Hyaluronic Acid Is an Effective Dermal Filler for Lip Augmentation: A Meta-Analysis

Introduction

The lips and the mouth have a crucial functional importance in vocalization and mastication. Additionally, they also play an important role in the aesthetics of the face (1, 2). Particularly, lip fullness is a key factor associated with attractiveness, beauty and youth (2, 3). A number of noxious and hereditary factors contribute to the deterioration of the perioral tissues with age (2, 4–7). Consequently, volume loss of the lips may occur with other signs of aging, such as the appearance of perioral lines, marionette lines and flattening of the cupid bow (2). There are several surgical and non-surgical reconstructive procedures aiming to restore oral competence, anatomical structures and to provide appealing aesthetic outcomes and in order to be more attractive (6, 8).

Theoretically, there is a wide range of possible reconstructive methods that can be applied to rebuild damaged tissues such as tissue engineering using stem cells (9–11), gene therapy (12, 13) and artificial biocompatible scaffolds (14, 15), but their use has been not well-established in routine clinical settings. Among the non-surgical regenerative and reconstructive procedures, hyaluronic acid (HA)-based dermal filling is one of the most frequently used treatments (16, 17). Its advantages over other filling materials include its natural occurrence, which provides non-immunogenic properties (18). It also exerts an antioxidant effect (19, 20), and anti-inflammatory activity (18, 21). Additionally, HA highly supports tissue regeneration and wound-healing by providing a suitable structure for cell ingrowth (22, 23). Due to its multiple advantageous properties, HA is also broadly used in other areas of tissue regeneration, such as orthopedics to treat osteoarthritis and rheumatoid arthritis (24, 25). Moreover, it is utilized in ophthalmology, dermatology (26), as well as in certain dental procedures (27–29).

The initial production of HA from animal sources was shifted to bacterial production. In this process, various genetically modified bacteria such as B. subtilis and Group A and C Streptococci are used to produce HA, which is then extracted and chemically further modified to create cross-links between HA polymers (30, 31). This advancement in production greatly contributed to its recent success with decreased manufacturing costs, increased purity of the products, and decreased immune reactions (32).

Since the approval of the first non-animal based HA in 2004 (8) several clinical trials aimed to reveal its true potentials. HA is believed to be an excellent candidate for soft tissue augmentation to restore lip fullness, cosmetic asymmetries and to deal with rhytids due to the loss of elasticity of connective tissue (7). However, clinical studies investigating effectiveness were conducted with small sample sizes and with short follow-up periods. Therefore, conclusions rely on weak evidence, including high levels of uncertainty.

No meta-analysis has been conducted to determine the effectiveness of HA for lip augmentation and to confirm its long-term aesthetic results. Thus, the main objective of the present meta-analysis and systematic review was to increase the power and precision of the estimated HA effect on lip augmentation. Secondarily, we investigated the number and nature of adverse effects (AEs) of HA published in the literature.

Materials and Methods

Protocol and Registration

This meta-analysis was reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement (33) using similar approaches that we have recently reported (34–36). The PRISMA checklist summarizing the content of this review is enclosed in the supporting information (Supplementary Table 1). The meta-analysis was registered in PROSPERO (International Prospective Register of Systematic Reviews), 10/12/2018, Registration Number: CRD42018102899. There were no deviations from the study protocol.

Eligibility Criteria

The PICO (patient characteristics, type of intervention, control, and outcome) format was applied to investigate the following clinical questions: (1) To what extent are hyaluronic acid dermal fillers effective for lip augmentation? (2) What are the common and also the rare treatment-related adverse effects of HA application?

For analysis, we considered records published in scientific journals meeting the requirements of our selected PICO. Patient characteristics: subjects above 18 years having a minimal, mild or moderate score on a validated lip fullness scale. Type of intervention: injecting hyaluronic acid dermal filler into the lips and perioral area to increase lip fullness and enhance aesthetic appearance. Control: base-line control—baseline values of lip fullness recorded before treatment. Lip fullness values recorded after treatment were compared to baseline values. The effectiveness was evaluated as the rate of responders. A responder was defined as a participant with at least one grade improvement on a validated lip fullness scale. Outcome, primary: effectiveness measurement, i.e., the number of responders at each check-up; secondary: number and type of AEs related to treatment.

Inclusion and Exclusion Criteria

Publications which met the following eligibility criteria were included: (1) randomized controlled trials, cohort studies or case series and case reports; (2) intervention: hyaluronic acid used for lip augmentation; (3) healthy adult participants; (4) records written in English or available in English translation; (5) site of injection: lips; (6) use of validated scale to measure outcome. Exclusion criteria were: (1) filling material other than hyaluronic acid; (2) site of injection other than lips and perioral area; (3) Previous facial surgery, permanent facial implants or any facial cosmetic procedure in the last 24 months.

Information Sources and Search

A systematic search limited to English language records was performed in three different major electronic databases [Cochrane Central Register of Controlled Trials (CENTRAL), Embase and MEDLINE (via PubMed)] on 31 December, 2018. Besides electronic databases, an extensive hand search in the reference list of relevant articles and included records were also performed to find eligible records. Gray and black literature was not considered for this meta-analysis. “Hyaluronic acid” and “lip” search terms and their synonyms were used in each database adapted to their specific search engines. Supplementary Table 2 contains the detailed search quey.

Study Selection

The EndNote (Clarivate Analytics, Philadelphia, US, version: X9.3.3) reference manager was used to organize and manage records. After removing duplicates, the remaining records were screened for suitability by two authors (L.M.C. and S.F.), in duplicate, based on the titles and abstracts of the published original papers. The eligibility of full texts of the remaining records was assessed by the same two review authors independently. Disagreements between reviewers were resolved by discussion or, if it was necessary, by consulting a third review author (G.V.).

Data Collection Process and Data Items

Data extraction was performed by two authors independently (L.M.C. and S.F.) using a preconstructed standardized data extraction form. The following information was extracted: first author's name, year of publication, sample size, age and gender distribution, study design, type of HA used, site of injection, follow-up period, type of validated scales used for evaluation, outcome (rate of responders, number and type of AEs). In case of disagreement, a third author (G.V.) was also involved.

Risk of Bias Assessment

Quality and risk of bias of the RCTs were evaluated by two authors (L.M.C. and S.F.) independently. Assessment was based on the recommendation of the Cochrane Collaboration, the Cochrane Risk of Bias assessment tool (37, 38). In case of disagreement a third author was involved (G.V.). Studies were evaluated according the domains specified in the Cochrane Handbook for Systematic Reviews of Interventions (38).

