Open access peer-reviewed chapter

Postoperative Analgesia in Plastic Surgery Procedures

Written By

Daniela Arévalo-Villa, Andrea Figueroa Morales, Roberto de Jesús Jiménez-Contreras and Víctor M. Whizar-Lugo

Submitted: 28 June 2023 Reviewed: 18 August 2023 Published: 30 September 2023

DOI: 10.5772/intechopen.112930

From the Edited Volume

Topics in Postoperative Pain

Edited by Victor M. Whizar-Lugo, Analucía Domínguez-Franco, Marissa Minutti-Palacios and Guillermo Dominguez-Cherit

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Abstract

Advances in the knowledge of the secondary effects of acute postoperative pain have motivated anesthesiologists and surgeons to pay special attention to its prevention and correct management. Surgical procedures in plastic surgery are very varied and produce postoperative pain in direct relation to the site, type, and extent of surgery, with facial interventions being the least painful (with the exception of rhinoplasty) and the most painful being breast surgery, abdominoplasty, and extensive liposuctions due to the possibility of trauma to peripheral nerves and greater secondary inflammation. The combination of surgeries produces more intense post-surgical pain. There is insufficient data on the frequency and severity of pain after plastic surgery, be it reconstructive or cosmetic. Although opioids have been considered to be the cornerstone in the treatment of postsurgical pain, their use in plastic surgery patients must be carefully evaluated for various reasons that interfere with the results of this type of surgery. Similar to other surgical specialties, multimodal analgesia is now the most appropriate way to prevent and treat pain in these patients. This chapter is a comprehensive review of the management of acute postoperative pain in certain plastic surgery procedures, with emphasis on the multimodal approach.

Keywords

  • plastic
  • surgery
  • postoperative
  • pain
  • analgesia

1. Introduction

Postoperative pain (POP) is a subjective phenomenon, without a useful biological function, which varies with several factors such as the patient themselves, type of surgery, experience with previous surgeries, duration and extent of surgery, anesthetic technique, kind of perioperative care, individual characteristics and experiences, fear, and anxiety. The latest global survey from International Society for Aesthetic Plastic Surgery published in January 2023 reports a considerable increase in esthetic surgery worldwide, showing an overall 19.3% increase in procedures performed by plastic surgeons in 2021 with more than 12.8 million surgical procedures and 17.5 million non-surgical procedures performed globally. This equates to an increase of 33.3% over the last 4 years [1]. Paradoxically, the COVID-19 pandemic has increased plastic surgery procedures around the world; although the frequency of scheduled plastic surgery has apparently decreased in many countries, some procedures have increased as patients have free time for their cosmetic plans [2, 3, 4, 5]. The top five most popular surgical procedures remain liposuction, breast augmentation, eyelid surgery, rhinoplasty, and abdominoplasty [1]. This notable increase in plastic surgeries has favored multiple advances not only in the surgical area, but in all anesthetic aspects, including the comprehensive management of POP. With increasing frequency, these types of surgeries are ambulatory or short stay, which tends to make the management of POP even more difficult, especially in the first post-surgical days.

Satisfactory POP management is mandatory for patient satisfaction. In patients undergoing thoracic and abdominal procedures, poor pain management has been related to pulmonary complications, cardiac ischemia, ileus, thromboembolism, and impaired immune function [6]. One of the greatest problems for adequate pain relief is due to inadequate physician familiarity with analgesic options available. Poorly controlled POP has been associated with deficient surgical outcomes, longer post-anesthesia care unit stays, poor pulmonary function, and higher readmission rates. The development of chronic pain after surgery, also called persistent postsurgical pain, is also related to uncontrolled acute POP and is recognized as a significant health problem [7]. On the one-day surgery basis, pain is one of the most prevalent problems, being as high as 58% 30 min after surgery in the undeveloped countries and up to 34.7% 48 h after discharge [6].

Up to date, multimodal analgesia is the most effective modality in the management of POP. This chapter reviews the importance of diagnosis, prevention, and timely management of POP in plastic surgery patients.

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2. Postoperative pain in plastic surgery

Postoperative pain in patients undergoing plastic surgery procedures is a problem that has not been resolved and that implies serious management challenges. On one side, these patients are extremely demanding, with little or no tolerance for complications, especially POP. A growing number are tourist patients who have traveled many hours and sometimes thousands of kilometers by train, plane, or car only to be operated in remote places, where another language is often spoken, and customs as well as food are different from their original countries [8, 9]. Transgender and gender diversity patients are a steadily growing group requesting plastic surgery that requires meticulous care in a humanitarian sense, avoiding pejorative comments [10]. These factors produce stressful situations that make the proper management of POP even more difficult. An empathic patient-centered intervention can reduce preoperative anxiety and favor a faster surgical recovery, wound healing, and patient satisfaction.

On the other hand, some plastic surgeons and anesthesiologists do not have enough knowledge and sensitivity to address the timely treatment of POP [11, 12]. If we add the challenges of the current global crisis on the inappropriate and sometimes illegal use of opioids and other narcotics, the problem is even more difficult to address [13].

