surgical safety checklist: implementation in an ambulatory ...dans un centre de chirurgie...
TRANSCRIPT
REPORTS OF ORIGINAL INVESTIGATIONS
Surgical safety checklist: implementation in an ambulatorysurgical facility
La liste de controle de la securite chirurgicale et sa mise en œuvredans un centre de chirurgie ambulatoire
Pamela J. Morgan, MD • Lisa Cunningham, BA (Hons) • Sohini Mitra, BSc •
Natalie Wong, BHSc • Wei Wu, MSc • Victoria Noguera, RN •
Mary Li, MSc • John Semple, MD
Received: 17 September 2012 / Accepted: 6 March 2013 / Published online: 16 March 2013
� Canadian Anesthesiologists’ Society 2013
Abstract
Purpose In 2007, the World Health Organization created
a Surgical Safety Checklist (SSC) that encompassed a
simple set of surgical safety standards. The threefold pur-
pose of this study was to add ambulatory-specific items to
the SSC, to introduce the items into an ambulatory surgical
facility, and to determine if patient outcomes regarding
postoperative pain and nausea/vomiting improved follow-
ing implementation. In addition, safety attitudes, antibiotic
timing, regional anesthesia/nerve blocks, preemptive pain
medications, prophylactic antiemetics, length of stay, and
hospital admission were also assessed.
Methods After Research Ethics Board approval, staff
complete a Safety Attitudes Questionnaire. Seven items
were added to the SSC. Data were then collected on 180
surgical cases before SSC implementation and 195 cases
following implementation. Compliance with each section of
the SSC was assessed.
Results On postoperative day one, the median (97.5%
confidence interval [CI]) difference between pre- and post-
implementation pain scores was 0.5 (97.5% CI, 0 to 1;
P = 0.13), and the median difference in the rate of post-
discharge nausea/vomiting was -8.4% (97.5% CI, -17.9
to 1.1; P = 0.06). There was no improvement in safety
attitudes or any of the secondary outcomes, with the
exception of the use of preemptive pain medications.
Compliance with the three sections of the checklist, i.e.,
BRIEFING, TIME OUT, and DEBRIEFING was 99.49%,
97.95%, and 96.92%, respectively. There was low com-
pliance in verbalization of the added ‘‘ambulatory-specific
items’’.
Conclusion Potential reasons for lack of uptake and
integration include poor ‘‘user’’ buy-in, an overly lengthy
checklist, and lack of prioritization of ambulatory-specific
items. A shortened SSC was developed based on the results
of this study. This trial was registered at ClinicalTrials.gov
ID: NCT00934310.
Author contributions Pamela J. Morgan was involved in theacquisition of funding for this study. Pamela J. Morgan LisaCunningham, Wei Wu, Victoria Noguera, and John Semple wereinvolved in the conception and design of the study. LisaCunningham, Sohini Mitra, Natalie Wong, and Mary Li wereinvolved in the acquisition of data for the study. Pamela J. Morganwas involved in the interpretation of the data. Pamela J. Morgan, WeiWu, and Mary Li analyzed the data. Pamela J. Morgan, LisaCunningham, and Mary Li were involved in drafting the article.Sohini Mitra, Natalie Wong, Wei Wu, Victoria Noguera, and JohnSemple were involved in the critical revision of the article.
This article is accompanied by an editorial. Please see Can J Anesth
2013; 60: this issue.
