ArticlePDF Available

EMLA Cream vs 10% Lidocaine Cream for Attenuating Venous Cannulation Pain – A Clinical Trial

Authors:
  • University of Lagos

Abstract and Figures

Background: Venous cannulation is a painful procedure that is associated with anxiety, distress and discomfort. But pain is frequently overlooked in adults. Aims and Objective: We compared the efficacy of 5% EMLA cream and 10% lidocaine cream in attenuating pain associated with peripheral venous cannulation. Methods: This prospective, randomized, placebo-controlled trial was conducted in 102 ASA I and II adults scheduled for elective surgery. They were randomly allocated by blind balloting to one of three groups: group E had 1.5 mL of EMLA cream, group L 1.5 mL of 10% lidocaine cream, and group P 1.5 mL KY gel. All cream was applied over a visible vein for 60 min with occlusive dressing. Pain was evaluated using visual analogue scale (VAS) and verbal rating scale (VRS). Results: The mean VAS score was significantly lower with either EMLA cream (2.62±1.76 cm) or 10% lidocaine cream (1.85±1.58 cm) than with placebo (4.78 ±1.88 cm), p
Content may be subject to copyright.
The ANNALS of AFRICAN SURGERY January 2019 Volume 16 Issue 1
4
EMLA Cream vs 10% Lidocaine Cream for Attenuating Venous
Cannulation Pain – A Clinical Trial
Oluwayemisi Bamidele Oluwadun,1 Oyebola Olubodun Adekola,2 Olufemi I.O. Dada,2 Simeon O. Olanipekun,1
Adebayo Sulaimon Adetunji,3 John Olutola Olatosi,2 Olushola Temitayo Kushimo2
1 Department of Anaesthesia, EKO Hospital, Lagos, Nigeria
2 Department of Anaesthesia, University of Lagos & Lagos University Teaching Hospital, Nigeria
3 Department of Anaesthesia, Lagos State University Teaching Hospital, Nigeria
Correspondence to: Dr OB Ogundun, Department of Anaesthesia, Eko Hospital, Ikeja, Lagos, Nigeria; email: gyogundun@yahoo.co.uk
Abstract
Background: Venous cannulation is a painful procedure
that is associated with anxiety, distress and discomfort.
But pain is frequently overlooked in adults. Aims and
Objective: We compared the ecacy of 5% EMLA cream
and 10% lidocaine cream in attenuating pain associated with
peripheral venous cannulation. Methods: This prospective,
randomized, placebo-controlled trial was conducted in
102 ASA I and II adults scheduled for elective surgery.
They were randomly allocated by blind balloting to one
of three groups: group E had 1.5 mL of EMLA cream,
group L 1.5 mL of 10% lidocaine cream, and group P 1.5
mL KY gel. All cream was applied over a visible vein for
60 min with occlusive dressing. Pain was evaluated using
visual analogue scale (VAS) and verbal rating scale (VRS).
Results: The mean VAS score was signicantly lower with
either EMLA cream (2.62±1.76 cm) or 10% lidocaine cream
(1.85±1.58 cm) than with placebo (4.78 ±1.88 cm), p<0.001.
Most patients who received EMLA cream (76.5%) or 10%
lidocaine cream (70.6%) compared with placebo (55.9%)
had mild pain during cannulation using VRS. Conclusion:
The eutectic mixture of local anesthetic cream and lidocaine
cream attenuated pain associated with peripheral venous
cannulation to varying degrees.
Key words: Venous cannulation pain, 10% lidocaine,
EMLA, VAS, VRS, Side eects
Ann Afr Surg. 2019; 16(1):4–10
DOI: http://dx.doi.org/10.4314/aas.v16i1.2
Conicts of Interest: None
Funding: None
© 2019 Author. This work is licensed under the Creative
Commons Attribution 4.0 International License.
Introduction
Crile Washington invented the cannula and used intravenous
therapy for the management of shock; this management
popularized venous cannulation (1). Peripheral venous
cannulation is a routine procedure during the delivery of
anesthesia, which many adults nd painful. Inadequate
pain relief is not only unpleasant for patients but may cause
anxiety about further treatment, deter patients from seeking
medical care in the future (2), and result in increase in
heart rate and blood pressure (3). The increase in heart rate
and blood pressure leads to increased myocardial oxygen
consumption and increased risk of myocardial infarction
in patients at risk, especially those with hypertension and
coronary artery disease (4). The use of topical anesthetic
agents for venous cannulation is on the increase (5). In
our institution, analgesia for cannulation is oered only
to children. We compared the ecacy of topical 5%
EMLA cream and 10% lidocaine cream in attenuating pain
associated with peripheral venous cannulation in adults.
Methods
This prospective, randomized, placebo-controlled study
was conducted between April 2013 and March 2014 after
institutional approval and informed consent were obtained
from all patients. Adult patients aged 18–60 years, with
the American Society of Anesthesiology (ASA) physical
status score I or II, scheduled for elective procedures under
anesthesia were studied. Criteria for exclusion were: refusal
to participate, past history of hypertension, arrhythmias,
chronic pain, and local skin infection, those on antiarrhytmic
agents such as calcium channel blockers and beta blockers,
analgesic use 24 hours before venous cannulation, allergy
or sensitivity to amide local anesthetic and glycerine, and
more than one attempt at cannulation. Power was analysed
for independent t test to determine an appropriate sample
size; the dierence in mean of the visual analogue scale
during venepuncture from a previous study was 13.3 (6). To
achieve a power of 80% and α = 0.05, a minimum sample
size of 34 was considered appropriate.
Original article
www.annalsofafricansurgery.com
AttenuAting venous cAnulAtion pAin—A clinicAl triAl
5
Study protocol
Routine preoperative anesthetic was review the day before
surgery. The study protocol was explained to the patients
and they were educated on the use of the visual analogue
scale (VAS) and verbal rating scale (VRS) that were used
to assess pain. The primary outcome compared the eects
of 10% lidocaine cream and of EMLA cream on VAS and
VRS. The secondary outcome compared the eects of 10%
lidocaine cream and of EMLA cream on the heart rate, blood
pressure and cutaneous skin manifestation.
