2.95 [-5.51,-0.39]) to the injection site were effective in reducing pain. Post-injection site massage reduced pain (SMD = -1.86 [-2.48,-1.24]) but this estimate was based on a single study.

Table 4
Sub-group analyses of IMI techniques applying pressure to the IMI site.
Meta-analysisNumber of studiesPooled SMD(95%CI)P valueHeterogeneity I2 (95%CI)
All pressure based studies10-1.44 (-1.99,-0.89)>0.00195% (92, 97)
Pressure techniques
    Manual pressure4-0.85 (-1.36,-0.33)0.00186% (65, 94)
    Helfer skin Tap3-2.95 (-5.51,-0.39)0.02498% (95, 99)
    ShotBlocker2-0.51 (-1.58,0.56)0.34796% (no estimate)
    Post injection massage1-1.86 (-2.48,-1.24)>0.001NA
Study design
    RCTs3-1.67 (-3.19,-0.14)0.03298% (96, 99)
    Quasi experimental7-1.36 (-1.94,-0.78)>0.00193% (87, 96)

NA—not assessed.

The study design (RCT vs quasi-experimental) did not affect the effect size (p = 0.842) when explored by a meta-regression (S1 Table), and the pooled estimate for RCTs (3 studies) and quasi-experimental studies (7 studies) were similar (SMD for RCTs = -1.67[-3.19,-0.14]; SMD for quasi-experimental studies = -1.36[-1.94, -0.78])—Table 4.

Asymmetry was observed in the funnel plot of the 10 studies investigating the application of local pressure to the injection site (Fig 8A). The asymmetry was further examined with a contour enhanced funnel plot and Egger’s meta-regression test for small study effect. Interventions from small studies were highly statistically significant (Fig 8B) and Egger’s test for small study bias was also statistically significant (coefficient of -9.09 [95%CI, -13.4, -4.78], p = 0.001).

Publication bias of meta-analysis of interventions applying pressure to injection site.
Fig 8

Publication bias of meta-analysis of interventions applying pressure to injection site.

(A) Funnel plots of studies (B) Contour enhanced funnel plot.

In S2 Table, sensitivity analyses were reported and the estimate of the intervention effect using a fixed effects meta-analysis for IMI techniques employing local pressure application differed considerably from the random effects estimate (fixed vs random effects SMD = - 0.74[-0.86,-0.63 vs 1.44[-1.99,-0.89]), reinforcing the likely bias from small studies in the meta-analysis. Because of this, four small studies [21, 22, 34, 39] (parallel studies with study size ≤ 100 and cross over studies with studies size ≤ 50) were excluded from a further meta-analysis of local pressure techniques resulting in the effect size estimate being reduced by 44% (All pressure studies vs large pressure studies only SMD = 1.44[-1.99,-0.89] vs—1.00[-1.56,-0.44]).

Studies investigating other IMI techniques

The Z track, acupressure, cold needle IMI technique and gluteal site injection meta-analyses lacked sufficient power to explore sub-group differences and biases. Only sensitivity analyses on the use of random effect and correlation in cross-over trials were explored.

The fixed and random effects estimates for the Z track were similar. The pooled estimates for the Z track technique were also similar regardless of the cross over design of included studies. Najafidolatbad et al. [27] was excluded from the meta-analysis of the Z track IMI intervention because the study compared two different techniques with no control arm. The inclusion of the Najafidolatbad et al. [27] study reversed the direction of the pooled estimate for the Z track IMI technique, indicating that the technique caused more pain than the comparator (with vs without Najafidolatbad et al. [27]; SMD = 0.22[-0.64,1.09] vs -0.20[-0.41,0.01]). The between study heterogeneity also increased by 93% points (S3 Table).

The fixed and random effects estimates, and the pooled estimates incorporating or ignoring the crossover design were similar in the meta-analysis of the acupressure technique (S4 Table).