We did not find sufficient epidemiological data on the frequency and intensity of POP after plastic surgery, although it is known that the most painful procedures are breast surgery, abdominoplasty, extensive liposuction, and combined surgeries. In some studies, it is mentioned that plastic surgery, neurosurgery, orthopedics, and general surgery have the highest prevalence of severe POP varying from 10 to 75% [14, 15, 16, 17].

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3. Management of POP in plastic surgery

The POP approach should be started before surgery. This stage, known as pre-emptive analgesia, is based on preventing the development of spinal hyperexcitability and behaviors related to pain. The measures to prevent POP are basic and very simple in plastic surgery. During the initial evaluation, the anesthesiologist must gain the patient’s trust by establishing a deep empathic relationship. The usual questioning and physical examination are not enough; the expectations of each patient must be known, and the reasons for their plastic surgery, and their personal and work environment are issues that facilitate this patient-anesthesiologist relationship. Pre-emptive analgesia includes the administration of an analgesic technique or drug with the aim of attenuating postoperative pain, hyperalgesia, and allodynia. In this phase, there is a wide range of possibilities, and several drugs must be used simultaneously. The preoperative combination of an NSAID, magnesium, ketamine, pregabalin, and an analgesic such as metamizole (dipyrone) or acetaminophen produces spectacular analgesic results [18, 19, 20, 21].

3.1 Pharmacological management of POP in plastic surgery

The pharmacological management of POP in plastic surgery plays a fundamental aspect since it reduces complications, long stays, and costs, and favors rapid recovery after surgery. Various drugs and locoregional analgesia, including the tumescent technique widely used in plastic surgery, are part of multimodal analgesia programs in these patients [6, 22, 23, 24].

3.1.1 Opioids

Although opioids are the cornerstone in the treatment of POP, unfortunately plastic surgeons prescribe almost twice as many opioids as are required after outpatient surgeries, which continues to be a major factor in the globalized crisis of legal and illegal use of these drugs [12, 25, 26, 27]. Just to mention an example, in body-contouring surgeries, opioid overprescription is a proven routine among plastic surgeons. Bennett et al. [28] examined health insurance claims between 2001 and 2015 of patients with no history of opioid use who underwent body-contouring surgeries (abdominoplasty/panniculectomy, breast reduction, mastopexy, brachioplasty, and thigh plasty). They found that 6.1% of patients who had not previously received opioids developed persistent new use and 12.9% were exposed to high-risk prescriptions. Persistent opioid use was higher in high-risk prescription patients (9.2%), being the highest in thigh plasty (17.7%; 95% CI, from 0.03 to 0. 33). These researchers found high rates of mood disorders, anxiety, smoking, alcohol intake, neck pain, arthritis, and other pain disorders. In a study [29] of 56,773 patients undergoing body-contouring surgery, it was found that hydrocodone with paracetamol was the most prescribed opioid with an average of 17.9 days. These authors examined the comorbidities in this group of patients, finding that the cases with peripheral vascular disease and smoking were prescribed more opioids than patient without peripheral vascular disease (871.97 vs. 535.41; p < 0.001) and smoking (1069.57 vs. 440.84; p < 0.001). Those patients who developed surgical site infection, disruption of wound, and venous thromboembolism were prescribed a considerably greater dose of opioids (1213.63 vs. 561.59; p < 0.001). Another example of opioid overuse is augmentation mammoplasty where up to 91.2% of surgeons prescribe opioids, the most recommended being oxycodone with acetaminophen 47%, and hydrocodone with acetaminophen 38.3% [30].

Opioids primarily act on mu, kappa, and delta opioid receptor modulating the algesic response. Mu opiate receptor properties also include euphoria, sedation, anorexia, nausea, vomiting, respiratory depression as well as tolerance and opioid addiction. When prescribing opioids, it is important to consider patients’ previous health conditions which could require chronic opioid use, or those conditions which may require higher doses in geriatric patients or patients with obstructive sleep apnea in which opioids may lead to airway obstruction.

Oliceridine is a new complex opioid, with potency similar to morphine, with no ceiling effect, which has fewer side effects than traditional opioids, although it can cause respiratory and CNS depression. It was approved by the US Food and Drug Administration in August 2020 for the intravenous treatment of moderate-to-severe acute pain in hospitalized patients. Although there is still not enough research on POP in plastic surgery, oliceridine could have a prominent place in these patients [31, 32].

3.1.2 Non-opioids

Acetaminophen (paracetamol) is one of the most frequently used analgesic agents. Despite the fact that it has been used for more than a century, its mechanism of action is not fully known, and is related to inhibition of CNS enzyme cyclooxygenase (COX) activities, with conflicting views on the COX isoenzyme/variant targeted by acetaminophen and on the nature of molecular interactions with these enzymes. It appears to selectively inhibit COX-2 by functioning as a reducing agent, although in vitro screening tests demonstrate low potency in inhibiting COX-1 and COX-2. In COX-1 transgenic mice, acetaminophen works through the inhibition of a variant of the COX-1 enzyme to mediate its analgesic and particularly thermoregulatory actions (antipyresis and hypothermia). Another possibility is that the descending inhibitory serotonergic pathway is potentiated to mediate the analgesic action of paracetamol, but without evidence of binding to serotonergic molecules. It has been proposed that AM404 (N-acylphenolamine), a paracetamol metabolite, activates the endocannabinoid1 and transient receptor potential vanilloid-1 (TRPV1) brain systems. Also, AM404 directly induces analgesia via TRPV1 receptors on terminals of C-fibers in the spinal dorsal horn [33, 34]. Consequently, acetaminophen induces analgesia by acting not only on the brain but also on the spinal cord.

