Objective: To determine the rate of post–face-lift hematoma among users of serotonin reuptake inhibitors (SSRIs) vs non-SSRI users. Selective serotonin reuptake inhibitors have come under recent scrutiny because of possible bleeding risks. However, cessation of SSRIs carries inherent risks.
Methods: The medical charts for 250 consecutive patients who underwent a modified deep-plane face-lift and 13 patients who underwent necklift from January 2010 to May 2011 were reviewed for the incidence of postoperative hematoma. Patients’ medical records were examined for medical comorbidities, coagulopathy, and medication list, with particular attention to any usage of SSRIs or serotonin norepinephrine reuptake inhibitors (SNRIs).
Results: Twenty-two percent of patients were taking SSRIs or SNRIs. We observed a total hematoma (major minor) rate of 1.95% for non–SSRI/SNRI users vs 1.72% for SSRI/ SNRI users. The minor hematoma rate was 1.95% among nonusers vs 0% for users. The major hematoma rate was 0% among nonusers vs 1.72% for users.
Conclusions: Usage of SSRIs was more common in this large series of face-lift patients than in the general population. In these patients, SSRIs in the perioperative period are found to be safe and did not seem to adversely affect outcome. We found no evidence to support discontinuing SSRIs perioperatively.
Hematoma formation is the most common complication of rhytidectomy,with an incidence of 0.2% to 8.1%.1 Expansilen hematomas require urgent evacuation because they pose risk of airway compromise. While larger expanding hematomas can be life threatening, smaller hematomas can result in flap necrosis, changes in pigmentation, persistent edema, prolonged ecchymosis, delayed wound healing, infection, and suboptimal aesthetic results. Decreasing the risk of hematomas is an important part of face-lift surgery. Several risk factors for hematoma formation have been evaluated in the literature. These have included operative technique, anesthetic type, perioperative blood pressure, lack of perioperative antiemetics, anticoagulant use, male sex, medical comorbidities, underlying coagulopathy, and age.211 Vacuum drains and the use of tissue sealant have also been evaluated as prophylactic measures.1,3,4,10,12 To further decrease the risk of hematoma, patients are instructed to stop taking all medications that increase the probability of bleeding, such as aspirin and nonsteroidal antiinflammatory drugs (NSAIDs).3
Recently, selective serotonin reuptake inhibitors (SSRIs) have come under scrutiny because of possible bleeding risks. The effect of SSRIs on bleeding has been evaluated in the literature, and the current theory proposes an inhibition of serotonin uptake into platelets, leading to an impairment in the platelet hemostatic response.1316 The effect of SSRIs on increased upper gastrointestinal (GI) tract bleeding has been suggested in the literature,1722 although the risks seemed to be higher among patients concomitantly taking aspirin or NSAIDs. In contrast, SSRIs do not seem to confer any significant bleeding risk for hemorrhage stroke, postpartum hemorrhage, or after invasive dental procedures.2326
Data on the effect of SSRIs on postoperative bleeding are limited. Three studies have evaluated the preoperative use of SSRIs in patients undergoing coronary artery bypass grafting (CABG) and found no additional risk of bleeding events, reoperations for bleeding, or inhospital mortality.2729 In contrast, Ga¨rtner et al30 found a 2.3 adjusted relative risk of reoperative for bleeding among SSRI users undergoing mastectomy. A study by Van Haelst et al31 reported an increased intraoperative blood loss among patients taking SSRIs who underwent hip arthroplasty; however, there was no increase in perioperative transfusion requirements.
Cessation of SSRI therapy is not without its risks. The World Health Organization has identified depression as the fourth leading cause of total disease burden and the leading cause of disability worldwide.32 Many patients experience physical, psychological, and somatic complaints shortly after the discontinuation of anti-depressants.3336 Stopping treatment can lead to depression during a time when patients require a high level of motivation and activity required for dressings, wound care, and visits to the surgeon for preoperative and postoperative care. Cessation of SSRIs can also lead to anxiety, which can be detrimental during the perioperative period. There is a need to understand how significant the risk of bleeding is in order to weigh its risk against that of cessation of SSRIs.
We performed this study to determine the rate of post– face-lift hematomas in patients taking SSRIs vs those who do not. To our knowledge, this is the first study of its kind in patients undergoing facial plastic surgery.