For the cold needle technique, the estimate from the fixed effect analysis was significant (fixed vs random effects; SMD = -0.73[-1.04,-0.42] vs—0.73[-1.83,0.37]). This difference in the CIs around the estimate is associated with the smaller calculated standard error in the fixed effect model compared to the random effect model, however given the large heterogeneity between studies (I2 = 92%[72,98]), the fixed effect meta-analyses may be an overestimation of the true effect. The pooled estimates were however similar regardless of the cross over design of included studies (S5 Table).

The fixed and random effects estimates for the gluteal injection site meta-analyses (ventrogluteal vs dorsogluteal) were similar (S6 Table). However, the 95%CI around the estimate for the acupressure and gluteal injection site meta-analyses were narrower when the cross-over design was ignored.

Discussion

Overall, we identified a variety of intramuscular injection (IMI) techniques which reduce injection site pain amongst diverse patient groups and healthcare settings. We found some evidence supporting the use of manual pressure at the site of injection (4 studies, SMD = -0.85[-1.36,-0.33]) and the Helfer skin tap (3 studies, SMD = -2.96 [-5.51,-0.39]). Manual pressure involves sustained application of pressure for 10 seconds with the thumb/fingers [34] while the Helfer skin tap generally involves short repeated pressure application (tapping) with the thumb/fingers for several seconds to relax the muscle prior to injection [22, 51, 52], this may either be preceded [40] or followed by [51, 52] making a large ‘V’ with the thumb and index finger [51] before inserting the injection needle. However, the evidence supporting these techniques was mostly from small non-randomised studies, and pooled estimates were characterised by significant unexplained heterogeneity which may reflect variations in the patient population and/or study design.

There were contradictory findings for the efficacy of the ShotBlocker technique—another local pressure type technique—on injection pain. Emel et al. [35] found injection associated pain to be similar in both the ShotBlocker and control arm, in contrast to a beneficial effect reported by Çelik and Khorshid [20, 35]. It is possible that the inconsistency in findings relates to the larger study population, smaller injection volume and healthier patient group in the Emel et al. [35] study. Post injection massage was found to be beneficial in reducing injection pain in a single unblinded, quasi-experimental study of 30 participants [21] but further larger studies are required to confirm any benefit.

A meta-analysis combining the ten studies with interventions based on applying local pressure suggests that this approach may be beneficial in reducing injection pain (10 studies, SMD -1.44 [-1.99,-0.89]). However, the estimate was associated with substantial inter study heterogeneity (I2 = 95% [92,97]) and there is a risk of overestimating the effect size given the inclusion of multiple studies with a small sample size. The effectiveness of applying local pressure on the injection site is supported by the findings of a systematic review in children where stroking the skin or applying pressure close to the injection site reduced IM vaccination pain [14]. Mechanistically the benefits of applying local pressure to the injection site may be explained by the gate-control theory of pain which hypothesises that the stimulation of Aβ afferent nerve fibres (mechanoreceptors) inhibit transmission of nociceptive input (pain) to second-order neurons through gating at the substantia gelatinosa in the dorsal root ganglion of the spinal cord [53, 54]. Our analysis of local pressure based IMI techniques on injection site pain updates and expands that of a previous systematic review in adults [15], and suggests that larger RCTs are required to strengthen the evidence for its use in routine practice. The application of local pressure over the injection site is potentially easy to teach and implement, however, standardisation of the amount of pressure and duration of applied pressure is required.

