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1.
Chinese Journal of Surgery ; (12): 430-442, 2021.
Article in Chinese | WPRIM | ID: wpr-878281

ABSTRACT

Prosthetic joint infection is one of the most serious complications after artificial joint replacement.Accurate diagnosis and proper standardized treatment are the keys to improve the cure rate of prosthetic joint infection,reduce the rate of recurrence and disability,and restore limb function.Regarding the diagnosis and treatment of prosthetic joint infection,although relevant research has progressed rapidly in recent years,there are still many problems that have not been well understood and explained,and there are still big differences and controversies in many aspects.This has brought a lot of confusion to clinicians during their daily practice.In order to make the diagnosis and treatment of prosthetic joint infection in China more standardized,a group of domestic experts in related fields was organized by the Joint Surgery Committee of the Chinese Orthopaedic Association to search the literature and integrate expert opinions,and compiled the "Guidelines for the diagnosis and treatment of prosthetic joint infection".Those most important and clinically concerned issues are elaborated,including the diagnostic criteria, standardized diagnostic algorithm,proper application of important tests,treatment principles,and the correct selection of various treatment options.Targeted and actionable recommendations are proposed.This guideline is expected to provide references for domestic colleagues in the diagnosis and treatment of prosthetic joint infection.


Subject(s)
Humans , Arthroplasty, Replacement/adverse effects , China , Prosthesis-Related Infections/therapy
2.
Braz. j. infect. dis ; 21(6): 613-619, Nov.-Dec. 2017. tab
Article in English | LILACS | ID: biblio-888916

ABSTRACT

ABSTRACT Purposes: Shoulder arthroplasty (SA) has been performed by many years for the treatment of several conditions, including osteoarthritis and proximal humeral fractures following trauma. Surgical site infection (SSI) following Shoulder arthroplasty remains a challenge, contributing to increased morbidity and costs. Identification of risk factors may help implementing adequate strategies to prevent infection. We aimed to identify pre- and intra-operative risk factors associated with deep infections after Shoulder arthroplasty. Methods: An unmatched case-control study was conducted to describe the prevalence, clinical and microbiological findings, and to evaluate patient and surgical risk factors for prosthetic shoulder infection (PSI), among 158 patients who underwent SA due to any reason, at a tertiary public university institution. Risk factors for PSI was assessed by uni- and multivariate analyses using multiple logistic regression. Results: 168 SA from 158 patients were analyzed, with an overall infection rate of 9.5% (16/168 cases). Subjects undergoing SA with American Society of Anesthesiologists (ASA) grade III or higher (odds ratio [OR] = 5.30, 95% confidence interval [CI] = 1.58-17.79, p < 0.013) and presenting local hematoma after surgery (odds ratio [OR] = 7.10, 95% confidence interval [CI] = 1.09-46.09, p = 0.04) had higher risk for PSI on univariate analysis. However, only ASA score grade III or higher remained significant on multivariate analysis (OR = 4.74, 95% CI = 1.33-16.92, p = 0.016). Gram-positive cocci and Gram-negative bacilli were equally isolated in 50% of cases; however, the most commonly detected bacterium was Pseudomonas aeruginosa (18.7%). Conclusion: This study provides evidence suggesting that patient-related known factors such as higher ASA score predisposes to shoulder arthroplasty-associated infection. Furthermore, unusual pathogens associated with PSI were identified.


Subject(s)
Humans , Female , Middle Aged , Aged , Aged, 80 and over , Shoulder Joint/surgery , Prosthesis-Related Infections/microbiology , Arthroplasty, Replacement/adverse effects , Joint Diseases/surgery , Joint Prosthesis/microbiology , Shoulder Joint/microbiology , Case-Control Studies , Logistic Models , Retrospective Studies , Risk Factors
3.
Clinics in Orthopedic Surgery ; : 288-297, 2016.
Article in English | WPRIM | ID: wpr-93984

ABSTRACT

BACKGROUND: Different implant designs are utilized in reverse shoulder arthroplasty. The purpose of this systematic review was to evaluate the results of reverse shoulder arthroplasty using a traditional (Grammont) prosthesis and a lateralized prosthesis for the treatment of cuff tear arthropathy and massive irreparable rotator cuff tears. METHODS: A systematic review of the literature was performed via a search of two electronic databases. Two reviewers evaluated the quality of methodology and retrieved data from each included study. In cases where the outcomes data were similar between studies, the data were pooled using frequency-weighted mean values to generate summary outcomes. RESULTS: Thirteen studies met the inclusion and exclusion criteria. Demographics were similar between treatment groups. The frequency-weighted mean active external rotation was 24° in the traditional group and 46° in the lateralized group (p = 0.0001). Scapular notching was noted in 44.9% of patients in the traditional group compared to 5.4% of patients in the lateralized group (p = 0.0001). The rate of clinically significant glenoid loosening was 1.8% in the traditional group and 8.8% in the lateralized group (p = 0.003). CONCLUSIONS: Both the traditional Grammont and the lateralized offset reverse arthroplasty designs can improve pain and function in patients with diagnoses of cuff tear arthropathy and irreparable rotator cuff tear. While a lateralized design can result in increased active external rotation and decreased rates of scapular notching, there may be a higher rate of glenoid baseplate loosening.


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Arthroplasty, Replacement/adverse effects , Postoperative Complications , Prosthesis Design , Rotator Cuff/surgery , Shoulder Prosthesis/adverse effects , Treatment Outcome
4.
Coluna/Columna ; 14(2): 85-87, Apr.-June 2015. tab, ilus
Article in English | LILACS | ID: lil-755850

ABSTRACT

OBJECTIVE:

To review the medical records of patients who underwent surgery for placement of cervical disc prosthesis after two years of postoperative follow-up, showing the basic epidemiological data, the technical aspects and the incidence of complications.

