An Enhanced Recovery After Surgery Protocol For Fa
An Enhanced Recovery After Surgery Protocol For Fa
An Enhanced Recovery After Surgery Protocol For Fa
a
Division of Plastic and Reconstructive Surgery, University of California Los Angeles, David Geffen School of
Medicine, Los Angeles, CA, United States
b
T.H. Chan School of Public Health, Harvard University, Boston, MA, United States
c
UCLA Gender Health Program, University of California Los Angeles, David Geffen School of Medicine, Los
Angeles, CA, United States
☆
This work was presented at the Plastic Surgery Research Council’s 67th Annual Meeting and the 100th Annual Meeting of the American
Association of Plastic Surgeons.
⁎
Correspondence to: Division of Plastic and Reconstructive Surgery, University of California, Los Angeles, 200 UCLA Medical Plaza, Suite
460, Los Angeles, CA 90095-6960, United States.
E-mail address: [email protected] (J.C. Lee).
https://doi.org/10.1016/j.bjps.2023.07.044
1748-6815/© 2023 British Association of Plastic, Reconstructive and Aesthetic Surgeons. Published by Elsevier Ltd. This is an open access
article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
M. Bedar, D. Dejam, R.M. Caprini et al.
versus 1.5 [1.0–2.1] MED/kg, p < 0.001), reported lower pain scores (2.5 ± 1.8 versus
3.7 ± 1.6, p = 0.002), and required a shorter hospital stay (median [IQR], 27.3 [26.3–49.8]
versus 32.4 [24.8–39.1] h, p < 0.001). When controlling for other contributing variables such as
previous gender-affirming surgeries, mental health diagnoses, and length of surgery using
multivariable linear regression analyses, ERAS protocol implementation independently pre
dicted reduced opioid use, lower pain scores, and shorter hospital stay after facial feminization
surgery.
Conclusions: The current work details an ERAS protocol for facial feminization surgery that
reduces perioperative opioid consumption, patient-reported pain scores, and hospital stays.
© 2023 British Association of Plastic, Reconstructive and Aesthetic Surgeons. Published by
Elsevier Ltd. This is an open access article under the CC BY license (http://creative
commons.org/licenses/by/4.0/).
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Journal of Plastic, Reconstructive & Aesthetic Surgery 85 (2023) 393–400
over-the-counter acetaminophen as needed. Nonsteroidal protocol and 38 patients (48.1%) were included in the pre-
anti-inflammatory drugs such as ketorolac and ibuprofen ERAS cohort. Age at surgery, body mass index, and medical
were not included in the regimen. comorbidities did not differ significantly between cohorts
(Table 1).
Approximately 73% of patients in each cohort had re
FFS ERAS protocol
ceived other gender-affirming surgeries prior to FFS, with
no differences in the types of procedures between groups.
Our FFS ERAS protocol was implemented in January 2021
All patients had previously been treated with hormone
with the primary goal of reducing postoperative opioid use.
therapy and the median (interquartile range, IQR) length of
Preoperatively, patients were counseled and educated re
hormone therapy was 3.0 (1.6–5.0) years in both cohorts.
garding the postoperative pain management protocol.
Mental health diagnoses were present in 60 patients
Intraoperatively, patients received a multimodal analgesia
(75.9%) in the cohort, with no differences between the pre-
regimen consisting of both opioid and nonopioid analgesics
ERAS and ERAS groups. Anxiety and depression were the
including local anesthetic injection of 0.25% bupivacaine
most frequently diagnosed mental health conditions, ac
with 1:200,000 epinephrine at each incision 10 min or more
counting for 64.6% and 63.3% of all patients, respectively.
prior to incision at each anatomic location sequentially,
8.9% of patients had a history of substance abuse with no
intravenous opioids as needed, intravenous ketorolac
differences between the pre-ERAS and ERAS groups. Of
(15–30 mg), and intravenous acetaminophen (1000 mg).
note, many patients had more than one mental health di
Postoperatively, patients received scheduled intravenous
agnosis.
