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1.
Bone Jt Open ; 3(3): 196-204, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35253478

ABSTRACT

AIMS: The aim of this study was to assess medium-term improvements following total hip arthroplasty (THA), and to evaluate what effect different preoperative Oxford Hip Score (OHS) thresholds for treatment may have on patients' access to THA and outcomes. METHODS: Patients undergoing primary THA at our institution with an OHS both preoperatively and at least four years postoperatively were included. Rationing thresholds were explored to identify possible deprivation of OHS improvement. RESULTS: Overall, 2,341 patients were included. Mean OHS was 19.7 (SD 8.2) preoperatively and 39.7 (SD 9.8) at latest follow-up. An improvement of at least eight-points, the minimally important change (MIC), was seen in 2,072 patients (88.5%). The mean improvement was 20.0 points (SD 10.5). If a rationing threshold of OHS of 20 points had been enforced, 90.8% of those treated would have achieved the MIC, but only 54.3% of our cohort would have had access to surgery; increasing this threshold to 32 would have enabled 89.5% of those treated to achieve the MIC while only depriving 6.5% of our cohort. The 'rationed' group of OHS > 20 had significantly better OHS at latest follow-up (42.6 vs 37.3; p < 0.001), while extending the rationing threshold above 32 showed postoperative scores were more significantly affected by the ceiling effect of the OHS. CONCLUSION: The OHS was not designed as a tool to ration healthcare, but if it had been used at our institution for this cohort, applying an OHS threshold of 20 to routine THA access would have excluded nearly half of patients from having a THA; a group in which over 85% had a significant improvement in OHS. Where its use for rationing is deemed necessary, use of a higher threshold may be more appropriate to ensure a better balance between patient access to treatment and chances of achieving good to excellent outcomes. Cite this article: Bone Jt Open 2022;3(3):196-204.

2.
Lancet ; 393(10172): 647-654, 2019 02 16.
Article in English | MEDLINE | ID: mdl-30782340

ABSTRACT

BACKGROUND: Total hip replacement is a common and highly effective operation. All hip replacements would eventually fail if in situ long enough and it is important that patients understand when this might happen. We aimed to answer the question: how long does a hip replacement last? METHODS: We did a systematic review and meta-analysis with a search of MEDLINE and Embase from the start of records to Sept 12, 2017. We included articles reporting 15-year survival of primary, conventional total hip replacement constructs in patients with osteoarthritis. We extracted survival and implant data and used all-cause construct survival as the primary outcome. We also reviewed reports of national joint replacement registries, and extracted data for a separate analysis. In the meta-analyses, we weighted each series and calculated a pooled survival estimate for each source of data. This study was registered with PROSPERO (CRD42018085642). FINDINGS: We identified 140 eligible articles reporting 150 series, and included 44 of these series (13 212 total hip placements). National joint replacement registries from Australia and Finland provided data for 92 series (215 676 total hip replacements). The 25-year pooled survival of hip replacements from case series was 77·6% (95% CI 76·0-79·2) and from joint replacement registries was 57·9% (95% CI 57·1-58·7). INTERPRETATION: Assuming that estimates from national registries are less likely to be biased, patients and surgeons can expect a hip replacement to last 25 years in around 58% of patients. FUNDING: National Institute for Health Research, National Joint Registry for England, Wales, Northern Ireland and Isle of Man, and The Royal College of Surgeons of England.


Subject(s)
Arthroplasty, Replacement, Hip/adverse effects , Prosthesis Failure , Registries , Reoperation , Follow-Up Studies , Humans , Osteoarthritis, Hip/surgery , Time Factors
3.
Lancet ; 393(10172): 655-663, 2019 02 16.
Article in English | MEDLINE | ID: mdl-30782341