In the operating theatre, the researcher randomly placed the
patients into three groups; each patient picked a prewritten
card from a bag. Group E treatment consisted of EMLA
cream, Group L 10% lidocaine cream and Group P used KY
gel; the placebo cream (KY gel) is reported not to have an
analgesic eect (7). The patients and research assistant were
blinded to the cream used. A multiparameter monitor was
attached to the patient to measure heart rate, non-invasive
blood pressure and oxygen saturation before and during
cannulation. The proposed cannulation site was cleaned
with alcohol swab, and the research assistant applied 1.5 mL
of the appropriate cream over the dorsum of the patient’s
hand. Next, an improvised occlusive dressing made of 4 by
4 gauze was applied and held in place with plaster for 60
min. The gauze was removed after 60 min and the researcher
assessed skin sensations such as itching, burning, tingling
and cold, after which the cream was removed gently using
a methylated spirit swab.
For uniformity, the researcher performed venous cannulation
using an 18G cannula on all patients, and the cannula was
secured with transparent plaster. Each patient’s reaction
during cannulation was noted by a second research assistant
and reported as expressionless, grimacing, hand withdrawal,
shouting or crying. Each patient was observed for features
of vaso-vagal reaction such as dizziness, light headedness,
sweating, or nausea.
Each patient was then asked to grade the cannulation pain
on the VAS, a 10-cm line marked 0 at one end and 10 at the
other (0 = no pain; 10 = worst pain imaginable). Assessments
of pain on the linear scale were measured to the nearest
centimeter. Each patient also assessed pain using the VRS
as none, mild, moderate, and severe.
Each patient’s immediate post-cannulation heart rate and
blood pressure were measured once the cannula was secured
with transparent plaster, then at every 1-minute interval for
10 minutes: before cannulation (baseline)-TB, immediate
post cannulation (T0), 1 min after cannulation (T1), 2 min
after cannulation (T2), 3 min after cannulation (T3), 4 min
after cannulation (T4), 5 min after cannulation (T5), 6 min
after cannulation (T6), 7 min after cannulation (T7), 8 min
after cannulation (T8), 9 min after cannulation (T9), and 10
min after cannulation (T10).
The cannulation site was continuously observed for local skin
reactions such as blanching, erythema, localized induration,
edema and urticaria hourly for the rst 2 hours and then at
6 hours, 12 hours, and 24 hours post cannulation. Allergic
reactions, if any, were noted and treated with standard rescue
measures.
Statistical analysis
Demographic, blood pressure, heart rate and visual analogue
scores were analyzed using analysis of variance, while
clinical data and VRS were analyzed with test of proportions
and Chi-square test; p <0.05 was considered statistically
signicant. Data obtained were analyzed using the Statistical
Package for Social Sciences (SPSS) Version 21 (SPSS Inc.,
Chicago, IL, USA).
Results
A total of 102 adult surgical patients were recruited. The
mean age, weight, height and BMI were comparable between
the 3 groups (Table 1).
Table 1: Demographic and clinical characteristics of patients
(n = 34 for each group)
Treatment groups
Variable EMLA Lidocaine Placebo p value
Age/years
(mean±SD)32.4±10.0 35.9± 9.2 35.4±9.3 0.27
Weight/kg
(mean±SD) 75.1±9.67 73.5±14.6 74±13.6 0.88
Height (m) 1.7±0.77 1.65±0.07 1.6±0.03 0.79
BMI (kg/m2) 27.8±3.4 27.1±6.2 27.6±5.1 0.83
Gender ratio
(M:F) 13:21 20:14 8:26 0.26
ASA (ratio
I:II) 19:15 20:14 24:10 0.23
Pain scores
The median VAS score at venous cannulation diered
signicantly between the three groups: group E 2 (0–8),
group L 2 (0–5) and group P 5 (1–8), p <0.001. VAS score
between groups E and L was similar, p = 0.45. On distribution
of pain between the group using VRS, more patients with
pain were in group P (34) than in groups E (32) and L (26),
p <0.001; pain distribution was similar between groups E
and L, p = 0.45.
The ANNALS of AFRICAN SURGERY January 2019 Volume 16 Issue 1
6
Reactions during cannulation
Table 2 shows the frequency distribution of patients with
dierent reactions to cannulation. In group E, 13(38.2%)
patients were expressionless during cannulation while
19(55.9%) grimaced. In group L, more than half of the
patients 18(52.9%) were expressionless while 14(41.2%)
grimaced. In group P, 6(17.6%) of the patients were
expressionless and 16(47.1%) grimaced. The dierence
in reactions during cannulation across the 3 groups was
statistically signicant, p=0.003.
Table 2: Mean visual analogue scale scores in the three groups
(n = 34 for each group)
EMLA Lidocaine Placebo p value
Mean±SD 2.6±1.8 1.9±1.5 4.8±1.9 0.001*
Median 2.0 2.0 5.0
* statistically signicant
Heart rate
Figure 1 shows the mean heart rates against time in the
dierent groups. The mean heart
rate in group E rose from baseline
value at T0. The mean heart rate
at T3 min fell below baseline and
remained steady below baseline
value throughout the study period.
In group L, mean heart rate fell
below baseline value immediate
post cannulation (T0) and remained
below baseline value till the end of
the study. The lowest value in heart
rate in group L was at T4. The mean
heart rate in the placebo group rose
above baseline value and remained
above baseline value throughout the
study period.
Figure 2 shows percentage changes
in mean heart rates from baseline
values with time. In groups E and
P, a rise of 1.78% and 7.17% was
observed when baseline values were
compared with immediate post-
cannulation values (T0). Group
L demonstrated a fall of –0.72%
from baseline values at (T0). The
placebo group demonstrated the
highest change with a 7.17% rise
from baseline values. Signicant
differences were observed in
percentage changes in mean HR from baseline values
between the groups during the study except at T8, p=0.10.
