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1.
J Glob Antimicrob Resist ; 8: 186-191, 2017 03.
Article in English | MEDLINE | ID: mdl-28213334

ABSTRACT

Reactive oxygen species (ROS) is a novel therapeutic strategy for topical or local application to wounds, mucosa or internal structures where there may be heavy bacterial bioburden with biofilm and chronic inflammation. Bacterial biofilms are a significant problem in clinical settings owing to their increased tolerance towards conventionally prescribed antibiotics and their propensity for selection of further antibacterial resistance. There is therefore a pressing need for the development of alternative therapeutic strategies that can improve antibiotic efficacy towards biofilms. ROS has been successful in treating chronic wounds and in clearing multidrug-resistant organisms, including methicillin-resistant Staphylococcus aureus (MRSA), and carbapenemase-producing isolates from wounds and vascular line sites. There is significant antifungal activity of ROS against planktonic and biofilm forms. Nebulised ROS has been evaluated in limited subjects to assess reductions in bioburden in chronically colonised respiratory tracts. The antibiofilm activity of ROS could have great implications for the treatment of a variety of persistent respiratory conditions. Use of ROS on internal prosthetic devices shows promise. A variety of novel delivery mechanisms are being developed to apply ROS activity to different anatomical sites.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Bacteria/drug effects , Bacterial Infections/drug therapy , Biofilms/drug effects , Reactive Oxygen Species/therapeutic use , Wound Infection/drug therapy , Administration, Topical , Animals , Drug Evaluation, Preclinical , Fungi/drug effects , Humans
2.
Auris Nasus Larynx ; 43(6): 595-601, 2016 Dec.
Article in English | MEDLINE | ID: mdl-26992272

ABSTRACT

Infantile middle ear capillary haemangiomas (MECH) are a rare entity with only five reported cases in the literature. At present there is no consensus regarding the management of such lesions. Extra-cutaneous haemangiomas have been successfully managed with oral propranolol but not yet reported in MECH. We present a further case and appraise the management options. At present oral propranolol has not been used in the treatment of MECH. The literature suggests that infantile MECH have a higher propensity to spontaneously involute and a greater likelihood of response to propranolol. Surgical excision is the best option in older children and adults.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Ear Neoplasms/therapy , Ear, Middle/surgery , Hemangioma, Capillary/therapy , Otologic Surgical Procedures , Propranolol/therapeutic use , Child , Ear Neoplasms/diagnostic imaging , Ear Neoplasms/pathology , Ear, Middle/diagnostic imaging , Ear, Middle/pathology , Hemangioma, Capillary/diagnostic imaging , Hemangioma, Capillary/pathology , Humans , Magnetic Resonance Imaging , Male , Tomography, X-Ray Computed , Watchful Waiting
4.
Eur Arch Otorhinolaryngol ; 272(6): 1371-6, 2015 Jun.
Article in English | MEDLINE | ID: mdl-24532083

ABSTRACT

Bone-anchored hearing aids (BAHAs) are based on the principle of osseointegration, which is fundamental to implant stability and survival. Previous exposure to ionising radiation may compromise this, as evidenced in relation to dental and craniofacial implants. There is a dearth of data, however, regarding BAHA implant systems in patients with previously irradiated implant sites. We sought, therefore, to investigate implant stability and survival in such patients. Patients were identified retrospectively from our electronic BAHA database. Hospital records were reviewed for demographics; operative technique; complications; and details regarding previous irradiation. Implant stability was assessed by resonance frequency analysis (RFA), generating a numerical value-implant stability quotient (ISQ). Extrapolating from dental studies, successfully loaded implants typically have ISQs of ≥60. Readings were, therefore, interpreted with respect to this. Seven patients were identified for inclusion. Mean time between irradiation and implant insertion was 33 months (range 16-72 months), and mean time from implant insertion to RFA measurement was 41 months (range 3-96 months). Operatively, all patients underwent single-stage procedures under local anaesthesia. One patient suffered a Holger's grade 2 skin reaction, while two suffered significant skin flap failure, requiring revision procedures. The implant survival rate was 100 %. All ISQ values were >60, with a mean of 66.9 (95 % confidence interval 63.1-70.6). Our data support sufficient osseointegration of BAHA implant systems in post-irradiated patients, but highlight issues with wound healing. Contemporary soft tissue preservation operative techniques will likely overcome this, facilitating safe and efficacious BAHA insertion in this ever-increasing group of patients.


Subject(s)
Bone-Implant Interface , Hearing Aids , Osseointegration/radiation effects , Prosthesis Failure/radiation effects , Radiotherapy/adverse effects , Bone-Implant Interface/physiopathology , Bone-Implant Interface/radiation effects , Female , Head and Neck Neoplasms/radiotherapy , Head and Neck Neoplasms/rehabilitation , Head and Neck Neoplasms/surgery , Humans , Male , Middle Aged , Retrospective Studies , Time Factors , Treatment Outcome , Wound Healing/radiation effects
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