ABSTRACT

BACKGROUND: Knee replacements are the mainstay of treatment for end-stage osteoarthritis and are effective. Given time, all knee replacements will fail and knowing when this failure might happen is important. We aimed to establish how long a knee replacement lasts. METHODS: In this systematic review and meta-analysis, we searched MEDLINE and Embase for case series and cohort studies published from database inception until July 21, 2018. Articles reporting 15 year or greater survival of primary total knee replacement (TKR), unicondylar knee replacement (UKR), and patellofemoral replacements in patients with osteoarthritis were included. Articles that reviewed specifically complex primary surgeries or revisions were excluded. Survival and implant data were extracted, with all-cause survival of the knee replacement construct being the primary outcome. We also reviewed national joint replacement registry reports and extracted the data to be analysed separately. In the meta-analysis, we weighted each series and calculated a pooled survival estimate for each data source at 15 years, 20 years, and 25 years, using a fixed-effects model. This study is registered with PROSPERO, number CRD42018105188. FINDINGS: From 4363 references found by our initial search, we identified 33 case series in 30 eligible articles, which reported all-cause survival for 6490 TKRs (26 case series) and 742 UKRs (seven case series). No case series reporting on patellofemoral replacements met our inclusion criteria, and no case series reported 25 year survival for TKR. The estimated 25 year survival for UKR (based on one case series) was 72·0% (95% CI 58·0-95·0). Registries contributed 299 291 TKRs (47 series) and 7714 UKRs (five series). The pooled registry 25 year survival of TKRs (14 registries) was 82·3% (95% CI 81·3-83·2) and of UKRs (four registries) was 69·8% (67·6-72·1). INTERPRETATION: Our pooled registry data, which we believe to be more accurate than the case series data, shows that approximately 82% of TKRs last 25 years and 70% of UKRs last 25 years. These findings will be of use to patients and health-care providers; further information is required to predict exactly how long specific knee replacements will last. FUNDING: The National Joint Registry for England, Wales, Northern Ireland, and Isle of Man and the Royal College of Surgeons of England.


Subject(s)
Arthroplasty, Replacement, Knee/adverse effects , Prosthesis Failure , Registries , Reoperation , Follow-Up Studies , Humans , Osteoarthritis, Knee/surgery , Time Factors
5.
Paediatr Anaesth ; 25(1): 36-43, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25280003

ABSTRACT

Recent studies have reported perioperative pulmonary aspiration in pediatric practice to be an uncommon problem associated with low morbidity and mortality. This paper examines the recent publications in both the adult and pediatric literature and looks at some of the potential risk factors involved, both patient and anesthetic, in the development of aspiration of gastric contents. We also look at the risk of severe morbidity following pulmonary aspiration and speculate on possible reasons behind the assertion that pulmonary aspiration in pediatric anesthetic practice is rare and a low-risk event.


Subject(s)
Anesthesia/adverse effects , Pneumonia, Aspiration/epidemiology , Respiratory Aspiration of Gastric Contents/epidemiology , Adult , Aging/physiology , Child , Humans , Perioperative Care , Pneumonia, Aspiration/mortality , Respiratory Aspiration of Gastric Contents/mortality , Risk
6.
Paediatr Anaesth ; 23(8): 702-11, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23763657

ABSTRACT

BACKGROUND: Pulmonary aspiration of gastric contents is a potentially devastating complication of anesthesia. AIMS: This prospective multicenter survey of specialist pediatric centers in the UK set out to elucidate the incidence, risk factors, and the outcome of such events. The survey took place over a twelve-month period via a web-based secure reporting system. RESULTS: Over the twelve-month period, 24 cases of pulmonary aspiration were reported. Over that time period, there were 118 371 cases performed at the eleven pediatric centers. The overall incidence of pulmonary aspiration is therefore 1 in 4932 cases or 2 in 10 000 cases. Over that time period, there were 18 cases during elective surgery and six cases in nonelective/emergency surgery. The incidence of pulmonary aspiration in the elective situation is therefore 1 in 5076 cases or 2.0 per 10 000 cases. The incidence in emergency procedures is 1 in 4498 cases or 2.2 per 10 000 cases. The timing and severity of deterioration were recorded. In the study period, 8 of 24 cases did not deteriorate, 13 of 24 deteriorated with immediate effect, and the further 3 of 24 deteriorated within the next hour. The deterioration was mild in 11 patients requiring medical management only, and the deterioration was severe in five patients. Those five patients required ventilation for varying durations of time. All patients made a full recovery. CONCLUSIONS: This multicenter survey of specialist pediatric centers in the UK over a one-year period reveals a low incidence of pulmonary aspiration in both elective and emergency cases. All patients made a full recovery.