Cohort studies were evaluated based on the Newcastle Ottawa Scale (NOS) for Cohort Studies (39). We slightly modified the original NOS scale. We removed “Ascertainment of exposure” subdomain from Selection domain. Thus, in the Selection domain three sub domains remained: “Representativeness of the exposed cohort,” “Selection of the non-exposed cohort,” and “Demonstration that outcome of interest was not present at start of study.” Scores for these subdomains were given according to the original NOS scale (39). Hence the maximum score was three, one and three stars for Selection, Comparability and Outcome domains, respectively. In the outcome 6 months or more of follow-up was considered acceptable. Drop-out below 10% was considered adequate. Supplementary Table 3 summarizes the modified NOS.

Summary Measures and Synthesis of Results

Untransformed proportions with 95% confidence intervals (CIs) were calculated for the rate of responders. A responder is defined as a participant with at least one grade improvement on a validated lip fullness scale compared to its baseline value. For analyzing AEs we used descriptive statistics, summing the sample sizes of included studies and the incidence of each AEs described in any of the included publications. The number of participants was chosen as statistical unit.

We only considered results credible if raw data for meta-analysis could be drawn from at least three records. We applied the random effect model with DerSimonian-Laird method. I² and chi-square tests were used to quantify statistical heterogeneity and gain probability-values, respectively; p < 0.1 indicated significant heterogeneity (38). All statistical analyses were performed using STATA 15.0.

Publication Bias

We constructed funnel plots and performed visual inspection of their results to check for publication bias.

Certainty of Evidence Pont

The GRADE approach was followed to evaluate the quality and certainty of evidence (37, 40). Assessment was performed independently by two review authors (L.M.C and S.F.).

Results

Study Selection

During the study selection process, we identified a total of 326 records. After removing duplicates, 259 items remained. During the screening process, 176 records were excluded due to various reasons such as filler material other than HA (n = 30) or different injection sites (n = 7), focusing on novel methods of injection (n = 24), investigating the effect of hyaluronic acid in special implications outside the scope of this meta-analysis (n = 64), review articles (n = 17) or miscellaneous (n = 34). Afterwards, 83 full text records were searched. Out of these publications, 32 were included in the qualitative synthesis and 10 in the quantitative synthesis assessing the effectiveness of lip augmentation (Figure 1).

FIGURE 1

Figure 1. PRISMA flow chart. Summarizing the study selection process.

Study Characteristics

Description of the Included Studies

We included 5 RCTs (41–45) and 5 cohort studies (46–50) to analyze the effects of HA on lip augmentation. Two additional RCTs (51, 52), six additional cohort studies (53–58) and 14 case reports (59–72) were included for assessing AEs.

In the effectiveness analysis, a total of 1,228 participants were included. Subjects aged 18 or older desiring lip augmentation, had lip fullness of minimal, mild or moderate on a validated lip fullness scale were included. In the study population all Fitzpatrick skin types have been represented. Exclusion criteria included a history of allergy to injectable HA, history to any semi-permanent or permanent tissue augmentation or aesthetic surgery or any temporary dermal filler treatments in the last 24 months in the facial region. Subjects with scarce or significant abnormalities of the lips were also excluded. The mean age of subjects in the studies varied between 41 and 54 years. Altogether 4 different injectable HA products were used, Juvéderm and Restylane were the two most commonly applied ones. Follow-up periods varied between 12 and 48 weeks. All included records utilized a validated lip fullness scale such as the Medicis Lip Fullness Scales (73) or the Allergan Lip Fullness Scale (74).

AEs were collected and assessed from a total of 32 records including 1,488 participants and more than 12 different HA products. In all includes studies the lips and perioral lines were the site of injection. A tabulated summary of the characteristics of the included studies and HA products is provided in Tables 1–3 and Supplementary Table 4.

TABLE 1

Table 1. Study characteristics of records included in effectiveness analysis.

TABLE 2

Table 2. Study characteristics of RCTs and cohort studies only included in adverse effect analysis.

TABLE 3

Table 3. Characteristics of hyaluronic acid dermal fillers assessed in the analysis.

Description of Excluded Studies

During full-text analysis, we excluded 51 records. Seven RCTs, nine cohort studies, 11 case reports and nine review articles. Three records had non-English texts. Additionally, in 11 cases we found no full text to the records and 1 record was a non-interventional study. Out of the 32 articles included in the analysis of AEs, we excluded 22 publications from the effectiveness analysis. Several excluded articles did not report sufficient information on effectiveness, while the others used incomparable scales to measure the effectiveness of lip augmentation.

Risk of Bias Within Studies

All RCTs applied means of random sequence generation. However, in the case of Carruthers et al. (52) and Dayan et al. (42) the methods used for allocation concealment were not clearly described. Due to the nature of the intervention, none of the studies applied blinding of personnel. On the other hand, the outcome assessment was performed by blinded evaluators in all studies. In the case of one study (42) attrition bias was unclear due to ambiguous reporting on lost to follow-ups. In another study (52) we found a high risk of attrition bias due to the 23% of dropouts. The level of reporting bias was low in all studies except three. Study protocols for Beer and coinvestigators (41), Carruthers et al. (52) and Glogau et al. (44) were not found. However, no intext evidence of reporting bias was found. Figure 2, Supplementary Figure 1, and Supplementary Table 5 contain the summary of the risk of bias assessment of the RCTs.

FIGURE 2

Figure 2. Risk of bias graph. Representing the portion of bias in each domain.

Bias in the observational studies was assessed based on the Newcastle Ottawa Scale (39). Observational studies did not have control groups. Instead, they measured the rate of responders only within the treatment group (baseline controlled). The average bias assessment score of the studies was 5.5 ± 1.3 stars on the modified seven-point scale. All 11 publications, earned three stars for selection (46–50, 53–58). Five studies received no starts for comparability (53–57). In three studies (54, 56, 58) the outcome assessments were only self-reports. One study (56) was considered to have inadequately short follow-ups for valuable results, while three studies (53, 55, 56) did not give any explanation for drop-outs. Supplementary Tables 6, 7 show the summary of the risk of bias assessment of observational studies.

Results of Individual Studies and Their Synthesis

Hyaluronic Acid Treatment Effectively Increases Lip Fullness

Two months after HA injection the overall pooled rate of responders, i.e., the percentage of participants with at least one grade improvement on a validated lip fullness scale [Medicis Lip Fullnes Scale (MLF) or Allergan Lip Fullness Scale (ALFS)] was 91% (95% CI: 0.85−0.96) (untransformed proportion, random-effects DerSimonian-Laird method). I²-values indicating statistical heterogeneity was 82.7% (p = 0.0). Data were pooled from 5 studies (41, 44, 46, 49, 50) (Figure 3).

FIGURE 3

Figure 3. Estimate of rate of responders at 2 months after treatment for the upper and lower lips. Overall, 92% (95% CI: 80–99%) and 90% (95% CI: 0.82–96%) of included participants had at least one grade improvement on a validated lip fullness scale regarding their upper and lower lips, respectively, after 2 months of initial treatment.

