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W H I T E  P A P E R

            HAND REVOLUMISATION                                                     aestheticmed.co.uk




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            bioresorbable.  PCL hydrolyses to hydroxycaproic acid and   DURATION OF IMPROVEMENT
            water, which is reabsorbed and excreted via a variety of  The assessment of hand volume was based on the hand
            metabolic pathways.                            severity scale reported ( ) and is summarised in Table 1.
                                                                              6,17
              CMC  gel  is  absorbed  by  macrophages  over  several  Four patients with severe volume loss (grade 3) achieved
            weeks. A CMC-based filler has been shown to effectively   improvement to moderate (grade 2) severity. Ten patients
                  15
            correct nasolabial hollows for up to six months in a  with moderate severity (grade 2) improved to mild severity
                                                       16
            bilateral period comparison study against an HA filler).    (grade 1). One patient with moderate volume loss did not
            PCL microspheres are not phagocytised but are thought  show improvement on clinician’s grade scores four months
            to  stimulate  neocollagenesis  via  fibroblast  activation,  after the first treatment but was slightly satisfied with
            perhaps by cytokine release during microsphere resorption   improvement. She elected to receive a second treatment.
            in the skin. Studies in animal model showed initial deposition
            of type-3 collagen with later deposition of type-1 collagen. 9
              Clinical  observations  have  confirmed  that  PCL-based
            microspheres are well tolerated for facial treatment. One
            previous pilot study of hand rejuvenation in five patients
            showed  improvement  of  patient  and  physician  reported
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            Global Esthetic Improvement Scale (GAIS) for six months.
            Comparative studies have shown that PCL-based fillers,
            when compared with a hyaluronic acid filler, showed greater
            persistence. 7

            MATERIALS AND METHODS
            15 female patients aged between 48 and 72 years of skin
            type 2 and 3 were evaluated for PCL filler injections to
            their hands because of dorsal hand volume loss (Ellansé
            typeM, Sinclair Pharmaceutical). They were provided with
            informed consent at least five days prior to treatment.
            They all had a minimum rating of three on a previously
            reported hand aging severity scale. 17  Their hands were
            photographed  before  and  following  treatment  with
            consistent  photography.  Clinical  examination  of  dorsal
            hand skin quality recorded severity of rhytides, skin laxity,
            and elasticity.

            METHODS OF INJECTIONS OF PCL
            PCL (Ellansé M) was selected for treatment based on
            past personal experience with Ellanse products for facial
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            volume loss (Lowe, NJ personal data and a pilot study).
            Hands were cleansed with chlorhexidine gluconate 4%.
            Local anesthetic (0.1 ml of 1% lidocaine) was drawn into a
            1ml syringe and mixed with PCL filler by luerlock connection
            with 20 transfers between the syringes.
              Entry points for cannulas were selected to avoid
            dorsal hand veins and entry areas injected with 0.3ml of
            1% lidocaine with adrenaline. 25G (50mm) cannula with
            introducer (SoftFil) was used for all patients. The cannula
            was inserted through an introducer to mid to upper
            subcutaneous depth and PCL injected using a retrograde
            technique while slowly withdrawing the cannula. A total
            of 1cc PCL was injected to the dorsal of each hand. The
            injected area was then massaged to smooth the area.
              Side effects and severity of pain and swelling were noted
            over the following five days. Presence of bruising and
            swelling was documented.

            RESULTS
            Results are summarised in Tables 1 and 2. Severity scores
            improved in all patients and were recorded as the degrees
                                                       6,17
            of improvements using the scales previously reported.
            This  improvement  was  statistically  significant  (Fisher
            exact test 0.0002. p < .05). Seven of the patients elected
            to have a second treatment between the two evaluation
            timepoints following their first treatment.    Figure 2. Pre and six months post-polycaprolactone


       58   Aesthetic Medicine • June 2020
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