ketorolac (15 mg) and oral acetaminophen (650 mg) every
6 h, until discharge. Breakthrough pain was addressed with
oral tramadol (50 mg). In severe pain, oral oxycodone (5 mg) Surgical characteristics
or intravenous hydromorphone was administered based on
clinical judgment. At discharge, patients were prescribed Overall, 93.7% of patients received one-stage FFS with no
oral acetaminophen (650 mg) and oral ibuprofen (400 mg) difference between pre-ERAS and ERAS groups (Table 2).
every 6 h alternating until no longer needed and were given Patients in each cohort underwent an average of 7.1 ± 1.9
a 5-day supply of tramadol (50 mg) for breakthrough pain. procedures, also with no differences between the pre-ERAS
and ERAS groups. With respect to the types of surgeries,
more patients within the pre-ERAS group received hairline
Statistical analyses lowering (81.6% vs. 58.5%; p = 0.03) and upper lip lift (55.3%
vs. 29.3%; p = 0.02) compared to the ERAS group, whereas
Descriptive statistics, chi-square analyses, and independent more patients in the ERAS group received mandibular re
samples t-tests were used to compare pre-ERAS and ERAS construction (95.1% vs. 78.9%, p = 0.03). Despite the dif
groups. The Shapiro–Wilk test was used to examine the ferences in surgical procedures, no difference in overall
normality of continuous data. Nonnormally distributed length of surgery was found between groups with a median
continuous data were compared using Mann–Whitney U (IQR) time of 7.8 (6.7–8.9) h for the entire cohort.
tests. Multivariable linear regression analyses were con
ducted to determine predictors of total perioperative
Comparison of perioperative analgesic medications,
opioid use, mean pain scores, and length of hospital stay.
Independent variables included for all three models were:
patient-reported pain scores, and length of hospital
implementation of the ERAS protocol, previous gender-af stay between Pre-ERAS and ERAS groups
firming surgeries, mental health diagnoses, and duration of
surgery. Additionally, length of hospital stay was included in The primary outcomes assessed in this work were total in
the models for perioperative opioid use and pain scores. All patient opioid use, patient-reported pain scores, and length
of the following assumptions were met for each model: of hospital stay (Table 3).
linearity and homoscedasticity using a residual versus pre
dicted values plot, collinearity using a variance inflation Perioperative analgesic medications
factor < 2 for all predictors for each model, independence In the total cohort, a combination of nonopioid and opioid
of residuals using Durbin–Watson criteria of 1.5–2.5, and analgesic medications were used in the perioperative, in
normality of residuals using a visual inspection of the P-P patient period with a median (IQR) of 1.1 (0.8–1.6) MED/kg
plot. Statistical significance was defined as a p-value less of total opioids and 33.2 (22.6–47.6) mg/kg of acet
than 0.05. Statistical analyses were performed using SPSS aminophen. The total opioid use differed between pre-
Statistics Version 27 (IBM Corp., Armonk, NY). ERAS and ERAS groups (median [IQR] 1.5 [1.0–2.1] vs. 0.8
[0.5–1.1] MED/kg, p < 0.001) in a manner that was driven
by the postoperative opioid medications administered,
with no differences in intraoperative opioid medications
Results between the groups. Postoperatively, the replacement of
oxycodone with tramadol as the first-line oral narcotic
Patient characteristics reduced MED/kg in the ERAS group significantly.
No differences between the groups were seen in the usage
A total of 96 patients were identified through retrospective of intravenous hydromorphone in the postoperative
chart review, and 79 patients met the inclusion criteria. A period. For nonopioid medications, ketorolac was one
total of 41 patients (51.9%) were treated with the ERAS of the mainstays of the ERAS protocol and, hence, was
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M. Bedar, D. Dejam, R.M. Caprini et al.
significantly higher compared to the pre-ERAS group where Patient-reported pain scores and length of hospital stay
no ketorolac was used. No differences were seen between In addition to the primary outcome of opioid usage, patient-
the groups for acetaminophen usage. In combination, reported pain scores and the length of hospital stay were
these data indicated that a reduction in perioperative evaluated. Compared to the pre-ERAS group, average pa
opioid use occurred with the implementation of the ERAS tient-reported pain scores during the course of the hospital
protocol. stay were significantly lower in the ERAS group (2.5 ± 1.8
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Journal of Plastic, Reconstructive & Aesthetic Surgery 85 (2023) 393–400
Table 3 Analgesic medications, patient-reported pain scores, and length of hospital stay between Pre-ERAS and ERAS groups.