The Z track technique has been widely recommended to reduce injection pain and drug leakage [2]. However, we found no evidence of the benefit of Z track on injection pain in the pooled estimates of 2 RCTs with low inter-study heterogeneity. Kara and Güneş [32] found a reduction in injection pain when the Z track technique was combined with positioning the patients in a prone position with ‘toes pointing down’ compared to the patient group in a prone position with ‘toes pointing down’ alone. However, this failed to reach statistical significance in our meta-analysis and the combined Z track technique with ‘toes pointing down’ was associated with more injection pain when compared to positioning the patient prone with an ‘internally rotated foot’ alone. Yilmaz et al. [36] also observed a reduction in IMI pain scores with the use of the Z track technique compared to standard IM technique, but again this failed to reach statistical significance in the primary analysis. There have been reported variations to performing the Z track technique in practice [55] and this may affect the observed effectiveness in different studies. It is possible that recommendations to use the Z track technique may have arisen from evidence gathered from descriptive studies and personal viewpoints [2]

Najafidolatbad et al. [27] found the airlock technique to be significantly more beneficial in reducing injection pain compared to the Z track IMI technique. The airlock technique is based on a similar principle to the Z track, where preventing drug leakage might reduce the risk of pain on injection. At present the benefits of the airlock method remain limited and the addition of an air bubble into the syringe may make delivering the correct volume of drug more difficult [56].

Some recommendations have been made in support of the ventrogluteal site over the dorsogluteal site with respect to injection pain and injection complications [12]. However, we found conflicting evidence for the use of the ventrogluteal site as an intervention to reduce injection pain. Yilmaz et al. [30] investigated the influence of using the dorso or ventrogluteal site on injection pain when combined with the airlock technique, and found a non-significant reduction of pain scores in those randomised to the ventrogluteal site compared to the dorsogluteal site. This trend was also observed when injections were administered without the airlock technique. Güneş et al. [31] found that injections administered with the airlock techniques were significantly less painful when given at the ventrogluteal site compared to the dorsogluteal site. Combining these studies in a meta-analysis suggest that the ventrogluteal site may be a better injection site when considering injection pain (2 studies, SMD, -0.43 [-0.81; -0.06]), but more studies are required to support this possibility.

The use of the acupressure technique was found to significantly reduce injection pain, especially when the acupressure point (UB31/UB32/BL32) was close to the injection site [4143], in which case the acupressure procedure becomes similar to the other manual pressure interventions–local injection site pressure and the Helfer skin tapping technique. The acupressure technique involves sustained application of pressure to the acupoint for 1 minute followed by short repeated application of pressure two to three times prior to injection [19, 41]. When the application of pressure was to an acupressure point site not local to the injection site, it did not appear to be effective [19]. The pooled estimate from the meta-analysis of acupressure was associated with significant heterogeneity, possibly reflecting variation in how the technique is delivered, study design and/or patient groups.

There was contradictory evidence on the benefits of the two-needle technique over the one needle technique. Aǧaç and Güneş [29] found the two-needle technique to be beneficial in reducing injection site pain, but the use of the two-needle or one-needle technique was combined with an additional intervention, the airlock technique. Rock [44] combined either two-needle or one-needle technique with Z track and did not find any significant benefit with the two-needle technique. However, since the airlock technique was found to reduce injection pain when compared to the Z track technique in a separate RCT [27], and there were differences in study design and patient groups of the Aǧaç and Güneş [29] and Rock [44] studies (Table 1), the benefit of changing the needle prior injection remains unclear.

The evidence for using a fast or slow injection speed is also unclear, owing to the differences in the design of the two relevant studies. Tuǧrul and Korshid [46] found that injection pain following IM injection of procaine penicillin diluted with 2ml of sterile water at speeds of 1ml/5s and 1ml/10s was similar, regardless of whether the injection site was dorsogluteal or ventrogluteal. However, Ozdemir et al. [45] found that a methylprednisolone injection diluted with 1ml sterile water injected over 10seconds was significantly more painful than administering the same injection over 30 seconds at the gluteal site. Both studies were small crossover quasi-experimental studies.