It does not have the same gastric complications as other NSAIDs. A single dose of acetaminophen may reduce pain by 50%. However, its administration should be reduced in patients with liver malfunction, limiting its total dose to 2000 mg/day. In healthy patients, its total dose in 24 h should not be over 4000/day mg. Liver damage from acetaminophen is a rare secondary effect related to overdose.

3.1.3 Non-steroidal anti-inflammatory drugs (NSAIDs)

It is a group of non-opioid analgesics widely used in POP, although its potency is less than that of opioids and its side effects are extensive, especially with long-term use. Selective COX-2 inhibitors are linked to greater cardiovascular risk, while non-selective COX inhibitors are associated with higher gastrointestinal hazard. NSAIDs with lower renal excretion with phase 2 metabolism are less likely to induce adverse effects and drug-drug interactions [35].

NSAIDs, which act in COX-1 and COX-2, have demonstrated a suitable analgesic effect. However, many patients have restrictions on their administration due to the higher risk of bleeding. In 2021, a meta-analysis showed that in 151,031 surgical procedures, including esthetic surgeries, the NSAIDs were unlikely the cause of postoperative bleeding. Even though NSAIDs have little to no effect on bleeding, the difference in COX-1 and COX-2 is evident when we analyze platelet dysfunction. For nonselective COX-1, the platelet dysfunction was greater than with COX-2 inhibitors. According to Schoenbrunner et al., the best NSAID for plastic surgery has been meloxicam due to its one-day administration basis and the affinity to COX-2, which decreases its action in platelet function [6, 22]. COX-2 selective inhibitors are contraindicated in those with preexisting coronary artery disease because of their association with higher rates of cardiac events. COX-2 selective inhibitors and NSAIDs should also be avoided in patients with chronic or acute renal disease [26].

It has been shown that diclofenac associated with beta-lactam antibiotics could be useful in surgical infections caused by methicillin-resistant Staphylococcus aureus (MRSA) where implants are used [36], which would represent a considerable advance in augmentation mammoplasty with implants.

3.1.4 Other types of analgesics and adjuvants in POP

There is a group of drugs that are used as adjuvants in postoperative analgesia that have proven to be useful, although their advantages are still controversial [37, 38, 39]. Some of these drugs are reviewed below.

3.1.4.1 Gabapentinoids

These drugs are specific ligands for the α2δ-1 subunit of voltage-gated calcium channels. Gabapentin, pregabalin, and mirogabalin have various pharmacological effects including antiepileptic, anti-anxiety, and analgesia, although this last effect is still controversial [40, 41]. A meta-analysis with 6201 patients found that the analgesic effect of both drugs is related to the doses used; pregabalin (≥150 mg) was more effective than 75 mg, and gabapentin (≥900 mg) if needed [38].

3.1.4.2 Ketamine

It is an extraordinary drug derived from phencyclidine. Synthesized in 1962 by Calvin Stevens at Parke Davis, it was first used in clinical anesthesia in 1965 by Corsen and Domino. It is a racemic mixture consisting of (S)- and (R)-ketamine, uncompetitive N-methyl-D-aspartate receptor antagonist. Although best characterized for its dissociative anesthetic properties, ketamine also has analgesic, anti-inflammatory, and antidepressant actions. It has been used as part of multimodal analgesia, from the pre-emptive phase, in the intraoperative period or in the immediate postoperative period. Sub-anesthetic doses of ketamine administered before induction or during trans-anesthesia have shown an analgesic effect in the postoperative period. It also has an important reduction in opioids and may reduce the hyperalgesia related to opioids [39]. Hallucinations are a disadvantage, although they are rare and can be prevented with a benzodiazepine administered as part of the preoperative medication.

3.1.4.3 Alpha-2 agonists

Alpha-2 adrenergic receptors are found in the central and peripheral nervous system, specifically in the pontine locus ceruleus, spinal cord tracts, rostral ventrolateral cord, and dorsal horn of the spinal cord. Clonidine, dexmedetomidine, and tizanidine are alpha-2 agonist drugs that modulate these centers, producing analgesia, sedation, bradycardia, and vasodilation without respiratory impairment. Its adjunctive effects to anesthesia are well known and are used as fundamental component of multimodal analgesia. In addition to their analgesic effect, they have been shown to reduce the use of perioperative opioids [18, 42, 43, 44, 45, 46].

3.1.4.4 Glucocorticoids

The use of glucocorticoids for postoperative pain is still controversial. They have a powerful anti-inflammatory effect through which their analgesic effect is hypothesized. Dexamethasone and methylprednisolone are the most used and can be administered perioperatively. They have also been used to reduce rebound pain that occurs with peripheral nerve blocks [47, 48, 49].

