94 results on '"Dierickx C"'
Search Results
2. Guidelines on the safety of light-based home-use hair removal devices from the European Society for Laser Dermatology
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Town, G., Ash, C., Dierickx, C., Fritz, K., Bjerring, P., and Haedersdal, M.
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- 2012
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3. A systematic review of light-based home-use devices for hair removal and considerations on human safety
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Thaysen-Petersen, D., Bjerring, P., Dierickx, C., Nash, J. F., Town, G., and Haedersdal, M.
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- 2012
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4. Surgical closure of nasoseptal perforations: predictive factors for success
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Dierickx, C, Van Gerven, L, and Jorissen, M
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NASAL SEPTAL PERFORATION ,Science & Technology ,Otorhinolaryngology ,Nasal mucosa ,nasal surgical procedure ,Life Sciences & Biomedicine ,acquired nose deformities - Abstract
ispartof: B-ENT vol:15 issue:3 pages:161-167 status: published
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- 2019
5. Problems with permanents make-up
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Dierickx, C. and De Cuyper, C.
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- 2003
6. Psoriasis
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Dierickx, C.
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- 2003
7. Indications for the high dose, lesion-targeted UVB treatment
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Dierickx, C.
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- 2003
8. Laser treatment of psoriasis
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Dierickx, C
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- 2002
9. SOME GEOGRAPHIC PROBLEMS OF THE BAHAMA ISLANDS
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Dierickx, C. Wallace
- Published
- 1953
10. Medische aspecten van slaapstoornissen bij kinderen
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null DIERICKX C and null VERHAAREN H
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General Medicine - Published
- 2003
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11. Guidelines on the safety of light-based home-use hair removal devices from the European Society for Laser Dermatology
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Town, Graham, Ash, C, Dierickx, C, Fritz, K, Bjerring, P, Haedersdal, M, Town, Graham, Ash, C, Dierickx, C, Fritz, K, Bjerring, P, and Haedersdal, M
- Abstract
In the past 5 years since their US introduction, there has been a rapid proliferation of light-based hair removal devices intended for home-use. In the last 2 years in Europe, sales already run into many tens of thousands of units with well-known multi-national companies entering the market. These guidelines provide a definition of light-based home-use technology, to inform healthcare professionals about home-use light-based technology and encourage manufacturers wishing to sell in Europe to adopt 'best practice'. The review presents the current status on standards and regulation issues and considers home-use safety issues, encompassing human, device and electrical safety, given risks to the eyes and skin from optical radiation both to the consumer and persons in the vicinity. Proposed technical measurement methodology is considered with focus on recognized critical parameters for the safe use of light-based hair removal technology including recording the technical performance and safety claims of a range of home-use hair removal devices. The literature review emphasizes potential adverse incidents and safety aspects of treating cosmetic conditions, such as unwanted hair growth. Although some regulations exist, they differ from region to region and there is a specific need for international common principles and guidelines relating to the manufacture, marketing and use of intense pulsed light and laser devices, including manufacturing standards for home-use products intended, amongst others, for cosmetic hair removal and photo-rejuvenation procedures. In these guidelines, the European Society for Laser Dermatology (ESLD) provides a professional view of what 'best practice' may imply for manufacturers and consumers alike.
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- 2012
12. A systematic review of light-based home-use devices for hair removal and considerations on human safety
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Thaysen-Petersen, D, Bjerring, P, Dierickx, C, Nash, J F, Town, Graham, Haedersdal, M, Thaysen-Petersen, D, Bjerring, P, Dierickx, C, Nash, J F, Town, Graham, and Haedersdal, M
- Abstract
Background Hair removal with professional light-based devices is established as an effective, mainstream treatment. The field of optical home-based hair removal is evolving and movement from control by physicians into hands of consumers warrants understanding efficacy and human safety. Objectives To systematically review and evaluate the efficacy and human safety of currently available home-based optical hair removal devices. Methods A comprehensive Pub Med literature search was conducted which systematically identified publications of relevance. Prospective clinical trials were included whether controlled, uncontrolled or randomized and with a sample size of at least 10 individuals. Results We identified a total of seven studies: one controlled (CT) and six uncontrolled trials (UCTs). No randomized controlled trials (RCT) were recognized. The best evidence was found for IPL (intense pulsed light) (three devices, one CT, five UCTs) and limited evidence for laser devices (one diode laser, one UCT). Most studies evaluated short-term hair reduction up to 3 and 6 months following light exposure at different body sites. Hair reduction percentages ranged from 6% to 72% after repetitive treatments. The most frequently reported side-effect was erythema, but oedema, blistering, crusting and pigment changes were also reported. Theoretical concerns about ocular damage and paradoxical hair growth have not been reported in any of the studies reviewed. Conclusions Available evidence from prospective, uncontrolled clinical trials indicates short-term hair removal efficacy of currently available home-use light-based hair removal devices. Additional controlled trials will be helpful to substantiate the efficacy and to better predict the incidence of adverse events associated with optical home-use hair removal.
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- 2012
13. A systematic review of light‐based home‐use devices for hair removal and considerations on human safety
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Thaysen‐Petersen, D., primary, Bjerring, P., additional, Dierickx, C., additional, Nash, J.F., additional, Town, G., additional, and Haedersdal, M., additional
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- 2011
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14. Milieuverstoringen in stedelijke gebieden
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van den Broeck, J., Dierickx, C., vande Sompele, K., Dhondt, André, and Matthysen, Erik
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- 1994
15. Best Practice Options for Hair Removal in Patients with Unwanted Facial Hair Using Combination Therapy with Laser: Guidelines Drawn up by an Expert Working Group
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Lapidoth, M., primary, Dierickx, C., additional, Lanigan, S., additional, Paasch, U., additional, Campo-Voegeli, A., additional, Dahan, S., additional, Marini, L., additional, and Adatto, M., additional
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- 2010
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16. 11th Meeting of the European Society for Pigment Cell Research 17-20 September 2003 Aula of Ghent University Voldersstraat 9, Gent, Belgium
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Naeyaert, J.M., primary, Lambert, J.L.W., additional, Naeyaert, J.M., additional, De Weert, J., additional, Ongenae, K., additional, Vossaert, K., additional, Brochez, L., additional, Verhaeghe, E., additional, Westbroek, W., additional, van Geel, N., additional, Dierickx, C., additional, Lambert, J., additional, Beermann, F., additional, Bennett, D., additional, Garcia-Borron, J.C., additional, Ghanem, G., additional, Goding, C., additional, Larue, L., additional, Pavel, S., additional, Picardo, M., additional, Roelandts, R., additional, Taieb, A., additional, Tobin, D.J., additional, Thody, A., additional, Verrando, P., additional, and Westerhof, W., additional
- Published
- 2003
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17. Contact cooling of the skin
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Altshuler, G B, primary, Zenzie, H H, additional, Erofeev, A V, additional, Smirnov, M Z, additional, Anderson, R R, additional, and Dierickx, C, additional
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- 1999
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18. Squamous cell carcinoma in chronic osteomyelitis
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Veekmans, P., primary and Dierickx, C., additional
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- 1991
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19. A patient bothered by unexpected sources of isothiazolinones
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Dooms-Goossens, A., primary, Morren, M., additional, Dierickx, C., additional, and Mariën, K., additional
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- 1990
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20. 11[sup th ] Meeting of the European Society for Pigment Cell Research 17–20 September 2003 Aula of Ghent University Voldersstraat 9, Gent, Belgium.
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Naeyaert, J.M., Lambert, J.L.W., De Weert, J., Ongenae, K., Vossaert, K., Brochez, L., Verhaeghe, E., Westbroek, W., van Geel, N., Dierickx, C., Lambert, J., Beermann, F., Bennett, D., Garcia-Borrón, J.C., Ghanem, G., Goding, C., Larue, L., Pavel, S., Picardo, M., and Roelandts, R.
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CONFERENCES & conventions ,CYTOLOGICAL research ,CHROMATOPHORES ,EPITHELIAL cells ,PROTOPLASM ,ASSOCIATIONS, institutions, etc. - Abstract
Reports on the 2003 meeting of the European Society for Pigment Cell Research in Ghent University in Gent, Belgium. Program of the meeting; List of speakers and topics discussed at the meeting.
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- 2003
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21. Ruby laser hair removal: evaluation of long-term efficacy and side effects.
