J Clin Aesthet Dermatol. 2019;12(6):E65–E72
by Giuseppe Sito, MD, PhD; Veronica Manzoni, MD; and Raffaella Sommariva, MD
Prof. Sito is with the Prof. Professor Giuseppe Sito Clinic in Turin, Italy. Dr. Manzoni is with the Istituto Auxologico Italiano in Milan, Italy. Dr. Sommariva is a specialist in plastic surgery practicing in Acqui Terme, Italy and Genoa, Italy.
ABSTRACT: Background. Vascular occlusion during the injection of facial fillers is uncommon, but can result in serious adverse events, including necrosis, blindness, and stroke.
Objectives. We explored factors that influence the frequency and severity of vascular complications during filler injections.
Methods. This was a meta-analysis that included case reports and case series published during the years 2004 to 2016 describing patients who experienced any type of vascular complication after an aesthetic procedure. In addition to the descriptive analysis of the variables retrieved, a logistic regression for predicting the outcome of the vascular event was performed.
Results: The analysis included 93 cases described in 30 articles. Blindness was the main consequence of the vascular complications (n=57; 61%). The reported outcome was partial or total recovery in 24 cases (28%) and no improvement in 61 cases (72%). Hyaluronic acid (HA) and autologous fat were the two fillers most frequently involved in vascular occlusions, with autologous fat showing a stronger trend toward no improvement than HA. Involvement of the ophthalmic and retinal arteries was most frequently associated with no improvement.
Conclusion: Injury to ophthalmic and retinal arteries during the injection of facial fillers can result in irreversible serious adverse events. Physicians performing facial filler injections should have a proficient knowledge of anatomy.
KEYWORDS: Dermal fillers, vascular complications, hyaluronic acid, autologous fat, collagen, adverse events
Nonsurgical cosmetic procedures are a growing trend worldwide. Included among these minimally invasive techniques are botulinum toxin and soft-tissue augmentation with fillers, which are used restore tissue loss and correct aging-related rhytides and folds. In 2011, dermal fillers were used in nearly 1.6 million aesthetic procedures, increasing to 2.3 million in 2013 and 5.5 million in 2014.1–3
Hyaluronic acid (HA) fillers are the most commonly used injectable fillers, followed by autologous fat. According to the American Society for Aesthetic Plastic Surgery, nearly 900,000 soft-tissue augmentation procedures were performed with HA in 2004.4,5 Other commonly used filler materials include bovine and human collagen (active for 1–3 months before degradation); poly-L-lactic acid, which stimulates endogenous collagen production for up to 15 months; and calcium hydroxylapatite, which offers up to 2 years of activity.3 These fillers can all be used for volume replacement and enhancement, such as cheek and chin augmentation, tear trough valley correction, nose reshaping (rhinoplasty), midface volumization, and lip enhancement.1,5–7 Although these procedures are generally considered safe, some local adverse events, aside from the relatively common site-injection reactions (e.g., swelling, tenderness, pain, bruising), have been observed.8–10 These include edema, erythema, scarring, granuloma formation, hyper- and hypopigmentation, infection, abscess formation, herpetic outbreaks, nodular masses, and paresthesia (if a nerve has been pinched during the procedure). While these adverse reactions are usually transient, the common use of three-dimensional facial volume restoration techniques, where the filler material can be injected at any depth, has brought about infrequent but serious and often irreversible vascular complications caused by symptomatic arterial occlusion.6,11–13 These vascular complications can result in persistent skin necrosis, ophthalmoplegia, permanent unilateral or bilateral vision loss, and stroke.11–13 Ocular and cerebral embolism occurs when the injected material travels from the distal to proximal retinal and ophthalmic arteries, causing sudden, excruciating pain, persistent blindness, and further tissue necrosis.11–13 In addition to fillers accessing the vessel lumen, vascular occlusion can occur by external compression of the stiff gel bolus deposited in direct contact with the vessel wall.14–16
Based on the available literature, some authors have suggested that the injection technique, site, and substance can have significant influence on the level of risk for an adverse vascular event.2,5,7,11,12,17 However, most of these reviews were not systematic, and the potential influence of other variables on the incidence of adverse events has not been addressed. Therefore, we reviewed the literature regarding vascular complications and performed a meta-analysis of the variables that potentially affect the frequency and severity of adverse events.