Total Cohort n = 79 Pre-ERAS ERAS p
n = 38 n = 41
Analgesic Medications
Total Opioids, median (IQR) MED/kg 1.1 (0.8–1.6) 1.5 (1.0–2.1) 0.8 (0.5–1.1) < 0.001
Intraoperative Total Opioids 0.6 (0.4–0.8) 0.6 (0.4–0.9) 0.6 (0.4–0.8) NS
Fentanyl, IV 0.3 (0.1–0.4) 0.2 (0.1–0.4) 0.3 (0.1–0.4) NS
Hydromorphone, IV 0.3 (0.2–0.4) 0.4 (0.2–0.5) 0.3 (0.2–0.4) NS
Postoperative Total Opioids 0.4 (0.1–0.9) 0.9 (0.4–1.5) 0.2 (0–0.5) < 0.001
Oxycodone, PO 0 (0–0.7) 0.8 (0.2–1.3) 0 (0–0) < 0.001
Tramadol, PO 0 (0–0.2) 0 (0) 0.1 (0–0.3) < 0.001
Hydromorphone, IV 0 (0–0.1) 0 (0–0.1) 0 (0–0.1) NS
Non-opioids, median (IQR) mg/kg
Ketorolac 0 (0–0.6) 0 (0–0) 0.6 (0.4–0.8) < 0.001
Acetaminophen 33.2 (22.6–47.6) 40.6 (21.9–57.6) 32.7 (24.8–39.1) NS
Pain Scores, (mean ± SD) 3.1 ± 1.8 3.7 ± 1.6 2.5 ± 1.8 0.002
Length of stay, hours (median, IQR) 29.4 (26.3–49.8) 32.4 (28.7–51.9) 27.3 (25.3–30.4) < 0.001
ERAS, enhanced recovery after surgery; NS, not significant; NA, not applicable; MED, morphine equivalent dose; IQR, interquartile range;
SD, standard deviation.
vs. 3.7 ± 1.6; p = 0.002). The reduction in pain scores was Total perioperative opioid use
accompanied by a decrease in the length of hospital stay The regression model explained 42.4% of the variance in
from a median (IQR) time of 32.4 (28.7–51.9) h in the pre- total opioid use in MED/kg [F(5,73) = 10.736, p < 0.001].
ERAS group to 27.3 (25.3–30.4) h in the ERAS group Among the independent variables included in the model,
(p < 0.001). the ERAS protocol independently predicted reduced opioid
use (β = −0.25, p = 0.01), whereas both previous gender-
Implementation of the FFS protocol as a predictor affirming surgeries (β = 0.21, p = 0.03) and a longer length
of hospital stay (β = 0.45, p < 0.001) independently pre
of perioperative opioid use, patient-reported pain
dicted increased opioid use.
scores, and length of hospital stay
Table 4 Implementation of the ERAS protocol as a predictor for perioperative opioid use, pain scores, and length of hospital
stay in multivariable linear regression models.
Opioid use Mean pain scores Length of hospital stay
R2 = 0.424 R2 = 0.224 R2 = 0.216
F (5,73) = 10.736, F (5,73) = 4.225, F (4,74) = 5.095,
P < 0.001 P = 0.002 P = 0.001
Predictors β p β p β p
ERAS protocol −0.25 0.01 −0.23 0.04 −0.37 < 0.001
Previous gender-affirming surgeries 0.21 0.03 0.09 NS 0.12 NS
Mental health diagnoses 0.04 NS 0.11 NS 0.05 NS
Length of surgery 0.04 NS 0.13 NS 0.20 NS
Length of hospital stay 0.45 < 0.001 0.24 0.04
NS, not significant; ERAS, enhanced recovery after surgery.