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Campos, Valeria B., Dierickx, Christine C., Farinelli, William A., Lin, Tai-Yuan D., Manuskiatti, Woraphong, Anderson, R. Rox, Campos, V B, Dierickx, C C, Farinelli, W A, Lin, T Y, Manuskiatti, W, and Anderson, R R
- Published
- 2000
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22. Prevention of Venous Thromboembolism after Hospital Discharge Continued Pharmacological Prophylaxis versus No Prophylaxis in Patients Undergoing Total Hip Replacement
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Haentjens, P., Delincé, P.H., Boghemans, J., Borms, T., Brabants, K., Bremen, J., Cuyvers, P., de Brouckére, G., De Groot, E, De Smet, K., Debiére, I, Delincé, Ph., Demedts, D., Dewijze, M., Dierckxsens, J., Dierickx, C., Eekhaut, M., Gohimont, A.-C., Haentjens, P., Hollaert, G., Meuris, S., Michaux, M., Peck, J., van Backlé, B., van Bouchaute, P., Van Gestel, J., van Hoye, M., van Overschelde, J., Vandevyver, D., Vanlommel, D., and Velghe, A.
- Abstract
After total hip replacement, continued pharmacological prophylaxis following hospital discharge is controversial.The primary objective of our study was to determine the safety and efficacy of continued prophylaxis with nadroparin three weeks after hospital discharge. The secondary objective was to evaluate the association between a confirmed venous thromboembolism and risk factors for deep venous thrombosis.This study was an open-label, randomized, multicentre, prospective trial. Patients were evaluated for deep venous thrombosis with duplex ultrasonography at discharge and 3 weeks later. Walking ability (mobility score) was assessed at the same times. Patients without deep venous thrombosis at discharge were randomly assigned to continued nadroparin (n=155) versus no pharmacologic prophylaxis (n=141) for three weeks.The rate of deep venous thrombosis three weeks post discharge was significantly lower in the nadroparin group: two patients (1.3%) versus nine (6.4%) without prophylaxis (p = 0.021; relative risk reduction = 79%). No significant difference in terms of safety was observed between groups and no major bleeding occurred.Three weeks after discharge, patients who developed deep venous thrombosis were significantly less mobile (p = 0.018).In conclusion, after total hip replacement, continued prophylaxis with nadroparin for 3 weeks after hospital discharge is beneficial.
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- 2001
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23. Computation of externally pressurized gas bearings characteristics via alternating directions methods
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UCL, Dierickx, C., Gorez, Raymond, Polome, Jocelyne, Simulation of Systems '79. Proceedings of the 9th IMACS Congress, UCL, Dierickx, C., Gorez, Raymond, Polome, Jocelyne, and Simulation of Systems '79. Proceedings of the 9th IMACS Congress
- Abstract
Computing the pressure distribution along the clearance of an externally pressurized gas bearing needs the solution of an elliptic partial differential equation. This is obtained via an alternating directions method combined with a special decomposition technique. The method can be implemented on digital and hybrid computers, and has some advantages from the point of view of computation speed and computer storage requirements. Three cases of practical interest are treated: numerical results are presented and problems of convergence are considered., Anglais
- Published
- 1980
24. Arrhythmia of the month. Variable atrioventricular block during atrial flutter: what is the mechanism?
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Duytschaever M, Dierickx C, Tavernier R, and Morady F
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- 2002
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25. Omgaan met ruimte: een vormingspakket over ruimtelijke ordening
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[et al.], Dierickx, C., Jacobson, Chris, Maes, John, and Verhetsel, Ann
- Published
- 1999
26. Melanin-dependent tissue interactions induced by a 755-nm picosecond-domain laser: complementary visualization by optical imaging and histology.
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Jacobsen K, Ortner VK, Fredman GL, Christensen RL, Dierickx C, Tanghetti E, Paasch U, and Haedersdal M
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- Animals, Swine, Skin diagnostic imaging, Skin pathology, Microscopy, Confocal methods, Tomography, Optical Coherence methods, Histological Techniques, Melanins, Lasers, Solid-State
- Abstract
Fractional picosecond-domain lasers (PSL) induce optical breakdown, which correlates histologically to vacuolization in the epidermis and dermis. In this ex vivo porcine study, we sought to establish a framework for the investigation of laser-tissue interactions and their dependence on melanin density. Light- (melanin index: 24.5 [0-100]), medium- (58.7), and dark-pigmented (> 98) porcine skin samples were exposed to a 755-nm fractional PSL and examined with dermoscopy, line-field confocal optical coherence tomography (LC-OCT), conventional OCT, and subsequently biopsied for digitally stained ex vivo confocal microscopy (EVCM) and histology, using hematoxylin and eosin (HE) and Warthin-Starry (WS) melanin staining. Dermoscopy showed focal whitening in medium- and dark-pigmented skin. Similarly, LC-OCT and OCT visualized melanin-dependent differences in PSL-induced tissue alterations. Vacuoles were located superficially in the epidermis in dark-pigmented skin but at or below the dermal-epidermal junction in medium-pigmented skin; in light-pigmented skin, no vacuoles were observed. Histology confirmed the presence of vacuoles surrounded by areas void of WS staining and disrupted stratum corneum in darker skin. The combined use of optical imaging for multiplanar visualization and histological techniques for examination of all skin layers may mitigate the effect of common artifacts and attain a nuanced understanding of melanin-dependent laser-tissue interactions., (© 2023. The Author(s).)
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- 2023
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27. Assessment of adverse events for a home-use intense pulsed light hair removal device using postmarketing surveillance.
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Hattersley AM, Kiernan M, Goldberg D, Dierickx C, Sliney DH, Haedersdal M, and Nash JF
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- Humans, Skin, Erythema etiology, Pain, Hair Removal adverse effects, Intense Pulsed Light Therapy methods
- Abstract
Background and Objectives: Home-use intense pulsed light (IPL) hair removal devices are convenient for consumers. Consumer safety associated with home-use IPL devices, however, remains a subject of interest. In this descriptive analysis, we assessed the most commonly reported adverse events (AEs) for a home-use IPL device from postmarketing surveillance and qualitatively compared these with AEs from clinical studies and medical device reports of home-use IPL treatments., Materials and Methods: For this analysis of voluntary reports, we queried a distributor's postmarketing database for IPL devices for the period beginning January 1, 2016, to December 31, 2021. All sources of comments, for example, phone, e-mail, company-sponsored web sites, were included in the analysis. AE data were coded according to the Medical Dictionary for Regulatory Activities (MedDRA) terminology. Also, we conducted a PubMed search to identify AE profiles from existing literature on home-use IPL devices and we searched the Manufacturer and User Facility Device Experience (MAUDE) database for reports on home-use IPL devices. These results were qualitatively compared to the data in the postmarketing surveillance database., Results: A total of 1692 cases involving IPL were identified from voluntary reports of AEs between 2016 and 2021. The shipment-adjusted reporting rate for AE cases (number of AE cases/100,000 shipped IPL devices) was 67/100,000 during this 6-year period. The most commonly reported AEs were pain of skin 27.8% (470/1692), "thermal burn" 18.7% (316/1692), and erythema 16.0% (271/1692). Among the top 25 AEs reported, no unexpected health events were observed. The reported AEs were qualitatively similar to the pattern seen in clinical studies and the MAUDE database associated with such home-use IPL treatments., Conclusion: This is the first such report documenting AEs for home-use IPL hair removal from a postmarketing surveillance program. These data are supportive of the safety of such home-use low-fluence IPL technology., (© 2023 The Authors. Lasers in Surgery and Medicine published by Wiley Periodicals LLC.)
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- 2023
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28. Standardised Tendon Fenestration with ITEC-Technique for Lateral Epicondylosis with Injection of Betamethasone versus Autologous Blood.
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Dierickx C, Goorens CK, Bellemans L, Goossens E, Mentens X, and Paulussen J
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- Humans, Betamethasone, Prospective Studies, Tendons, Adrenal Cortex Hormones therapeutic use, Pain, Tennis Elbow drug therapy
- Abstract
Background: Infiltration is one of the treatment options for lateral epicondylosis, a degenerative process in the tendon of the musculus extensor carpi radialis brevis. The aim of this study was to evaluate the clinical outcome of a standardised fenestration technique, the Instant Tennis Elbow Cure (ITEC) technique, with injection of betamethasone versus autologous blood. Methods: A prospective comparative study was performed. Twenty-eight patients received an infiltration with 1 mL betamethasone, in combination with 1 mL 2% lidocaine. Twenty-eight patients received an infiltration with 2 mL autologous blood. Both infiltrations were administered using the ITEC-technique. The patients were evaluated at baseline, 6 weeks, 3 months and 6 months using Visual Analogue Scale (VAS), Patient-Rated Tennis Elbow Evaluation (PRTEE) and Nirschl staging. Results: At the 6-week follow-up, the corticosteroid group showed significantly better results for VAS. At the 3-month follow-up, no significant differences were observed for all three scores. At the 6-monthfollow-up, the autologous blood group showed significantly better results for all three scores. Conclusions: Standardised fenestration using the ITEC-technique with corticosteroid infiltration is more effective in reducing pain at the 6-week follow-up. At the 6-month follow-up, the use of autologous blood is more effective in pain reduction and functional recovery. Level of Evidence: Level II.