We performed an institutional review board–approved retrospective review of all patients having undergone a complete, platysma muscle suspension, deep-plane face-lift by the senior surgeon (D.B.R.) from January 1, 2010, to May 1, 2011. The technique used is a modification of a deep-plane rhytidectomy, in which the platysma muscle is isolated and identified within the face and neck. To isolate the facial component of the platysma, a No. 10 blade scalpel is used to dissect the superficial musculoaponeurotic system (SMAS) laterally from the line created by the true zygomatic insertion point to the angle of the mandible. Dissection deep to the platysma muscle occurs approximately 1 cm posterior to the nasolabial fold along the face and 8 cm below the mandible. Midline platysmaplasty with subplatysmal dissection is also performed. All but 13 patients underwent the complete, platysma muscle suspension, deep-plane face-lift (either primary or revision) as described. Thirteen patients underwent subplatysmaplasty alone and were included in the study.
There were no exclusion criteria for the study. Patients’ medical records were examined for their age, medical comorbidities, medication list, surgical history, and postoperative course. Medication lists were examined in particular for the usage of any NSAID, aspirin, warfarin, clopidogrel, or anti-depressants. anti-depressants were categorized as SSRIs, serotonin norepinephrine reuptake inhibitors(SNRIs),and“other”classofantidepressantagents. SSRIs included fluoxetine hydrochloride, citalopram hydrobromide, fluvoxamine maleate, paroxetine hydrochloride, sertraline hydrochloride, fluvoxamine maleate, escitalopram oxalate, and clomipramine hydrochloride. SNRIs such as venlafaxine hydrochloride, desvenlafaxine succinate, and duloxetine hydrochloride were also included in the study due to their mechanism of serotonin reuptake inhibition. The “other” class of agents, including trazodone hydrochloride and buproprion hydrochloride, was excluded from analysis of bleeding risk owing to lack of clinically significant serotonin reuptake inhibition.
All patients were instructed to discontinue the use of aspirin and NSAIDs 2 weeks prior to surgery. All patients were also instructed to discontinue supplements associated with bleeding, such as vitamin E, fish oil, omegas, glucosamine, flax seed, herbal medications, and green tea 2 weeks prior to surgery. Aspirin, NSAIDS, and supplements were restricted until 2 weeks postoperatively. No patients were taking warfarin or clopidogrel. Patients were also advised to take Arnica montana tablets daily for 5 days before surgery to minimize ecchymosis. Smoking cessation was advised. No tissue sealant or vacuum drains were used. Pressure dressings were placed, which were removed the subsequent morning. Perioperative blood pressure parameters were instituted with a goal systolic blood pressure lower than 140 mm Hg and diastolic blood pressure lower than 90 mm Hg, and antihypertensive medications were administered by the anesthesiologists if necessary. All patients also were given 3 intraoperative prophylactic antiemetics: dexamethasone, metoclopramide hydrochloride, and ondansetron hydrochloride. Patients received general anesthesia, and deep extubation was performed to minimize coughing or bucking.
Patient medical records were examined for any bleeding complications and intervention. Patients were evaluated on postoperative days 1, 5, and 8. Major hematomas were defined as expansile collections that required urgent surgical evacuation. Minor hematomas contained 10 mL or less of blood and were treated by needle aspiration in the office.
A total of 263 consecutive patients were included in the study, with a mean age of 61 years (range, 4480 years). There were 5 male and 258 female patients. A total of 181 patients underwent primary deep-plane rhytidectomy and subplatysmaplasty; 69 patients underwent revision rhytidectomies; and 13 patients underwent subplatysmaplasty alone.
Group 1 comprised 205 patients (78%) not taking SSRIs/SNRIs. Group 2 comprised 58 patients (22%) who were taking SSRIs or SNRIs. SSRIs constituted most of these anti-depressants (67%). While several patients were taking an SSRI or SNRI in conjunction with another class of anti-depressants (ie, trazodone or buproprion), only 1 patient was taking both an SSRI and an SNRI. Two patients had mild von Willebrand disease and were given desmopressin acetate preoperatively. No other coagulopathies were present.