3.1.4.5 Metamizole (Dipyrone)

It is a non-opioid analgesic that has been demonized in some European countries and in the USA due to the possibility of death secondary to agranulocytosis, although it is one of the most used analgesics in the world since 1970. Its mechanism of action continues to be a question, having attributed to the inhibition of prostaglandin synthesis in peripheral tissues and in the central nervous system. Another recent theory mentions the modulation of CB1 and CB2 cannabinoid receptors [50, 51]. A randomized, double-blind, multiple-dose study in plastic surgery patients compared intramuscular metamizole 1 g (every 8 h) versus intramuscular diclofenac 75 mg (every 12 h), observing that dipyrone considerably decreased the requirement for meperidine as rescue analgesic in the first 18 h after surgery. This was also associated with significantly lower pain scores in patients receiving metamizole. Diclofenac had reduced side effects with thrombocytopenia and prolonged bleeding time in most patients [52].

At Lotus Med Group—a center specialized in plastic surgery—we use the analgesic management shown in Table 1, adjusting the doses according to the type of surgery, patient, analgesic response, and secondary effects. We believe that pre-emptive, intraoperative, and preventive multimodal analgesia is the best approach for the correct management of POP in plastic surgery. Of course, the analgesic approach must always consider an empathetic and pleasant environment for each patient, offering continuous follow-up in the immediate and mediate postoperative period. Using this analgesic approach, we have not had cases of persistent postoperative pain.

Pre-surgeryIntraoperativeFirst 24–48 hAnalgesics at home**
Etoricoxib 90 mg oralFentanyl 50 up to 250 μgNalbuphine 5–10 mg i.v. /6 hTramadol 25–300 mg/day
Codeine 15–60 mg/day
Oxycodone 5–15 mg/6 h
Acetaminofen 500 mg/4–6 h
Etoricoxib 90–120 mg/day
Celecoxib 100–400 mg/day
Ibuprofen 200–400 mg/6–8 h
Diclofenac 25, 50 or 100 mg/6 h
Pregabaline 75 mg/12 h
Clonidine 0.1 mg oralMorphine 10–30 mgMetamizole 2 gr iv drip/12 h
Melatonine 10 mg oralNalbuphine up to 30 mgKetorolac 30 i.v./8 h
Magnesium sulfate 2 g i.v.Clonidine 75–250 μg*Pregabaline 75 mg/12 h. oral
Metamizole 1 gr i.v.
Dexamethasone 8 mg i.v.

Table 1.

Perioperative analgesia plan for adult patients in plastic surgery.

Added to bupivacaine during spinal anesthesia.


Combination of 1 opioid, 1 NSAID or acetaminofen, plus pregabaline.


3.1.4.6 Local anesthetics

Local anesthetics (LA) inhibit neuronal action potentials via voltage-gated sodium channel blockade. LA for postoperative analgesia is a safe option as long as the total doses administered are monitored to avoid dangerous side effects, including death. These drugs can be administered by injection into the wound, subcutaneously, by tumescent infiltration, intravenously, by the neuroaxial route, in peripheral nerve blocks, interpleural, or in transdermal patches. Local infiltration of LA is a simple technique widely used by plastic surgeons; from the various tumescent solutions where local anesthetics are mixed—primarily lidocaine—to some regional blocks. LA toxicity is a controversial issue among anesthesiologists and plastic surgeons. The maximum safe doses of tumescent lidocaine have been reported to be 28 mg/kg without liposuction and 45 mg/kg with liposuction, doses that produce serum lidocaine concentrations below toxic levels [53]. The American Society of Plastic Surgeons Practice Advisory on Liposuction recommends not to exceed a maximum dose of 35 mg/kg and only as part of a wetting solution [54]. Intravenous perioperative lidocaine decreases the incidence and intensity of chronic postoperative pain: initial bolus dose of 1.5 mg/kg followed by a continuous lidocaine infusion of 1.5 mg/kg during surgery.

3.2 Regional analgesia

The role of regional anesthesia to treat POP in plastic surgery procedures has been widely discussed [22, 23, 24, 55, 56]. Some authors suggest that this method of analgesia may reduce the incidence of pain by many mechanisms. Blocking the nerves interferes the transmission of nociceptive input from peripheral nerves, giving as result the reduced inflammation of the nerves and the activation of glial cells. This technique also reduces the opioid consumption during and after surgery, decreases PONV, and cuts lengths of stay as well as costs. Regional blocks as well as neuroaxial analgesia are extensively used in many specialties and have become a component of many Enhanced Recovery After Surgery (ERAS) protocols. Epidural analgesia has demonstrated to improve pain management at 1 year after surgery, and recent studies have shown that peripheral nerve blocks have the same analgesic outcomes [57].

3.2.1 Peripheral nerve blocks

The increasingly frequent use of ultrasound-guided peripheral blocks favors the anesthetic and analgesic effects, decreasing side effects and complications, improves comfort and quality of recovery of the patient, and decreases chronic post-surgical pain and dependence on opioid drugs. In plastic surgery, the most used for mammary surgery are PEC I and II, erector spinae plane block, and thoracic paravertebral blocks, and some surgeons like to perform proximal intercostal nerve blockade.