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M. Bedar, D. Dejam, R.M. Caprini et al.
p < 0.001), while no other predictors were found to affect thoughtful opioid-reduction strategies are highly important
the length of hospital stay. in this patient population.
In the extant literature, only two opioid-sparing perio
perative protocols have been described for gender-affirming
surgeries, both for gender-affirming vaginoplasty. Salgado
Discussion et al. reported that the addition of epidural anesthesia
improved pain control16 and Tirrell et al. reported that the
In this work, we described the implementation and out replacement of intravenous patient-controlled opioid an
comes of an ERAS protocol for gender-affirming FFS to re algesia with pro re nata oral opioid medications resulted in
duce postoperative opioid use in an at-risk patient a reduced total quantity of opioid administration as well as
population. The two main differences in patients treated a reduced hospital stay.17 Both former reports differ sig
under the ERAS protocol compared to pre-ERAS were: (1) nificantly from the current report due to differences in
the addition of scheduled ketorolac and (2) the replacement anatomic location. Unlike vaginoplasty surgery, FFS is fre
of postoperative oral oxycodone with oral tramadol as the quently associated with sensory neuropraxia in the V1 and
primary pro re nata narcotic oral analgesic. The effects of V3 distributions of the trigeminal nerve due to the extensive
the ERAS protocol were then assessed using three primary fronto-orbital and mandibular osseous reconstruction.
outcome measures: total perioperative opioid usage, pa Hence, standard trigeminal nerve blocks are unlikely to
tient-reported pain scores, and total length of inpatient assist in postoperative pain control. In contrast to the latter
stay. All three measures demonstrated a reduction in the study, the length of hospital stay for facial gender-affirming
ERAS cohort compared to the pre-ERAS cohort. surgery patients is significantly shorter and the need for
Furthermore, when controlling for other potential factors opioid analgesics is also lower overall. Hence, the oral
that may influence any of the three outcomes such as pre opioid used in the current ERAS protocol, tramadol, was
vious gender-affirming surgeries, mental health diagnoses, chosen specifically due to its potency, approximately 20%
and complexity of the specific surgery, the implementation that of oral morphine18 as well as its lower risk of misuse.27
of the ERAS protocol independently predicted decreased In contrast to the majority of reported ERAS protocols,
opioid use, decreased patient-reported pain scores, and we consciously chose against incorporating gabapentin as
decreased length of hospital stay. part of the multimodal analgesia regimen.12,14,17 The ra
Over the past decade, the contribution of postsurgical tionale to omit gabapentin was, in part, to limit the number
prescription opioids to opioid misuse has been increasingly of simultaneous changes in the perioperative pain regimen
clarified. Following elective surgical procedures, persistent as well as to prevent the potential for gabapentin misuse,
opioid use has been estimated by Waljee, Brummett, and an increasingly recognized entity.28–30 Motivations for ga
colleagues to be approximately 6%−13% of all opioid-naïve bapentinoid misuse have been attributed to a myriad of
adult patients and approximately 5% of all opioid-naïve effects, such as auditory hallucinations, euphoric mood,
adolescent patients with variations based on the type of and dissociation.31 The alarming effect of gabapentin as a
surgery.7,19–21 These effects are potentially cumulative as potentiator of opioid-induced deaths28,32 has resulted in its
Agarwal et al. demonstrated that both prior noncontinuous reclassification to a Class C controlled substance in the
and continuous opioid exposure for 3 months or longer United Kingdom as well as tighter regulation at the state
predicted higher odds of persistent opioid use.22 Among the level in the United States. The hazards of gabapentinoid
transgender patient population, the risks of opioid use fol misuse suggest that re-evaluation for its inclusion in ERAS
lowing surgery may be higher secondary to other existing protocols overall may be indicated.