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- 2023
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29. Highlighting nuances of blue light phototherapy: Mechanisms and safety considerations.
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Uzunbajakava NE, Tobin DJ, Botchkareva NV, Dierickx C, Bjerring P, and Town G
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- Humans, Skin radiation effects, Ultraviolet Rays, Apoptosis, Phototherapy, Light
- Abstract
The efficacy of blue light therapy in dermatology relies on numerous clinical studies. The safety remains a topic of controversy, where potentially deleterious effects were derived from in vitro rather than in vivo experiments. The objectives of this work were (1) to highlight the nuances behind "colors" of blue light, light propagation in tissue and the plurality of modes of action; and (2) to rigorously analyze studies on humans reporting both clinical and histological data from skin biopsies with focus on DNA damage, proliferation, apoptosis, oxidative stress, impact on collagen, elastin, immune cells, and pigmentation. We conclude that blue light therapy is safe for human skin. It induces intriguing skin pigmentation, in part mediated by photoreceptor Opsin-3, which might have a photoprotective effect against ultraviolet irradiation. Future research needs to unravel photochemical reactions and the most effective and safe parameters of blue light in dermatology., (© 2022 The Authors. Journal of Biophotonics published by Wiley-VCH GmbH.)
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- 2023
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30. Energy-based devices for the treatment of Acne Scars: 2022 International consensus recommendations.
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Salameh F, Shumaker PR, Goodman GJ, Spring LK, Seago M, Alam M, Al-Niaimi F, Cassuto D, Chan HH, Dierickx C, Donelan M, Gauglitz GG, Haedersdal M, Krakowski AC, Manuskiatti W, Norbury WB, Ogawa R, Ozog DM, Paasch U, Victor Ross E, Clementoni MT, Waibel J, Bayat A, Goo BL, and Artzi O
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- Cicatrix etiology, Cicatrix pathology, Cicatrix therapy, Consensus, Humans, Treatment Outcome, Acne Vulgaris complications, Low-Level Light Therapy
- Abstract
Background and Objectives: Acne scars are one of the most distressing and long-term consequences of acne vulgaris, with damaging effect on a person's physical, mental, and social well-being. Numerous treatment options are available including surgical and nonsurgical techniques, depending on the clinical presentation. Although considerable advances in the development of new treatment technologies and applications have been made in the last decade, international treatment guidelines and reimbursement schemes have not yet caught up with current knowledge and practice in many centers. The authors intend to highlight the potential utility of energy-based devices (EBDs) for acne scarring, offer recommendations for safe and efficacious treatment, and provide consensus-based EBD treatment options based on varying presentations demonstrated in a series of real-life clinical photographs., Study Design/materials and Methods: An international panel of 24 dermatologists and plastic surgeons from 12 different countries and a variety of practice backgrounds was self-assembled to develop updated consensus recommendations for the treatment of acne scars. A two-step modified Delphi method took place between March 2020 and February 2021 consisting of two rounds of emailed questionnaires. The panel members approved the final manuscript via email correspondence., Results: The manuscript includes a comprehensive discussion and panel recommendations regarding the following topics: 1. the role of EBD in mitigating and treating acne scars in a patient with active acne, 2. the use of various EBDs for the treatment of different acne scar types with special focus on commonly used laser platform such as vascular lasers, ablative fractional lasers (AFLs) and non-AFLs (NAFLs), 3. treatment combinations, and 4. acne scar treatments in skin of color. The last part comprised of 10 photos of real-life clinical cases with the panel recommendation treatment plan to achieve best aesthetic outcome., Conclusion: Panel members were unanimous in their view that EBDs have a role in the management of acne scars, with AFLs, NAFLs, vascular lasers, and RF devices preferentially selected by most of the panel experts. EBDs are considered a first-line treatment for a variety of acne scar types and patients without access to these treatments may not be receiving the best available care for optimal cosmetic results. Future high-quality research and updated international treatment guidelines and reimbursement schemes should reflect this status., (© 2021 Wiley Periodicals LLC.)
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- 2022
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31. Thermo-Mechanical Fractional Injury Enhances Skin Surface- and Epidermis- Protoporphyrin IX Fluorescence: Comparison of 5-Aminolevulinic Acid in Cream and Gel Vehicles.
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Foged C, Haedersdal M, Bik L, Dierickx C, Phillipsen PA, and Togsverd-Bo K
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- Epidermis, Humans, Protoporphyrins, Aminolevulinic Acid pharmacology, Photochemotherapy
- Abstract
Background and Objectives: Thermo-mechanical fractional injury (TMFI) impacts the skin barrier and may increase cutaneous drug uptake. This study investigated the potential of TMFI in combination with 5-aminolevulinic acid (ALA) cream and gel formulations to enhance Protoporphyrin IX (PpIX) fluorescence at the skin surface and in the skin., Study Design/materials and Methods: In healthy volunteers (n = 12) a total of 144 test areas were demarcated on the upper back. Test areas were randomized to (i) TMFI (6 milliseconds, 400 µm at a single pass) or no pretreatment and (ii) 20% ALA in cream or gel formulations. Skin surface PpIX fluorescence was quantified by PpIX fluorescence photography and photometry in 30-minute intervals until 3 hours. PpIX fluorescence microscopy quantified separate PpIX fluorescence in the epidermis, and in superficial-, mid-, and deep- dermis from punch biopsies sampled after 3 hours of ALA incubation. Local skin reactions (LSR) and pain intensities (numerical rating scale 0-10) were evaluated immediately, at 3 hours and 14 days after the intervention., Results: TMFI exposure before photosensitizer application significantly increased skin surface PpIX fluorescence, both for ALA cream (TMFI-ALA-cream 7848 arbitrary units [AU] vs. ALA-cream 5441 AU, 3 hours, P < 0.001) and ALA gel (TMFI + ALA-gel 4591 AU vs. ALA-gel 3723 AU, 3 hours, P < 0.001). The TMFI-mediated increase in PpIX fluorescence was similar for ALA-cream and -gel formulations (P = 0.470) at the skin surface. In the epidermis, PpIX fluorescence intensities increased from combination treatment with TMFI and ALA-cream (TMFI + ALA-cream 421 AU vs. ALA-cream 293 AU, P = 0.034) but not from combination with TMFI and ALA-gel (TMI + ALA-gel 264 AU vs. ALA-gel 261 AU, P = 0.791). Dermal fluorescence intensities (superficial-, mid-, or deep dermis) were unaffected by TMFI pretreatment in both ALA-cream and ALA-gel exposed skin (P = 0.339). ALA-cream generally induced higher PpIX fluorescence intensities than ALA-gel (skin surface P < 0.001 and epidermis P < 0.03). TMFI induced low pain intensities (median 3) and mild LSR that were resolved at 14 days follow-up., Conclusion: Given the present study design, TMFI, in combination with the standardized application of 20% ALA cream and gel formulations, significantly enhanced skin surface PpIX fluorescence compared to no pretreatment. Additionally, TMFI increased epidermal PpIX fluorescence combined with 20% ALA cream vehicle. Thus, TMFI pretreatment and formulation characteristics exert influence on PpIX fluorescence intensities in normal skin. Lasers Surg. Med. © 2020 Wiley Periodicals LLC., (© 2020 Wiley Periodicals LLC.)
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- 2021
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32. Are clinical outcomes of frozen shoulder linked to pain, structural factors or pain-related cognitions? An explorative cohort study.