When the rate of responders for volume increase in the upper and lower lips were compared, only a very minor, 2% difference was observed between them 2 months after HA application (41, 44, 46, 49, 50). Upper lips: ES = 0.92, 95% CI: 0.88−0.99; I² = 88.46%, p = 0.00 and lower lips: ES = 0.90, 95% CI: 0.82−0.96; I² = 74.02%, p = 0.01 (Figure 3).

An additional analysis was also performed using data of the three available studies (41, 42, 44) investigating lip fullness augmentation in non-treated controls. Even among these subjects, who received no HA injection, 21% were demonstrated to be responders 2 months after baseline assessment indicating a possible placebo effect in HA injection studies (ES = 0.21, 95% CI: 0.06−0.40; I² = 89.95%, p = 0.00) (Figure 4).

FIGURE 4

Figure 4. Estimate of overall rate of responders at 2 months in the no treatment group. Overall, 21% (95% CI: 6–40%) of included participants had at least one grade improvement on a validated lip fullness scale after 2 months in the no treatment group.

The rate of responders to HA treatment, i.e., the percentage of participants with at least one grade improvement on the MLF or ALF scales after 3 months, was also calculated including eight studies (42, 43, 45–50). The untransformed proportion (random-effects DerSimonian-Laird method) of the pooled data showed that 71% of the HA-treated participants were responders, meaning that 71 out of 100 experienced a substantial, at least one grade increase in lip fullness 3 months after the initial treatment (ES = 0.71, 95% CI: 0.55−0.87; I² = 97.91%, p = 0.00) (Figure 5).

FIGURE 5

Figure 5. Estimate of overall rate of responders at 3 months after treatment. Overall, 71% (95% CI: 55–87%) of included participants had at least one grade improvement on a validated lip fullness scale after 3 months of initial treatment.

Six months after the HA injection, the overall rate of responders, i.e., again the percentage of those who still have an increase of lip fullness scale by one grade or higher, were synthetized from five studies (42, 43, 47, 48, 50). This analysis revealed that 74% of those who received the one dose HA treatment maintained their increase of lip volume (ES = 0.74, 95% CI: 0.66−0.82; I² = 66.88%, p = 0.02) (Figure 6).

FIGURE 6

Figure 6. Estimate of overall rate of responders at 6 months after treatment. Overall, 74% (95% CI: 66–82%) of included participants had at least one grade improvement on a validated lip fullness scale after 6 months of initial treatment.

The lip volume data 12 months after HA application were available only in four studies (42, 43, 47, 48). Our meta-analysis revealed that rate of responders was 46% even after 1 year of a single HA injection (ES = 0.46, 95% CI: 0.28−0.65; I² = 93.21%, p = 0.00) (Figure 7).

FIGURE 7

Figure 7. Estimate of overall rate of responders at 12 months after treatment. Overall, 46% (95% CI: 28–65%) of included participants had at least one grade improvement on a validated lip fullness scale after 12 months of initial treatment.

Adverse Effects of Hyaluronic Acid Injection

Studies reporting the AEs related to HA injections were included in this analysis. Data were pooled from six RCTs (41–43, 45, 51, 52), 11 cohort studies (46–50, 53–58) and 14 case reports (59–72) including 1,488 participants overall.

The results revealed that the five most common AEs were tenderness (n = 1,320, 88.7%), injection site swelling (n = 1,105, 74.3%), contusion (n = 725, 48.7%), injection site mass (n = 406, 27.3%), and injection site pain (n = 293, 19.7%). The appearance of herpes labialis (n = 9, 0.6%) was identified in a few cases, while filler-associated necrosis of the lips was also found very rarely in case reports. More serious AEs such asgranulomatous foreign body reaction (n = 9, 0.6%), were infrequent. Life-threatening angioedema was reported only in four cases out of the 1,488 patients (0.3%) included in the studies on HA injection into the lip (Supplementary Table 8).

Publication Bias

Funnel plot constructed from studies with 3 months follow-up shows asymmetry of published records suggesting small-study effect (Supplementary Figure 2). Due to the small number of studies included, no further statistical analysis could be performed to test for small-study effect.

Certainty of Evidence

The assessement based on the GRADE approach revealed that the final level of evidence for the effectiveness of HA treatment on lip augmentation is very low. This is explained by some low level of study designs (cohort studies), the significant inconsistency due to statistical heterogeneity indicating confounding factors, imprecision indicated by wide range of confidence intervals and suspected publication bias due to small study effect.

In the case of EAs the level of evidence is also very low due to study design, the high risk of bias and the lack of consistent reporting on EAs (Supplementary Table 9).

Discussion

Summary of Evidence

As it is the entrance of the gastrointestinal tract, the health and esthetics of lips are important for the well-being of the human body. Although HA is a frequently used dermal filler for non-surgical aesthetic treatment (8, 17), its benefits and possible AEs for lip augmentation have not been assessed quantitatively by meta-analysis. Although several primary studies existed on the matter, their relatively small sample size did not allow to draw strong conclusions. Our study is the first meta-analysis to integrate the available data from individual primary studies for the effectiveness of HA for lip augmentation after HA injections. In our analysis, we included studies which used validated scales to assess changes in lip fullness. We also included case reports to find-long term and rare events of treatment-related AEs. We found that HA injection effectively increases lip fullness up to 6 months among the majority of treated patients. Moreover, our analysis revealed that approximately half of the successfully treated participants still had a significantly increased lip fullness after 12 months. Most AEs related to the treatment were consistent across prospective studies. AEs were mostly mild or moderate, but rare severe AEs could also be observed in a very small number of cases.

Although our meta-analysis clearly showed the effectiveness of HA injection on the lip, the variability of the individual studies was also very obvious (41–45). This heterogeneity suggests that there were significant confounding factors that might influence the outcome of HA treatments. Several factors have been suggested to influence the outcome of lip augmentation, such as the injected volume, the number of touch-up treatments, the type of injection technique, the number of cross-links in HA product, and also the skin type of the patients, the experience of investigators, as well as the evaluation method (42, 44, 45, 80). In our analysis of effectiveness, more than 8 HA products using 5 different HA concentrations were included. The different papers reported several injection techniques and various injection volumes. Due to the high variability and the low number of studies containing identical subgroups, it was not possible to perform a comprehensive statistical analysis to investigate the effects of such confounding factors. Raspaldo and coinvestigators found that live assessment yielded more precise results compared to photo analysis based on 3D images. They argued that photographs can alter shadows and smaller rhytids, thereby altering evaluation outcomes (45). On the contrary, Moragas et al. argued that the use of a validated scale is most appropriate for evaluating lip augmentation outcomes. Yet, in their review, they suggested that anthropometric measures were far from being perfect. Therefore, they did not evaluate natural appearance or changes in the shape of the lips (80).