Subject(s)
Anesthesiology/statistics & numerical data , Pediatrics/statistics & numerical data , Respiratory Aspiration of Gastric Contents/epidemiology , Respiratory Aspiration of Gastric Contents/therapy , Adolescent , Age Factors , Anesthesiology/standards , Bronchoscopy , Child , Child, Preschool , Comorbidity , Disease Progression , Elective Surgical Procedures , Emergency Medical Services , Female , Health Care Surveys , Humans , Infant , Infant, Newborn , Intraoperative Complications/epidemiology , Laryngoscopy , Male , Prospective Studies , Respiration, Artificial , Risk Factors , Sex Factors , Treatment Outcome , United Kingdom/epidemiology
7.
Paediatr Anaesth ; 22(8): 745-51, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22672476

ABSTRACT

AIM: To assess the effect of bone marrow transplantation (BMT), enzyme replacement therapy (ERT), and a fiberoptic endotracheal intubation technique in patients with mucopolysaccharidosis type I (MPS I, Hurler syndrome). BACKGROUND: The mucopolysaccharidoses are inherited metabolic conditions with a well-documented association with difficult airway management. We present the largest series to date of patients with Hurler syndrome (MPS I) and look at the impact of new treatments, such as BMT and ERT, on anesthesia and airway management. METHODS/MATERIALS: We carried out a retrospective chart review of patients with MPSI undergoing anesthesia over 9 years at the Royal Manchester Children's Hospital. Data were collected on incidence of difficult and failed intubation and airway difficulties under anesthesia. RESULTS: There were 39 patients identified, of which 20 had the attenuated form of MPS I and received ERT, 18 were treated by BMT and one patient received neither treatment. These patients had a total of 114 general anesthetics for 141 procedures. The incidence of airway complications overall is lower than previously reported at 31%. Patients with the attenuated form of the disease on ERT still have a high incidence of airway problems at 57% and a failed intubation rate of 3%. BMT patients on the other hand have a much lower incidence of airway complications at 14%, and there were no failed intubations in this group. CONCLUSIONS: Managing the MPS1 patient continues to be a challenge but with treatment and newer forms of airway management it is improving.


Subject(s)
Airway Management/methods , Anesthesia , Bone Marrow Transplantation/methods , Enzyme Replacement Therapy , Mucopolysaccharidosis I/therapy , Adolescent , Child , Child, Preschool , Female , Fiber Optic Technology , Humans , Infant , Laryngeal Masks , Laryngoscopy , Male , Mucopolysaccharidosis I/physiopathology , Mucopolysaccharidosis I/surgery , Retrospective Studies , Treatment Failure
8.
Paediatr Anaesth ; 19 Suppl 1: 77-87, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19572847

ABSTRACT

This article looks at the current techniques and equipment recommended for the management of the difficult intubation scenario in pediatric practice. We discuss the general considerations including preoperative preparation, the preferred anesthetic technique and the use of both rigid laryngoscopic and fiberoptic techniques for intubation. The unanticipated scenario is also discussed.


Subject(s)
Anesthesia, Inhalation/methods , Intubation, Intratracheal , Anesthesia, Inhalation/instrumentation , Child , Child, Preschool , Guidelines as Topic , Humans , Infant , Infant, Newborn , Laryngeal Masks , Laryngoscopes , Optical Fibers , Preanesthetic Medication , Preoperative Care , Respiration, Artificial
11.
Paediatr Anaesth ; 17(7): 697-702, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17564654

ABSTRACT

Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these patients. We present our experience of regional anesthetic blocks used in five patients with the infantile form of glycogen storage disease type II with and without sedation for 11 surgical procedures during a clinical trial of replacement therapy for this condition. Both femoral nerve blockade and caudal epidural blockade were used with good result. The relative merits of the type of block are discussed in addition to the choice of sedation and risks of general anesthesia. The avoidance of general anesthesia in the newly presenting patient with Pompe's disease may reduce potential morbidity until enzyme replacement has been established.


Subject(s)
Anesthesia, Conduction , Anesthesia, General , Glycogen Storage Disease Type II/pathology , Anesthetics, Combined , Biopsy , Catheters, Indwelling , Child, Preschool , Conscious Sedation , Female , Femoral Nerve , Glycogen/metabolism , Glycogen Storage Disease Type II/diagnosis , Humans , Infant , Lidocaine , Lidocaine, Prilocaine Drug Combination , Male , Muscle, Skeletal/metabolism , Muscle, Skeletal/pathology , Nerve Block , Prilocaine , Treatment Outcome
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