One major bleeding complication occurred in a 62yearold woman who underwent revision rhytidectomy. The patient had no history of coagulopathy and was not taking any known NSAIDs or aspirin. The hematoma manifested within the first 12 postoperative hours, requiring surgical evacuation. This patient was also taking a lowdose SSRI. This was the only hematoma in group 2. Thus, group 2 had a resulting hematoma rate of 1.72% (1 in 58) (Table 1). Group 1 did not have any major hematomas. Therefore, the major hematoma rate in group 1 was 0% compared with 1.72% in group 2, with an overall hematoma rate of 0.38% (1 in 263).
In group 1, 4 patients (a rate of 1.95%) experienced a minor hematoma treated successfully by needle aspiration (Table 2). Minor hematomas manifested on postoperative days 2 to 14. One of these patients had mild von Willebrand disease. There were no minor hematomas in group 2. Therefore, the minor hematoma rate in group 1 was 1.95% compared with 0% in group 2. Overall, the total hematoma (major minor) rate was 1.95% in group 1 and 1.72% in group 2. Differences in hematoma rates between both groups were statistically insignificant using unpaired t test (P =.87).
Table 1. Incidence of Postrhytidectomy Hematomaa
Table 2. Cases of Minor Hematoma in Group 1a
Controversy still exists as to whether there are bleeding risks associated with SSRIs. While there are observational studies and case reports of hemorrhagic risks associated with SSRIs,1722 clinical trials and level I evidence are lacking. SSRIs are believed to impair platelet aggregation by down regulating the serotonin (5HT) receptors on blood platelets. Because serotonin is not synthesized in platelets, this receptor down regulation blocks the reuptake of serotonin from the circulation, resulting in intraplatelet serotonin depletion.21,37 Serotonin released from platelets at the site of vascular injury facilitates platelet aggregation and hemostatic thrombus formation.38 In the study by Hergovich et al,16 platelet serotonin concentration decreased by 83% after 14 days of paroxetine use. SSRIs are also believed to have broad antiplatelet effects by decreasing platelet binding affinity, inhibiting calcium mobilization, and reducing platelet secretion in response to collagen.20
While SSRIs may decrease platelet serotonin, the causal relationship between SSRIs and clinically significant bleeding is unclear. In the study by Hougardy et al,39 only 6 of 43 paroxetine users had abnormal platelet function, which could not be definitively attributed to SSRI usage. In another study of 12 healthy young men, there was no difference in platelet activity and serotonin uptake between sertraline and placebo.40 The concern over hemorrhagic complications began with several case reports noting epistaxis, purpura, ecchymosis, retroperitoneal hematoma, and GI tract bleeding while using SSRIs.19 Several observational studies have since reported an increased risk of GI tract bleeding due to SSRIs, with an increased relative risk ranging from 1.24 to 3.60.1722 This effect was found to be potentiated by concurrent use of NSAIDs or low-dose aspirin, with an increased relative bleeding risk of 5.2 to 12.2,17,18,22 and relieved by concurrent use of proton pump inhibitors.22 Critics of these studies assert that they do not demonstrate direct causality. In addition, these retrospective case control and cohort studies are derived from computerized databases that are possibly lacking in clinical detail and may not control for other risk factors for GI tract bleeding.21 Other studies have demonstrated no significant increase in GI tract bleeding with SSRIs.41 SSRIs have also been found to confer no increased risk of hemorrhagic stroke.23,24,42
Data on postoperative bleeding effects are limited and mixed. A retrospective study of patients having undergoing CABG found no increased risk of rates of re-operation for bleeding or rates of red blood cell (RBC) transfusion among SSRI users.28 However, among those receiving transfusions, the median volume of RBC units transfused was higher in the SSRI group (5 U vs 4 U). In contrast, 2 other studies found no increased RBC transfusion requirement among SSRI users undergoing CABG.27,29 Kim et al27 also noted no difference in any bleeding events, 30day mortality, or reoperations for bleeding. While SSRI users were 2.3 times more likely to need reoperation for bleeding after mastectomy in one study,30 they had no increased frequency of oral bleeding complications after invasive dental procedures.26
None of these latter studies discontinued SSRI use in the perioperative period. Cessation of SSRIs has been associated with clinically significant risk. Numerous studies have described withdrawal symptoms in patients after discontinuation of SSRIs, including psychological, physical, and somatic complaints. A diverse set of symptoms has been reported, most commonly dizziness, vertigo, nausea, vomiting, fatigue, and malaise. Patients have also experienced gastrointestinal symptoms, agitation, insomnia, tremors, nightmares, headaches, irritability, anxiety, and paresthesias.3336 More serious symptoms have included relapses in significant depression, aggression, hypomania, and suicide. A study by Valuck et al43 noted a 61% increased risk of suicide attempt in the 2 weeks following discontinuation of anti-depressants. Discontinuation symptoms have been reported in 12% to 50% of antidepressant users, can begin within 3 to 5 days of treatment cessation, and have been reported to last up to 3 weeks.3336 Symptoms improve once medications are restarted.