Although some studies have mentioned the possibility that PECS blockade combined with multimodal analgesia does not reduce intraoperative and/or PACU opioid consumption in women undergoing ambulatory breast surgery [58], the meta-analysis by Grape et al. [59] including 1026 patients in 16 trials concludes that there is moderate-to-high-level evidence that PECS blocks provide postoperative analgesia after breast surgery when compared with no regional technique. Ahiskalioglu et al. [60] evaluated the use of bilateral ultrasound-guided serratus plane block in 40 patients undergoing breast reduction, concluding that it is a safe technique in the treatment of POP, in addition to reducing the consumption of opioids.

Intercostal blocks are easy to perform, although they have some complications such as rapid absorption of LAs and, of course, the possibility of pneumothorax, as shown in Figure 1.

Figure 1.

Left pneumothorax secondary to intraoperative intercostal block for POP in breast implants.

For abdominoplasty, the transversus abdominis plane (TAP) block, rectus abdominis muscle block, and erector spinae plane block [60, 61, 62], as well as analgesia by tumescent infiltration using lidocaine, ropivacaine, or levobupivacaine [63, 64], produce excellent relief of POP.

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4. Conclusions

The prevention and treatment of POP are mandatory in the comprehensive management of patients undergoing plastic surgery—be it cosmetic or reconstructive—since moderate-to-intense post-surgical pain generates negative physiological changes that affect rapid recovery, prolong hospitalization, higher readmission rates, high costs, and interference with patient satisfaction. Multimodal analgesia has proven to be the best regimen in the comprehensive management of these patients, requiring an approach that includes medications combined with non-pharmacological techniques. Although opioids have been the cornerstone in the treatment of pain secondary to surgery, the indiscriminate use of opioids for POP should be avoided.

Proper management of POP is an important determinant in the rapid recovery of patients and the return to their daily activities.

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Conflict of interest

The authors declare no conflict of interest.