Mean arterial pressure
Figure 3 shows the mean arterial pressure (MAP) against
time. MAP decreased in all the groups at T3 with that of the
treatment groups dropping below baseline values. Figure 4
shows the mean percentage change in mean arterial pressure
from baseline values over the study period. MAP increased
in all the 3 groups immediate post cannulation (T0). The
increases from baseline values were 2.92%, 2.10% and
6.01% in groups E, L and P respectively. These changes
were not statistically signicant, p=0.39. Throughout the
study period there was no statistical dierence between the
3 groups when considering percentage change in MAP from
baseline values.
Mean rate pressure product
Figure 5 shows the mean rate pressure product over the
study period. Statistical dierence was observed only at T3,
olAwudAn et Al.
Figure 1: Mean heart rate (bpm) at different time points
TB
0
–2
–4
2
4
6
8
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
% change from baseline
T5 T6 T7 T8 T9 T10
TB
74
76
78
80
82
84
86
88
90
94
92
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
Mean heart rate (mmHg beats/minute)
T5 T6 T7 T8 T9 T10
TB
85
87
89
91
93
95
97
99
101
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
Mean MAP (mmHg)
T5 T6 T7 T8 T9 T10
Figure 2: Percentage change in mean heart rate from baseline
TB
0
–2
–4
2
4
6
8
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
% change from baseline
T5 T6 T7 T8 T9 T10
TB
74
76
78
80
82
84
86
88
90
94
92
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
Mean heart rate (mmHg beats/minute)
T5 T6 T7 T8 T9 T10
TB
85
87
89
91
93
95
97
99
101
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
Mean MAP (mmHg)
T5 T6 T7 T8 T9 T10
www.annalsofafricansurgery.com
AttenuAting venous cAnulAtion pAin—A clinicAl triAl
7
p=0.01. Group P showed the highest rise of 12,365 mmHg.
beat.min–1 in the immediate post cannulation period while
the least rise was in the EMLA group at 5,997.1 mmHg.
beat.min–1 at T7 post cannulation.
Side effects
In group E, 1 patient (2.9%) had burning skin sensation; in
group L, 2 patients (5.9%) had burning skin sensation and
1 patient (2.9%) tingling sensation. In assessing local skin
reactions in all 3 groups, 1 patient (2.9%) in each group
was observed to have blanching
of the skin when treatment
creams ceased. Blanching was
no longer observed 1 hour post
cannulation.
Discussion
We have demonstrated
that VAS was lower after
application of EMLA and
10% lidocaine cream 60 min
before venous cannulation than
after application of KY gel.
However, VAS was comparable
with EMLA and 10% lidocaine
cream. A similar observation
with EMLA and lidocaine
creams was reported earlier;
however, a comparison was
not made with the placebo
(8). The observation in the
two studies may suggest that
lidocaine and EMLA creams
have equipotent analgesic
effect during venepuncture,
while KY gel had inferior
analgesic property. Miller et al.
compared the analgesic eect
of SC 1% lidocaine (0.3–0.5
mL), 2.5 g EMLA cream and
1 mL Iontocaine (a mixture of
2% lidocaine and 1:100,000
epinephrine) on pain at
application of agent and during
venous cannulation in adults
scheduled for ambulatory
surgery (5). The authors
observed that at application
of topical anesthetic agent,
patients who received SC
1% lidocaine had a higher
VAS (15.6±9.4) mm than
those receiving either EMLA
cream (VAS 0.2 ±0.4) mm or
Figure 5: Mean rate pressure product at different time points
SVC
RPA
SVC
RPA
IVC
Soft
IVC
Loss of conciousness
Frequency
Clinical presentation
012345678
Quadriplegia
Abasia
Gait disturbances
Overt neck wound
Bleeding from the ear
Quadriparesis
Aphasia
Urine stool incontinence
Otorrhea
TB
0
2,000
4,000
6,000
8,000
10,000
12,000
14,000
T0 T1 T2 T3 T4
Time (minutes)
EMLA
LIDOCAINE
PLACEBO
Mean RPP change (mmHg.beats/min)
T5 T6 T7 T8 T9 T10
TB
0
–2
–4
–5
2
4
6
8
10
T0 T1 T2 T3 T4
Time (minutes)
EMLA
LIDOCAINE
PLACEBO
% change from baseline
T5 T6 T7 T8 T9 T10
Figure 4: Percentage change in mean BP from baseline
Figure 3: Mean arterial blood pressure at different time points
TB
0
–2
–4
2
4
6
8
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
% change from baseline
T5 T6 T7 T8 T9 T10
TB
74
76
78
80
82
84
86
88
90
94
92
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
Mean heart rate (mmHg beats/minute)
T5 T6 T7 T8 T9 T10
TB
85
87
89
91
93
95
97
99
101
T0 T1 T2 T3 T4
Time in minutes
EMLA
LIDOCAINE
PLACEBO
Mean MAP (mmHg)
T5 T6 T7 T8 T9 T10
The ANNALS of AFRICAN SURGERY January 2019 Volume 16 Issue 1
8
Iontocaine (VAS 2.5 ±4) mm. During venous cannulation,
patients who received EMLA cream had a higher VAS
(22.3±20.1) mm than those who had either SC 1% lidocaine
(VAS 6.4±8.5) mm or Iontocaine (VAS 4.2±7.2) mm. The
authors concluded that Iontocaine (Numby Stu system
using ionotophoresis) had superior analgesic eect during
application and at venous cannulation. This is because
ionotophoresis uses a mild electrical current to deliver the
ions of medication and drive medication through the skin,
hence ensuring that the block is localized and dense. The
limitation of Miller et al.’s study was the relatively small size
of 10 individuals per group; future studies are encouraged
with larger sample sizes (5).
In another study among adult volunteers, either EMLA or 4%
lidocaine cream was shown to be eective in reducing pain
associated with pinprick when compared with placebo (9).
However, the anesthetic ecacy of 4% lidocaine cream and
EMLA cream was comparable, though the use of occlusive
lidocaine had a faster onset of action than EMLA cream.
Similarly, no adverse events were seen (9). The authors
concluded that a topical preparation with 4% lidocaine is an
eective and safe treatment option for supercial anesthesia,
with faster onset of action.