P. J. Morgan, MD (&) � L. Cunningham, BA (Hons) �S. Mitra, BSc � N. Wong, BHSc � M. Li, MSc
Department of Anesthesia, Women’s College Hospital,
University of Toronto, 76 Grenville St., Toronto,
ON M5S 1B2, Canada
e-mail: [email protected]
W. Wu, MSc
Women’s College Research Institute,
University of Toronto, Toronto, ON, Canada
V. Noguera, RN
Department of Nursing, Women’s College Hospital,
University of Toronto, Toronto, ON, Canada
J. Semple, MD
Department of Surgery, Women’s College Hospital,
University of Toronto, Toronto, ON, Canada
123
Can J Anesth/J Can Anesth (2013) 60:528–538
DOI 10.1007/s12630-013-9916-8
Resume
Objectif En 2007, l’Organisation mondiale de la Sante a
cree une Liste de controle de la securite chirurgicale (LCSC)
couvrant un ensemble simple de normes de securite pour la
chirurgie. L’objectif triple de cette etude etait d’ajouter des
elements specifiques au contexte ambulatoire a la LCSC,
d’introduire ces elements dans un centre de chirurgie
ambulatoire, et de determiner si les devenirs des patients
en matiere de douleur et de nausees et vomissements
postoperatoires etaient ameliores suite a la mise en œuvre
de la LCSC. En outre, les attitudes face a la securite,
l’administration opportune des antibiotiques, l’anesthesie
regionale / blocs nerveux, les medicaments de prevention de la
douleur, les antiemetiques en prophylaxie, la duree du sejour
et les admissions a l’hopital ont egalement ete evalues.
Methode Apres avoir recu le consentement du Comite
d’ethique de la recherche, le personnel de l’etablissement a
rempli un Questionnaire sur les attitudes face a la securite,
a la suite duquel sept elements ont ete ajoutes a la LCSC.
Les donnees ont ensuite ete colligees sur la base de 180 cas
chirurgicaux avant la mise en œuvre de la LCSC et de 195
cas apres sa mise en œuvre. Le respect de chaque section
de la LCSC a ete evalue.
Resultats Au premier jour postoperatoire, la difference
mediane (intervalle de confiance [IC] 97,5 %) entre les
scores de douleur avant et apres mise en œuvre etait de 0,5
(IC 97,5 %, 0 a 1; P = 0,13), et la difference mediane dans
l’incidence de nausees et vomissements apres le conge etait
de -8,4 % (IC 97,5 %, -17,9 a 1,1; P = 0,06). Il n’y a eu
aucune amelioration dans les attitudes face a la securite ou
dans toute autre mesure secondaire, a l’exception de
l’utilisation de medicaments de prevention de la douleur. Le
respect des trois sections de la liste de controle, soit Reunion
preparatoire, Temps mort et Reunion-bilan (BRIEFING,
TIME OUT, DEBRIEFING) etait de 99,49 %, 97,95 %, et
96,92 %, respectivement. Le respect etait peu maintenu au
niveau de la verbalisation des « elements specifiques au
contexte ambulatoire » ajoutes.
Conclusion Parmi les raisons potentielles ayant freine
l’adoption et l’integration de cette liste amelioree, citons le
manque de conviction des « utilisateurs », la longueur de
la liste de controle, et le manque de priorisation des
elements specifiques au contexte ambulatoire. Une LCSC
raccourcie a ete mise au point sur la base des resultats de
cette etude. Cette etude est enregistree sous ClinicalTrials.
gov, ID: NCT00934310.
It has been more than ten years since the Institute of
Medicine published the pivotal report, To Err is Human:
Building a Safer Health System.1 The patient safety
movement has made significant strides, and the develop-
ment of the World Health Organization’s (WHO) Surgical
Safety Checklist (SSC) was the first major international
collaboration to improve perioperative patient safety. The
SSC was piloted in eight hospitals around the world from
October 2007-September 2008.2 The death rate was 1.5%
before the checklist was introduced, and the rate declined
to 0.8% afterward (P = 0.003). Furthermore, inpatient
complications occurred in 11.0% of patients at baseline and
in 7.0% of patients after the checklist was introduced
(P \ 0.001).2 Subsequent studies have supported the find-
ings in this hallmark publication.3-7
The significant improvement in morbidity and mortality was
shown in inpatient hospitals. During the past decade, however,
there has been a 300% increase in the number of surgical/
diagnostic procedures performed in ambulatory surgical cen-
tres in the United States. In ambulatory surgical centres, there is
a much lower incidence in morbidity and mortality and a dif-
ferent set of complications.8 In a report by Kurrek and Twersky,
the authors studied the literature published during 1997-2008
for incidences of mortality and morbidity in out-of-hospital
facilities.9 Their findings indicated a mortality rate of 0.00008-
0.05% and a complication rate of 0.7-1.3%.