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De Baets L, Matheve T, Dierickx C, Bijnens E, Jans D, and Timmermans A
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- Cognition, Cohort Studies, Female, Humans, Pain, Bursitis, Shoulder Joint
- Abstract
Background: In frozen shoulder (FS), inflammatory-fibrotic adaptations in capsuloligamentous structures are typically linked to perceived glenohumeral stiffness, glenohumeral range of motion (ROM) restrictions and decreased arm function. However, ROM restrictions based on muscle guarding are suggested as well., Objectives: To assess differences between pain, perceived stiffness, ROM restrictions and arm function at time of diagnosis and at four months follow-up and to assess whether perceived stiffness, ROM restrictions and arm function relate to pain, structural and/or cognitive factors., Design: observational cohort study., Methods: In persons with idiopathic FS, pain intensity at rest/at night/during activities (Numeric Rating Scale), perceived stiffness (Numeric Rating Scale), abduction/external rotation ROM (goniometry), and function (Disabilities of the Arm, Shoulder and Hand Questionnaire) were compared between both time points (Wilcoxon-signed rank tests). Spearman correlation coefficients assessed the relation between perceived stiffness, ROM and function on the one hand and structural factors (coracohumeral ligament (CHL) thickness and inferior glenohumeral recess (IGR) perimeter - arthroMRI), pain intensity and pain-related cognitions (Pain Catastrophizing Scale, Tampa Scale for Kinesiophobia) on the other hand., Results: Twenty persons participated (14 female; 56±8yrs) and three persons dropped out at 4 months. Pain intensity, perceived stiffness, ROM and arm function improved over time. ROM was related to CHL-thickness and IGR-perimeter; perceived stiffness was related to pain intensity; and arm function was related to pain intensity and pain-related cognitions., Conclusion: Objectively measured ROM is related to structural factors, while patient-reported outcomes are related to pain intensity and/or pain-related cognitions. Perceived stiffness does not relate to structural factors., (Copyright © 2020 Elsevier Ltd. All rights reserved.)
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- 2020
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33. Outcomes of reverse total shoulder arthroplasty with postoperative scapular fracture. A systematic review.
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Loomans L, Debeer P, and Dierickx C
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- Disability Evaluation, Fractures, Bone diagnostic imaging, Humans, Pain Measurement, Postoperative Complications diagnostic imaging, Scapula diagnostic imaging, Arthroplasty, Replacement, Shoulder methods, Fractures, Bone etiology, Postoperative Complications etiology, Scapula injuries
- Abstract
Postoperative scapular fractures are infrequent complications of reverse total shoulder arthroplasty (RTSA). The aim of this study is to discuss the functional outcome, clinical outcome and pain scores of these fractures and to analyze these outcome results based on fracture location. A systematic review in accordance with the PRISMA guidelines was conducted. Pubmed, EMBASE, Web of Science, Cochrane library and Ovid have been screened. A total of 78 RTSA in 12 articles were retained for qualitative analysis. The average minimum follow- up was 33.3 ± 14.4 months (range 12-60 months) and the mean age was 74.4 ± 5.6 years (range 63-85 years) with a mean female percentage of 90.9%. Overall, the mean DASH score was 39.8 ± 9.4 points (range 29.5- 48.0 points), ASES score 53.4 ± 23.3 points (range 13.3-95.0 points), SST 3.2 ± 2.2 points (range 0.0- 5.1 points), the only OSS 28.0 points and Constant- Murley shoulder score 50.5 ± 20.0 points (range 31.5- 69.0). The mean anterior elevation was 91.5° ± 30.7° (range 46.0°-160.0°), abduction 87.8° ± 21.8° (range 55.0°-125.0°), external rotation 33.2° ± 22.2° (range 9.0°-85°) and the only internal rotation was 60.0°. The VAS score averaged of 3.8 ± 2.8 points (range 0.8-9.0 points). A subgroup analysis of acromial and scapular spine fractures was performed. Acromial and scapular spine fractures have an undeniable effect on RTSA outcomes, however patients still improve compared to their preoperative state. We advise to consider acromial and scapular fractures as different problems, as prognosis is worse for more medial fractures.
- Published
- 2020
34. Assessment of Scapulothoracic, Glenohumeral, and Elbow Motion in Adhesive Capsulitis by Means of Inertial Sensor Technology: A Within-Session, Intra-Operator and Inter-Operator Reliability and Agreement Study.
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De Baets L, Vanbrabant S, Dierickx C, van der Straaten R, and Timmermans A
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- Female, Humans, Male, Middle Aged, Reproducibility of Results, Task Performance and Analysis, Biosensing Techniques, Bursitis physiopathology, Elbow physiopathology, Range of Motion, Articular physiology, Shoulder Joint physiopathology
- Abstract
Adhesive capsulitis (AC) is a glenohumeral (GH) joint condition, characterized by decreased GH joint range of motion (ROM) and compensatory ROM in the elbow and scapulothoracic (ST) joint. To evaluate AC progression in clinical settings, objective movement analysis by available systems would be valuable. This study aimed to assess within-session and intra- and inter-operator reliability/agreement of such a motion capture system. The MVN-Awinda® system from Xsens Technologies (Enschede, The Netherlands) was used to assess ST, GH, and elbow ROM during four tasks (GH external rotation, combing hair, grasping a seatbelt, placing a cup on a shelf) in 10 AC patients (mean age = 54 (± 6), 7 females), on two test occasions (accompanied by different operators on second occasion). Standard error of measurements (SEMs) were below 1.5° for ST pro-retraction and 4.6° for GH in-external rotation during GH external rotation; below 6.6° for ST tilt, 6.4° for GH flexion-extension, 7.1° for elbow flexion-extension during combing hair; below 4.4° for GH ab-adduction, 13° for GH in-external rotation, 6.8° for elbow flexion-extension during grasping the seatbelt; below 11° for all ST and GH joint rotations during placing a cup on a shelf. Therefore, to evaluate AC progression, inertial sensors systems can be applied during the execution of functional tasks., Competing Interests: The authors declare no conflicts of interest.
- Published
- 2020
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35. Laser Treatment of Traumatic Scars and Contractures: 2020 International Consensus Recommendations.
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Seago M, Shumaker PR, Spring LK, Alam M, Al-Niaimi F, Rox Anderson R, Artzi O, Bayat A, Cassuto D, Chan HH, Dierickx C, Donelan M, Gauglitz GG, Leo Goo B, Goodman GJ, Gurtner G, Haedersdal M, Krakowski AC, Manuskiatti W, Norbury WB, Ogawa R, Ozog DM, Paasch U, Victor Ross E, Tretti Clementoni M, and Waibel J
- Subjects
- Delphi Technique, Humans, Wound Healing, Cicatrix therapy, Contracture therapy, Laser Therapy methods
- Abstract
Background and Objectives: There is currently intense multidisciplinary interest and a maturing body of literature regarding laser treatments for traumatic scars, but international treatment guidelines and reimbursement schemes have not yet caught up with current knowledge and practice in many centers. The authors intend to highlight the tremendous potential of laser techniques, offer recommendations for safe and efficacious treatment, and promote wider patient access guided by future high-quality research., Study Design/materials and Methods: An international panel of 26 dermatologists and plastic and reconstructive surgeons from 13 different countries and a variety of practice backgrounds was self-assembled to develop updated consensus recommendations for the laser treatment of traumatic scars. A three-step modified Delphi method took place between March 2018 and March 2019 consisting of two rounds of emailed questionnaires and supplementary face-to-face meetings. The panel members approved the final manuscript via email correspondence, and the threshold for consensus was at least 80% concurrence among the panel members., Results: The manuscript includes extensive detailed discussion regarding a variety of laser platforms commonly used for traumatic scar management such as vascular lasers and ablative and non-ablative fractional lasers, special considerations such as coding and laser treatments in skin of color, and 25 summary consensus recommendations., Conclusions: Lasers are a first-line therapy in the management of traumatic scars and contractures, and patients without access to these treatments may not be receiving the best available care after injury. Updated international treatment guidelines and reimbursement schemes, additional high-quality research, and patient access should reflect this status. Lasers Surg. Med. © 2019 Wiley Periodicals, Inc., (Published 2019. This article is a U.S. Government work and is in the public domain in the USA.)
- Published
- 2020
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36. Fractional 1,927 nm Thulium Laser Plus Photodynamic Therapy Compared and Combined for Photodamaged Décolleté Skin: A Side-by-Side Randomized Controlled Trial.