Selby and Bowles (10) compared the analgesic eect of three
agents. Patients were randomly allocated to 4 groups before
venous cannulation: SC lidocaine, ethyl chloride spray,
EMLA cream applied for 5 min, and control (no analgesia).
Pain during venepuncture was assessed using a VAS of 100
mm. They observed that lidocaine and ethyl chloride were
very eective in removing venepuncture pain (95% CI for
the dierence between the control and spray groups was
7.0–23 mm, and between the control and lignocaine groups
10–25 mm). EMLA cream had a limited, but insignicant,
eect (95% CI for dierence between control and EMLA
groups was 2–15 mm). They concluded that the analgesic
eect of lignocaine and ethyl chloride was better than that of
EMLA cream applied for 5 min before venous cannulation
(10). This is contrary to our observation with lidocaine and
EMLA creams; the dierence may be because EMLA was
applied 60 min before venepuncture in our study.
In another study (11), the VRS in patients who received
EMLA cream 60 min before cannulation was lower than
VRS with lidocaine iontophoresis (20 mA) during venous
cannulation with a large bore catheter (18G). However, the
onset of analgesia was short with iontophoresis; similarly,
erythema and paraesthesia were transient and common (11).
The authors concluded that EMLA provided a dense and
superior analgesia than ionotophoresis. This was contrary
to the observation made by Miller et al. (5). The former
researchers attributed their observations to the use of a low
iontophoretic dose. The variation in these observations may
reect a dierent patient group, dierent iontophoretic dose
and a smaller stimulus (5, 11).
The dierence in mean pain score in studies on pain during
venous cannulation has been attributed to dierences in size
of cannula, site of venous cannulation, dosage and duration
of application of topical agent, use of premedication, and
gender (2, 9, 10, 12).
Hemodynamic parameters
We observed a signicant increase in heart rate immediate
post cannulation (T0) from baseline values in groups E and
P but a decrease in heart rate in group L.
Similarly, a 1.5% decrease in heart rate in patients treated
with lidocaine injection prior to cannulation was reported
earlier (4), despite the dierence in the route of administration
and concentration of lidocaine in the two studies. While this
study used 4% lidocaine cream, the latter study administered
0.25 mL of 1% lidocaine directly in the subcutaneous layer
(4).
A prospective, randomized clinical trial assessed the
efficacy and side effects of commonly used topical
anesthesia methods in adults receiving peripheral venous
cannulation. The study was double-blinded to the degree
that the methodologies allowed. One hundred and fty
healthy adults undergoing elective surgery were randomly
allocated to ve groups: EMLA cream, ethylchloride spray,
intracutaneous inltration with 2% lidocaine, placebo cream,
and no treatment. Venepuncture was performed with a 18G
cannula on the dorsal side of the hand. Puncture pain and
pain caused by the topical treatment itself were measured
using VAS (range: 0–100 mm). Hemodynamic response,
diculties in performing the puncture and side-eects were
recorded. All analgesic techniques were well tolerated.
Hemodynamic response and degree of puncture diculty
showed no dierences between the groups. Puncture pain
(median mm VAS) following inltration (1.0) and EMLA
(10.0) was signicantly lower than in no treatment (30.0)
or in placebo (30.0). The benet of local inltration was
altered by injection pain (11.5). Spray did not signicantly
lower puncture pain (26.5) and, in addition, was associated
with discomfort (10.5). In adults, EMLA cream signicantly
reduces puncture pain and represents an acceptable alternate
method for topical anesthesia in venous cannulation. Local
lidocaine inltration is impaired by applicational pain,
whereas spraying the puncture site with ethylchloride has
no analgesic benet.
The percentage change in mean heart rate at cannulation in
olAwudAn et Al.
www.annalsofafricansurgery.com
AttenuAting venous cAnulAtion pAin—A clinicAl triAl
9
group P (7.17%) is comparable with that in the placebo group
(7.25%) in the latter study (3). However, the percentage
increase in mean HR was sustained for 10 min in our
study but for 3 min in another study (4). We attributed our
observation to lack of premedication while some researchers
premedicated all their patients with 20 mg temazepam one
hour before venepuncture (4). On the contrary, a decrease
in heart rate 15 min post cannulation following the use of
EMLA cream before cannulation was reported in another
study (13). The observed decrease was recorded 15 min
post cannulation, which may not be a good representation
of what occurred immediate post cannulation.
We reported a sudden increase in MAP at the 10th min
(T10) only in group E patients. The percentage change
from baseline value in MAP at this time (T10) was also
increased. This increase may be due to reduced analgesic
eect with early manifestation in the MAP. It is possible
that other hemodynamic parameters may also have shown
an increase had the duration of study been extended. In this
study, 10% lidocaine cream provided a consistent protective
eect against signicant increase in heart rate and MAP
accompanying venous cannulation. These eects may not
be unrelated to the degree of pain attenuation that lidocaine
delivers. 10% lidocaine gave the lowest pain scores and also
the lowest level of alteration in hemodynamic variables.
Langham et al. (4) observed a 10–15% increase in MAP
in the placebo group. In this study, MAP rose by 6.01%
in group P. This disparity may be due to the dierent sites
of blood pressure measurement. Langham et al. measured
blood pressure on the finger using the finapres (4),
while we measured at the upper arm using an electronic
sphygmomanometer. The napres technique has been shown
to have low precision for systolic and MAP measurements,
and is thus not permitted for absolute blood pressure
measurements in individual patients (14). Finger arteries
are aected by contraction and dilatation in response to
psychological and physical stress and these in turn aect the
readings from the napres (14). An awake patient must be
relaxed for accurate readings to be obtained from the napres
(14). An electronic sphygmomanometer with an appropriate
size cu applied to the upper arm is more likely to give
readings close to those obtained were invasive monitoring
used (14). Therefore, the napres might have given an
exaggerated MAP in the placebo group.