Post-discharge nausea and vomiting (PDNV) is an impor-
tant contributor to postoperative morbidity in the ambulatory
surgical population.10 Similarly, postoperative pain is under-
managed, with as many as 86% of patients experiencing
moderate to severe pain.11 The purpose of this study was to
examine the effectiveness of the SSC in the context of an
ambulatory surgical facility by adding ambulatory care-spe-
cific items to the checklist, assessing adherence to the safety
checklist items, and examining the impact of the SSC on
safety attitudes and important patient outcomes.
Methods
After Research Ethics Board approval, all operating room and
postoperative anesthetic care unit personnel in an ambulatory
surgical facility were asked to complete a 58-item validated
Safety Attitudes Questionnaire (SAQ).12,13 Questions pertain-
ing to communication and collaboration were assessed using a
five-point scale with 1 = very low and 5 = very high, and the
individual’s ‘‘experience’’ in the work environment was
assessed using a five-point scale with 1 = disagree strongly
and 5 = agree strongly.
Champions committee and checklist development
A committee was formed comprising representatives of all
perioperative disciplines, including anesthesiology, sur-
gery, and nursing. The committee consisted of three nurse
Safety checklist in ambulatory surgery 529
123
administrators, a clinical nurse educator, eight registered
nurses (RN), four surgeons (plastics, urology, orthopedics,
and gynecology), three staff anesthesiologists, and an
anesthesia resident. The mandate of the committee was to
determine the specific items to add to the SSC that would
reflect patient outcomes in an ambulatory surgical facility
and to determine how the checklist would be implemented.
The Canadian version of the SSC (adapted from the
World Health Organization’s Surgical Safety Checklist by
the Canadian Patient Safety Institute) was downloaded
from the Canadian Patient Safety Institute Web site and
used as the preliminary template (Appendix A: reproduced
with permission) (http://signup.patientsafetyinstitute.ca/English/
toolsResources/sssl/Pages/SurgicalSafetyChecklist.aspx) This
checklist consists of 59 items. ‘‘Items’’ were defined as any
phrase preceded by either a checkbox or a dash. A litera-
ture review was then conducted to determine the most
important postoperative outcomes in the ambulatory sur-
gical population. Items related to these outcomes that had
the potential to improve postoperative morbidity and could
be added to the checklist were developed and presented to
the committee for discussion. Items were added to the
checklist if committee consensus was achieved. Seven
additions were made to the WHO SSC. In the BRIEFING
section: under ‘‘Surgeon(s) review(s)’’, i.)intraoperative
local anesthetic infiltration was added; under ‘‘Anesthesi-
ologist(s) review(s)’’, ii.)general anesthesia versus regional
anesthesia, iii.)nerve block, and iv.)intraoperative antie-
metics (as a single item) were added; and under ‘‘Special
precautions’’, v.)preemptive pain medication was added. In
the TIME OUT section, vi.)allergies was added, and in the
DEBRIEFING section, vii.) local anesthetic infiltration was
added. The added items were specifically identified by
using a red, italicized, and underlined font, and they were
indicated with an asterisk. As a result, the BRIEFING
section consisted of 41 items; the TIME OUT section
consisted of ten items, and the DEBRIEFING section
consisted of 15 items for a total of 65 items (Appendix B:
reproduced with permission). In addition, a 17-item HAND
OFF section was added; however, this section was not
verbally included in the SSC and compliance data were not
collected on this section. Rather, it was included as a
guideline that the RN could use in handing over either
during the procedure or in the postanesthetic care unit.
