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PDO threads, calcium hydroxyapatite, and l-polylactic acid for vulvar flaccidity - indications, technique, and results

Vivian de Carvalho Amaral

DOI: https://doi.org/10.5935/scd1984-8773.2023150192

Financial support: None
Conflict of interest: None
How to cite this article: Amaral VC. PDO threads, calcium hydroxyapatite, and l-polylactic acid for vulvar flaccidity - indications, technique, and results. Surg Cosmet Dermatol. 2023;15:e20230192.


Abstract

The labia majora become saggy with aging. Although filling with hyaluronic acid provides significant rejuvenation, it can also lead to the formation of true vulvar testicles if poorly indicated, especially in excessively flaccid vulvas, which do not support any further volumization. In these cases of excessive flaccidity, we believe that collagen biostimulators would be the best initial treatment, as their injection would lead to the replacement of dermal collagen and improvement in laxity, without a significant increase in volume. We have been using calcium hydroxyapatite, l-polylactic acid, and PDO threads since 2019, with good results.


Keywords: Vulva; Collagen; Genitalia, Female; Rejuvenation


INTRODUCTION

The external female genitalia loses elasticity and volume with age,1,2 causing the labia majora (LM) to become flaccid and pendulous. Although volumetric replacement of the LM with hyaluronic acid (HA) can provide significant rejuvenation,1, 2, 3, 4 when poorly indicated, it can also form vulvar testicles.5 We believe that such aesthetic failure occurs due to large volumes of high molecular weight products or when the injection is poorly indicated and performed in excessively flaccid vulvas that cannot support additional volume.

In cases of excessive flaccidity, we believe that collagen biostimulators (CB) would be the best initial treatment, as their injection would lead to the replacement of dermal collagen, improving flaccidity without excessive increase in volume. For this purpose, since 2019, we have been using the injection of calcium hydroxyapatite (CaHA), l-polylactic acid (PLLA), and PDO threads (PDO), with good results.

 

METHODS

Since 2019, we selected 21 women between 30 and 60 years with vulvar flaccidity and bulky and/or hanging labia majora (LM) for collagen biostimulators (CB) injection.

The choice of treatment was based on the criteria below:

- Bulky LM, which should not have received any additional volume, received PDO;

- LM that needed initial volumization, received CaHA;

- PLLA was the product of choice to treat the entire genital area, involving LM and mons pubis.

We inserted the three products into the superficial subcutaneous tissue.

CaHA and PLLA injections were performed using the fan technique, by retroinjection, with a 22 G, 5 cm cannula.

We used a syringe with carboxymethylcellulose gel 70% and CaHA 30% for CaHA injection, diluted in the saline solution until reaching four times the initial volume of the syringe. Half the final volume obtained was injected into each LM (about 3.0 ml per side) (Figure 1).

We used 150 mg or 210 mg bottles for PLLA injections, initially diluted in 16 ml and 24 ml of distilled water, respectively, plus 4 ml of lidocaine1%. A PLLA concentration of 7.5 mg/ml was reached in both dilutions: 5 ml was injected in each LM and 10 ml in the mons pubis (Figure 2).

For PDO insertion, we used five threads on screws (29 G, 52 mm) in the upper 1/3 and five monofilament threads (30 G, 50 mm) in the lower 2/3 of each LM, totaling ten threads per side (Figure 3).

Patients who received PDO were only re-approached four months after the initial procedure, if necessary. In the case of CaHA or PLLA treatment, one to two sessions were performed, with a minimum interval of 30 days.

 

RESULTS

All treated patients were satisfied with their results after 90 days (Figures 4, 5, and 6). However, we observed greater initial satisfaction among patients who received CaHA.

As complications, we noted the formation of a palpable nodule, not visible, with CaHA, and an infection treated with oral antibiotic therapy with PDO, without the need to remove the threads. Patients injected with PLLA had no major complications. Intercurrences, such as small bruises, edema, and local discomfort, were common to all procedures and resolved spontaneously within seven days.