Literature search and article selection. This meta-analysis included data from case reports and case series of patients experiencing any type of vascular complication after an aesthetic procedure published during the years 2004 to 2016. The main source for article retrieval was the PubMed. Additional sources included Google Scholar, where the search was restricted to the article title, and a case series by Park et al,18 which provided details from 19 cases previously published as case reports. The database search, performed on December 2016, combined the term filler with the following terms: injection (or injected), blindness, visual loss, ophthalmoplegia, artery occlusion, embolism, ischemia (or ischemic), necrosis, and complication. Only full-text articles written in English were considered for eligibility. To be included in the analysis, cases had to report a vascular event occurring after an aesthetic procedure on the human face.
Data extraction and management. Data for the meta-analysis were extracted from each case and transferred to a predefined form containing the following variables: case reference, age, sex, injected product, aesthetic procedure, needle diameter, injected volume, person who injected the product, injection site, blood vessel affected, main consequence(s) of the vascular event, concomitant symptoms, time to symptom onset, intervention performed to treat the vascular complication, and outcome. Additionally, diagnostic tests performed to confirm the occurrence of vascular complications were recorded to address the quality of the articles included in our review. The main consequences of a vascular complication were blindness, visual loss, necrosis, and other. Blindness was only considered when explicitly stated in the text, whereas visual loss included a reduction in visual acuity, the perception of light only, and the perception of hand movement only. Time-to-onset values were grouped into three categories: less than one hour postprocedure, 1 to 24 hours postprocedure, and more than 24 hours postprocedure. The final outcome was categorized as no change, partial recovery, or full recovery based on the progress of the main consequence of the vascular complication.
Statistical analysis. Categorical variables were described as frequency and percentage, whereas quantitative variables were described as means and standard deviations (SDs). To assess the factors possibly influencing the outcome of vascular complications, the percentages of cases with no improvement and those showing partial or full recovery were compared using the chi-squared test. For variables showing statistically significant differences, a post-hoc analysis was performed by computing the chi-squared values of the adjusted residuals and applying the Bonferroni correction, as described by Beasley et al.19 A prediction model (multivariate analysis) for the vascular event outcomes was built using logistic regression. The multivariate analysis included all variables regarding events occurring prior to any vascular complication, which showed significant differences when comparing patients without improvement and those with partial or total recovery. The significant threshold was set at alpha=0.05 and all analyses were performed using the Statistical Package for the Social Sciences version 22.0 for Windows software program (IBM Corp., Armonk, New York).
Study selection. The initial search (including articles retrieved from additional sources) yielded 143 articles, published during the years 2004 to 2016, on vascular events potentially associated with the use of injected fillers (Figure 1). After removing duplicates and excluding non-English articles and those without full-text availability, 86 were considered eligible. Of these, 56 either reported results at injection sites other than the face or did not report any vascular complication, and thus were discarded. The final selection included 30 full-text articles reporting 93 cases: 22 case reports (i.e., articles containing a full description of one or more cases),2,8,13,20–39 seven case series (i.e., articles containing a tabulated description of various cases with vascular complications),18,40–44 and one observational trial (i.e., an article retrieving data from a cohort of patients, including at least one patient experiencing a vascular complication).45 Most cases (n=62; 66.7%) were reported in Korea, while 14 (15.1%) were reported in China, 10 (10.8%) were reported in the United States, three (3.2%) were reported in Germany, three (3.2%) were reported in Taiwan, and one (1.1%) was reported in Japan.
All cases had information regarding the injection site and main consequences of vascular complications. Other key variables, such as injected substance, outcome, and affected blood vessel were reported in 92 (98.9%), 85 (91.4%), and 82 (88.2%) cases, respectively. In 80 cases (86.0%), the vascular complication and identity of the affected blood vessel were confirmed by at least one of the following imaging techniques: optical coherence tomography, magnetic resonance imaging, ultrasonography, or fundoscopy. In six cases, the affected vessel was deduced from the signs (e.g., necrosis affecting a skin area clearly irrigated by the facial artery) or the treatment outcome (e.g., prostaglandins injected into a vein, leading to the improvement of signs and symptoms). Conversely, in four cases, the physician failed to identify the affected vessel despite performing imaging diagnostic tests. Needle diameter, injected volume, and the professional who performed the injection were only reported in 11, 17, and 13 cases, respectively; due to their low representation in the study sample, these variables were excluded from analysis.