Data collection
A dedicated research assistant attended surgical procedures
with the principal investigator and completed the SSC data
form until the principal investigator was satisfied with the
accuracy of data collection. University students (n = 12)
were then recruited to participate as observers and data
collectors over the course of the one-year study. All students
received an introduction and explanation of the study pro-
tocol by the principal investigator and research assistant.
The research assistant accompanied each student in the
operating room until fidelity of data collection was
achieved. Students were instructed to leave the answer blank
if they weren’t able to determine the answer to a question.
Once completed, the research assistant reviewed all data
collection forms for missing data. Chart reviews were con-
ducted to fill in missing data points where possible.
Before introduction of the adapted SSC, trained person-
nel attended a random sample of ambulatory surgical
procedures and prospectively collected data. Operating
room personnel were not informed as to the specific reason
for the observer’s presence in the operating room. All
ambulatory surgical procedures were eligible for inclusion
in the study. Once data collection was completed on the
calculated sample size and following a multidisciplinary
education session, the SSC was introduced into all operating
rooms and a period of three weeks was given to allow per-
sonnel to adapt to its use. A laminated copy of the adapted
SSC was posted and available in every operating room, and
descriptors of the individual items were located on the
reverse side of the laminated SSC. The committee decided
that the surgeon would conduct the BRIEFING section, the
RN, anesthesiologist, or surgeon would conduct the TIME
OUT section, and the circulating RN would conduct the
DEBRIEFING section using the laminated SSC as a guide.
After the introductory time period, trained observers
again collected the same information as prior to SSC
implementation as well as data regarding adherence to the
three sections of the SSC (BRIEFING, TIME OUT, and
DEBRIEFING) and to the individual items within these
sections. Operating room personnel were not aware of the
specific data being collected by the observers. The data
collector checked off those items in each section that were
verbally discussed during each surgical procedure. After all
data were collected, perioperative personnel were again
asked to complete the SAQ.
The primary outcome was the incidence of pain and
nausea/vomiting on postoperative day one, which was
obtained by telephone interview. Post-discharge pain was
assessed using a scale of 1-10: 1 = no pain and 10 = the
worst possible pain. Nausea and vomiting was assessed
using a four-point scale: 0 = no nausea/vomiting,
1 = mild, 2 = moderate, 3 = severe nausea/vomiting.
Secondary outcomes included the timing of perioperative
antibiotic administration (antibiotic administration to inci-
sion time), the use of preemptive nonsteroidal anti-
inflammatory medications (yes/no), the use of prophylactic
antiemetics (yes/no), the use of regional anesthesia (yes/no),
the use of regional nerve blocks (yes/no), the length of stay
in the surgical facility, and the number of patients requiring
admission.
530 P. J. Morgan et al.
123
Statistical analyses
Sample size calculation
The standard deviation (SD) of postoperative pain scores
following outpatient surgery was 2.4,14 and the incidence
of postoperative nausea and vomiting (PONV) ranged from
20-30%.15 Based on this information and to detect a min-
imum difference of one point in pain score and a 15%
incidence rate, the sample size was calculated as 160 per
group with an alpha = 0.025 and power = 0.80.
Data analysis
The data were analyzed using descriptive statistics. For
continuous variables, the Shapiro-Wilk and Kolmogorov-
Smirnov tests were used to test the hypothesis of normal
distribution. Non-normally distributed data were reported
as median (interquartile range [IQR]) and were evaluated
with a Mann-Whitney U test. Categorical variables were
presented as count (percentages) and were evaluated using
Fisher’s exact test. For primary outcomes, P val-
ues \ 0.025 were regarded as significant, corresponding to
the Bonferroni correction to control the familywise error
rate at 0.05 for the two tests performed. The 97.5% con-
fidence intervals (CI) were calculated for the differences in
median and percentages. For secondary outcomes, P val-
ues \ 0.007 were regarded as significant, corresponding to
the Bonferroni correction for the seven tests performed.