- Author
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Hendel K, Mogensen M, Wenande E, Dierickx C, Haedersdal M, and Togsverd-Bo K
- Subjects
- Aged, Combined Modality Therapy, Female, Follow-Up Studies, Humans, Middle Aged, Skin Aging pathology, Lasers, Solid-State therapeutic use, Photochemotherapy methods, Photosensitizing Agents therapeutic use, Skin Aging drug effects, Skin Aging radiation effects, Thulium
- Abstract
Background and Objectives: Décolleté photodamage is a common condition typically treated with light and energy-based devices. This study investigated the efficacy and safety of a fractional 1,927 nm thulium laser (TL) alone and combined with photodynamic therapy (PDT)., Study Design/materials and Methods: In a 12-week follow-up study, participant décolletés were divided into four treatment areas and randomized to receive a single treatment with field-directed TL, PDT, combination TL-PDT, or lesion-directed curettage control. All actinic keratoses (AKs) underwent lesion-directed curettage before randomization. TL was delivered at 20 mJ/mb, 500 mJ/cm
2 fluence, 5 W, and 8 (n = 6 pts.) or 16 (n = 6 pts.) passes. PDT was performed with 16% methyl aminolevulinate (MAL) creme incubated for 3 h, followed by red light-emitting diode light at 37 J/cm2 . Outcome measures included clinical assessment of overall photodamage and specific subcomponents, assisted by optical coherence tomography (OCT) imaging., Results: Twelve women with moderate to severe photodamage on the décolleté and a cumulative total of 184 thin grade I AKs were included. Field-directed treatments TL and combination TL-PDT equally improved the overall photodamage, mottled pigmentation, and rhytides compared with lesion-directed control (P < 0.05). The skin texture improved by TL alone and was further improved by combining TL and PDT (P < 0.05). Median AK complete responses were similar for field-directed interventions TL-PDT (100%), TL (90%), PDT (82%), and lesion-directed curettage control (52%) (P = 0.464). Patients presented with mild local skin responses, slightly more pronounced when combining TL with PDT versus individual treatments (P < 0.05). No scarring or adverse events were observed., Conclusions: The 1,927 nm fractional thulium laser is an effective, tolerable, and safe field-directed treatment for décolleté photodamage. Provided alone, TL proved to be as effective as combined TL-PDT for overall photodamage, while a greater improvement in skin texture was achieved using TL and PDT in combination. Lasers Surg. Med. © 2019 Wiley Periodicals, Inc., (© 2019 Wiley Periodicals, Inc.)- Published
- 2020
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37. A New Method for Percutaneous Drug Delivery by Thermo-Mechanical Fractional Injury.
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Shavit R and Dierickx C
- Subjects
- Administration, Cutaneous, Adult, Aged, Female, Humans, Male, Middle Aged, Skin Absorption, Aminolevulinic Acid, Drug Delivery Systems methods, Levulinic Acids administration & dosage, Photochemotherapy methods, Photosensitizing Agents administration & dosage
- Abstract
Background and Objectives: Percutaneous drug delivery (PDD) is a means of increasing the uptake of topically applied agents into the skin. Successful delivery of a photosensitizer into the skin is an important factor for effective photodynamic therapy. To evaluate the efficacy of pretreatment by thermomechanical fractional injury (TMFI) (Tixel®, Novoxel®, Israel) at low-energy settings in increasing the permeability of the skin to a known hydrophilic-photosensitizer medication, 5-amino-levulinic-acid hydrochloride (ALA) in compounded 20% ALA gel. To compare the effect of TMFI on ALA permeation into the skin in compounded gel to three commercial photosensitizing medications in different vehicles: ALA microemulsion gel, methyl-amino-levulinic-acid hydrochloride (MAL) cream, and ALA hydroalcoholic solution., Study Design/materials and Methods: Five healthy subjects were treated in two separate experiments and on a total of 136 test sites, with four topical photosensitizer preparations as follows: compounded 20% ALA gel prepared in a good manufacturing practice (GMP)-certified pharmacy (Super-Pharm Professional, Israel), 10% ALA microemulsion gel (Ameluz®, Biofrontera Bioscience GmbH, Leverkusen, Germany), 16.8% MAL cream (Metvix®, Galderma, Lausanne, Switzerland), and 20% ALA hydroalcoholic solution (Levulan Kerastick®, DUSA Pharmaceuticals, Inc., Wilmington, MA, USA). The dermal sites were pretreated by Tixel® (Novoxel® Ltd., Israel) prior to topical drug application. One site was untreated to serve as control. Protoporphyrin IX (PpIX) fluorescence intensity readouts were taken immediately and 1, 2, 3, 4, and 5 hours posttreatment., Results: The highest average PpIX fluorescence intensity measurements were obtained for the compounded 20% ALA gel following pre-treatment by TMFI at 6 milliseconds pulse duration. After 2 and 3 hours, TMFI-treated sites exhibited an increased hourly rate in readouts of FluoDerm units, which were 156-176% higher than the control rates (P ≤ 0.004). TMFI pre-treatment did not enhance the percutaneous permeation of either ALA or MAL following the microemulsion gel, hydroalcoholic solution, and cream applications., Conclusions: Pretreatment with low-energy TMFI at a pulse duration of 6 milliseconds increased the percutaneous permeation of ALA linearly over the first 5 hours from application when the compounded 20% ALA gel was used. Formulation characteristics have substantial influence on the ability of TMFI pretreatment to significantly increase the percutaneous permeation of ALA and MAL. Lasers Surg. Med. © 2019 Wiley Periodicals, Inc., (© 2019 Wiley Periodicals, Inc.)
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- 2020
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38. Light-based home-use devices for hair removal: Why do they work and how effective they are?
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Town G, Botchkareva NV, Uzunbajakava NE, Nuijs T, van Vlimmeren M, Ash C, and Dierickx C
- Subjects
- Humans, Hair Removal, Intense Pulsed Light Therapy
- Abstract
Objectives: This review has the following objectives: Firstly, it provides an explanation of the evolution of laser/intense pulsed light (IPL) hair reduction modalities from high fluence professional devices to low fluence home-use appliances. Secondly, it summarises published literature reviews on home-use devices (HUDs) as evidence of their growing credibility. Thirdly, it proposes mechanistic differences in light delivery regimes and the resulting divergences in mode of action., Materials and Methods: An extensive literature search was performed to review the progress of laser/IPL-induced hair reduction and determine what evidence is available to explain the mode of action of professional and HUDs for hair removal. Establishing the likely biological mode of action of professional high-fluence systems versus home-use low-fluence appliances was performed by combining data obtained using ex vivo hair follicle (HF) organ culture and the clinical results involving human participants., Results: Significant basic science and clinical evidence has been published to confirm the clinical efficacy and technical safety of many laser and IPL home-use devices for hair removal. Clearly, HUDs are different compared to professional systems both in terms of fluence per pulse and in terms of biological mechanisms underlying hair removal. Here we presented data showing that a single low fluence pulse of both 810 nm laser (6.6 J/cm
2 , 16 ms) and IPL (9 J/cm2 , 15 ms and 6.8 J/cm2 , 1.9 ms) leads to induction of catagen transition. Catagen transition was characterized by morphological changes similar to what occurs in vivo with occasional detection of apoptosis in the dermal papilla and outer root sheath cells. This suggests that high hair reduction can be expected in vivo and longer-term treatment might result in HF miniaturization due to a cumulative effect on the dermal papilla and outer root sheath cells. In line with this hypothesis, in this review we demonstrate that long-term application of a commercially-available home-use IPL appliance resulted in persistent hair reduction (80%) one year after last treatment. These data are in line with what was previously reported in the literature, where clinical studies with home-use IPL appliances demonstrated high efficacy of hair reduction on female legs, armpits and bikini zones, with full hair regrowth after four treatments following cessation of IPL administration. Limitations of HUDs include lack of hair clearance for very dark skin types and low speed of treatment compared with professional devices. Numerous uncontrolled and controlled clinical efficacy studies and technical safety investigations on consumer-use appliances support many of the leading manufacturers' claims., Analysis & Conclusions: Manufacturers make consumer appliances safe and easy to use by considering "human factors," needs and capabilities of a variety of users. Safety is of primary concern to manufacturers, regulators and standards bodies as these appliances may be accessible to children or their use attempted on unsuitable skin types without full awareness of potential side effects. Consumer cosmetic appliances are provided with warnings and obvious safety notices describing the nature of any ocular or dermal hazard and precautions for reducing risk of accidental injury, infection, etc. HUDs employing optical energy are provided with design and engineering controls such as safety switches, alarms and sensors to prevent their incorrect operation or eye exposure. In-vivo studies demonstrated that low fluence home-use hair removal devices can result in high hair reduction efficacy after a short treatment regime, while prolonged and less frequent (once in six weeks) maintenance treatment over a year can lead to high and sustained hair reduction even one year after cessation of treatment. Home-use hair removal devices can be a useful adjunct to professional in-office treatments with high professional awareness. There are sufficient positive arguments for practitioners to make the case to patients for HUDs as "companion" products to professional treatments. In addition, devices for hair removal can be used effectively as stand-alone products by the consumer if they are willing to adopt a regime of regular or frequent use. Further clinical studies involving dynamic observation of HF cycle stage and type (terminal vs. vellus) over the total duration of treatment, for example, using biopsies or non-invasive imaging are necessary to confirm the proposed mode of action of low fluence pulses in a combination with treatment and maintenance regimes. Lasers Surg. Med. 51:481-490, 2019. © 2019 Wiley Periodicals, Inc., (© 2019 Wiley Periodicals, Inc.)- Published
- 2019
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39. Topical brimonidine reduces IPL-induced erythema without affecting efficacy: A randomized controlled trial in patients with facial telangiectasias.