The rate–pressure product (RPP: a product of systolic blood
pressure and heart rate) is a good index of myocardial oxygen
consumption, and the maximum recommended range is
12,000 to 23,000 mmHg.beat.mm–1 (14). Values above this
are commonly associated with myocardial ischemia and
angina. In our study, the mean RPP throughout in the placebo
group was 10, 970 mmHg.beat.mm–1, in the EMLA group
10,328 mmHg.beat.mm–1, and in the lidocaine group 11,881
mmHg.beat.mm–1. None of the groups had RPP range that
fell within the maximum range expected; as such, there
may not be signicant increase in oxygen consumption in
normotensive patients following venous cannulation.
In the perioperative period, Rao et al. (15) recommend not
greater than 20% uctuation in heart rate and systolic blood
pressure in patients with cardiac morbidity going for non-
cardiac surgery. The increase in baseline values observed
of 7.17% for heart rate and 6.01% for MAP in the placebo
group in response to venous cannulation were lower than
the allowable uctuation. These values were further reduced
in the two treatment groups E (HR, 1.78%; MAP, 2.92%)
and L (HR, 0.72%; MAP, 2.10%). This implies that with
the attenuation of venous cannulation pain, hemodynamic
uctuations can be minimized. Therefore, in patients with
cardiac morbidity (those with hypertension and coronary
artery disease) who may show exaggerated hemodynamic
response to pain, it is imperative that these uctuations are
avoided by attenuating cannulation pain.
Side effects
We observed minimal side eects on application of treatment
creams. During cream application 1 patient in the EMLA
group and 2 patients in the lidocaine group complained of
burning. Tingling sensation was also reported by 1 patient
in the lidocaine group. Other authors, however, did not
have similar experience with lidocaine application (4). The
sensations reported by these patients subsided once the
creams were removed. Browne et al. (6) reported mild
pruritus following the use of amethocaine.
Blanching of the skin after removal of treatment creams
was observed in 1 patient in each group. A higher incidence
had been reported earlier in a similar study; in the EMLA
cream group, 3 patients (8.8%) had blanching of skin while
10 patients (29.8%) had erythema (16). EMLA cream is
known to cause initial local vasoconstriction, leading to
blanching; this is followed by vasodilatation, resulting in
erythema and induration (17). We reported no erythema and
only 1 patient blanched, this we attributed to the dark skin
of our studied population unlike other studies with light-
skinned patients. Kano et al. (18) noticed local erythema
in 8 out of 24 patients treated with lidocaine for venous
cannulation pain. Browne et al. (6) compared EMLA with
topical Amethocaine for cannulation and observed that
blanching occurred more with the EMLA group (23 patients
out of 32 patients) while erythema was observed more in the
The ANNALS of AFRICAN SURGERY January 2019 Volume 16 Issue 1
10
Amethocaine group (11 patients out of 32). The cutaneous
manifestation observed resolved within an hour. Sakamoto et
al. (16) observed a reduction in the number of patients with
local reaction 30 min after cream removal (blanching from
8.8% to 2.9%, erythema from 29.4% to 8.8%), suggesting
that these cutaneous manifestations are local and transient.
This study is limited by the paucity of literature on 10%
lidocaine for comparison and critical analysis with our study.
Nevertheless, we have demonstrated that EMLA and 10%
lidocaine creams attenuated pain and the associated pressor
response to venous cannulation to varying degrees. Lidocaine
cream gave lower pain score and better cardiovascular
stability during cannulation than EMLA cream. Both were
associated with transient, localized cutaneous manifestations.
References
1. Herman RE. Shock, physiological surgery and George
Washington Crile: Innovation in the progressive era. Ann
Surg. 1981; 194:121–2.
2. Bond M, Crathrone L, Peters JL, et al. First, Do No Harm:
Pain relief for the peripheral venous cannulation of adults—a
systematic review and network meta-analysis. BMC
Anesthesiol. 2016; 16(1):81.
3. Jagadamba A, Karthiyanee K, Shankar MS, et al. Gender
variation in pain perception after intravenous cannulation in
adults. IJA.2011; 28(1).
4. Langham BT, Harrison DA. The pressor responsetovenous
cannulation: Attenuation by prior inltration with local
anaesthetic. Br J Anaesth. 1993; 70:519–21.
5. Miller KA, Balakrishman G, Eichbauer G, et al. 1% lidocaine
injection, EMLA cream, or ‘Numby Stu’ for topical analgesia
associated with peripheral intravenous cannulation. AANA
Journal. 2001;69(3):185–7.
6. Browne J, Awad I, Plant R, et al. Topical Amethocaine
(AmetopTM) is superior to EMLA for intravenous cannulation.
Can J Anaesth. 1999; 46:1014–18.
7. Li HWR, Wong CYG, Lo SST, et al. Eect of local lignocaine
for pain relief during suction termination of rst trimester
pregnancy: A randomized controlled trial. Hum Reprod. 2006;
21:1461–6.
8. Armagan E, Kocabas E, Koksal O, et al. Comparison of the
ecacies of topical anaesthetics in the reduction of the pain
during peripheral intravenous cannulation: A randomised trial.
Hong Kong J. Emerg Med. 2012; 19(3):183–8.
9. Herberger K, Krause K, Maier K, et al. Local anesthetic
eects of lidocaine cream: Randomised controlled trial using
a standardised prick pain. J DermTreat. 2012; 23(6):437–42.
10. Selby I, Bowles BJ. Analgesic for venous cannulation: A
comparison of EMLA (5 minutes application), lignocaine,
ethyl, and nothing. J R Soc Med. 1995; 88:264–7.
11. Moppett IK, Szypula K, Yeoman PM. Comparison of EMLA
and lidocaine iontophoresis for cannulation analgesia. Eur J
Anaesthesiol. 2004; 21(3):210–3.
12. Macario A, Weinger M, Troung P, et al. Which clinical
anaesthesia outcomes are both common and important to avoid?
The perspective of a Panel of Experts’ Anaesthesiologists.
Anesth Analg. 1999; 88:1085–91.
13. Speirs AF, Taylor KH, Joanes DN, Girdler NM, et al.A
randomised, double-blind, placebo-controlled comparative
study of topical skin analgesics and the anxiety and discomfort
associated with venous cannulation. Br D J. 2001; 190:444–9.