The 99.3% CI of differences were calculated.
SAQ
This is a 58-item questionnaire to assess staff safety atti-
tudes, which includes an assessment of communication and
collaboration among staff. A repeated measures analysis of
variance was used to assess the results. Statistical signifi-
cance was defined as P \ 0.05.
Analyses were performed using SAS� version 9.2 (SAS
Institute, Inc., Cary, NC, USA).
Results
Pre-implementation data collection occurred over a period
of seven months and post-implementation data collection
occurred over a period of five months, for a total study
period of one year.
In the pre-implementation phase, SAQs were distributed
to 86 perioperative personnel, 70 of which were returned.
Due to the departure of a surgical program, 14 surgeons
were not present in the post-implementation phase, which
left 56 SAQs for distribution, 50 of which were completed.
The mean (SD) value for communication and collaboration
was high in both groups (mean 3.99 (0.66) and 4.09 (0.61),
respectively; P = 0.36), but there was no improvement
after implementation of the SSC. The assessment of the
staff’s ‘‘experience’’ in the working environment was also
good (mean 3.69 (0.29) and 3.76 (0.35), respectively;
P = 0.09), but again showed no statistical difference
between time periods. There was no improvement in the
six items related to teamwork and safety climate that
Haynes identified as most likely to respond to a checklist
intervention16 (Table 1).
Data on 180 patients were obtained prior to implemen-
tation of the SSC, and data on 195 patients were obtained
following implementation. There was no statistically sig-
nificant difference in age, sex, or type of surgical procedure
between the patient populations before and after SSC
implementation (Table 2). The median difference in pain
scores between groups was 0.5 (97.5% CI, 0 to 1;
P = 0.13). Since the incidence of nausea/vomiting was
Table 1 Safety Attitudes Questionnaire
Characteristics Pre (n=50) Post (n=50) P value
I would feel safe being treated here as a patient 4.44 (0.61) 4.40 (0.76) 0.3
Briefing operating room (OR) personnel before a surgical procedure is important for patient safety 4.76 (0.48) 4.79 (0.50) 0.82
I am encouraged by my colleagues to report any patient safety concerns I may have 4.24 (0.85) 4.24 (0.90) 0.99
In the ORs here, it is difficult to speak up if I perceive a problem with patient care 2.26 (1.09) 1.98 (1.03) 0.7
The physicians and nurses here work together as a well-coordinated team 4.20 (0.64) 4.30 (0.71) 0.39
Personnel frequently disregard rules or guidelines (e.g., handwashing, treatment
protocols/clinical pathways, sterile field, etc.) that are established for the OR
2.13 (1.00) 2.28 (1.22) 0.60
Total 4.22 (0.41) 4.25 (0.52) 0.71
Responses were scored on a five-point scale with 1 = strongly disagree and 5 = strongly agree. All values are mean (standard deviation). The
total value is the mean of responses, with negative statements (‘‘In the ORs here…’’ and ‘‘Personnel frequently disregard…’’) reverse-scored
Safety checklist in ambulatory surgery 531
123
low, comparison was made between those experiencing no
nausea/vomiting and those experiencing some nausea/
vomiting (mild, moderate, or severe). The difference in the
incidence rate of nausea/vomiting between the pre- and
post-implementation groups was -8.4% (97.5% CI, -17.9
to 1.1; P = 0.06) (Table 3).
Ninety-eight of 180 (54.4%) patients received prophy-
lactic antibiotics pre-implementation, and 105 of 195
(53.8%) patients received antibiotics post-implementation.