- Author
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Vissing AE, Dierickx C, Karmisholt KE, and Haedersdal M
- Subjects
- Administration, Topical, Female, Humans, Male, Middle Aged, Single-Blind Method, Treatment Outcome, Adrenergic alpha-2 Receptor Agonists administration & dosage, Brimonidine Tartrate administration & dosage, Edema prevention & control, Erythema prevention & control, Face, Laser Therapy methods, Postoperative Complications prevention & control, Telangiectasis surgery
- Abstract
Background: Laser and intense pulsed light (IPL) are standard symptomatic treatments for superficial telangiectasias, but postoperative erythema, oedema, and pain may prolong downtime., Objectives: To investigate whether topical brimonidine reduces IPL-induced inflammation in patients with moderate to severe facial telangiectasias., Methods: A randomized, two-centre, single-blinded, split-face trial on adjuvant brimonidine and air-cooling versus air-cooling alone (control) in 19 patients treated in Denmark (n = 10 patients) and Belgium (n = 9). Brimonidine was applied to the allocated side after each of three facial IPL-treatments, given at 3-week intervals. Patients were assessed up to 1 month after the final treatment. Outcome measures included blinded clinical on-site evaluation of erythema and oedema (5-point-scales), objective erythema-scores (red-filter analysis), patient-evaluated pain (Visual Analogue Scale), IPL-efficacy (blinded photo-evaluation of telangiectasia clearance), and patient preference., Results: In total, 19 patients were enrolled and completed the study. IPL induced moderate to severe erythema after each treatment. Application of brimonidine, reduced erythema to baseline values compared to air-cooling alone and sustained efficacy 24 hours after treatment (median difference reduction: score 1 at each assessment, P ≤ 0.022). Objective erythema-scores supported clinical findings, demonstrating a median erythema reduction of 50-95% after application of brimonidine and air-cooling compared to 9-28% reduction after air-cooling alone (P ≥ 0.002). No difference in reduction of IPL-induced oedema was observed between facial sides (P ≥ 0.227). Brimonidine and air-cooling slightly and consistently reduced postoperative pain compared to air-cooling alone (VAS 1.0 after brimonidine versus VAS 1.5-2.0 after air-cooling alone at treatment 1-3, P ≤ 0.032). At 1-month follow-up, patients experienced excellent clearance of telangiectasias (75-100% clearance) on both facial sides (P = 1.000). Patient preference supported clinical data and 79% of patients preferred brimonidine to control (P = 0.019)., Conclusion: Compared to air-cooling alone, adjuvant brimonidine reduces IPL-induced erythema and associated pain while maintaining a high IPL-efficacy. Lasers Surg. Med. 50:1002-1009, 2018. © 2018 Wiley Periodicals, Inc., (© 2018 Wiley Periodicals, Inc.)
- Published
- 2018
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40. Effectiveness and Safety of Acne Scar Treatment With Nonanimal Stabilized Hyaluronic Acid Gel.
- Author
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Dierickx C, Larsson MK, and Blomster S
- Subjects
- Adult, Atrophy, Cicatrix etiology, Cicatrix pathology, Dermal Fillers adverse effects, Female, Gels, Humans, Hyaluronic Acid adverse effects, Hyaluronic Acid therapeutic use, Male, Patient Satisfaction, Self Concept, Self Efficacy, Severity of Illness Index, Acne Vulgaris complications, Cicatrix drug therapy, Dermal Fillers therapeutic use, Hyaluronic Acid analogs & derivatives, Skin pathology
- Abstract
Background: Acne scarring affects most patients with acne and have a negative impact on quality of life. New effective treatment options offering minimal downtime are therefore needed., Objective: To evaluate improvement in overall facial appearance after hyaluronic acid (HA) treatment of atrophic acne scars., Methods: Twelve subjects with moderate-to-severe acne scars were treated at 3 sessions 4 weeks apart. At each session, up to 2-mL HA gel was injected into each side of the face. Acne scar severity, global facial aesthetic improvement, and subject satisfaction were assessed up to 36 weeks after treatment. Safety assessments included subject diaries and adverse events., Results: The overall facial appearance and the appearance of atrophic acne scars improved after treatment. Scar severity and subject satisfaction with the overall facial appearance and with the sensation and perception of the skin improved in most subjects. Subjects' self-esteem and self-confidence also improved. Adverse events were typically mild to moderate, expected, and procedure-related., Conclusion: Hyaluronic acid gel injections were effective and safe for treatment of moderate-to-severe atrophic acne scars. The treatment effect developed gradually over time with the highest improvement observed at the end of the study.
- Published
- 2018
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41. Selective Suprascapular and Axillary Nerve Block Versus Interscalene Plexus Block for Pain Control After Arthroscopic Shoulder Surgery: A Noninferiority Randomized Parallel-Controlled Clinical Trial.
- Author
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Neuts A, Stessel B, Wouters PF, Dierickx C, Cools W, Ory JP, Dubois J, Jamaer L, Arijs I, and Schoorens D
- Subjects
- Adult, Arthroscopy adverse effects, Axilla diagnostic imaging, Axilla surgery, Brachial Plexus diagnostic imaging, Brachial Plexus surgery, Brachial Plexus Block methods, Female, Humans, Male, Middle Aged, Pain, Postoperative diagnostic imaging, Scapula diagnostic imaging, Scapula surgery, Shoulder diagnostic imaging, Single-Blind Method, Ultrasonography, Interventional methods, Arthroscopy trends, Brachial Plexus Block trends, Pain, Postoperative prevention & control, Shoulder surgery, Ultrasonography, Interventional trends
- Abstract
Background and Objectives: This randomized trial aimed to assess if a combined suprascapular-axillary nerve block (SSB) is noninferior (margin = 1.3 on a 0- to 10-point scale) to interscalene block (ISB) in treating pain after arthroscopic shoulder surgery. Secondary end points included opioid consumption, dyspnea, discomfort associated with muscle weakness, and patient satisfaction., Methods: One hundred patients undergoing arthroscopic shoulder surgery were randomized to receive ultrasound-guided ISB (n = 50) or SSB (n = 50). Pain intensity at rest, dyspnea, and discomfort were recorded upon arrival in the recovery room, discharge to the ward, and at 4, 8, and 24 hours after surgery. Piritramide consumption was recorded for the first 24 hours. Patient satisfaction was assessed on the second postoperative day., Results: During the first 4 hours after surgery, the difference in mean pain score between SSB and ISB was higher than 2.5 (±0.8). The difference gradually decreased to 1.1 (±1.0) at 8 hours before resulting in noninferiority during the night and at 24 hours. Piritramide consumption was significantly higher in the SSB group in the first 8 hours. The incidence of dyspnea and discomfort was higher after ISB. Treatment satisfaction was similar in both groups., Conclusions: Suprascapular-axillary nerve block is inferior to ISB in terms of analgesia and opioid requirement in the immediate period after arthroscopic shoulder surgery but is associated with a lower incidence of dyspnea and discomfort. The difference in pain and opioid consumption gradually decreases as the blocks wear off in order to reach similar pain scores during the first postoperative night and at 24 hours., Clinical Trial Registration: This study was registered at ClinicalTrials.gov, identifier NCT02415088.
- Published
- 2018
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42. Using normal and high pulse coverage with picosecond laser treatment of wrinkles and acne scarring: Long term clinical observations.
