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1.
J Burn Care Res ; 44(2): 381-392, 2023 03 02.
Article in English | MEDLINE | ID: mdl-35486925

ABSTRACT

Long-term laryngotracheal complications (LTLC) after inhalation injury (II) are an under-recognized condition in patients with burns. The purpose of this study was to systematically review all available evidence on LTLC after II and identify gaps in knowledge to guide the direction of future research. A scoping review was performed to synthesize all available evidence on LTLC after II, as guided by the question, "What are the LTLC after II, in patients with or without a history of translaryngeal intubation and/or tracheostomy?". MEDLINE, Web of Science, Ovid Embase, Cochrane Library, and Google Scholar were searched for publications on this topic. Of the 3567 citations screened, a total of 153 full-text articles were assessed for eligibility and 49 were included in the scoping review. The overall level of evidence was low, with case reports constituting 46.7% of all included human studies. The lesions were most frequently in the trachea (36.9%), followed by the glottis (34.7%) and subglottis (19.0%). LTLC occur in 4.8 to 6.5% of patients after II and these complications are under-recognized in burns patients. The risk factors for LTLC include high-grade II, elevated initial inflammatory responses, prolonged translaryngeal intubation, and a history of tracheostomy. The goal of management is to restore airway patency, preserve voice quality, and restore normal diet and swallow function. There is limited high-level evidence on LTLC, particularly with regards to long-term functional morbidity in voice and swallow. Large, prospective studies are required to address this gap in knowledge.


Subject(s)
Burns , Laryngostenosis , Larynx , Humans , Laryngostenosis/etiology , Laryngostenosis/surgery , Burns/complications , Tracheostomy/adverse effects , Prospective Studies
2.
J Knee Surg ; 35(6): 653-660, 2022 May.
Article in English | MEDLINE | ID: mdl-32927494

ABSTRACT

Multiple intraoperative strategies are described to achieve full extension in total knee arthroplasty, but only a few studies have assessed the effect of the flexion gap on intraoperative improvement in flexion contracture. The aim of this study was to determine whether posterior condylar offset, in isolation, independently affects extension at the time of total knee arthroplasty.Two hundred and seventy-eight patients who underwent total knee arthroplasty for knee osteoarthritis and flexion contracture ≥ 5 degrees between January 2008 and July 2018 were included in this study. Patients with other factors that could affect knee extension at the time of surgery were excluded. We recorded the thickness of posterior femoral condyle bone resected as well as the thickness of the posterior femoral component chosen for each patient. Patients' knee extension was recorded under anesthetic, prior to resection and intraoperatively after total knee replacement.Average thickness of bone resection for the posteromedial femur was 12.64 ± 1.65 mm and for the posterolateral femur was 10.38 ± 1.52 mm. Using a linear regression model, we found that changes in posterior offset and implant downsizing influenced correction of fixed flexion deformity at the time of surgery. When patients had a combined posteromedial and posterolateral offset 2 mm thinner than the thickness of bone resected, there was an average correction of 3.5 degrees of flexion contracture.Our study demonstrated that posterior femoral condyle offset is an independent variable affecting correction of flexion contracture at the time of surgery in a gap balanced cruciate-retaining total knee arthroplasty. This is a level IV evidence study.


Subject(s)
Arthroplasty, Replacement, Knee , Contracture , Knee Prosthesis , Osteoarthritis, Knee , Contracture/etiology , Contracture/surgery , Femur/surgery , Humans , Knee Joint/surgery , Osteoarthritis, Knee/surgery , Range of Motion, Articular
3.
J Robot Surg ; 15(5): 813-819, 2021 Oct.
Article in English | MEDLINE | ID: mdl-33389627

ABSTRACT

Robot-assisted arthroplasty (RAA) is increasingly practised in orthopaedic surgery. The aim of this study was to perform a bibliometric analysis of all published primary research into RAA and to apply the Progressive Scholarly Acceptance (PSA) model to evaluate its acceptance as an orthopaedic surgical technique. A literature search was performed that included all peer-reviewed, primary, English language publications on RAA from its introduction in 1992 up to 2019. RAA was defined as robot-assisted hip or knee arthroplasty. A bibliometric analysis was performed to categorise articles by type of study and level of evidence. Studies were also categorised as initial investigations (II) or refining studies (RS). A PSA analysis was performed, with the end-point being defined as the point in time when the number of RS exceeded the number of II. Of the 199 studies originating from 19 countries and 101 institutions, only 16 (8.04%) were randomised-controlled trials. Fifty-one percent of studies had been published since 2015. Using PSA analysis, 161 (80.9%) studies were categorised as II and 38 (19.1%) were categorised as RS. This demonstrates that RAA has not yet reached the point of scholarly acceptance. Scholarly acceptance of RAA as an orthopaedic surgical technique has yet to be reached. However, there has been an exponential increase in the number of publications on RAA in the last 5 years, reflecting renewed interest this technique. We predict that, for the next 5 years, RAA will remain in the experimental phase due to the rapid development of new technology in this field.


Subject(s)
Arthroplasty, Replacement, Knee , Robotic Surgical Procedures , Robotics , Bibliometrics , Humans , Robotic Surgical Procedures/methods
4.
Int J Pediatr Otorhinolaryngol ; 133: 110015, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32229365

ABSTRACT

OBJECTIVES: To demonstrate the safety and feasibility of the first reported case of a 3 Tesla MRI scan in a paediatric 3 Tesla-compatible cochlear implant recipient under general anaesthesia. MATERIALS AND METHODS: A three-year-old child with bilateral optic pathway glioma treated with chemotherapy, who subsequently received a right sided 3 Tesla-compatible cochlear implant for sensorineural hearing loss was examined. The CI device chosen was implanted due to its purported MRI compatibility. Following informed consent and hospital executive approval, the child underwent a 3 Tesla MRI scan to assess for growth of the optic pathway glioma. RESULTS: A 3 Tesla MRI scan of the brain was performed under general anaesthesia. There was expected artefact due to the magnet of the receiver stimulator. There was no malfunction of the implant noted after the procedure, and no neurological or otological complications. The child had five more uneventful 3 Tesla MRI scans of the brain without complications. CONCLUSION: This is the first reported case of a child with a 3 Tesla-compatible cochlear implant undergoing a 3 Tesla MRI scan of the brain under general anaesthesia. Provided manufacturer guidelines are adhered to, 3 Tesla MRI scanning should not be contraindicated in paediatric cochlear implant recipients with a compatible device.


Subject(s)
Cochlear Implants , Magnetic Resonance Imaging/methods , Nervous System Neoplasms/diagnostic imaging , Optic Nerve Glioma/diagnostic imaging , Anesthesia, General , Child, Preschool , Hearing Loss, Sensorineural/surgery , Humans , Male , Neuroimaging/methods
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