 

DISCUSSION

Collagen biostimulators (CBs) act by increasing the production of dermal collagen by fibroblasts.

Inserting PDO threads results in neocollagenesis, proportional to the number of threads injected,6 neovascularization, fat reduction, and higher tissue contracture.7 Based on this information, we followed the injection criteria:

• Due to the effect of fat compaction, we chose the most voluminous LM for PDO insertion;

• We never inject less than ten threads in each LM, for effective neocollagenesis;

• For a greater lifting effect, we used screw threads, which deliver a higher concentration of polydioxanone, with consequent higher tissue retraction in the upper 1/3;

• We did not use screw wires inferiorly, as they could bring about discreet volumization, which is undesirable in this location;

• We did not associate HA local injection before six months, under the risk of hydrophilic degradation of PDO.8

Hyperdiluted CaHA stimulates neocollagenesis with safety,9, 10, 11 efficacy, and long duration.12 Due to the presence of the carboxymethylcellulose gel vehicle, the treatment can be used as an adjuvant to volume increase.13 The most reported complications are nodules, which disappear without intervention in most cases.13 Its occurrence increases in areas of thinner skin and very superficial injections of less diluted CaHA.14 Based on this information, we follow the criteria for injecting CaHA:

• We opted for CaHA for LM that already needed some initial volumization, with intense skin flaccidity and prominent grooves in the area;

• We hyperdiluted the CaHA to 400% and kept the injection in the cutaneous portion of the LM, away from the mucosa, to avoid the formation of nodules;

• We vigorously massage the area after the injection and guide home massage for five minutes five times a day for five days;

• In general, only one session was performed, followed, after 60 days, by actual volumization with HA.

PLLA is considered a biocompatible and biodegradable polymer, effective, safe, with lasting effects and a high level of satisfaction among patients.15, 16, 17 PLLA injections induce the neoformation of type 1 and type 3 collagen, TGF-β1, TGF-β2, and TGF-β3, histologically perceptible as early as two weeks after injection and with a decrease in 12 weeks,18 but with clinically visible therapeutic effects for up to two years.19 The efficacy and safety of PLLA are influenced by the correct product reconstitution, dilution, and administration. Unwanted adverse events such as papules and nodules can result from incorrect product reconstitution, uneven distribution, superficial injection, or lack of post-treatment massage.20 Based on this information, we follow the criteria for PLLA injection:

• We followed the recommendation described in the medical literature for an injection of approximately 3mg/cm21, which allowed us to treat larger areas that included not only the LM but also the mons pubis;

• We avoided injecting patients with excessive volume in the mons pubis;

• We stopped the injection when 3/4 of the cannula was visible to avoid superficialization of the product and the appearance of papules and nodules 21;

• We performed the immediate reconstitution of the PLLA without major complications 22;

• We conducted, on average, two sessions with intervals of 30 days;

• We proceeded with the local massage as described for CaHA.

 

CONCLUSIONS

Although the use of collagen biostimulators (CBs) in non-genital areas is well established, the literature on such substances in vulvar rejuvenation is still scarce.23 However, the intense search for genital beautification procedures, associated with the good results obtained with the injection of CBs in other body areas has encouraged its use in the vulvar region.

We consider the treatments described to be safe and effective. The patients were instructed regarding the delayed effects of non-volumizing injections, which was crucial for achieving the expectations of the results. The most common adverse events of the three procedures were injection-related and included bruising, swelling, and mild discomfort. The encouraging results obtained should inspire further studies.

 

AUTHORS' CONTRIBUTION:

Vivian de Carvalho Amaral 0000-0002-5379-652X
Statistical analysis; approval of the final version of the manuscript; study design and planning; preparation and writing of the manuscript; data collection, analysis, and interpretation; active participation in research orientation; intellectual participation in propaedeutic and/or therapeutic conduct of studied cases; critical literature review; critical revision of the manuscript.

 

REFERENCES:

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