An important observation of our analysis is the considerable decrease in lip fullness over a 12-month period as HA treatment remained effective in only about the half of the treated patients after 1 year. Although HA is regarded to be a temporary filler, its longevity on lip volume have not been investigated with statistical methods. The decreased number of augmented lips at 12 months follow-up period could be ascribed to the natural biodegradation of HA (26). Cross-linking slows down the biodegradation of HA (81), but it is unclear to what level the concentration and degree of cross-links of HA affects its long-term effectiveness.

Unfortunately, no studies are available on the effectivness of hydratization of the lips in response to hyaluronic acid treatment. HA fillers were described to increase not only the volume, but also hydratize the treated tissue when applied (82). Namely, Seok and coinvestigators observed increased skin hydration levels after HA injections into various parts of the face (83). For AEs, we found that similar event rates were reported from the included RCTs (41–45) and other prospective studies (46–50). However, case reports revealed additional AEs (59–72), which were not reported in clinical trials. Our analysis revealed that the most frequent AEs were injection-related, such as tenderness, injection site swelling, bruising, injection site mass, injection site pain. All of these AEs resolved without the need of treatment within a few weeks. Similar AE rates were found in earlier studies for lips (3, 80, 84) and for other anatomical sites as well (8, 17).

Remarkably, in one study (51), herpes labialis was found to be the most common AE (17%). The reason for this is unclear since the prevalence of this viral infection was much lower in the other included studies (0.6%). Most probably, in the work of Downie et al. the needle puncture could have triggered the reactivation of herpes virus infection (51, 85). In this context. a systematic review on HA filling of nasolabial folds found that the correct injection technique (avoiding fan-like injection) applying slow rate injection (0.3 ml/min) can minimize the risk of injection-related effects (8).

Moreover, our analysis uncovered some AEs that have been reported only in case reports, such as foreign granulomatous reactions with histology (0.6%), tumor-like nodule (0.3%). Angioedema (0.3%) was reported in one RCT (42) and in three case reports (60, 62, 70). Filler-associated necrosis of the lips were noted in three case reports (86–88). The available systematic reviews have not identified such AEs in similar prevalence (3, 8, 17, 80, 89). Additionally, vocalization and mastication may also be disturbed but no reports are available about this.

Impurities in HA could be a potential explanation for immune system-related AEs. HA itself is a non-allergic and a non-toxic molecule (90). However, in health industry products HA is manufactured from various xenogeneic sources. Also, there are differences between the various HA manufacturing procedures (31, 80, 91). In our meta-analysis all included studies used HA produced by bacterial transduction. HA products originating from bacterial transduction, using advanced purification technologies are thought to reduce the risk of host immune response compared to HA products from animal sources (80). Rough HA preparations may be further modified chemically to create the cross-links that extend the lifespan of the injected HA (80, 91). However, impurities, residual proteins and nucleic acid fragments leading to immune reactions may still exist after purification (31, 32, 91). It is unclear whether the few cases of angioedema and granulomas were due to impurities in the used HA products or by the possible contamination of the needle with bacteria used to puncture the skin (92–94). But a recent systematic review investigated the incidence of delayed inflammatory reactions associated with HA injection (17). That work concluded that although the estimated incidence is relatively low, preceding skin tests could be still relevant before HA injection to prevent certain types of granulomas, such as the ones caused by delayed-type hypersensitivity reaction (17).

Limitations

A major limitation of the present work is the relatively small number of RCTs found on the topic. Although our analysis revealed the importance of confounding factors, no sub-group analysis could be performed due to the limited reported data, and to uncomprehensive data-reporting. For example, the volume of HA injection and the injection technique were not given, and subdivision of the results according to skin types were not always provided. Additionally, different studies used different reporting schemes and wording for detecting AEs. Hence, due to the lack of clear definition, we had to merge certain reported AEs based on our estimation.

In several papers, the documentation of AEs was not optimal for comparison. Additionally, most of the prospective studies had a short follow-up period, up to a maximum of 1 year. Moreover, our analysis was based on reported events, unreported events could not be taken into account. This may cause underestimation of the number and type of AEs associated with lip augmentation.

Conclusion

In conclusion, our meta-analysis provided evidence that hyaluronic acid injections are highly efficient at least up to 6 months. Even after 1 year following HA injections, in almost half of the patients, the lip volume was still significantly increased. Additionally, we found that most of the AEs after HA treatment were mild or moderate. But the lack of longer follow-ups could not reveal possible delayed reactions. Based on our present meta-analysis, we suggest that more high quality RCTs are needed to strengthen the certainty of evidence and firmly establish the long-term effect of HA injection for lip augmentation.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author Contributions

LC, SF, AL, VG, SK, PH, and GV devised the project, the main conceptual ideas, and planned the research. LC, SF, NG, DC, SK, and GV worked out the methodology. LC, SF, and GV performed the data collection: literature search, study selection, and data extraction. LC, AM, and DC also organized and maintained research data for analysis. NG performed analytic calculations, applied statistical models for synthetizing data, and visualized synthetized data into forest plots. AM, DC, and SK also aided the research by interpretation of raw and synthetized data. LC and SF worked on summarizing results into figures and tables. SK and GV were responsible for managing and coordinating the research activity. PH and GV took leadership responsibility for the research activity, provided resources, and acquired financial support for the research project. SK, PH, and GV validated reproducibility of the results. LC, NG, AM, DC, and GV wrote the manuscript with input from all authors. SF, AL, VG, SK, PH, and GV extensively reviewed the work and further edited the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by the Hungarian Human Resources Development Operational Program (EFOP-3.6.2-16-2017-00006). Additional support was received from the Thematic Excellence Program (2020-4.1.1.-TKP2020) of the Ministry for Innovation and Technology in Hungary, within the framework of the Therapy thematic program of the Semmelweis University. Support was also received from an Economic Development and Innovation Operative Program Grant (GINOP 2.3.2-15- 2016-00048) and an Institutional Developments for Enhancing Intelligent Specialization Grant (EFOP-3.6.1-16-2016-00022) of the National Research, Development and Innovation Office. All funds issued by the Hungarian government with cooperation of the European Union. Funders did not have any role in the research. For open access publication support was received through the Central Library of Semmelweis University. The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fsurg.2021.681028/full#supplementary-material

References

1. Larrabee YC, Moyer JS. Reconstruction of mohs defects of the lips and chin. Facial Plastic Surg Clin North Am. (2017) 25:427–42. doi: 10.1016/j.fsc.2017.03.012