14. Imholz BPM, Weiling W, Montfrans GAV, et al. Fifteen years’
experience with nger arterial pressure monitoring: Assessment
of the technology. Cardiovasc Res. 1998; 38:605–16.
15. Rao TLK, Jacobs KH. Reinfarction following anaesthesia in
patients with myocardial infarction. Anesthesiology. 1983;
59:499–04.
16. Sakamoto M, Kano T, Sadanaga M, et al. Dermal patch
anaesthesia: Comparison of 10% lignocaine gel with absorption
promoter and EMLA cream. Anaesthesia 1993; 48:390–2.
17. Yeoh CN, Lee CY. Pain during venous cannulation: Double-
blind, randomized clinical trial of analgesic eect between
topical Amethocaine and eutectic mixture of local anaesthetic.
J Anaesthesiol Clin Pharmacol. 2012; 28:205–9.
18. Kano T, Hashiguuchi A, Nakamura M, et al. Comparative
study of transdermal 10% lidocaine gel with and without
glycrrhentinic acid monohemiphthalate disodium for pain
reduction at cannulation. Anaesth Analg. 1992; 74:535–8.
olAwudAn et Al.
... [14][15][16] Current literature suggests that lidocaine reduces the pain associated with peripheral IV catheterization and improves patient satisfaction. 8,17,18 To date, there has been no published research on the use of benzocaine for peripheral IV catheterization. Nevertheless, previous research aimed at reducing the discomfort associated with inferior alveolar nerve block injections has demonstrated the effectiveness of topical anesthetic benzocaine spray for pain management. ...
... Similar studies have reported that lidocaine, used before peripheral intravenous catheterization, effectively reduces pain associated with the procedure and increases patient satisfaction. 17,18 The results of this study align with those findings. Topical analgesics like lidocaine primarily pass through the skin surface by passive diffusion. ...
... Topical anaesthetics are agents that bring about topical anaesthesia, or a reversible loss of sensation in a circumscribed area of the skin or mucous membranes, by reversibly blocking the conduction of nerve impulses at free nerve endings [9]. Some of the topical anaesthetic agents that have been employed to achieve topical anaesthesia before peripheral venous cannulation include the Eutectic Mixture of Local Anaesthetics (5% EMLA): a mixture of 2.5% Lidocaine and 2.5% Prilocaine in an emulsion base; 4% Amethocaine gel, 10% Lidocaine, coolants such as ethyl chloride, alkane mixtures, and fluorohydrocarbons [10][11][12][13]. Although reviews [7,14], evaluating the reduction in PVC insertion/venipuncture pain with the use of topical anaesthetic agents compared to placebo, had been conducted globally, none had been undertaken in Africa. ...
Preprint
Full-text available
Introduction:Pain associated with peripheral venous catheter (PVC) insertion and venipuncture can be a significant source of discomfort, particularly for children. The use of topical anaesthetic preparations before PVC insertion can reduce discomfort and enhance health-seeking behaviour. Objective:This review was aimed at assessing the efficacy of topical anaesthesia to reduce pain during PVC insertion compared to placebo or no treatment, and the associated adverse effects with the use of topical anaesthetic preparations among the African population. Methods:This review was conducted using a systematic literature search of the following databases and registers:: PubMed, NDLTD, OATD, TROVE, LILACS, Scopus, The Cochrane Library, CINAHL & MEDLINE [via EBSCOhost], Africa Journal Online (AJOL), Google Scholar, and MedNar was conducted between November and December 2023. Prospective observational studies, randomised controlled trials, case-control studies, longitudinal studies, theses and dissertations were considered in these searches. A total of four studies and 448 respondents participated in the review. Result:All studies investigated the efficacy of various topical agents, including 5% EMLA and 10% lidocaine cream, and demonstrated a significant reduction in pain with topical anaesthesia compared to placebo or no treatment. The adverse/side effect profile was generally favourable, with no major adverse reactions reported. Conclusion:Topical anaesthesia is a valuable tool in reducing procedural pain during peripheral venous catheterization and venipuncture in the African population. This review establishes its superiority over placebo or no treatment. Specifically, 10% lidocaine outperforms 5% EMLA in minimizing procedural pain with minimal side effects. Further research is needed to explore alternative preparations for cases of adverse reactions and ineffective anaesthesia.
... Minimally invasive surgeries should be encouraged as this leads to shorter operating time, shorter hospital stays and fewer complications (16). A paper by Olwadun et al. in this issue proposes a way of reducing pain during cannulation procedures (17). Were such innovations with proved patient benefits rewarded, surgeons would incorporate them in care provision. ...
Article
Full-text available
Health care financing takes several forms. In Kenya, most health care costs are financed as out-of-pocket payments by patients and their families (1). Penetration of private health insurance is low and covers mainly those in formal employment in the major urban centers (1, 2). The National Health Insurance Fund (NHIF) is the national state corporation tasked with public health care financing. Membership of NHIF is mandatory for all employees in the public and private sectors but is voluntary for those in the informal sector. By September 2018, at least 25 million Kenyans had NHIF cover, courtesy of 7.6 million principal subscribers (3). In the past, NHIF concentrated on providing ambulance services and paying for bed charges for inpatients. It recently started financing surgical care, previously financed by private insurance or out-ofpocket payments that led to medical impoverishment, increased morbidity and mortality, and poor quality of care (4, 5). Financial barriers to care include direct and indirect costs: direct costs relate to care—surgical fees, supplies laboratory tests, drugs, transport, stay at hospital, and food; indirect costs are costs amassed because of the sickness or absence of the patient (6).