- Author
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Dierickx C
- Subjects
- Adult, Aged, Cicatrix etiology, Cicatrix pathology, Face, Female, Follow-Up Studies, Humans, Male, Middle Aged, Patient Satisfaction, Pilot Projects, Skin Aging pathology, Time Factors, Treatment Outcome, Acne Vulgaris complications, Cicatrix radiotherapy, Lasers, Solid-State therapeutic use, Low-Level Light Therapy, Skin Aging radiation effects
- Abstract
Objective: The picosecond 755 nm alexandrite laser using a diffractive lens array has demonstrated consistent clinical efficacy for improving the appearance of acne scarring and wrinkles amongst other benefits. This small pilot study is to assess the difference, if any, in clinical benefit if a higher than the standard protocol for number of pulses delivered to a tissue area is used compared to the standard protocol guidelines., Method: Seven subjects received treatment to one side of the face with a standard protocol number of laser pulses with the other side of the face receiving higher than standard number of pulses from the same 755 nm picosecond laser using an additional diffractive lens array. Photographs at final follow up were compared to baseline by two blinded Board Certified Dermatologists and assessed for improvements to acne scarring using a 6-point grading score, for wrinkles using the Fitzpatrick Wrinkle & Elastosis 3-point grading scale and a Global Aesthetic Improvement Scale assessment. Subjects also completed a satisfaction questionnaire., Results: For the acne scarring subjects, the average improvement from baseline to final follow up was 4.0 +/- 1.0 for the standard treated side and 4.5 +/- 0.5 for the high pulse side. There was no statistically significant difference between the two treated sides (P > 0.05, n = 3 paired t-test). For the wrinkle subjects, the average grading of the standard pulse side improved from 2.0 +/- 0.82 to 1.75 +/- 1.0 from baseline to final follow-up. The high pulse side improved from 1.5 +/- 1.0 to 1.125 +/- 0.25 from baseline to final follow-up. There was no statistically significant difference between the improvement of the standard and high pulse treatment sides (P > 0.05, n = 4 paired t-test). The comparison of baseline to final follow-up images of each subject found both sides to be Much or Very Much improved with no statistically significant difference between the standard and high pulse sides (P > 0.05, n = 7 paired t-test). Six of the seven subjects did not note any difference between the effect on different sides of the face and four of the seven rated their overall improvement after treatment as Good, three subjects as Reasonable and one subject with Slight Improvement. All subjects found the treatment comfortable and easy to tolerate and there was no increased incidence of side effects other than the mild occurrences typically observed for this type of treatment., Conclusion: This is a small pilot study with limited subject numbers and further data is needed to be able to make firm conclusions of observed trends, which suggest that the use of higher than standard suggested protocol number of pulses with the diffractive lens array and the 755 nm picosecond laser does not appear to offer any additional benefit over that that can already be achieved with the standard number of pulses, but also does not increase risk of detrimental post treatment effects either. Lasers Surg. Med. 50:51-55, 2018. © 2017 The Authors. Lasers in Surgery and Medicine Published by Wiley Periodicals, Inc., (© 2017 The Authors. Lasers in Surgery and Medicine Published by Wiley Periodicals, Inc.)
- Published
- 2018
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43. Prebending of osteosynthesis plate using 3D printed models to treat symptomatic os acromiale and acromial fracture.
- Author
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Beliën H, Biesmans H, Steenwerckx A, Bijnens E, and Dierickx C
- Abstract
Background: A symptomatic os acromiale can lead to impingement syndrome and rotator cuff tendinopathy. An acromion fracture is often part of a more complex scapular trauma that needs stabilisation., Methods: We developed a new technique using a three-dimensional (3D) model and a distal clavicle reconstruction plate to treat os acromiale and acromion fractures. Our hypothesis was that such an approach would be a useful addition to the existing techniques. First, a 3D model of the acromion was printed, then an osteosynthesis plate was pre-bent to fit the exact shape and curve of the acromion. We tested this technique and present reports on five patients, three with os acromiales and two with acromial fractures. We followed these patients during their rehabilitation and evaluated them using the Constant-Murley and the Disabilities of the Arm, Shoulder and Hand scores., Results: In every case the fracture or non-union healed. If the surgery was performed before additional damage (such as an impingement syndrome) occurred, we saw that the patient's pain completely disappeared. This new technique also has other advantages because the surgeon can prepare the entire operation in advance, which reduces the duration of surgery. Another advantage of using a 3D model is that it can also be used to inform the patient and the surgical team about the planned operation., Conclusion: This new technique using a preoperative patient-customized plate is a good alternative for use in open reduction and internal fixation, particularly if the patient has no other conditions.
- Published
- 2017
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44. New and Advanced Picosecond Lasers for Tattoo Removal.
- Author
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Adatto MA, Amir R, Bhawalkar J, Sierra R, Bankowski R, Rozen D, Dierickx C, and Lapidoth M
- Subjects
- Cicatrix etiology, Cicatrix therapy, Color, Dermatologic Surgical Procedures adverse effects, Dermatologic Surgical Procedures methods, Humans, Ink, Laser Therapy adverse effects, Lasers, Solid-State adverse effects, Lasers, Solid-State therapeutic use, Laser Therapy methods, Tattooing adverse effects
- Abstract
Early methods of tattoo removal ultimately resulted in unacceptable cosmetic outcomes. While the introduction of laser technology was an improvement over the existing chemical, mechanical, and surgical procedures, the use of nonselective tattoo removal with carbon dioxide and argon lasers led to scarring. Q-switched lasers with nanosecond (10-9) pulse domains were considered to have revolutionized tattoo treatment, by selectively heating the tattoo particles, while reducing the adverse sequelae to adjacent normal skin. Theoretical considerations of restricting pulse duration, to heat tattoo particles to higher temperatures, proposed the use of sub-nanosecond pulses to target particles with thermal relaxation times lower than the nanosecond pulses in Q-switched lasers. Initial studies demonstrated that picosecond (10-12) pulses were more effective than nanosecond pulses in clearing black tattoos. Advances in picosecond technology led to the development of commercially available lasers, incorporating several different wavelengths, to further refine pigment targeting., (© 2017 S. Karger AG, Basel.)
- Published
- 2017
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45. A randomized side-by-side study comparing alexandrite laser at different pulse durations for port wine stains.
- Author
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Carlsen BC, Wenande E, Erlendsson AM, Faurschou A, Dierickx C, and Haedersdal M
- Subjects
- Adolescent, Adult, Aged, Biopsy, Needle, Denmark, Dose-Response Relationship, Radiation, Female, Follow-Up Studies, Hospitals, University, Humans, Immunohistochemistry, Male, Middle Aged, Port-Wine Stain pathology, Prospective Studies, Radiation Dosage, Severity of Illness Index, Time Factors, Treatment Outcome, Young Adult, Lasers, Dye therapeutic use, Lasers, Solid-State therapeutic use, Low-Level Light Therapy methods, Port-Wine Stain radiotherapy
- Abstract
Background and Objectives: Pulsed dye laser (PDL) represents the gold-standard treatment for port wine stains (PWS). However, approximately 20% of patients are poor responders and yield unsatisfactory end-results. The Alexandrite (Alex) laser may be a therapeutic alternative for selected PWS subgroups, but optimal laser parameters are not known. The aim of this study was to assess clinical PWS clearance and safety of Alex laser at a range of pulse durations., Materials and Methods: Sixteen individuals (14 previously PDL-treated) with deep red (n = 4), purple macular (n = 5) and purple hypertrophic (n = 7) PWS were included. Four side-by-side test areas were marked within each lesion. Three test areas were randomized to Alex laser at pulse durations of 3, 5, or 10 ms (8 mm spot, DCD 60/40), while the fourth was untreated. The lowest effective fluence to create purpura within the entire test spot was titrated and applied to intervention areas. Standardized clinical photographs were taken prior to, immediately after laser exposure and at 6-8 weeks follow up. Clinical PWS clearance and laser-related side effects were assessed using clinical photos., Results: Alex laser at 3, 5, and 10 ms pulse durations demonstrated significant clearance compared to untreated controls (P < 0.001). Three milli second pulse duration exhibited improved clearance versus 5 ms (P = 0.016) and 10 ms (P = 0.004), while no difference between five and 10 ms was shown (P = 0.063). Though not significant, good responders (>50% clearance) were more likely to have purple hypertrophic PWS (5/7) compared to purple macular (2/5) and deep red lesions (1/4). Eight laser-exposed test areas (17%) developed hypopigmented atrophic scarring. Side effects tended to be more frequently observed with 5 ms (n = 4) and 10 ms (n = 3) versus 3 ms pulse duration (n = 1). Correspondingly, 3 ms was associated with a superior (n = 6) or comparable (n = 10) overall cosmetic appearance for all individuals., Conclusion: Alex laser at 3 ms pulse duration offers superior clinical clearance and safety compared to 5 and 10 ms, and seems best suited for purple hypertrophic PWS. Treatment should be restricted to experienced personnel due to a particularly narrow therapeutic window. Lasers Surg. Med. 49:97-103, 2017. © 2016 Wiley Periodicals, Inc., (© 2016 Wiley Periodicals, Inc.)