Using a cold needle for the injection procedure reduced injection pain compared to the use of room temperature needle, but this was not found to be statistically significant when the data from studies were pooled (Fig 6). Bartell et al. [47] found no significant benefit on injection pain when the cold needle (-20°C) was used in administering vaccines to the deltoid muscle in healthy volunteers and this was also the case when saline was administered, although saline injections were generally less painful compared to vaccines. In contrast, Thomas et al. [48] found the cold needle (0–2°C) technique to be significantly beneficial in reducing injection pain following benzathine penicillin injection. It is possible that the variation in temperature of the needles, the injection site or difference in substance injected may influence the benefit of the cold needle technique. More studies are warranted to confirm the benefits of the cold needle technique.

Other studies explored IMI techniques related to modifying the temperature of injectate [49] or injection site [50]. Warming the injectate to ~27 to 29°C did not alter the severity of injection pain [49]. However, Farhadi and Esmailzadeh [50] found that cooling the injection site with ice for 30 seconds prior to injection, significantly reduced pain. This may relate to the potential benefit of ice-therapy on pain following soft tissue (including muscular) injury [57] but, further studies are required to substantiate this.

Our systematic review and meta-analysis provides updates on the evidence on intramuscular injection techniques beyond the systematic review of Şanlialp et al. [15]. We identified additional evidence on the manual pressure, Z track, ShotBlocker, and acupressure techniques and report on other IMI techniques including the Helfer Skin tap, application of ice to injection site, and altering the temperature of the injectate. Şanlialp et al. [15] found the ventrogluteal site, Z track technique, and manual pressure to be the most effective IMI techniques in reducing injection pain, but also found that the two-needle technique, post injection massage and ShotBlocker IMI techniques were beneficial in reducing injection pain. The benefits of the manual pressure technique and post injection massage are similar to our assessment, however, our findings on ShotBlocker, acupressure, two-needle technique and Z track are in contrast to the findings of Şanlialp et al. [15]. We identified more studies on the acupressure and ShotBlocker IMI techniques which have influenced our assessments of these techniques. However, both our study and Şanlialp et al. [15] assessed the same evidence on the two-needle and the Z track technique. In Şanlialp et al. [15], the data from the Rock [44] study was transformed, and the two-needle technique was reported to be significantly beneficial in reducing IMI pain, in contrast to the primary findings. Similarly the data from Najafidolatabad et al. [27] was transformed in Şanlialp et al. [15] and the Z track intervention reported to be significantly beneficial in reducing injection pain compared to the air-lock method, again conflicting with the report of the original study. It is likely that the difference in the number of included studies, methodological differences in combining studies for meta-analysis and interpretation of the direction of effect between our study and that of Şanlialp et al. [15] have account for the difference in our inferences.

A risk of bias assessment found poor reporting of essential design elements including blinding and randomisation in most of the identified RCTs. The risk of bias for the non-randomised studies was moderate in the majority of studies. None of the included experimental studies carried out baseline assessment of pain prior to IMI or commented on how patients receiving an IMI for pain relief might interpret injection pain differently to those who were healthy volunteers and presumed to be pain free. The outcome measures, although similar, differed in their precise wording and how they were delivered across studies. This lack of consistency is potentially important when making comparisons between studies particularly for a subjective outcome measure such as pain. We also identified marked variation in standard IM injection practice—for example, the standard technique in Ozturk et al. [28] involved a two needle technique, for Kara and Güneş [32] it included a two-needle technique, airlock technique, aspiration and injection speed of lml /10sec, and Yilmaz et al. [36] included the airlock technique. This may reflect a non-standard approach in how clinicians are initially taught or subsequently learn about IMI technique.