Case characteristics. Table 1 summarizes the main characteristics of the cases described in the selected articles. In most cases (n=57; 61.3%), blindness was the main consequence of vascular complication. In five cases (5.4%), the patients experienced blindness and skin necrosis simultaneously. Whereas blindness was typically assumed to be a consequence of a vascular embolization of the filler material, necrosis was sometimes attributed to compression (Figure 2).2,39,45 However, none of these cases reported evidence regarding the etiology of skin necrosis, and compression was suggested based on the time-to-onset or necrosis progression. Nine patients (9.7%) experienced neither necrosis nor visual loss or blindness despite a diagnosis of vascular occlusion. Eight patients (8.6%) reported mild consequences (e.g., pain, erythema), all of which resolved completely. One patient that was injected with autologous fat in the glabella experienced occlusion of the retinal artery with concomitant brain infarction, which resulted in hemiplegia and death.43
Theoretically, multiple blood vessels and nerves can be reached by the needle during filler injection (Figure 3). However, the paths of facial, nasal, temporal, and ophthalmic arteries define anatomical areas with increased risk of injury during filler injection (Figure 4). In the case of the ophthalmic artery, the increased risk included occlusion of one of its most important branches: the retinal artery. In our analysis, the ophthalmic retinal arteries accounted for 79.3 percent of the cases in which the affected blood vessel was reported. In addition to the nasociliary artery, other blood vessels affected by the aesthetic procedure were the choroid vessels, the internal carotid artery, the middle cerebral artery, and the facial vein and artery. The occlusion of the ophthalmic artery was mostly due to injections in the nose (n=18, 42.9% of all cases affecting the ophthalmic artery). Conversely, the occlusion of the retinal artery was mostly due to injections in the glabella (n=18, 55% of all cases affecting the retinal artery).
In 12 cases (12.9%), vascular occlusion progressed to brain infarction, identified by magnetic resonance imaging. Two of these were associated with ophthalmic artery occlusion, whereas eight were associated with retinal artery occlusion. With the exception of two cases—one leading to the patient’s death and another resulting in neurological sequelae—blindness was the main consequence for all patients affected by brain infarction.
Full recovery was reported in seven cases (8.2%): one case of blindness, one of visual loss, and five cases of vascular occlusion with minor consequences. Temporary blindness was caused by an HA injection in the eyebrow. The patient reported foggy and hazy vision immediately after the filler injection; 10 days later, the filler was successfully removed by irrigation and aspiration after creating a temporal limbal incision in the affected eye. Eight days after removal, visual acuity was restored.27
Hyaluronidase was used only in 10 of 40 cases in which HA was the cause of vascular occlusion. The time between symptom onset and hyaluronidase injection exceeded three hours in all cases. The dose of hyaluronidase injected, reported only in five cases, ranged from 1,000 to 9,000 units. In five of these cases, blindness was the main consequence of the vascular event; only one patient experienced partial recovery,25 whereas the rest remained blind despite attempts to remove the HA obstruction by injecting hyaluronidase.
Factors influencing outcome. To explore possible baseline factors influencing the outcome, cases with either visual loss or blindness as the main consequence were grouped into two categories based on the outcome: total or partial recovery and no improvement (Table 2). A chi-squared test revealed significant differences in the injected substance, the affected blood vessel, and the time to symptom onset. The post-hoc analysis of the injected substance showed that both HA and autologous fat were significantly associated with no improvement (p=0.003 and p<0.001 for the chi-squared adjusted residuals of HA and autologous fat, respectively; the significance threshold after Bonferroni correction was set at alpha=0.005). Regarding the affected vessel, only the ophthalmic artery was significantly associated with no improvement (p=0.001 for the chi-squared adjusted residuals; the significant threshold after the Bonferroni correction was set at alpha=0.006). A post-hoc analysis of time-to-onset did not reveal significant differences in any of the three categories.
The injected substance, the affected blood vessel, and the time to symptoms onset were included in a logistic regression analysis. The resulting model explained 22 percent of the outcome’s variance, categorized as “no improvement” and “total or partial recovery” (R2=0.219; p=0.027). However, only the affected blood vessel significantly contributed to the overall model (Table 3).
In this systematic review and meta-analysis of patients with vascular complications occurring after aesthetic procedures, we found that unilateral blindness was the most frequent vascular adverse event associated with cosmetic fillers for facial tissue augmentation. Of these, autologous fat tended to cause more cases of permanent vascular damage. Among all blood vessels affected, the ophthalmic artery was significantly associated with irreversible blindness.