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Wollina U. Perioral rejuvenation: restoration of attractiveness in aging females by minimally invasive procedures. Clin Interv Aging. (2013) 8:1149–55. doi: 10.2147/CIA.S48102

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Stojanovič L, Majdič N. Effectiveness and safety of hyaluronic acid fillers used to enhance overall lip fullness: a systematic review of clinical studies. J Cosmet Dermatol. (2019) 18:436–43. doi: 10.1111/jocd.12861

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Stolic D, Jankovic M, Draskovic M, Georgiev S, Stolic M. The surgical lips deformity corrected with hyaluronic fillers: a case report. Macedonian J Med Sci. (2015) 3:423–5. doi: 10.3889/oamjms.2015.067

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Schweiger ES, Riddle CC, Tonkovic-Capin V, Aires DJ. Successful treatment with injected hyaluronic acid in a patient with lip asymmetry after surgical correction of cleft lip. Dermatol Surg. (2008) 34:717–9. doi: 10.1111/j.1524-4725.2008.34133.x

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Yamasaki A, Lee LN. Facial fillers in lip reconstruction. Oper Tech Otolaryngol Head Neck Surg. (2020) 31:38–44. doi: 10.1016/j.otot.2019.12.009

CrossRef Full Text | Google Scholar

7. Luthra A. Shaping lips with fillers. J Cutaneous Aesthet Surg. (2015) 8:139–42. doi: 10.4103/0974-2077.167269

CrossRef Full Text | Google Scholar

8. Cohen JL, Dayan SH, Brandt FS, Nelson DB, Axford-Gatley RA, Theisen MJ, et al. Systematic review of clinical trials of small- and large-gel-particle hyaluronic acid injectable fillers for aesthetic soft tissue augmentation. Dermatol Surg. (2013) 39:205–31. doi: 10.1111/dsu.12036

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Racz GZ, Kadar K, Foldes A, Kallo K, Perczel-Kovach K, Keremi B, et al. Immunomodulatory and potential therapeutic role of mesenchymal stem cells in periodontitis. J Physiol Pharmacol. (2014) 65:327–39.

PubMed Abstract | Google Scholar

10. Grimm WD, Dannan A, Becher S, Gassmann G, Arnold W, Varga G, et al. The ability of human periodontium-derived stem cells to regenerate periodontal tissues: a preliminary in vivo investigation. Int J Periodontics Restorative Dent. (2011) 31:e94–101. doi: 10.11607/prd.00.1020

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Földes A, Kádár K, Kerémi B, Zsembery Á, Gyires K, Zádori ZS, et al. Mesenchymal stem cells of dental origin-their potential for antiinflammatory and regenerative actions in brain and gut damage. Curr Neuropharmacol. (2016) 14:914–34. doi: 10.2174/1570159X14666160121115210

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Farkas K, Yeruva S, Rakonczay Z Jr, Ludolph L, Molnár T, Nagy F, et al. New therapeutic targets in ulcerative colitis: the importance of ion transporters in the human colon. Inflam Bowel Dis. (2010) 17:884–98. doi: 10.1002/ibd.21432

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Rakonczay Z Jr, Hegyi P, Hasegawa M, Inoue M, You J, Iida A, et al. CFTR gene transfer to human cystic fibrosis pancreatic duct cells using a Sendai virus vector. J Cell Physiol. (2008) 214:442–55. doi: 10.1002/jcp.21220

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Juriga D, Nagy K, Jedlovszky-Hajdú A, Perczel-Kovách K, Chen YM, Varga G, et al. Biodegradation and osteosarcoma cell cultivation on poly(aspartic acid) based hydrogels. ACS Appl Mater Interfaces. (2016) 8:23463–76. doi: 10.1021/acsami.6b06489

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Hegedus O, Juriga D, Sipos E, Voniatis C, Juhász Á, Idrissi A, et al. Free thiol groups on poly(aspartamide) based hydrogels facilitate tooth-derived progenitor cell proliferation and differentiation. PLoS ONE. (2019) 14:e0226363. doi: 10.1371/journal.pone.0226363

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Taylor SC, Downie JB, Shamban A, Few J, Weichman BM, Schumacher A, et al. Lip and perioral enhancement with hyaluronic acid dermal fillers in individuals with skin of color. Dermatol Surg. (2019) 45:959–67. doi: 10.1097/DSS.0000000000001842

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Chung KL, Convery C, Ejikeme I, Ghanem AM. A systematic review of the literature of delayed inflammatory reactions after hyaluronic acid filler injection to estimate the incidence of delayed type hypersensitivity reaction. Aesthet Surg J. (2020) 40:NP286–300. doi: 10.1093/asj/sjz222

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Dahiya P, Kamal R. Hyaluronic acid: a boon in periodontal therapy. N Am J Med Sci. (2013) 5:309–15. doi: 10.4103/1947-2714.112473

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Litwiniuk M, Krejner A, Speyrer MS, Gauto AR, Grzela T. Hyaluronic acid in inflammation and tissue regeneration. Wounds. (2016) 28:78–88.

PubMed Abstract | Google Scholar

20. Waddington RJ, Moseley R, Embery G. Reactive oxygen species: a potential role in the pathogenesis of periodontal diseases. Oral Dis. (2000) 6:138–51. doi: 10.1111/j.1601-0825.2000.tb00325.x

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Jentsch H, Pomowski R, Kundt G, Gocke R. Treatment of gingivitis with hyaluronan. J Clin Periodontol. (2003) 30:159–64. doi: 10.1034/j.1600-051X.2003.300203.x

CrossRef Full Text | Google Scholar

22. Necas J, Bartosikova L, Brauner P, Kolar J. Hyaluronic acid (hyaluronan): a review. Vet Med. (2008) 53:397–411. doi: 10.17221/1930-VETMED

CrossRef Full Text | Google Scholar

23. Kim JE, Sykes JM. Hyaluronic acid fillers: history and overview. Facial Plast Surg. (2011) 27:523–8. doi: 10.1055/s-0031-1298785

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Barbucci R, Lamponi S, Borzacchiello A, Ambrosio L, Fini M, Torricelli P, et al. Hyaluronic acid hydrogel in the treatment of osteoarthritis. Biomaterials. (2002) 23:4503–13. doi: 10.1016/S0142-9612(02)00194-1

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Moreland LW. Intra-articular hyaluronan (hyaluronic acid) and hylans for the treatment of osteoarthritis: mechanisms of action. Arthritis Res Ther. (2003) 5:54–67. doi: 10.1186/ar623

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Salwowska NM, Bebenek KA, Zadło DA, Wcisło-Dziadecka DL. Physiochemical properties and application of hyaluronic acid: a systematic review. J Cosmet Dermatol. (2016) 15:520–6. doi: 10.1111/jocd.12237

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Bertl K, Bruckmann C, Isberg PE, Klinge B, Gotfredsen K, Stavropoulos A. Hyaluronan in non-surgical and surgical periodontal therapy: a systematic review. J Clin Periodontol. (2015) 42:236–46. doi: 10.1111/jcpe.12371

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Baldini A, Zaffe D, Nicolini G. Bone-defects healing by high-molecular hyaluronic acid: preliminary results. Ann Stomatol (Roma). (2010) 1:2–7.