The review has a number of limitations. First, the search terms chosen were based on scoping searches and prior knowledge of the literature on IMI. The use of additional search terms may have increased the number of records returned, but would have made the number of records requiring review unfeasible and was considered unlikely to identify other highly relevant studies. Searches were limited to the main bibliographic databases and citation searching, without review of potential grey literature. The meta-analyses combined data across studies in order to estimate effect size with more precision than is possible in a single study. The patient population, IMI techniques and outcome measures were not identical across studies and therefore caution is required in the meta-analysis interpretation. Publication bias might account for some of the effect we observed. Smaller trials are, in general, analysed with less methodological rigor than larger studies [58], and an asymmetrical funnel plot suggests that selective reporting may have led to an overestimation of effect size in small trials. However, our assessment is restricted to 10 studies, and publication bias assessment can be limited when evaluating a small number of studies [59]. We also performed a meta-regression on the influence of the experimental design of the studies on local pressure IMI techniques (10 studies), and it is possible that we did not have sufficient power to detect an association between study design and effect size, however, the sub-group analysis shows that the estimates from the combined RCT or quasi-experimental studies were similar in both direction and level of significance (Table 4).

Our review would support future research to further explore whether local pressure based IMI techniques, in combination or individually, can reduce IMI pain. The existing evidence is based on small sample sizes (for instance, n = 340 [manual pressure] and n = 242, [Helfer skin tap]) with a significant risk of bias, and larger randomised controlled trials are therefore warranted.

In conclusion, the current evidence suggests that the application of local pressure, especially manual pressure and/or rhythmic tapping of the injection site prior to injection may be beneficial in reducing IMI pain, but any conclusions are limited by small study sizes, non-standardised interventions, imprecise control groups and wide inter-study heterogeneity.

References

World Health Organization. WHO guideline on the use of safety-engineered syringes for intramuscular, intradermal and subcutaneous injections in health care settings. 2016.

DWynaden, ILandsborough, RChapman. Establishing best practice guidelines for administration of intra muscular injections in the adult: a systematic review of the literature. Contemporary Nurse: A Journal for the Australian Nursing Profession. 2005;20(2):26777. 10.5172/conu.20.2.267 . Language: English. Entry Date: 20060505. Revision Date: 20150820. Publication Type: Journal Article.

DJGreenblatt, MAllen. Intramuscular injection-site complications. JAMA. 1978;240(6):5424. 10.1001/jama.1978.03290060044011

LHNicoll, AHesby. Intramuscular injection: An integrative research review and guideline for evidence-based practice. Applied Nursing Research. 2002;15(3):14962. 10.1053/apnr.2002.34142

SKBardal, JEWaechter, DSMartin. Chapter 2—Pharmacokinetics. In: SKBardal, JEWaechter, DSMartin, editors. Applied Pharmacology. Philadelphia: Content Repository Only!; 2011. p. 1734. 10.1016/j.cbpa.2011.05.033

M.Shatsky Evidence for the use of intramuscular injections in outpatient practice. American family physician. 79(4):297.

GABrazeau, BCooper, KASvetic, CLSmith, PGupta. Current perspectives on pain upon injection of drugs. Journal of Pharmaceutical Sciences. 2000;87(6):66777. 10.1021/js970315l

HSMarshall, MFClarke, SEvans, LPiotto, RJGent. Randomized trial using ultrasound to assess intramuscular vaccination at a 60° or 90° needle angle. Vaccine. 2013;31(23):264752. 10.1016/j.vaccine.2013.03.037

OAyinde, JDCRoss. Factors associated with severity and resolution of intramuscular injection site pain following treatment for uncomplicated gonorrhoea: a prospective cohort study of GToG trial participants. Sexual Health. 2020;17(3):25561. 10.1071/SH19176

10 

YNir, APaz, ESabo, IPotasman. Fear of injections in young adults: prevalence and associations. Am J Trop Med Hyg. 2003;68(3):3414. Epub 2003/04/11. .

11 

KEBoerner, KABirnie, CTChambers, ATaddio, CMMcMurtry, MNoel, et al. Simple Psychological Interventions for Reducing Pain From Common Needle Procedures in Adults: Systematic Review of Randomized and Quasi-Randomized Controlled Trials. The Clinical journal of pain. 2015;31:S90S8. 10.1097/AJP.0000000000000270 00002508-201510001-00009.