The antibiotics were administered after the incision to 5 of
98 (5.1%) patients pre-implementation and to 6 of 105
(5.71%) patients post-implementation (P = 0.85). The
remainder of the patients in both groups received antibi-
otics within 60 min before the incision. The median
difference in minutes in the timing of antibiotic adminis-
tration was 1 (99.3% CI, -2 to 4; P = 0.45). Before and
after implementation of the SSC, the difference in the use
of regional anesthesia was -3.4% (99.3% CI, -9.4 to 2.5;
P = 0.11), and the difference in the use of regional blocks
was 1.0% (99.3% CI, -11.5 to 13.0; P = 0.89). A higher
Table 2 Demographic data
Characteristics Before implementation
(n = 180)
After implementation
(n = 195)
Age: mean (standard deviation) 41.5 (14.3) 40.2 (13.4)
Female: n (%) 120 (67%) 135 (69%)
Procedure: n (%)
Gynecology 61 (34%) 57 (29%)
General surgery 34 (19%) 36 (18%)
Plastic surgery 18 (10%) 38 (19%)
Urology 7 (4%) 11 (6%)
Orthopedic surgery 60 (33%) 53 (27%)
Table 3 Primary outcomes
Characteristics Before
implementation
(n=180)
After
implementation
(n=195)
Difference
(97.5% confidence
interval)
P value
Pain (POD1): median [Interquartile
range] 1 = no pain; 10 = worst possible pain
3 [2-5] 3 [2-5] 0.5 (0 to 1) 0.13
Nausea and/or vomiting (POD1)
Some (mild, moderate, severe): n (%) 32 (17.8%) 51 (26.2%) -8.4% (-17.9 to 1.1) 0.06
POD = postoperative day
Table 4 Secondary outcomes
Characteristics Before
implementation
(n = 180)
After
implementation
(n = 188)
Difference
(99.3% confidence
interval)
P value
Antibiotic to incision time Minutes: median, [IQR] 10 [5-17] 10 [7-16] 1 (-2 to 4) 0.45
Preoperative NSAIDS given: n (%) 16 (8.9%) 61(32.4%) -23.3% (-35.5 to -11.1) B 0.001
Received PONV prophylaxis, n (%) 156 (86.7%) 149 (79.3%) 8.0% (-3.4 to 19.4) 0.05
Regional anesthesia n (%) 10 (5.6%) 4 (2.1%) -3.4% (-9.4 to 2.5) 0.11
Regional blocks: n (%) 32 (17.8%) 34 (18.1%) 1.0% (-11.5 to 13.0) 0.89
Length of stay in facility Hours: median, [IQR] 3.1 [2.4-3.9] 3.2 [2.6-3.9] -0.1 (-0.4 to 0.2) 0.38
Patients admitted to hospital: n (%) 1 (0.6%) 3 (1.6%) -1.1% (-4.2 to 2.1) 0.62
IQR = interquartile range; NSAIDS = nonsteroidal anti-inflammatory drugs; PONV = postoperative nausea and vomiting
532 P. J. Morgan et al.
123
percentage of patients received PONV prophylaxis in the
pre-implementation group than in the post-implementation
group (86.7% vs 79.3%, respectively) with a difference of
8.0% (99.3% CI, -3.4 to 19.4; P = 0.05). There was a
significant increase in the use of preemptive pain medica-
tions after implementation of the SSC (difference -23.3%;
99.3% CI, -35.5 to -1.1) (Table 4).
Items on the SSC
Compliance with the three sections on the checklist,
BRIEFING, TIME OUT, and DEBRIEFING was 99.49%,
97.95%, and 96.92% respectively. Compliance was defined
as a verbal discussion of at least one item in the section.
The median [IQR] number of items verbalized was: 19 [15-
22] items in the 41-item BRIEFING section, 5 [4-6] items
in the ten-item TIME OUT section, and 9 [7-11] items in
the 15-item DEBRIEFING section.