- Published
- 2017
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46. Predictive factors of speech understanding in adults with cochlear implants.
- Author
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Dierickx C, Jacquemin L, Boon E, Dierckx A, Debruyne F, Wouters J, Desloovere C, and Verhaert N
- Subjects
- Adult, Female, Humans, Male, Prospective Studies, Retrospective Studies, Cochlear Implants, Speech Perception
- Abstract
Objective: The aim of this study was to analyse the factors that influenced speech recognition scores in quiet conditions and speech reception threshold levels (SRT) in fixed noise conditions, after cochlear implant (CI) surgery in adults with postlinguistic deafness., Study Design: Combined retrospective and prospective study in a tertiary referral centre., Methods: We included 66 patients that received implants between 2002 and 2013. We retrospectively collected speech recognition scores and 14 demographic, audiological, and technical factors, including gender, age at implantation, aetiology, hearing loss progression, preoperative Pure Tone Average (PTA), hearing loss onset age and duration, duration and use of hearing aids (HAs); implantation in the best or worst ear; implantation on the right or left side; use of HA after implantation; and the duration and type of CI. We prospectively tested a subgroup of 21 patients for SRT in fixed noise., Results: The hearing loss duration significantly affected speech recognition scores in quiet conditions (H (4) = 10.567, p =0.032) and SRTs in fixed noise conditions (rs = 0.466, p = 0.033). The PTA of the better ear significantly affected only the SRT in fixed noise conditions (rs = 0.57 1, p = 0.007)., Conclusion: The duration of hearing loss and the PTA of the best ear had significant effects on the outcomes of speech recognition and SRT in quiet and fixed noise conditions, respectively. These findings are important for counselling CI candidates. Further studies in larger study populations are warranted.
- Published
- 2016
47. Non-ablative fractional laser provides long-term improvement of mature burn scars--a randomized controlled trial with histological assessment.
- Author
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Taudorf EH, Danielsen PL, Paulsen IF, Togsverd-Bo K, Dierickx C, Paasch U, and Haedersdal M
- Subjects
- Adult, Burns pathology, Cicatrix etiology, Cicatrix pathology, Female, Follow-Up Studies, Humans, Male, Middle Aged, Patient Satisfaction, Time Factors, Treatment Outcome, Young Adult, Burns complications, Cicatrix therapy, Laser Therapy, Lasers, Solid-State therapeutic use
- Abstract
Background and Objectives: Non-ablative fractional laser-treatment is evolving for burn scars. The objective of this study was to evaluate clinical and histological long-term outcome of 1,540 nm fractional Erbium: Glass laser, targeting superficial, and deep components of mature burn scars., Materials & Methods: Side-by-side scar-areas were randomized to untreated control or three monthly non-ablative fractional laser-treatments using superficial and extra-deep handpieces. Patient follow-up were at 1, 3, and 6 months. Primary outcome was improvement in overall scar-appearance on a modified-Patient-and-Observer-Scar-Assessment-Scale (mPOSAS, 1 = "normal skin", 10 = "worst imaginable scar"). Secondary outcomes included histology, patient satisfaction (0-10), patient-assessed improvement, and safety., Results: Study was completed by 17 of 20 randomized patients with normotrophic (n = 11), hypertrophic (n = 5) or atrophic (n = 1) scars. Scar-appearance improved from laser-treatments (P < 0.001 vs. untreated) and histology at 6 months supported collagen-remodeling. Improvement appeared continuously during the post-operative period (mPOSAS baseline: 7 [5-8], 6 months: 4 [3-5] P = < 0.001). At 6 months, patients were satisfied with treatment (6 [3-9]) and 82% reported improved scar-texture. Treatments caused mild to moderate pain (4 [2-7]). Adverse effects decreased during follow-up and at final assessment, discrete erythema, hyperpigmentation or imprints from laser-grid were present in 11 patients. No patients experienced worsening of scar-appearance., Conclusions: Combined superficial and deep non-ablative fractional laser-treatments induce long-term clinical and histological improvement of mature burn scars., (© 2014 Wiley Periodicals, Inc.)
- Published
- 2015
- Full Text
- View/download PDF
48. Intra-articular shoulder infiltrations. A study of Dutch and Flemish shoulder specialists.
- Author
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Smeets K, Appermans W, Feyen L, and Dierickx C
- Subjects
- Humans, Netherlands, Ultrasonography, Injections, Intra-Articular methods, Orthopedics, Practice Patterns, Physicians', Shoulder Joint diagnostic imaging, Specialization
- Abstract
Unlabelled: It has been demonstrated that the use of echography during intra-articular shoulder infiltrations provides superior results. The correct infiltration technique and the related (contra-) indications are still under discussion. The authors' objective was to ascertain how intra-articular shoulder infiltrations are done in Holland and Flanders. An electronic questionnaire was answered by 35 members of the FLESSS (Flanders) and 30 members of the WSE (Netherlands) and was then processed statistically., Results: 21.54% of those questioned think they have sufficient experience with the use of echography during intra-articular infiltrations. 87.7% of the orthopaedists give a normal dose of corticoids to diabetes patients and more than 71% infiltrate when anticoagulants are used. Whereas 68.57% of the Flemish use posterior infiltration, 76.67% of the Dutch give an anterior injection., Conclusions: Echography is not used enough as an aid for intra-articular shoulder infiltrations. Neither diabetes mellitus nor anticoagulants are considered to be contra-indications. The Flemish shoulder specialists mainly administer posterior infiltration with methylprednisolone. The Dutch orthopaedists mainly administer anterior infiltration with triamcinolone.
- Published
- 2014
49. Regarding "Aberrant origin of the long head of the biceps: a case series".
- Author
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Dierickx C, Ceccarelli E, Conti M, Vanlommel J, and Castagna A
- Subjects
- Humans, Male, Arthralgia diagnosis, Arthroscopy methods, Muscle, Skeletal abnormalities, Musculoskeletal Abnormalities diagnosis, Shoulder Joint surgery, Tendons abnormalities
- Published
- 2012
- Full Text
- View/download PDF
50. Variations of the intra-articular portion of the long head of the biceps tendon: a classification of embryologically explained variations.
- Author
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Dierickx C, Ceccarelli E, Conti M, Vanlommel J, and Castagna A
- Subjects
- Adolescent, Adult, Aged, Female, Humans, Joint Instability etiology, Joint Instability physiopathology, Joint Instability surgery, Male, Middle Aged, Muscle, Skeletal anatomy & histology, Prognosis, Prospective Studies, Retrospective Studies, Risk Assessment, Shoulder Impingement Syndrome etiology, Shoulder Impingement Syndrome physiopathology, Shoulder Joint abnormalities, Shoulder Joint embryology, Tendon Injuries surgery, Tendons anatomy & histology, Tendons embryology, Young Adult, Arthroscopy, Muscle, Skeletal abnormalities, Shoulder Joint anatomy & histology, Tendon Injuries classification, Tendons abnormalities
- Abstract
Background: Although the intra-articular portion of the long head of the biceps (LHB) usually runs free, different types of fusions with the inferior surface of the capsule are known to be possible. Anatomic variations of this part of the LHB have been previously described and were nearly always considered to be innocent., Materials and Methods: Out of 2 populations of 1500 arthroscopies each, we collected prospectively and retrospectively all possible variations of the proximal portion of the LHB., Results: We included 57 cases (1.91%) of this total population in an attempt to describe the complete range of these form variants: the simple vinculum or pulley-like sling, the partial or complete mesotenon between biceps and capsule, the complete adherent LHB, the double-tendon origin, the reversed-type split-tendon, and the complete absence of the LHB. We suggest a classification of 12 variations of the intra-articular portion of the LHB., Discussion: By taking into account an extensive literature review, we suggest that these conditions are congenital and consider them as a result of partial detachment from the mesothelial or synovial fusion with the inferior surface of the capsule. The incidence of these variants and their associated pathologies are investigated., Conclusion: By offering this new classification and a physiopathologic hypothesis, we try to explain why some of these anatomic variants may also acquire a pathologic significance.
- Published
- 2009
- Full Text
- View/download PDF
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