12 

S.Ogston-Tuck Intramuscular injection technique: an evidence-based approach. Nursing standard (Royal College of Nursing (Great Britain): 1987). 2014;29(4):529. 10.7748/ns.29.4.52.e9183.

13 

VShah, ATaddio, CMMcMurtry, SAHalperin, MNoel, RPillai Riddell, et al. Pharmacological and Combined Interventions to Reduce Vaccine Injection Pain in Children and Adults: Systematic Review and Meta-Analysis. The Clinical journal of pain. 2015;31(10 Suppl):S38S63. Epub 2015/09/17. 10.1097/AJP.0000000000000281 .

14 

ATaddio, ALIlersich, MIpp, AKikuta, VShah. Physical interventions and injection techniques for reducing injection pain during routine childhood immunizations: Systematic review of randomized controlled trials and quasi-randomized controlled trials. Clinical Therapeutics. 2009;31:S48S76. 10.1016/j.clinthera.2009.07.024

15 

AŞanlialp Zeyrek, ŞTakmak, NKKurban, SArslan. Systematic review and meta-analysis: Physical-procedural interventions used to reduce pain during intramuscular injections in adults. Journal of advanced nursing. 0(0). 10.1111/jan.14183

16 

SHDowns, NBlack. The feasibility of creating a checklist for the assessment of the methodological quality both of randomised and non-randomised studies of health care interventions. Journal of epidemiology and community health. 1998;52(6):37784. Epub 1998/10/09. 10.1136/jech.52.6.377

17 

JASterne, MAHernán, BCReeves, JSavović, NDBerkman, MViswanathan, et al. ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ. 2016;355:i4919. 10.1136/bmj.i4919

18 

PWhiting, JSavović, JPTHiggins, DMCaldwell, BCReeves, BShea, et al. ROBIS: A new tool to assess risk of bias in systematic reviews was developed. J Clin Epidemiol. 2016;69:22534. Epub 06/16. 10.1016/j.jclinepi.2015.06.005 .

19 

YRaddadi, MAdib-Hajbaghery, ZGhadirzadeh, DKheirkhah. Comparing the effects of acupressure at LI4 and BL32 points on intramuscular injection pain. European Journal of Integrative Medicine. 2017;11:638. 10.1016/j.eujim.2017.01.015.

20 

NÇelik, LKhorshid. The Use of ShotBlocker for Reducing the Pain and Anxiety Associated With Intramuscular Injection: A Randomized, Placebo Controlled Study. Holistic Nursing Practice. 2015;29(5):26171. 10.1097/HNP.0000000000000105

21 

HKKanika, PSRani. Effect of massage on pain perception after administration of Intramuscular Injection among adult patients. Nursing Research & Midwifery Journal. 2011;7(3):1308.

22 

RKhanra S Asokan, Lenka A. Helfer Skin Tap Technique on Pain Associated With Intramuscular Injection among Adult Patients. International Journal of Nursing Education. 2018;10(3):127. 10.5958/0974-9357.2018.00058.2 . Language: English. Entry Date: 20181006. Revision Date: 20181204. Publication Type: Article. Journal Subset: Continental Europe.

23 

DRElbourne, DGAltman, JPHiggins, FCurtin, HVWorthington, AVail. Meta-analyses involving cross-over trials: methodological issues. International Journal of Epidemiology. 2002;31(1):1409. 10.1093/ije/31.1.140

24 

ALJennings, ANDavies, JPTHiggins, JAnzures‐Cabrera, KEBroadley. Opioids for the palliation of breathlessness in advanced disease and terminal illness. The Cochrane database of systematic reviews. 2001;(3). 10.1002/14651858.CD002066 CD002066.

25 

JPTHiggins, SGreen. Cochrane Handbook for Systematic Reviews of Interventions 2011.

26 

JPHiggins, SGThompson. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):153958. Epub 2002/07/12. 10.1002/sim.1186 .