In the BRIEFING, TIME OUT, and DEBRIEFING
sections, there were 17, two, and two items, respectively,
that were verbalized \ 33% of times. After consensus of
the original champions’ committee members, the SSC used
in this study was adapted in the following way: 15 items
were deleted from the BRIEFING section; five items were
deleted from the TIME OUT section, and one item was
deleted from the DEBRIEFING section. This resulted in a
final 45-item checklist for use in an ambulatory surgical
centre (Figs. 1, 2). Items relating to the prevention of
postoperative pain and nausea were highlighted on the final
version by using capital letters and underlining (available
from the authors upon request).
Discussion
The purpose of this study was to adapt an already devel-
oped checklist to include items relevant to the ambulatory
surgical population. Ambulatory surgery has low rates of
major morbidity and mortality so outcomes, such as post-
operative pain and PONV or post-discharge nausea and
vomiting (PDNV), are more relevant in this population.17
There is evidence to suggest that attention to certain
measures can significantly decrease the severity of post-
operative pain and PONV/PDNV, including such
interventions as preemptive pain medications, the use of
regional anesthesia or regional nerve blocks, and the use of
prophylactic antiemetics, especially in high-risk surgical
procedures/patients.15 Despite adding items to the SSC that
pertain to these specific interventions, verbalization of
these items occurred in \ 10% of observed cases. Conse-
quently, it is not surprising that there was no improvement
in post-discharge pain and nausea/vomiting on the first
postoperative day before and after checklist introduction.
We also did not show a difference in the use of regional
anesthesia or prophylactic antiemetics. There was a sig-
nificant increase in the use of preemptive analgesics after
SSC introduction. This difference resulted from a change in
process whereby orthopedic patients began to receive
preoperative nonsteroidal medications on a routine basis
during this period of time; this change was unrelated to the
introduction of the SSC.
Checklist use has been a mainstay of safety practices in
the aviation industry for years. The use of checklists in
health care, however, has been much slower to evolve
despite evidence that their use improves patient outcomes
and/or improves team behaviours and communica-
tion.5,18-23 Specifically, use of the WHO SSC has shown a
decrease in inpatient morbidity and mortality2,4-7,24 as well
as improvement in teamwork skills, communication, and
adherence to process measures.1,23,25-27 Nevertheless, Ko
et al.’s recent systematic review of checklist use in medi-
cine has shown limited evidence of their effectiveness.28
Analysis of the studies indicated that many were of poor
quality with low levels of evidence and a high rate of bias.
In summary, the authors determined that it was not feasible
to provide an accurate summary of any trends across all
studies.
Similar to the study by Vogts and Fourcade, compliance
with BRIEFING and TIME OUT was high in our study, but
our study also showed a high compliance with the
DEBRIEFING section.29,30 The three items most com-
monly discussed were: Allergies, Site and procedure, and
ASA Class (American Society of Anesthesiologists’ class).Fig. 1 Checklist generation
Safety checklist in ambulatory surgery 533
123
There is, however, a need for caution when interpreting
compliance rates. Compliance is often defined as some
discussion having occurred with respect to the three sec-
tions of the SSC; however, not all items may have been
addressed within each section. Levy et al. recently reported
that individual items were either not executed as designed
or not executed at all despite the documented 100% com-
pletion of the SSC BRIEFING section.31 Therefore, some
studies report on ‘‘completeness’’ of the SSC. The evidence
suggests that rate of ‘‘completeness’’ of the SSC is sig-
nificantly lower than the rate of compliance.5,30,32 Our
study has shown that 21 items were discussed\33% of the
time.
There are a number of reports of low compliance with
healthcare checklists.33,34 In this study, several factors
may have contributed to the low compliance within
certain areas of the SSC and the failure to use the
checklist to improve the primary and secondary out-
comes. For a checklist to be effective, users at the
‘‘sharp end’’ must appreciate its value.35 If the users are
told simply that the checklist is an institutional require-
ment and they are not given or are not interested in the
rationale for its implementation, adherence to the
checklist may be suboptimal. Certainly, in the case of
the SSC, its implementation was an institutional
requirement and an institution’s adherence to the SSC
was posted on a provincial Web site with public access.