Article
Background: The eutectic mixture of local anesthetics (EMLA) is an effective cutaneous anesthetic, although its application is time consuming and poses a risk of methemoglobinemia. Currently, the efficacy of topical 10% lidocaine cream is unclear. Objective: To compare the onset, anesthesia depth, and duration of topical 10% lidocaine and EMLA cream. Methods: The randomized, split-body, comparative trial performed on 40 participants who received a topical 10% lidocaine cream or EMLA on forearms for 15-150 min. Pain was stimulated using a 21-gauge needle insertion and evaluated with the Verbal Pain Score. Adverse effects were recorded. Results: EMLA conferred significantly better efficacy than 10% lidocaine (p < 0.001). For acceptable pain at 4-mm depth, the minimal application times were 40.88 and 45.38 min of EMLA and 10% lidocaine creams, respectively. With 60/120-min application, the maximal needle-insertion depths with acceptable pain were 6.61/9.47 mm (EMLA) and 6.01/8.94 mm (10% lidocaine). EMLA's anesthetic effect showed an early increase after removal which was sustained for 60-90 min. Both creams caused adverse effects, with EMLA showing higher proportions, although the differences were statistically insignificant. Conclusion: The efficacy of EMLA was superior to 10% lidocaine cream, especially regarding anesthesia onset and duration.
Article
Full-text available
Background Peripheral venous cannulation is an everyday practice in hospitals, which many adults find painful. However, anaesthesia for cannulation is usually only offered to children. Inadequate pain relief is not only unpleasant for patients but may cause anxiety about further treatment and deter patients from seeking medical care in the future. The aim of this study is to discover the most effective local anaesthetic for adult peripheral venous cannulation and to find out how the pain of local anaesthetic application compares with that of unattenuated cannulation. Methods These aims are addressed through a systematic review, network meta-analysis and random-effects meta-analysis. Searching covered 12 databases including MEDLINE and EMBASE from 1990 to August 2015. The main included study design was RCTs. The primary outcome measure is self-reported pain, measured on a 100 mm visual analogue scale. ResultsThe systematic review found 37 includable studies, 27 of which were suitable for network meta-analysis and two for random-effects meta-analysis. The results of the network meta-analysis indicate that none of the 17 anaesthetic considered had a very high probability of being the most effective when compared to each other; 2 % lidocaine had the highest probability (44 %). When the anaesthetics were compared to no treatment, the network meta-analysis showed that again 2 % lidocaine was estimated to be the most effective (mean difference −25.42 (95 % CI −32.25, −18.57). Other members of the ‘caine’ family were also estimated to be more effective than no treatment as were Ametop®, EMLA® and Rapydan® patch. The meta-analysis compared the pain of anaesthetic application with the unattenuated pain of cannulation. This found that all applications of local anaesthetic were less painful than cannulation without local anaesthetic. In particular a 1 % lidocaine injection was estimated to be −12.97 (95 % CI −15.71, −10.24) points (100 mm VAS) less painful than unattenuated cannulation. Conclusions The pain of peripheral venous cannulation in adults can be successfully treated. The pain of application of any local anaesthetic is less than that of unattenuated cannulation. Local anaesthetic prior to cannulation should become normal practice and a marker of high quality care. Protocol registrationThe protocol for the larger study was registered with PROSPERO no. CRD42012002093.
Article
Full-text available
Objective This study aimed to compare the efficacies of two different topical anesthetic agents and placebo in the reduction of the pain observed during intravenous (IV) cannulation. Methods Study enrolled a total of 129 healthy male donors and IV cannulation was performed to antecubital region. The donors were assigned into three groups. Prilocaine-lidocaine mixture cream (E), lidocaine spray (X) and Placebo cream (P) were given to patients. After the administration the donors were waited for approximately 45 minutes. The pain experienced by the donors after the insertion of 16 gauge cannula in arms was recorded as “pain experienced at minute 0, 5 and 15” on 100 mm visual analog scale (VAS). Results In the first group, there was no significant difference between mean VAS scores recorded after the administration of prilocainelidocaine mixture cream and lidocaine spray before IV cannulation. Mean VAS value was 9.1 mm with prilocaine-lidocaine mixture cream and 9.3 mm with lidocaine spray. In the second group, we detected significant difference between mean VAS scores recorded after the administration of lidocaine spray and placebo cream. Mean VAS value was 9.8 mm with lidocaine spray and 24.3 mm with placebo (p<0.05). In the third group, we found statistically significant difference between VAS scores recorded after the administration of prilocaine-lidocaine mixture cream and placebo cream. Mean VAS value was 8.8 mm with prilocaine-lidocaine mixture cream and 33.0 mm with placebo cream (p<0.05). Conclusion Although both agents administrated before IV cannulation were superior to placebo in adult patients in this study, we can state that these drugs were not superior to each other and showed similar efficacy.
Article
Full-text available
Purpose A eutectic mixture of local anesthetics (EMLA) is commonly used to provide topical anesthesia for intravenous (iv) cannulation. One of its side effects is vasoconstriction, which may render cannulation more difficult. A gel formulation of amethocaine (Ametop™) is now commercially available. The aim of this study was to compare EMLA and Ametop™ with regard to the degree of topical anesthesia afforded, the incidence of vasoconstriction and the ease of iv cannulation. Methods Thirty two ASA 1 adult volunteers had a # 16 gauge iv cannula inserted on two separate occasions using EMLA and Ametop™ applied in a double blind fashion for topical anesthesia. Parameters that were recorded after each cannulation included visual analogue pain scores (VAPS), the presence of vasoconstriction and the ease of cannulation, graded as: 1 = easy, 2 = moderately difficult, 3 = difficult and 4 = failed. Results The mean VAPS ± SD after cannulation with Ametop™ M was 12 ± 9.9 and with EMLA was 25.3 ± 16.6 (P = 0.002). Vasoconstriction occurred after EMLA application on 17 occasions and twice after Ametop™ (P = 0.001). The grade of difficulty of cannulation was 1.44 ± 0.88 following EMLA and 1.06 ± 0.25 with Ametop™ (P = 0.023). Conclusions Intravenous cannulation was less painful following application of Ametop™ than EMLA. In addition, Ametop™ caused less vasoconstriction and facilitated easier cannulation. Its use as a topical anesthetic agent is recommended, especially when iv access may be problematic.