References

  1. 1. Global Survey 2021. Full report and press releases [Internet]. Isaps.org. [cited 2023 Sep 28]. Available from: https://www.isaps.org/discover/about-isaps/globalstatistics/reports-and-pressreleases/globalsurvey-2021-full-reportand-press-releases/
  2. 2. Mortada H, Alawaji ZH, Aldihan RA, Alkuwaiz LA, Alshaalan SF, et al. Impact of the Coronavirus Disease 2019 pandemic on the patterns and characteristics of plastic surgery practice: A retrospective comparative study of before and during the pandemic. Cureus. 2022;14(9):e29722. DOI: 10.7759/cureus.29722
  3. 3. Moss WD, Pires GR, Samlowski E, Webb J, DeAngelo MM, et al. Characterizing the volume of surgery and post-operative complications during the COVID-19 pandemic. Langenbeck’s Archives of Surgery. 2022;407(8):3727-3733. DOI: 10.1007/s00423-022-02605-6
  4. 4. Qiao Z, Deng Y, Wang X, Sun Y, Xiong X, et al. The impact of COVID-19 on plastic and reconstructive surgery in China: A single-centre retrospective study. Journal of Plastic, Reconstructive & Aesthetic Surgery. 2023;76:160-168. DOI: 10.1016/j.bjps.2022.10.033
  5. 5. Che K, Wang K, Yuan Y, Zhang Z, Li F, Li Q. Trend of academic productivity in plastic surgery and the impact of COVID-19: A bibliometric analysis. The Journal of Craniofacial Surgery. 2023;34(2):454-460. DOI: 10.1097/SCS.0000000000009021
  6. 6. Schoenbrunner AR, Joshi GP, Janis JE. Multimodal analgesia in the aesthetic plastic surgery: Concepts and strategies. Plastic and Reconstructive Surgery. Global Open. 2022;10(5):e4310. DOI: 10.1097/GOX.0000000000004310
  7. 7. Richebé P, Capdevila X, Rivat C. Persistent postsurgical pain: Pathophysiology and preventative pharmacologic considerations. Anesthesiology. 2018;129(3):590-607. DOI: 10.1097/ALN.0000000000002238
  8. 8. Whizar-Lugo V, Flores-Carrillo JC, Campos-León J, Parra-Beltrán P, Azamar-Llamas D. Perioperative care of tourist-patients. Journal of Anesthesia and Critical Care: Open Access. 2015;3(6):00119. DOI: 10.15406/jaccoa.2015.03.00119
  9. 9. May DM. Ambulatory anesthesia for cosmetic surgery in Brazil. Current Opinion in Anaesthesiology. 2016;29(4):493-498. DOI: 10.1097/ACO.0000000000000361
  10. 10. Lai A, Johnson R. World professional association for transgender health guidelines: 2022 surgical treatment updates in the standards of care for transgender and gender diverse people. Neurourology and Urodynamics. 2022;42(5):900-902. DOI: 10.1002/nau.25099
  11. 11. Torabi R, Bourn L, Mundinger GS, Saeg F, Patterson C, et al. American Society of Plastic Surgeons member post-operative opioid prescribing patterns. Plastic and Reconstructive Surgery. Global Open. 2019;7(3):e2125. DOI: 10.1097/GOX.0000000000002125
  12. 12. Oberhofer HM, Rao A, Carlson JT, Mast BA, Simmons CJ, et al. Opioid prescribing practices among plastic surgeons: Results of the 2019 American Society of Plastic Surgeons opioid survey. Annals of Plastic Surgery. 2022;88(6):665-673. DOI: 10.1097/SAP.0000000000003145
  13. 13. Wang AMQ , Retrouvey H, Wanzel KR. Addressing the opioid epidemic: A review of the role of plastic surgery. Plastic and Reconstructive Surgery. 2018;141(5):1295-1301. DOI: 10.1097/PRS.0000000000004332
  14. 14. Cabedo N, Valero R, Alcón A, Gomar C. Prevalence and characterization of postoperative pain in the postanaesthesia care unit. Revista Española de Anestesiología y Reanimación. 2017;64(7):375-383. DOI: 10.1016/j.redar.2016.11.006
  15. 15. Domínguez HG, Sandoval LCG, Domínguez CLG. Prevalencia de dolor postquirúrgico. Acta Médica Grupo Ángeles. 2016;14(2):84-89
  16. 16. Gramke HF, de Rijke JM, van Kleef M, Raps F, Kessels AG, et al. The prevalence of postoperative pain in a cross-sectional group of patients after day-case surgery in a university hospital. The Clinical Journal of Pain. 2007;23(6):543-548. DOI: 10.1097/AJP.0b013e318074c970
  17. 17. Chung F, Ritchie E, Su J. Postoperative pain in ambulatory surgery. Anesthesia and Analgesia. 1997;85(4):808-816. DOI: 10.1097/00000539-199710000-00017
  18. 18. Nair A, Rangaiah M, Borkar N. Efficacy and safety of oral tizanidine premedication as pre-emptive analgesia in adult patients undergoing elective surgeries—A systematic review. Saudi Journal of Anaesthesia. 2023;17(2):214-222. DOI: 10.4103/sja.sja_780_22
  19. 19. Klifto KM, Elhelali A, Payne RM, Cooney CM, Manahan MA, Rosson GD. Perioperative systemic nonsteroidal anti-inflammatory drugs (NSAIDs) in women undergoing breast surgery. Cochrane Database of Systematic Reviews. 2021;11(11):CD013290. DOI: 10.1002/14651858.CD013290.pub2
  20. 20. Dahl JB, Møiniche S. Pre-emptive analgesia. British Medical Bulletin. 2004;71:13-27. DOI: 10.1093/bmb/ldh030
  21. 21. Whizar LV, Cisneros CR, Reyes AMA, Campos LJ. Anestesia para cirugía facial cosmética. Anest Mex. 2005;17:117-131
  22. 22. Schoenbrunner AR, Janis JE. Pain management in plastic surgery. Clinics in Plastic Surgery. 2020;47(2):191-201. DOI: 10.1016/j.cps.2019.12.001
  23. 23. Mahaalit-Aribawa GN, Wiryana M, Agung-Senapathi T, Parami P. Pain management in plastic surgery. In: Whizar-Lugo VM, editor. Anesthesia Topics for Plastic and Reconstructive Surgery. London, UK: Intechopen; 2018. pp. 102-128. DOI: 10.5772/intechopen.79302. Chapter 6