To our knowledge, this is the first study evaluating the effects of SSRIs on postoperative bleeding in the facial plastics literature. Among our 263 patients who underwent rhytidectomy, 58 (22%) were using SSRIs or SNRIs. One major bleeding complication occurred, requiring surgical intervention, resulting in a total hematoma rate of 0.38%. Since this patient was using an SSRI, this yielded a 1.72% hematoma rate among group 2 vs 0% for group 1. The minor hematoma rate was 1.95% among group 1 vs 0% for group 2. Total hematoma rate (major minor) was 1.95% for group 1 vs 1.72% for group 2.
This study is limited by its low power, and we cannot establish a causal relationship between SSRI use and postoperative bleeding. While this study cannot definitely rule out a small increased risk of postoperative bleeding with the usage of SSRIs, we can conclude that the rate of hematoma among SSRI users is small and comparable with published rates of major hematoma. In addition, the rates of total hematoma between non–SSRI users and SSRI users are comparable. This is in the context of what is considered to be extensive dissection by the senior author (D.B.R.) both above and below the platysma and SMAS. This is also the first study that reports the prevalence of SSRI use in face-lift surgery. A rate of 22% is significant and reflects the prevalence of depression and anxiety in this group of patients. Given the risk of cessation of SSRIs, the low hematoma rate among users and the lack of level I evidence supporting bleeding, our study does not find good reason to stop SSRIs in the perioperative period.
In conclusion, SSRI usage is common among face-lift patients. Data on increased bleeding risks with SSRIs are limited and mixed. Given our major hematoma rate of 1.72% and minor hematoma rate of 0% among SSRI users, SSRIs in the perioperative period did not seem to adversely affect bleeding.
- Zoumalan R, Rizk SS. Hematoma rates in drainless deep-plane face-lift surgery with and without the use of fibrin glue. Arch Facial Plast Surg. 2008;10(2):103107.
- Kamer FM, Song AU. Hematoma formation in deep plane rhytidectomy. Arch Facial Plast Surg. 2000;2(4):240242.
- Baker DC, Stefani WA, Chiu ES. Reducing the incidence of hematoma requiring surgical evacuation following male rhytidectomy: a 30year review of 985 cases. Plast Reconstr Surg. 2005;116(7):19731985.
- Grover R, Jones BM, Waterhouse N. The prevention of haematoma following rhytidectomy: a review of 1078 consecutive face-lifts. Br J Plast Surg. 2001;54(6): 481486.
- Rees TD, Lee YC, Coburn RJ. Expanding hematoma after rhytidectomy: a retrospective study. Plast Reconstr Surg. 1973;51(2):149153.
- Barker DE. Prevention of bleeding following a rhytidectomy. Plast Reconstr Surg. 1974;54(6):651653.
- Straith RE, Raju DR, Hipps CJ. The study of hematomas in 500 consecutive face lifts. Plast Reconstr Surg. 1977;59(5):694698.
- Lawson W, Naidu RK. The male face-lift: an analysis of 115 cases. Arch Otolaryngol Head Neck Surg. 1993;119(5):535539.
- Rees TD, Barone CM, Valauri FA, Ginsberg GD, Nolan WB III. Hematomas requiring surgical evacuation following face lift surgery. Plast Reconstr Surg. 1994; 93(6):11851190.
- Perkins SW, Williams JD, Macdonald K, Robinson EB. Prevention of seromas and hematomas after face-lift surgery with the use of postoperative vacuum drains. Arch Otolaryngol Head Neck Surg. 1997;123(7):743745.