The risk of vascular complications associated with facial aesthetic procedures has been addressed previously in case reports, case series, and literature reviews. In an attempt to further understand the factors influencing the risks and outcomes of vascular complications, we extracted data from individual cases to provide a quantitative approach. Moreover, considering that the number of products available for soft-tissue augmentation has been progressively and continuously increasing for the last 10 years, our review aimed to present an updated picture of vascular complications associated with these fillers. All analyses based on case reports are constrained by the amount and accuracy of the information published. Eighty-six percent of cases reported using imaging diagnostic techniques to verify the diagnosis of vascular occlusion, and most of them provided details regarding key variables such as the injected substance, the blood vessel affected, the outcome of the vascular complication, and the time to symptom onset.
In terms of clinical correlation, one of the most relevant variables was the filler injected. In our study selection, the absolute number of cases with vascular complications after the use of HA and autologous fat was similar. However, considering that HA is, by far, the most used filler in the world for aesthetic procedures,4,5 this observation suggests that autologous fat is more often associated with vascular complications than HA. Regarding the recovery rate of vascular complications, both HA and autologous fat were significantly associated with a lower frequency of improvement, but the latter showed a stronger trend towards more severe outcomes. This result is consistent with that of previous reviews, which concluded that autologous fat is the filler material that most frequently causes permanent blindness.12,17,46 In a previous review by Beleznay et al,12 autologous fat was responsible for 47.9 percent of cases of unilateral permanent blindness, followed by HA (23.5%), collagen (8.2%), poly-L-lactic acid (3.1%), and calcium hydroxylapatite (2%). The increased risk of major vascular complications associated with autologous fat injections could be explained by its large particle size, enabling it to occlude relatively large vessels, such as the ophthalmic artery.12,17
Regarding safety, one of the advantages of HA is the availability of an effective rescue procedure (i.e., hyaluronidase injection into or around the occluded blood vessel).45,47,48 This is one of the reasons why HA has been claimed as the safest substance indicated for tissue augmentation.48,49 However, in our review, the number of cases in which hyaluronidase was administered accounted for only a quarter of all cases in which HA was used (10 vs. 40). Furthermore, although the reduced number of cases limited our statistical analysis, it is worth mentioning that only half of these cases resulted in the total recovery of the main outcome related to vascular occlusion. The low recovery rate despite the use of hyaluronidase could be partially explained by the excessive time gap between symptoms onset and hyaluronidase injection, ranging from 3 to 24 hours, with five over seven cases exceeding the four-hour threshold, below which significant differences are seen.45 These observations suggest that the safer profile of HA compared with autologous fat might be better explained by the properties of the filler material rather than the availability of a rescue procedure. Due to the different physical properties of each substance, the injector’s ability to inject the filler using the right pressure might become an overriding factor influencing the risk of vascular complications.12,50 Rapid injections not only result in greater amounts of filler but also limit the capacity of the injector to identify and amend any vascular occlusion. Furthermore, various authors have proposed that, when exerting too much pressure on the plunger, even during the injection of small amounts of filler, arterial pressure can easily be overcome, with the filler reaching deeper arteries.6,12 Of course, injection pressure and rate cannot be monitored unless the professional performing the injection uses a motorized injector to deliver the filler; hence, this information could not be included in our analysis. Motorized injectors have been proposed as a means to reduce injection risks, as they provide a comfortable flow rate and allow physicians to keep their attention on the patient.50,51
Considering that shorter onset times are more likely to prompt early interventions, we expected time to symptom onset to influence the outcome. However, no significant differences were found between the times before and after one hour. The importance of the time gap between the vascular complication and the intervention was investigated in animal models by Kim et al38 and Cavallini et al,47 who found that rescue procedures performed less than four hours after a filler injection significantly reduced the area of necrotic ear skin. However, these studies were based on hyaluronidase injections as rescue procedures, which were barely used in our case collection. Notwithstanding the lack of correlation with other studies, two important drawbacks limited our analysis of the potential influence of the time-to-onset on symptom recovery. First, our dataset did not include time frames more accurate than a 24-hour interval. Second, most of these cases were reported by ophthalmologists with patients showing sudden blindness concurrent with filler injections; therefore, the time from the aesthetic intervention to the onset of vision loss or blindness was assessed retrospectively.