risk factors for substance use.7,23–25 While improvement in pain outcomes during the perio
In addition to behavioral and mental health-related risk perative period is encouraging, ultimately, assessment of
factors, the quantity and frequency of gender-affirming the current ERAS protocol requires long-term evaluation of
surgeries may also place transgender individuals at an in opioid misuse in the outpatient setting. The high prevalence
creased risk of opioid misuse compared to their cisgender of mental health diagnoses in the transgender patient po
peers. The US Transgender Survey data indicated that many pulation overall,24,25 as well as in the current cohort
transgender individuals seek to undergo more than one (75.9%), suggests that the risk profile for persistent opioid
gender-affirming surgery, and the perceived psychosocial use after gender-affirming surgery may be uniquely higher.7
benefits of these surgeries may encourage patients to un Further analysis using statewide prescription tracking da
dergo multiple procedures in a short time span to alleviate tabases similar to the report by Chao and colleagues on
dysphoria-related stressors.26 An uptick in health insurance breast reconstruction14 will be necessary to determine the
coverage for various gender-affirming procedures may also success of the current ERAS protocol.
alleviate financial barriers to surgery, thus allowing trans
gender patients to undergo more procedures with con
sequent opioid exposures and less recovery time between Conclusions
procedures. While the relationship of gender-affirming sur
geries to opioid misuse has not been well-studied, the cur We describe an ERAS protocol to reduce opioid usage in
rent work suggests that prior gender-affirming surgeries patients undergoing gender-affirming FFS. Our analysis
predicted higher quantities of total perioperative opioid suggests that this regimen reduced perioperative opioid
consumption after FFS (Table 4). In combination, these lines consumption, decreased patient-reported pain, and shor
of evidence would suggest that vigilance in opioid admin tened the time to discharge after surgery. The implications
istration following gender-affirming surgeries as well as of these findings are particularly important among
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Journal of Plastic, Reconstructive & Aesthetic Surgery 85 (2023) 393–400
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Funding Psychiatric disorders in the US transgender population. Ann
Epidemiol 2019;39(1–7):e1.
7. Brummett CM, Waljee JF, Goesling J, et al. New persistent
This work was supported by the Bernard G. Sarnat opioid use after minor and major surgical procedures in US
Endowment for Craniofacial Biology (JCL) and the Jean adults. JAMA Surg 2017;152(6):e170504. https://doi.org/10.
Perkins Foundation (JCL). JCL is additionally supported by 1001/jamasurg.2017.0504.
the National Institutes of Health/National Institute of 8. Bartlett EL, Zavlin D, Friedman JD, Abdollahi A, Rappaport NH.
Dental and Craniofacial Research R01 DE029234 and R01 Enhanced recovery after surgery: the plastic surgery paradigm
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Ethical approval org/10.1001/jamasurg.2016.4952.
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We have obtained ethical approval for this study involving after surgery pathway for microsurgical breast reconstruc
human subjects through the University of California Los tion: a systematic review and meta-analysis. Plast Reconstr
Angeles Institutional Review Board protocol 11-000925. Surg 2019;143(3):655–66. https://doi.org/10.1097/prs.
0000000000005300.
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duction in elective plastic surgery: a randomized prospective
Financial disclosure statement study. 02 01 Plast Reconstr Surg 2021;147(2):325e–30e.
https://doi.org/10.1097/PRS.0000000000007592.
All authors have no financial interests, including in pro 12. Dietz N, Sharma M, Adams S, et al. Enhanced Recovery After
Surgery (ERAS) for spine surgery: a systematic review. World
ducts, devices, or drugs associated with this manuscript.
Neurosurg 2019;130:415–26. https://doi.org/10.1016/j.wneu.
JCL is a medical education consultant for Stryker. All
2019.06.181.
sources of funds supporting the completion of this manu 13. Johnson AC, Colakoglu S, Reddy A, et al. Perioperative blocks
script are under the auspices of the University of California, for decreasing postoperative narcotics in breast reconstruc
Los Angeles. tion. Anesth Pain Med 2020;10(5):e105686. https://doi.org/
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Enhanced recovery after surgery protocols decrease outpatient
Appendix A. Supporting information opioid use in patients undergoing abdominally based microsurgical
breast reconstruction. Plast Reconstr Surg 2020;145(3):645–51.
Supplementary data associated with this article can be https://doi.org/10.1097/prs.0000000000006546.
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