- Jones BM, Grover R, Hamilton S. The efficacy of surgical drainage in cervicofacial rhytidectomy: a prospective, randomized, controlled trial. Plast Reconstr Surg. 2007;120(1):263270.
- Por YC, Shi L, Samuel M, Song C, Yeow VK. Use of tissue sealants in face-lifts: a metaanalysis. Aesthetic Plast Surg. 2009;33(3):336339.
- McCloskey DJ, Postolache TT, Vittone BJ, et al. Selective serotonin reuptake inhibitors: measurement of effect on platelet function. Transl Res. 2008;151(3): 168172.
- De Clerck F. The role of serotonin in thrombogenesis. Clin Physiol Biochem. 1990; 8(suppl 3):4049.
- Meijer WE, Heerdink ER, Nolen WA, Herings RMC, Leufkens HGM, Egberts ACG. Association of risk of abnormal bleeding with degree of serotonin reuptake inhibition by anti-depressants. Arch Intern Med. 2004;164(21):23672370.
- Hergovich N, Aigner M, Eichler HG, Entlicher J, Drucker C, Jilma B. Paroxetine decreases platelet serotonin storage and platelet function in human beings. Clin Pharmacol Ther. 2000;68(4):435442.
- Dall M, Schaffalitzky de Muckadell OB, Lassen AT, Hansen JM, Hallas J. An association between selective serotonin reuptake inhibitor use and serious upper gastrointestinal bleeding. Clin Gastroenterol Hepatol. 2009;7(12):13141321.
- Dalton SO, Johansen C, Mellemkjaer L, Nørga˚rd B, Sørensen HT, Olsen JH. Use of selective serotonin reuptake inhibitors and risk of upper gastrointestinal tract bleeding: a populationbased cohort study. Arch Intern Med. 2003;163 (1):5964.
- Turner MS, May DB, Arthur RR, Xiong GL. Clinical impact of selective serotonin reuptake inhibitors therapy with bleeding risks. J Intern Med. 2007;261(3): 205213.
- Serebruany VL. Selective serotonin reuptake inhibitors and increased bleeding risk: are we missing something? Am J Med. 2006;119(2):113116.
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- Kharofa J, Sekar P, Haverbusch M, et al. Selective serotonin reuptake inhibitors and risk of hemorrhagic stroke. Stroke. 2007;38(11):30493051.
- Douglas I, Smeeth L, Irvine D. The use of anti-depressants and the risk of haemorrhagic stroke: a nested case control study. Br J Clin Pharmacol. 2011;71(1): 116120.
- Salkeld E, Ferris LE, Juurlink DN. The risk of postpartum hemorrhage with selective serotonin reuptake inhibitors and other anti-depressants. J Clin Psychopharmacol. 2008;28(2):230234.
- Napen˜as JJ, Hong CHL, Kempter E, Brennan MT, Furney SL, Lockhart PB. Selective serotonin reuptake inhibitors and oral bleeding complications after invasive dental treatment. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011; 112(4):463467.
- Kim DH, Daskalakis C, Whellan DJ, et al. Safety of selective serotonin reuptake inhibitor in adults undergoing coronary artery bypass grafting. Am J Cardiol. 2009; 103(10):13911395.
- Xiong GL, Jiang W, Clare RM, et al. Safety of selective serotonin reuptake inhibitor use prior to coronary artery bypass grafting. Clin Cardiol. 2010;33(6):E9498.
- Andreasen JJ, Riis A, Hjortdal VE, Jørgensen J, Sørensen HT, Johnsen SP. Effect of selective serotonin reuptake inhibitors on requirement for allogeneic red blood cell transfusion following coronary artery bypass surgery. Am J Cardiovasc Drugs. 2006;6(4):243250.
- Ga¨rtner R, CroninFenton D, Hundborg H, et al. Use of selective serotonin reuptake inhibitors and risk of reoperation due to postsurgical bleeding in breast cancer patients: a Danish populationbased cohort study. BMC Surg. 2010;10:3.
- van Haelst IMM, Egberts TCG, Doodeman HJ, et al. Use of serotonergic anti-depressants and bleeding risk in orthopedic patients. Anesthesiology. 2010;112 (3):631636.
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