Our results also showed that the affected blood vessel significantly influenced the outcome of the vascular complication. Based on the statistical analysis, ophthalmic artery occlusion was more frequently associated with no improvement than that of other blood vessels, particularly the nasociliary artery. However, individual case examinations revealed that the most dangerous adverse events (i.e., cerebral infarctions) occurred as an ultimate consequence of retinal artery occlusion. Since the retinal artery is a final branch of the ophthalmic artery, it could be assumed that an occlusion of the retinal artery is not likely to have consequences at more central areas. However, as previously discussed, when the tip of the needle penetrates the artery and pressure is applied to the plunger, the filler can reverse the flow in it, moving as a column proximal to the origin of the retinal artery. If the injector exerts more pressure on the plunger for a longer time, the column can reach the origin of the ophthalmic artery, and part of the filler embolus can access the internal carotid artery and subsequently reach cerebral circulation (Figure 2).6,12 The use of motorized devices, which enable accurate pressure control, has been proposed to minimize this risk.50,51 We found no differences in the outcome when the occlusion occurred in other blood vessels, particularly the nasociliary and facial arteries. Although this observation is consistent with the larger diameter of these vessels, due to the limited number of cases in which there was occlusion in blood vessels other than the ophthalmic and retinal arteries, no firm conclusions could be reached.
Finally, we addressed the influence of the injection site on the outcome of the vascular event. Previous studies reported the glabella and the forehead as areas more frequently associated with blindness and visual loss than the nose.5,7,11 However, in our analysis, injections in the nose accounted for nearly half of the cases of vascular complications and had a similar frequency to that of injections in the glabella. These observations indicated that the nose might not be a safer injection site than the glabella. Lazzeri et al11 suggested that the dorsal nasal artery (i.e., the second terminal branch of the ophthalmic artery) might be responsible for the transmission of emboli following injections in either the glabella or the area proximal to the nasal root. Other injection sites did not yield significant results upon comparing the outcomes of the vascular procedures. However, it is worth mentioning that our analysis was compromised by the fact that a single patient could be injected at various sites, which precludes the identification of the precise injection responsible for the vascular complication.
Limitations. The fact that our meta-analysis was based mostly on case reports implies some limitations that should not be dismissed. Case reports do not always provide all details of the procedures performed. This was particularly notable for some variables identified as risk factors for vascular complications, such as injection technique, injected volume, pressure applied, and needle diameter, which were omitted in most cases. Some of these factors were investigated by Glogau et al,5 who concluded that low injection pressures (i.e., flow rates of less than 0.3mL/minute) and small volume injections (i.e., less than 0.5mL) might prevent retrograde embolization of the filler; the authors also recommended avoiding the fan-like technique, which was identified as the main cause of iatrogenic vascular occlusion. Other variables that could not be analyzed because of data omission, despite their potential interest, include the specialty of the person performing the injection, the characteristics of the device (e.g., needle, cannula), and the concentration of hyaluronidase used in the rescue procedure. In addition to a few poor-quality case reports, some of the cases analyzed were not reported by the physician injecting the filler but rather by the ophthalmologist who treated the complication, thus omitting details of the initial aesthetic procedure. The variables most affected by this lack of data were time-to-onset, initial rescue treatment, and concomitant symptoms, which, in most cases, were retrospectively reported by the physician treating the complication. Another potential source of inaccuracy was the ad-hoc data transformation. The heterogeneity in the way the various case reports reported the data prevented the use of pure, raw data for the analysis, which would have been a factor adding simplicity and clarity to our conclusion.
In addition to presenting an updated and quantitative perspective of vascular complications associated with filler injections, the results obtained in our analysis might serve to support a few recommendations to help clinicians who perform filler augmentation procedures avoid vascular adverse events or minimize their consequences. Table 4 provides a list of key recommendations for preventing and minimizing vascular adverse events when performing filler injections. However, as mentioned before, our analysis has important limitations associated with the accuracy and diversity of data presentation in the source articles. Hence, the recommendations we present in Table 4 should not be interpreted as being strictly supported by the results of our meta-analysis; our recommendations are also based on our own insights gained from our extensive experience as plastic surgeons.
This meta-analysis provides an up-to-date overview of vascular complications associated with the injection of facial fillers. Our results support the hypothesis that autologous fat is more likely to cause serious vascular events than HA, irrespective of the use of hyaluronidase to treat the vascular occlusion. In light of the information published in the literature, it seems that accidental injection in the terminal branches of the facial artery, particularly the retinal artery, almost invariably leads to unilateral, and occasionally bilateral, blindness. The incidental occlusion of the retinal artery most frequently occurs when treating the nose, but this artery can also be reached from the glabella. Thus, to prevent vascular adverse effects, it is essential that the physician performing the filler injections has a proficient knowledge of anatomy.
The authors gratefully acknowledge the time and effort of Dr. Patrice Delobel, Dr. Kévin Legent, and Dr. Luana Consolini, who provided scientific advice and helped with laying the groundwork of this research. The authors also thank the i2e3 Biomedical Research Institute team for providing statistical and medical writing assistance.
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