PubMed Abstract | Google Scholar

29. Mandel I, Farkasdi S, Varga G, Nagy ÁK. Comparative evaluation of two hyaluronic acid gel products for the treatment of interdental papillary defects. Acta Stomatol Croat. (2020) 54:227–37. doi: 10.15644/asc54/3/1

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Sze JH, Brownlie JC, Love CA. Biotechnological production of hyaluronic acid: a mini review. 3 Biotech. (2016) 6:67. doi: 10.1007/s13205-016-0379-9

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Schuurmans CCL, Mihajlovic M, Hiemstra C, Ito K, Hennink WE, Vermonden T. Hyaluronic acid and chondroitin sulfate (meth)acrylate-based hydrogels for tissue engineering: synthesis, characteristics and pre-clinical evaluation. Biomaterials. (2021) 268:120602. doi: 10.1016/j.biomaterials.2020.120602

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Boeriu CG, Springer J, Kooy FK, van den Broek LAM, Eggink G. Production methods for hyaluronan. Int J Carbohydr Chem. (2013) 2013:624967. doi: 10.1155/2013/624967

CrossRef Full Text | Google Scholar

33. Moher D, Shamseer L, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev. (2015) 4:1. doi: 10.1186/2046-4053-4-1

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Czumbel LM, Kiss S, Farkas N, Mandel I, Hegyi A, Nagy Á, et al. Saliva as a candidate for COVID-19 diagnostic testing: a meta-analysis. Front Med (Lausanne). (2020) 7:465. doi: 10.3389/fmed.2020.00465

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Tóth B, Hegyi P, Lantos T, Szakács Z, Kerémi B, Varga G, et al. The efficacy of saffron in the treatment of mild to moderate depression: a meta-analysis. Planta Med. (2019) 85:24–31. doi: 10.1055/a-0660-9565

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Czumbel LM, Kerémi B, Gede N, Mikó A, Tóth B, Csupor D, et al. Sandblasting reduces dental implant failure rate but not marginal bone level loss: a systematic review and meta-analysis. PLoS ONE. (2019) 14:e0216428. doi: 10.1371/journal.pone.0216428

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Cumpston M, Li T, Page MJ, Chandler J, Welch VA, Higgins JP, et al. Updated guidance for trusted systematic reviews: a new edition of the cochrane handbook for systematic reviews of interventions. Cochrane Database Syst Rev. (2019) 10:Ed000142. doi: 10.1002/14651858.ED000142

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Higgins JPT, Altman DG, Gøtzsche PC, Jüni P, Moher D, Oxman AD, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ. (2011) 343:d5928. doi: 10.1136/bmj.d5928

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Deeks JJ, Dinnes J, D'Amico R, Sowden AJ, Sakarovitch C, Song F, et al. Evaluating non-randomised intervention studies. Health Technol Assess. (2003) 7:iii-x, 1–173. doi: 10.3310/hta7270

CrossRef Full Text | Google Scholar

40. Schünemann HBJ, Guyatt G, Oxman A editors. GRADE Handbook for Grading Quality of Evidence and Strength of Recommendations. Hamilton, ON (2015). Available online at: https://Gradepro.org

41. Beer K, Glogau RG, Dover JS, Shamban A, Handiwala L, Olin JT, et al. A randomized, evaluator-blinded, controlled study of effectiveness and safety of small particle hyaluronic acid plus lidocaine for lip augmentation and perioral rhytides. Dermatol Surg. (2015) 41(Suppl. 1):S127–36. doi: 10.1097/DSS.0000000000000199

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Dayan S, Bruce S, Kilmer S, Dover JS, Downie JB, Taylor SC, et al. Safety and effectiveness of the hyaluronic acid filler, HYC-24L, for lip and perioral augmentation. Dermatol Surg. (2015) 41(Suppl. 1):S293–301. doi: 10.1097/DSS.0000000000000540

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Geronemus RG, Bank DE, Hardas B, Shamban A, Weichman BM, Murphy DK. Safety and effectiveness of VYC-15L, a hyaluronic acid filler for lip and perioral enhancement: one-year results from a randomized, controlled study. Dermatol Surg. (2017) 43:396–404. doi: 10.1097/DSS.0000000000001035

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Glogau RG, Bank D, Brandt F, Cox SE, Donofrio L, Dover J, et al. A randomized, evaluator-blinded, controlled study of the effectiveness and safety of small gel particle hyaluronic acid for lip augmentation. Dermatol Surg. (2012) 38:1180–92. doi: 10.1111/j.1524-4725.2012.02473.x

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Raspaldo H, Chantrey J, Belhaouari L, Eccleston D, Saleh R, Acquilla R, et al. Lip and perioral enhancement: a 12-month prospective, randomized, controlled study. J Drugs Dermatol. (2015) 14:1444–52.

PubMed Abstract | Google Scholar

46. Chopra R, Graivier M, Fabi S, Nestor M, Meuse P, Mashburn J. A multi-center, open-label, prospective study of cannula injection of small-particle hyaluronic acid plus lidocaine (SPHAL) for lip augmentation. J Drugs Dermatol. (2018) 17:10–6.

PubMed Abstract | Google Scholar

47. Eccleston D, Murphy DK. Juvéderm® volbella™ in the perioral area: a 12-month prospective, multicenter, open-label study. Clin Cosm Investig Dermatol. (2012) 5:167–72. doi: 10.2147/CCID.S35800

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Fagien S, Maas C, Murphy DK, Thomas JA, Beddingfield FC. Juvéderm ultra for lip enhancement: an open-label, multicenter study. Aesthetic Surg J. (2013) 33:414–20. doi: 10.1177/1090820X13478609

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Solish N, Swift A. An open-label, pilot study to assess the effectiveness and safety of hyaluronic acid gel in the restoration of soft tissue fullness of the lips. J Drugs Dermatol. (2011) 10:145–9.