  24. 24. Saffari TM, Saffari S, Brower KI, Janis JE. Management of acute surgical pain in plastic and reconstructive surgery. Plastic and Reconstructive Surgery [Internet]. 2023. Publish Ahead of Print. DOI: 10.1097/prs.0000000000010694
  25. 25. Rose KR, Christie BM, Block LM, Rao VK, Michelotti BF. Opioid prescribing and consumption patterns following outpatient plastic surgery procedures. Plastic and Reconstructive Surgery. 2019;143(3):929-938. DOI: 10.1097/PRS.0000000000005351
  26. 26. Barker JC, Joshi GP, Janis JE. Basics and best practices of multimodal pain management for the plastic surgeon. Plastic and Reconstructive Surgery. Global Open. 2020;8(5):e2833. DOI: 10.1097/GOX.0000000000002833
  27. 27. Martínez CF, Hernández CE. ¿Sabes que es realmente el fentanilo? Anest Mex. 2023;35(2):345-349
  28. 28. Bennett KG, Kelley BP, Vick AD, Lee JS, Gunaseelan V, et al. Persistent opioid use and high-risk prescribing in body contouring patients. Plastic and Reconstructive Surgery. 2019;143(1):87-96. DOI: 10.1097/PRS.0000000000005084
  29. 29. Mundra L, Garossi K, Iorio M, Mathes D, Winocour J, Kaoutzanis C. Opioid-prescribing patterns in body contouring surgery. Aesthetic Surgery Journal [Internet]. 2023;43(9):978-985. DOI: 10.1093/asj/sjad117
  30. 30. Crystal DT, Cuccolo NG, Plewinski MJ, Ibrahim AMS, Sinkin JC, et al. Assessment of opioid-prescribing practices in breast augmentation: Future directions for prescribing guidelines. Annals of Plastic Surgery. 2021;86(1):11-18. DOI: 10.1097/SAP.0000000000002430
  31. 31. Singla NK, Skobieranda F, Soergel DG, Salamea M, Burt DA, et al. APOLLO-2: A randomized, placebo and active-controlled phase III study investigating oliceridine (TRV130), a G protein-biased ligand at the μ-opioid receptor, for management of moderate to severe acute pain following abdominoplasty. Pain Practice. 2019;19(7):715-731. DOI: 10.1111/papr.12801
  32. 32. Simpson KN, Fossler MJ, Wase L, Demitrack MA. Cost–effectiveness and cost-benefit analysis of oliceridine in the treatment of acute pain. Journal of Comparative Effectiveness Research. 2021;10(15):1107-1119
  33. 33. Ayoub SS. Paracetamol (acetaminophen): A familiar drug with an unexplained mechanism of action. Temperature (Austin). 2021;8(4):351-371. DOI: 10.1080/23328940.2021.1886392
  34. 34. Mallet C, Desmeules J, Pegahi R, Eschalier A. An updated review on the metabolite (AM404)-mediated central mechanism of action of paracetamol (acetaminophen): Experimental evidence and potential clinical impact. Journal of Pain Research. 2023;16:1081-1094. DOI: 10.2147/JPR.S393809
  35. 35. Ribeiro H, Rodrigues I, Napoleão L, Lira L, Marques D, et al. Non-steroidal anti-inflammatory drugs (NSAIDs), pain and aging: Adjusting prescription to patient features. Biomedicine & Pharmacotherapy. 2022;150:112958. DOI: 10.1016/j.biopha.2022.112958
  36. 36. Zhang S, Qu X, Tang H, Wang Y, Yang H, et al. Diclofenac resensitizes methicillin-resistant Staphylococcus aureus to β-lactams and prevents implant infections. Advanced Science. 2021;8(13):2100681. DOI: 10.1002/advs.202100681
  37. 37. Low YH, Gan TJ. NMDA receptor antagonists, gabapentinoids, α-2 agonists, and dexamethasone and other non-opioid adjuvants: Do they have a role in plastic surgery? Plastic and Reconstructive Surgery. 2014;134(4 Suppl. 2):69S-82S. DOI: 10.1097/PRS.0000000000000703
  38. 38. Hu J, Huang D, Li M, Wu C, Zhang J. Effects of a single dose of preoperative pregabalin and gabapentin for acute postoperative pain: A network meta-analysis of randomized controlled trials. Journal of Pain Research. 2018;11:2633-2643. DOI: 10.2147/JPR.S170810
  39. 39. O’Neill RC, Hayes KD, Davison SP. Safety of postoperative opioid alternatives in plastic surgery: A systematic review. Plastic and Reconstructive Surgery. 2019;144(4):991-999. DOI: 10.1097/PRS.0000000000006074
  40. 40. Verret M, Lauzier F, Zarychanski R, Perron C, Savard X, et al. Perioperative use of gabapentinoids for the management of postoperative acute pain: A systematic review and meta-analysis. Anesthesiology. 2020;133(2):265-279. DOI: 10.1097/ALN.0000000000003428
  41. 41. Dauri M, Faria S, Gatti A, Celidonio L, Carpenedo R, et al. Gabapentin and pregabalin for the acute post-operative pain management. A systematic-narrative review of the recent clinical evidences. Current Drug Targets. 2009;10(8):716-733. DOI: 10.2174/138945009788982513
  42. 42. Whizar LV, Gómez-Ramírez IA, Cisneros-Corral R, Martínez-Gallegos N. Intravenous dexmedetomidine vs. intravenous clonidine to prolong bupivacaine spinal anaesthesia. A double blind study. Anest Mex. 2007;19:143-146
  43. 43. Whizar-Lugo V, Flores-Carrillo J, Preciado-Ramírez S. Intrathecal clonidine as spinal anaesthesia adjuvant - is there a magical dose? In: Topics in Spinal Anaesthesia. London, UK, Croatia: Intechopen; 2014. pp. 97-121. DOI: 10.5772/58712. Chapter 5
  44. 44. Kaye AD, Chernobylsky DJ, Thakur P, Siddaiah H, Kaye RJ. Dexmedetomidine in enhanced recovery after surgery (ERAS) protocols for postoperative pain. Current Pain and Headache Reports. 2020;24(5):21. DOI: 10.1007/s11916-020-00853-z