27 

SNajafidolatabad, JMalekzadeh, ZMohebbinovbandegani. Comparison of the pain severity, drug leakage and ecchymosis rates caused by the application on tramadol intramuscular injection in Z-track and air-lock techniques. Investigacion & Educacion en Enfermeria. 2010;28(2):1715. . Language: English. Entry Date: 20110114. Revision Date: 20170831. Publication Type: Journal Article.

28 

DOzturk, ZGBaykara, AKaradag, EEyikara. The effect of the application of manual pressure before the administration of intramuscular injections on students’ perceptions of postinjection pain: a semi-experimental study. Journal of clinical nursing. 2017;26(11–12):16328. 10.1111/jocn.13530

29 

EAgac, UYGunes. Effect on pain of changing the needle prior to administering medicine intramuscularly: a randomized controlled trial. Journal of advanced nursing. 2011;67(3):5638. 10.1111/j.1365-2648.2010.05513.x .

30 

DKYilmaz, YDikmen, FKokturk, YDedeoglu. The effect of air-lock technique on pain at the site of intramuscular injection. Saudi medical journal. 2016;37(3):3048. 10.15537/smj.2016.3.13113

31 

ÜGüneş, DKara Yılmaz, SArı, OCeyhan. Which site is more painful in intramuscular injections? The dorsogluteal site or the ventrogluteal site? A case study from Turkey. Clinical Nursing Studies. 2013;1. 10.5430/cns.v1n4p74

32 

DKara, UYapucu Gunes. The effect on pain of three different methods of intramuscular injection: A randomized controlled trial. International journal of nursing practice. 2016;22(2):1529. 10.1111/ijn.12358

33 

EAgac, UYGunes. Effect on pain of changing the needle prior to administering medicine intramuscularly: a randomized controlled trial. Journal of advanced nursing. 2011;67(3):5638. 10.1111/j.1365-2648.2010.05513.x

34 

BJBarnhill, MDHolbert, NMJackson, RSErickson. Using pressure to decrease the pain of intramuscular injections. Journal of pain and symptom management. 1996;12(1):528. 10.1016/0885-3924(96)00049-8

35 

TEmel, CNese, KLeyla. Effects of ShotBlocker on Relief of Pain Due to Hepatitis B Vaccine Injection into Deltoid Muscle. International Journal of Caring Sciences. 2017;10(3):166975. . Language: English. Entry Date: 20180227. Revision Date: 20180618. Publication Type: Article.

36 

DYilmaz, LKhorshid, YDedeoglu. The Effect of the Z-Track Technique on Pain and Drug Leakage in Intramuscular Injections. Clinical nurse specialist CNS. 2016;30(6):E7E12. 10.1097/NUR.0000000000000245

37 

MFKeen. Comparison of intramuscular injection techniques to reduce site discomfort and lesions. Nursing research. 1986;35(4):20710.

38 

JWYChung, WMYNg, TKSWong. An experimental study on the use of manual pressure to reduce pain in intramuscular injections. Journal of Clinical Nursing. 2002;11(4):45761. 10.1046/j.1365-2702.2002.00645.x

39 

GZore, RDias. Effectiveness of Nursing Interventions on Pain Associated With Intramuscular Injection. International Journal of Science and Research. 2014;3(6):19952000.

40 

AAHassnein, HMMSoliman. Efficacy of Helfer Skin Tapping Technique on Pain Intensity as perceived by the patients receiving Intramuscular Injection. International Journal of Nursing Didactics. 2016;6:12. 10.15520/ijnd.2016.vol6.iss2.135.12–22

41 

NMAlavi. Effectiveness of acupressure to reduce pain in intramuscular injections. Acute Pain. 2007;9(4):2015. 10.1016/j.acpain.2007.09.002

42 

ZSuhrabi, HTaghinejad. Effect of acupressure (UB32) on pain intensity in intramuscular injections. Iranian journal of nursing and midwifery research. 2014;19(1):247. .