Article
Full-text available
Venous cannulation is often a painful procedure for the patient. Eutectic mixture of local anesthetic (EMLA) is the commonest topical analgesic used but suffers from disadvantages such as slow onset and skin blanching, which may interfere with venous cannulation. Amethocaine is a newer topical analgesic which seems to be devoid of such problems. This prospective randomized double-blind study compared the analgesic efficacy of EMLA with amethocaine during venous cannulation in adults. Eighty ASA I-II patients, aged 18-65 years, were recruited. The test drug was applied on the designated site of venous cannulation and covered with an occlusive dressing for at least 60 min prior to the procedure. Data collected included visual analogue score (VAS) during first attempt at venous cannulation, the ease and success rate at cannulation, and cutaneous changes at the application site. Mean and median VAS for the EMLA group were 27.9 ± 9.8 and 30 mm, respectively; while for the Amethocaine group were 19.1 ± 14.1 and 20 mm, respectively. Differences in VAS did not reach statistical significance. No statistically significant differences were observed in the ease and success rate at cannulation. Cutaneous changes in the form of local induration and erythema (three patients in the Amethocaine group) and blanching (eight patients in the EMLA group) were mild, localized, and required no further treatment. No patient developed severe allergic reactions. Topical EMLA and amethocaine were comparable in terms of analgesic efficacy and ease of venous cannulation in adult patients.
Article
Abstract Background: ELA-max (4% Lidocaine) and EMLA cream (Lidocaine-Prilocaine 2.5%) are topicals used for superficial anesthesia. Only few studies have been published on their comparative effectiveness in close-to-practice pain models. Objective: 1) To evaluate the analgesic efficacy of Lidocaine cream compared with Lidocaine-Prilocaine cream and placebo. 2) To assess the safety and tolerability. Methods: Randomized, three-arm, double-blind trial in 40 healthy volunteers comparing the anesthetic effects of Lidocaine and Lidocaine-Prilocaine cream to placebo at various time points (0-120 min). A standardized pain was induced by lancet pricks and measured by a visual analogue scale. Intra-individual comparison between the test areas was performed in a cross-over design. Results: Lidocaine showed significantly reduced pain compared to placebo at all assessment points. Pain reduction was achieved significantly earlier using Lidocaine occlusively (30 min). No significant differences were found concerning the anesthetic efficacy of Lidocaine and Lidocaine-Prilocaine cream. There were no relevant adverse events. Conclusion: This study confirms that a topical preparation with 4% Lidocaine is an effective and safe treatment option for superficial anesthesia. It supports the claim that an occlusive application is more rapid in action. 4% Lidocaine is of value as a rapidly-acting local anesthetic for the treatment of minor surgical procedures.
Article
Three commonly available local anaesthetics were compared, in a controlled trial, for use before venous cannulation. The pain of application of the local anaesthetic, the pain of cannulation, and the rate of successful cannulations were compared. The value of EMLA cream applied for 5 min was questioned. Venous cannulation with a 20G venflon was found to be significantly more painful than the application of any of the local anaesthetics (P < 0.01). Lignocaine 1%, injected subcutaneously, and ethyl chloride spray significantly reduced the pain of venous cannulation (P < 0.01). The use of lignocaine did not result in significantly more failed cannulations than the control group. It was concluded that local anaesthesia should be used before venous cannulation, even for 20G cannulae.
Article
We have compared the cardiovascular response to insertion of an 18-gauge venous cannula in 40 healthy patients. In 20 of the patients, cannulation was preceded by infiltration of local anaesthetic. Both rate-pressure product and mean arterial pressure increased significantly (? <0.01) compared with baseline when no local infiltration was used, but there was no significant change from baseline when infiltration with local anaesthetic preceded cannulation. We conclude that there is a significant pressor response to venous cannulation which is obtunded by prior infiltration with local anaesthetic. We recommend, therefore, that s.c. injection of lignocaine should be considered before insertion of an i. v. cannula, especially in the high risk patient. (Br. J. Anaesth. 1993; 70: 519–521)
Article
The analgesic effects of transdermally applied 10% lignocaine aquagel containing 3% glycyrrhetinic acid monohemiphthalate disodium (as an absorption enhancer) and EMLA cream were compared on the forearms of 34 adult volunteers in a double-blind fashion. The mean pinprick pain scores (graded by noting the number of painful pinpricks out of five) at 30, 60 and 90 min after application and 30 min after removal of the anaesthetics were 3.3 (0.3) (mean SE), 1.2 (0.3), 0.3 (0.1) and 0.3 (0.1) respectively, in the lignocaine gel group. Corresponding scores were 3.5 (0.3), 1.5 (0.3), 0.7 (0.2) and 0.1 (0.1) respectively, in the EMLA group. Insertion of a 26-gauge needle into the treated skin to a depth of 1 mm at 90 min after application was not painful in 91% of the volunteers in the lignocaine gel group and 88% of those in the EMLA group. There was no significant difference in any of the corresponding pain scores between the two groups.
Article
Unlabelled: Anesthesia groups may need to determine which clinical anesthesia outcomes to track as part of quality improvement efforts. The goal of this study was to poll a panel of expert anesthesiologists to determine which clinical anesthesia outcomes associated with routine outpatient surgery were judged to occur frequently and to be important to avoid. Outcomes scoring highly in both scales could then be prioritized for measurement and improvement in ambulatory clinical practice. A mailed survey instrument instructed panel members to rate 33 clinical anesthesia outcomes in two scales: how frequently they believe the outcomes occur and which outcomes they expect patients find important to avoid. A feedback process (Delphi process) was used to gain consensus rankings of the outcomes for each scale. Importance and frequency scores were then weighted equally to qualitatively rank order the outcomes. Of the 72 anesthesiologists, 56 (78%) completed the questionnaire. The five items with the highest combined score were (in order): incisional pain, nausea, vomiting, preoperative anxiety, and discomfort from IV insertion. To increase quality of care, reducing the incidence and severity of these outcomes should be prioritized. Implications: Expert anesthesiologists reached a consensus on which low-morbidity clinical outcomes are common and important to the patient. The outcomes identified may be reasonable choices to be monitored as part of ambulatory anesthesia clinical quality improvement efforts.