  45. 45. Chen R, Sun S, Li Y, Dou X, Dai M, et al. Efficacy and safety evaluation of dexmedetomidine for postoperative patient controlled intravenous analgesia: A systematic review and meta-analysis. Frontiers in Pharmacology. 2022;13:1028704. DOI: 10.3389/fphar.2022.1028704
  46. 46. Fernández Martin MT, Alvarez Lopez S, Aldecoa A-SC. Role of adjuvants in regional anesthesia: A systematic review. Revista Española de Anestesiología y Reanimación. 2023;70(2):97-107. DOI: 10.1016/j.redare.2021.06.006
  47. 47. Jensen KK, Brøndum TL, Leerhøy B, Belhage B, Hensler M, et al. Preoperative, single, high-dose glucocorticoid administration in abdominal wall reconstruction: A randomized, double-blinded clinical trial. Surgery. 2020;167(4):757-764. DOI: 10.1016/j.surg.2019.12.007
  48. 48. Jensen KK, Brøndum TL, Belhage B, Hensler M, Arnesen RB, et al. Preoperative steroid in abdominal wall reconstruction: Protocol for a randomised trial. Danish Medical Journal. 2016;63(8):A5260
  49. 49. Gao M, Li Y, Yu J, Li W, Qin S, et al. The effects of intravenous dexamethasone on rebound pain after nerve block in patients with ankle fracture: A randomized controlled trial. Journal of Pain Research. 2023;16:1127-1136. DOI: 10.2147/JPR.S399660
  50. 50. de Oliveira DR, Maia RC, de Carvalho França PR, Fernandes PD, Barbosa G, et al. 2-arylpropionic acid pyrazolamides as cannabinoid CB2 receptor inverse agonists endowed with anti-inflammatory properties. Pharmaceuticals (Basel). 2022;15(12):1519. DOI: 10.3390/ph15121519
  51. 51. Stessel B, Lambrechts M, Evers S, Vanderstappen C, Callebaut I, et al. Non-opioid analgesics and the endocannabinoid system. Balkan Medical Journal. 2020;37(6):309-315. DOI: 10.4274/balkanmedj.galenos.2020.2020.6.66
  52. 52. Saray A, Büyükkocak U, Cinel I, Tellioglu AT, Oral U. Diclofenac and metamizol in postoperative analgesia in plastic surgery. Acta Chirurgiae Plasticae. 2001;43(3):71-76
  53. 53. Klein JA, Jeske DR. Estimated maximal safe dosages of tumescent lidocaine. Anesthesia and Analgesia. 2016;122(5):1350-1359. DOI: 10.1213/ANE.0000000000001119
  54. 54. Iverson RE, Lynch DJ. American Society of Plastic Surgeons Committee on Patient Safety. Practice advisory on liposuction. Plastic and Reconstructive Surgery. 2004;113(5):1478-1490; discussion 1491-5. DOI: 10.1097/01.prs.0000111591.62685.f8
  55. 55. Bagatin D, Bagatin T, Šakić K, Deutsch J, Nemrava J, Šimičević D. Optimal analgesia for breast surgery enhanced recovery in day surgery. Acta Clinica Croatica. 2022;61(Suppl. 2):49-56. DOI: 10.20471/acc.2022.61.s2.06
  56. 56. ElHawary H, Joshi GP, Janis JE. Practical review of abdominal and breast regional analgesia for plastic surgeons: Evidence and techniques. Plastic and Reconstructive Surgery. Global Open. 2020;8(12):e3224. DOI: 10.1097/GOX.0000000000003224
  57. 57. Homsy C, Lindsey JT. Regional anesthetic blocks in plastic surgery using portable ultrasound: A simplified approach. Annals of Plastic Surgery. 2019;82(6S Suppl. 5):S374-S379. DOI: 10.1097/SAP.0000000000001805
  58. 58. Uribe AA, Weaver TE, Echeverria-Villalobos M, Periel L, Pasek J, et al. Efficacy of PECS block in addition to multimodal analgesia for postoperative pain management in patients undergoing outpatient elective breast surgery: A retrospective study. Frontiers in Medicine (Lausanne). 2022;9:975080. DOI: 10.3389/fmed.2022.975080
  59. 59. Grape S, Jaunin E, El-Boghdadly K, Chan V, Albrecht E. Analgesic efficacy of PECS and serratus plane blocks after breast surgery: A systematic review, meta-analysis and trial sequential analysis. Journal of Clinical Anesthesia. 2020;63:109744. DOI: 10.1016/j.jclinane.2020.109744
  60. 60. Ahiskalioglu A, Yayik AM, Demir U, Ahiskalioglu EO, Celik EC, Ekinci M, et al. Preemptive analgesic efficacy of the ultrasound-guided bilateral superficial serratus plane block on postoperative pain in breast reduction surgery: A prospective randomized controlled study. Aesthetic Plastic Surgery. 2020;44(1):37-44. DOI: 10.1007/s00266-019-01542-y
  61. 61. Williams L, Iteld L. Moving toward opioid-free breast surgery: Regional blocks and a novel technique. Clinics in Plastic Surgery. 2021;48(1):123-130. DOI: 10.1016/j.cps.2020.09.003
  62. 62. Liheng L, Siyuan C, Zhen C, Changxue W. Erector spinae plane block versus transversus abdominis plane block for postoperative analgesia in abdominal surgery: A systematic review and meta-analysis. Journal of Investigative Surgery. 2022;35(9):1711-1722. DOI: 10.1080/08941939.2022.2098426
  63. 63. Bagatin D, Bagatin T, Nemrava J, Ivelj MŠ, Deutsch J, Šakić K. Influence of local infiltration analgesia on postoperative pain in abdominoplasty patients. Acta Clinica Croatica. 2019;58(Suppl. 1):23-28. DOI: 10.20471/acc.2019.58.s1.03
  64. 64. Šakić K, Bagatin D, Bagatin T, Šakić L, Jeleč V, et al. Comparison of different surgical procedures with local infiltration analgesia in day surgery. Acta Clinica Croatica. 2019;58(Suppl. 1):67-73. DOI: 10.20471/acc.2019.58.s1.10

Written By

Daniela Arévalo-Villa, Andrea Figueroa Morales, Roberto de Jesús Jiménez-Contreras and Víctor M. Whizar-Lugo

Submitted: 28 June 2023 Reviewed: 18 August 2023 Published: 30 September 2023