43 

SSNajafi, SNazaribin, MMomennasab, AKordi Yoosefinejad. The Effect of Manual Acupressure (Point UB32) on Pain Associated with Intramuscular Injections of Magnesium Sulfate. JAMS Journal of Acupuncture and Meridian Studies. 2018. 10.1016/j.jams.2018.07.002.

44 

D.Rock Does drawing up technique influence patients’ perception of pain at the injection site? The Australian and New Zealand journal of mental health nursing. 2000;9:14751. 10.1046/j.1440-0979.2000.00176.x

45 

LOzdemir, EPιnarcι, BNAkay, AAkyol. Effect of Methylprednisolone Injection Speed on the Perception of Intramuscular Injection Pain. Pain Management Nursing. 2013;14(1):310. 10.1016/j.pmn.2010.03.002

46 

ETuğrul, LKhorshıd. Effect on pain intensity of injection sites and speed of injection associated with intramuscular penicillin. International Journal of Nursing Practice. 2014;20(5):46874. 10.1111/ijn.12161

47 

JCBartell, KARoberts, NJSchutte, KCSherman, DMuller, MSHayney. Needle temperature effect on pain ratings after injection. The Clinical journal of pain. 2008;24(3):2604. 10.1097/AJP.0b013e31816111c0 .

48 

NThomas, RAndrews, SKaur, RJuneja, ASaxena. Needle temperature and pain perception in the treatment of rheumatic heart disease. British Journal of Cardiac Nursing. 2019;14(3):1348. 10.12968/bjca.2019.14.3.134

49 

MMaiden, GBenton, RBourne. Effect of warming adult diphtheria-tetanus vaccine on discomfort after injection: A randomised controlled trial. The Medical journal of Australia. 2003;178:4336. 10.5694/j.1326-5377.2003.tb05284.x

50 

AFarhadi, MEsmailzadeh. Effect of local cold on intensity of pain due to Penicillin Benzathin intramuscular injection. International Journal of Medicine and Medical Sciences. 2011;3(11):3435.

51 

SShah, ANarayanan. Effect of Helfer Rhythmic skin tap technique on procedural pain among patients receiving intramuscular injection. Manipal Journal of Nursing and Health Sciences. 2016;2(1):39.

52 

J.Helfer Painless injections: Heifer Skin Tap Technique. Nurse educator. 2000;25:2723.

53 

RMelzack, PDWall. Pain Mechanisms: A New Theory. Science. 1965;150(3699):971. 10.1126/science.150.3699.971

54 

FJRopero Peláez, STaniguchi. The Gate Theory of Pain Revisited: Modeling Different Pain Conditions with a Parsimonious Neurocomputational Model. Neural Plasticity. 2016;2016:4131395. 10.1155/2016/4131395

55 

PStrohfus, OPaugh, CTindell, PShaver. Evidence calls for practice change in intramuscular injection techniques. Journal of Nursing Education and Practice. 2017;8:83. 10.5430/jnep.v8n2p83

56 

MARodger, LKing. Drawing up and administering intramuscular injections: a review of the literature. Journal of advanced nursing. 2000;31(3):57482. Epub 2000/03/16. 10.1046/j.1365-2648.2000.01312.x .

57 

DCMAuley. Ice Therapy: How Good is the Evidence? Int J Sports Med. 2001;22(05):37984. 10.1055/s-2001-15656

58 

MEgger, GDavey Smith, MSchneider, CMinder. Bias in Meta-Analysis Detected by a Simple, Graphical Test. BMJ. 1997;315:629. 10.1136/bmj.315.7109.629

59 

JASterne, DGavaghan, MEgger. Publication and related bias in meta-analysis: power of statistical tests and prevalence in the literature. J Clin Epidemiol. 2000;53(11):111929. Epub 2000/12/07. 10.1016/s0895-4356(00)00242-0 .