PubMed Abstract | Google Scholar

50. Yazdanparast T, Samadi A, Hasanzadeh H, Nasrollahi SA, Firooz A, Kashani MN. Assessment of the efficacy and safety of hyaluronic acid gel injection in the restoration of fullness of the upper lips. J Cutaneous Aesthetic Surg. (2017) 10:101–5. doi: 10.4103/JCAS.JCAS_115_16

CrossRef Full Text | Google Scholar

51. Downie J, Mao Z, Rachel Lo TW, Barry S, Bock M, Siebert JP, et al. A double-blind, clinical evaluation of facial augmentation treatments: a comparison of PRI 1, PRI 2, Zyplast® and Perlane®. J Plastic Reconst Aesthetic Surg. (2009) 62:1636–43. doi: 10.1016/j.bjps.2008.06.056

CrossRef Full Text | Google Scholar

52. Carruthers A, Carruthers J, Monheit GD, Davis PG, Tardie G. Multicenter, randomized, parallel-group study of the safety and effectiveness of onabotulinumtoxinA and hyaluronic acid dermal fillers (24-mg/ml smooth, cohesive gel) alone and in combination for lower facial rejuvenation. Dermatol Surg. (2010) 36(Suppl. 4):2121–34. doi: 10.1111/j.1524-4725.2010.01705.x

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Artzi O, Loizides C, Verner I, Landau M. Resistant and recurrent late reaction to hyaluronic acid-based gel. Dermatol Surg. (2016) 42:31–7. doi: 10.1097/DSS.0000000000000562

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Carruthers J, Klein AW, Carruthers A, Glogau RG, Canfield D. Safety and efficacy of nonanimal stabilized hyaluronic acid for improvement of mouth corners. Dermatol Surg. (2005) 31:276–80. doi: 10.1097/00042728-200503000-00004

CrossRef Full Text | Google Scholar

55. Fischer TC, Sattler G, Gauglitz GG. Hyaluron filler containing lidocaine on a CPM basis for lip augmentation: reports from practical experience. Facial Plast Surg. (2016) 32:283–8. doi: 10.1055/s-0036-1583534

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Philipp-Dormston WG, Hilton S, Nathan M. A prospective, open-label, multicenter, observational, postmarket study of the use of a 15 mg/mL hyaluronic acid dermal filler in the lips. J Cosmet Dermatol. (2014) 13:125–34. doi: 10.1111/jocd.12085

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Rzany B, Cartier H, Kestemont P, Trevidic P, Sattler G, Kerrouche N, et al. Full-face rejuvenation using a range of hyaluronic acid fillers: efficacy, safety, and patient satisfaction over 6 months. Dermatol Surg. (2012) 38:1153–61. doi: 10.1111/j.1524-4725.2012.02470.x

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Samuelson U, Fagrell D, Wetter A, Kuusk S, Hamilton L, Haglund P. An open-label, multicenter, evaluator-blinded study to assess the efficacy and safety of a new hyaluronic acid-based gel product for lip enhancement. Dermatol Surg. (2015) 41:1052–9. doi: 10.1097/DSS.0000000000000432

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Anatelli F, Chapman MS, Brennick J. Amorphous basophilic deposit in the superficial dermis of the lip in an 80 year old. Am J Dermatopathol. (2010) 32:306–9. doi: 10.1097/DAD.0b013e3181b9e5ab

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Bulam H, Sezgin B, Tuncer S, Findikcioglu K, Cenetoglu S. A severe acute hypersensitivity reaction after a hyaluronic acid with lidocaine filler injection to the lip. Arch Plastic Surg. (2015) 42:245–7. doi: 10.5999/aps.2015.42.2.245

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Curi MM, Cardoso CL, Curra C, Koga D, Benini MB. Late-onset adverse reactions related to hyaluronic acid dermal filler for aesthetic soft tissue augmentation. J Craniofac Surg. (2015) 26:782–4. doi: 10.1097/SCS.0000000000001358

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Dougherty AL, Rashid RM, Bangert CA. Angioedema-type swelling and herpes simplex virus reactivation following hyaluronic acid injection for lip augmentation. J Am Acad Dermatol. (2011) 65:e21–2. doi: 10.1016/j.jaad.2010.11.043

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Duhovic C, Duarte-Williamson E. Delayed granulomatous reaction to dermal fillers treated with intralesional triamcinolone and oral minocycline. Br J Dermatol. (2016) 175:90. doi: 10.1111/bjd.14651

CrossRef Full Text

64. Edwards PC, Fantasia JE, Iovino R. Foreign body reaction to hyaluronic acid (restylane): an adverse outcome of lip augmentation. J Oral Maxillofac Surg. (2006) 64:1296–9. doi: 10.1016/j.joms.2006.04.028

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Eversole R, Tran K, Hansen D, Campbell J. Lip augmentation dermal filler reactions, histopathologic features. Head Neck Pathol. (2013) 7:241–9. doi: 10.1007/s12105-013-0436-1

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Farahani SS, Sexton J, Stone JD, Quinn K, Woo SB. Lip nodules caused by hyaluronic acid filler injection: report of three cases. Head Neck Pathol. (2012) 6:16–20. doi: 10.1007/s12105-011-0304-9

PubMed Abstract | CrossRef Full Text | Google Scholar

67. Feio PS, Gouvea AF, Jorge J, Lopes MA. Oral adverse reactions after injection of cosmetic fillers: report of three cases. Int J Oral Maxillofac Surg. (2013) 42:432–5. doi: 10.1016/j.ijom.2012.05.022

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Fernández-Aceñero Ma J, Zamora E, Borbujo J. Granulomatous foreign body reaction against hyaluronic acid: report of a case after lip augmentation. Dermatol Surg. (2003) 29:1225–6. doi: 10.1097/00042728-200312000-00018

PubMed Abstract | CrossRef Full Text | Google Scholar

69. Grippaudo FR, Di Girolamo M, Mattei M, Pucci E, Grippaudo C. Diagnosis and management of dermal filler complications in the perioral region. J Cosmet Laser Ther. (2014) 16:246–52. doi: 10.3109/14764172.2014.946048

PubMed Abstract | CrossRef Full Text | Google Scholar

70. Leonhardt JM, Lawrence N, Narins RS. Angioedema acute hypersensitivity reaction to injectable hyaluronic acid. Dermatol Surg. (2005) 31:577–9. doi: 10.1097/00042728-200505000-00017

PubMed Abstract | CrossRef Full Text | Google Scholar

71. Martin L, Hunter K, Speight P, Farthing P, Khurram SA. Beauty is only mucosa deep-an analysis of oral lumps and bumps caused by cosmetic fillers. Virchows Archiv. (2018) 473:s104. doi: 10.26226/morressier.5b4709886f4cb30010951cec

PubMed Abstract | CrossRef Full Text | Google Scholar

72. Wolfram D, Tzankov A, Piza-Katzer H. Surgery for foreign body reactions due to injectable fillers. Dermatology (Basel, Switzerland). (2006) 213:300–4. doi: 10.1159/000096193

CrossRef Full Text | Google Scholar

73. Kane MA, Lorenc ZP, Lin X, Smith SR. Validation of a lip fullness scale for assessment of lip augmentation. Plast Reconstr Surg. (2012) 129:822e−8e. doi: 10.1097/PRS.0b013e31824a2df0