Although attempts were made to inform all stakeholders
of the process and the rationale behind the use of the
SSC, the lack of improvement suggests that the SSC was
not implemented effectively.
This particular point is reinforced by our results from
testing safety attitudes. Safety culture has been recognized
as an important strategy in the improvement of the deficits
Fig. 2 Checklist details
534 P. J. Morgan et al.
123
identified in healthcare safety.36 Culture has been identified
as a factor affecting absenteeism, employee turnover,
length of stay, and readmission rates. The SAQ is a vali-
dated tool designed specifically for operating room teams
and is an adaptation of the Flight Management Attitudes
Questionnaire developed for aviation teams.37 Using six
items from the SAQ, Haynes showed an improvement in
safety attitudes before and after introduction of the SSC.38
Our study did not show an improvement in safety attitudes
using these same six items, which may be accounted for by
the higher values seen in our pre-intervention group
(Table 1).
The checklist may have been too lengthy for use in an
ambulatory surgical facility where turnover pressure is
high. Limiting the length of a checklist is considered cru-
cial for its feasibility and usefulness. In the nuclear
industry, it has been stated that ‘‘…as the list of items
grows, there may be a higher probability of overlooking
any given item.’’39 Had we pilot tested the initial adapta-
tion of the checklist at an early stage, we may have been
able to identify the checklist items that were not consis-
tently noted, allowing for an initial modification and
obviating the need for a revised checklist at the end of the
study.
The Pareto principle may be employed with respect to
checklist content. It assumes that 20% of adverse events
will account for 80% of injuries, allowing tailoring of a
checklist to focus on priority areas. If potential adverse
events are not prioritized, healthcare workers may end up
addressing 80% of the adverse events that account for only
20% of the injuries.35 In this study, addition of more items
to an already lengthy checklist was likely compounding the
lack of prioritization of SSC items. Although morbidity
from post-discharge pain and nausea/vomiting occurs,
major adverse events more likely to profit from a
‘‘checklist’’ discussion would include four items: correct
patient, correct operation, correct side, and allergy identi-
fication. In fact, despite the length of the SSC used in this
study, these four ‘‘big ticket’’ items were identified in [90% of cases. All operating room staff may have clearly
understood the rationale for discussion of these items and
were therefore compliant. Other items, however, may not
have been perceived as relevant by all users and therefore
were not mentioned. Similar to the comments of Vats et al.,
some items on the SSC were simply not relevant to cases in
an ambulatory facility and were therefore ignored.33
Another potential confounding factor in the lack of
effective SSC implementation was the fact that the sur-
geons involved in the study were not all based primarily at
our centre. They would therefore have been exposed to a
different checklist at another institution and may not have
recognized the differences between their home-based hos-
pital SSC and our ambulatory facility SSC. Hierarchy may
also have played a role in that some RNs may have been
reluctant to ‘‘step in’’ if items were not mentioned by the
attending surgeon.
In summary, the SSC was not effectively implemented
in our ambulatory facility. A number of potential reasons
have been cited. Specifically, items added to the SSC in
an attempt to improve the primary outcomes of post-
discharge pain and nausea/vomiting were ineffective,
suggesting that the SSC may not be the optimal strategy
to address these issues. Due to poor compliance with the
adapted version (Appendix B) used in this study, a final
abbreviated checklist has been developed for use in an
ambulatory surgical facility and is available from the
authors.
Acknowledgments This study was funded by a grant from the
Alternate Funding Plan Innovation Fund, Ministry of Health and
Long Term Care and Department of Anesthesia, University of Tor-
onto Merit Award.
Competing interests None declared.
Appendix A
Surgical Safety Checklist
Safety checklist in ambulatory surgery 535
123
Appendix B
Modified Surgical Safety Checklist
536 P. J. Morgan et al.
123
Safety checklist in ambulatory surgery 537
123
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