PubMed Abstract | CrossRef Full Text | Google Scholar

74. Werschler WP, Fagien S, Thomas J, Paradkar-Mitragotri D, Rotunda A, Beddingfield FC III. Development and validation of a photographic scale for assessment of lip fullness. Aesthet Surg J. (2015) 35:294–307. doi: 10.1093/asj/sju025

PubMed Abstract | CrossRef Full Text | Google Scholar

75. Kühne U, Esmann J, von Heimburg D, Imhof M, Weissenberger P, Sattler G. Safety and performance of cohesive polydensified matrix hyaluronic acid fillers with lidocaine in the clinical setting - an open-label, multicenter study. Clin Cosmetic Investig Dermatol. (2016) 9:373–81. doi: 10.2147/CCID.S115256

PubMed Abstract | CrossRef Full Text | Google Scholar

76. Allergan. Directions for Use, Juvéderm Volbella with Lidocaine. Internet: Allergan (Route de Promery Zone Artisanale de Pré-Mairy 74370 PRINGY-FRANCE) (2016). Available online at: https://allergan-web-cdn-prod.azureedge.net/allergan/allergannewzealand/media/allergannewzealand/products/current-approved-volbella-with-lidocaine-dfu_01feb2016.pdf (accessed September 17, 2020).

77. Allergan. Final Labeling Amendment, Juvéderm Volbella XC: FDA. (2016). Available online at: https://www.accessdata.fda.gov/cdrh_docs/pdf11/p110033s018d.pdf (accessed September 17, 2020).

78. WebMD. PERLANE-L Internet: RxList. (2013). Available online at: https://www.rxlist.com/perlane-l-drug.htm#description (accessed December 16, 2020).

79. Medicis A Inc. Restylane-L Patient Brochure: FDA. (2012). Available online at: https://www.accessdata.fda.gov/cdrh_docs/pdf4/P040024S056c.pdf (accessed September 17, 2020).

80. San Miguel Moragas J, Reddy RR, Hernandez Alfaro F, Mommaerts MY. Systematic review of “filling” procedures for lip augmentation regarding types of material, outcomes and complications. J Cranio-maxillo-facial Surg. (2015) 43:883–906. doi: 10.1016/j.jcms.2015.03.032

PubMed Abstract | CrossRef Full Text | Google Scholar

81. Ali MJ, Ende K, Maas CS. Perioral rejuvenation and lip augmentation. Facial Plastic Surg Clin North Am. (2007) 15:491–500, vii. doi: 10.1016/j.fsc.2007.08.008

CrossRef Full Text | Google Scholar

82. Bukhari SNA, Roswandi NL, Waqas M, Habib H, Hussain F, Khan S, et al. Hyaluronic acid, a promising skin rejuvenating biomedicine: a review of recent updates and pre-clinical and clinical investigations on cosmetic and nutricosmetic effects. Int J Biol Macromol. (2018) 120:1682–95. doi: 10.1016/j.ijbiomac.2018.09.188

PubMed Abstract | CrossRef Full Text | Google Scholar

83. Seok J, Hong JY, Choi SY, Park KY, Kim BJ. A potential relationship between skin hydration and stamp-type microneedle intradermal hyaluronic acid injection in middle-aged male face. J Cosmet Dermatol. (2016) 15:578–82. doi: 10.1111/jocd.12244

PubMed Abstract | CrossRef Full Text | Google Scholar

84. Pascali M, Quarato D, Carinci F. Filling procedures for lip and perioral rejuvenation: a systematic review. Rejuvenation Res. (2018) 21:553–9. doi: 10.1089/rej.2017.1941

PubMed Abstract | CrossRef Full Text | Google Scholar

85. Grinde B. Herpesviruses: latency and reactivation—viral strategies and host response. J Oral Microbiol. (2013) 5:10.3402/jom.v5i0.22766. doi: 10.3402/jom.v5i0.22766

PubMed Abstract | CrossRef Full Text | Google Scholar

86. Hirsch P, Infanger M, Kraus A. A case of upper lip necrosis after cosmetic injection of hyaluronic acid soft-tissue filler-Does capillary infarction play a role in the development of vascular compromise, and what are the implications? J Cosmet Dermatol. (2020) 19:1316–20. doi: 10.1111/jocd.13391

PubMed Abstract | CrossRef Full Text | Google Scholar

87. Narins RS, Jewell M, Rubin M, Cohen J, Strobos J. Clinical conference: management of rare events following dermal fillers–focal necrosis and angry red bumps. Dermatol Surg. (2006) 32:426–34. doi: 10.1097/00042728-200603000-00018

PubMed Abstract | CrossRef Full Text | Google Scholar

88. Robati RM, Moeineddin F, Almasi-Nasrabadi M. The risk of skin necrosis following hyaluronic acid filler injection in patients with a history of cosmetic rhinoplasty. Aesthet Surg J. (2018) 38:883–8. doi: 10.1093/asj/sjy005

PubMed Abstract | CrossRef Full Text | Google Scholar

89. Wang C, Luan S, Panayi AC, Xin M, Mi B, Luan J. Effectiveness and safety of hyaluronic acid gel with lidocaine for the treatment of nasolabial folds: a systematic review and meta-analysis. Aesthetic Plastic Surg. (2018) 42:1104–10. doi: 10.1007/s00266-018-1149-3

PubMed Abstract | CrossRef Full Text | Google Scholar

90. Liu L, Liu Y, Li J, Du G, Chen J. Microbial production of hyaluronic acid: current state, challenges, and perspectives. Microb Cell Fact. (2011) 10:99. doi: 10.1186/1475-2859-10-99

PubMed Abstract | CrossRef Full Text | Google Scholar

91. Selyanin M, Boykov P, Khabarov V, Polyak F. Methods of Hyaluronic Acid Production. Chichester: John Wiley & Sons, Ltd (2015). p. 77–95.

92. Wang Y, Leng V, Patel V, Phillips KS. Injections through skin colonized with Staphylococcus aureus biofilm introduce contamination despite standard antimicrobial preparation procedures. Sci Rep. (2017) 7:45070. doi: 10.1038/srep45070

PubMed Abstract | CrossRef Full Text | Google Scholar

93. Dumitraşcu DI, Georgescu AV. The management of biofilm formation after hyaluronic acid gel filler injections: a review. Clujul Med. (2013) 86:192–5.

PubMed Abstract | Google Scholar

94. Gottfried L. No Proof that biofilm bacteria are causing dermal filler granulomas. Am J Biomed Sci Res. (2019) 4:17–22. doi: 10.34297/AJBSR.2019.04.000749

CrossRef Full Text | Google Scholar