METHODS:

Medical records of seven patients who underwent surgery for placement of cervical disc prosthesis were reviewed after two years of follow-up, at the Institute of Orthopedics and Traumatology, Faculty of Medicine, University of São Paulo.

RESULTS:

The average age of patients participating in this study was 43.86 years. Six patients (85.7%) had one level approached while one patient (14.3%) had two levels addressed. The level C5-C6 has been approached in one patient (14.3%) while the C6-C7 level was addressed in five patients (71.4%). One patient (14.3%) had these two levels being addressed, C5-C6 and C6-C7. The mean operative time was 164.29±40 minutes. Three patients were hospitalized for 2 days and four for 3 days making an average of 2.57±0.535 days. Two patients (28.6%) underwent a new surgical intervention due to loosening of the prosthesis. The mean follow-up was 28.14±5.178 months (23-35 months).

CONCLUSIONS:

Although cervical arthroplasty appears to be a safe procedure and present promising results in our study as well as in many other studies, it requires long-term studies.

.

OBJETIVO:

Revisar las historias clínicas de los pacientes que se sometieron a cirugía para colocación de prótesis de disco cervical después de dos años de seguimiento postoperatorio, que muestran los datos epidemiológicos básicos, los aspectos técnicos y la incidencia de complicaciones.

MÉTODOS:

Fueron revisados los registros médicos de siete pacientes que se sometieron a cirugía para colocación de prótesis de disco cervical después de dos años de seguimiento en el Instituto de Ortopedia y Traumatología de la Facultad de Medicina de la Universidad de São Paulo.

RESULTADOS:

La edad media de los pacientes que participaron en este estudio fue de 43,86 años. Seis pacientes (85,7%) tuvieron un nivel a ser abordado mientras que un paciente (14,3%) tuvo dos niveles abordados. El nivel C5-C6 ha sido tratado por separado en un paciente (14,3%), mientras que el nivel de C6-C7 fue tratado en cinco pacientes (71,4%). Un paciente (14,3%) tuvo dos niveles abordados, C5-C6 y C6-C7. El tiempo quirúrgico promedio fue de 164,29 ± 40 minutos. Tres pacientes fueron hospitalizados por 2 días y cuatro por 3 días, lo que hace una media de 2,57 ± 0,535 días. Dos pacientes (28,6%) fueron sometidos a una nueva intervención quirúrgica debido al aflojamiento de la prótesis. El promedio de seguimiento fue de 28,14 ± 5,178 meses (23-35 meses).

CONCLUSIONES:

Aunque la artroplastia cervical parezca un ser procedimiento seguro y que presente resultados prometedores en nuestro estudio, así como en muchos otros estudios, necesita estudios a largo plazo.

.

OBJETIVO:

Revisar os prontuários de pacientes que foram submetidos à cirurgia para colocação de prótese de disco cervical, após dois anos de seguimento pós-operatório, evidenciando os dados epidemiológicos básicos, os aspectos da técnica e a incidência de complicações.

MÉTODO:

Foram revisados os prontuários de sete pacientes submetidos à cirurgia para colocação de prótese de disco cervical após dois anos de seguimento no Instituto de Ortopedia e Traumatologia da Faculdade de Medicina da Universidade de São Paulo.

RESULTADO:

A média de idade dos pacientes participantes no presente estudo foi 43,86 anos. Seis pacientes (85,7%) tiveram um nível abordado enquanto um paciente (14,3%) teve dois níveis abordados. O nível C5-C6 foi abordado isoladamente em um paciente (14,3%) enquanto o nível C6-C7 em cinco pacientes (71,4%). Um paciente (14,3%) teve dois níveis abordados sendo estes C5-C6 e C6-C7. A média de tempo cirúrgico foi de 164,29 ± 40 minutos. Três pacientes ficaram internados por 2 dias e quatro por 3 dias, perfazendo uma média de 2,57 ± 0,535 dias. Dois pacientes (28,6%) foram submetidos a reintervenção cirúrgica devido à soltura da prótese. O acompanhamento médio foi de 28,14 ± 5,178 meses (23-35 meses).

CONCLUSÕES:

A artroplastia cervical, apesar de parecer ser um procedimento seguro e apresentar resultados promissores em nosso estudo, bem como em diversos estudos da literatura, necessita de estudos a longo prazo.

.


Subject(s)
Humans , Arthroplasty, Replacement/adverse effects , Postoperative Period , Prostheses and Implants , Intervertebral Disc Degeneration
5.
Clinics in Orthopedic Surgery ; : 359-364, 2015.
Article in English | WPRIM | ID: wpr-127319

ABSTRACT

BACKGROUND: The delta reverse shoulder replacement system was developed for the treatment of rotator cuff arthropathy so that the deltoid can substitute for the deficient rotator cuff. To evaluate the results of delta reverse shoulder replacement for functional improvement and complications in a consecutive series by a single surgeon over a period of six years with a minimum follow-up of 2 years. METHODS: The data were collected retrospectively from electronic theatre records. Over a period of 6 years (2006-2012), 46 cases that fulfilled the inclusion criteria were identified. There were 34 females and 12 males. The average age of patients was 76.2 years (range, 58 to 87 years). A single surgeon performed all procedures using the anterosuperior approach. The mean follow-up time was 49 months (range, 24 to 91 months). All cases had preoperative and postoperative Constant scores. We collected the data on indications, hospital stay, and change in the Constant score, complications, and reoperation rates. RESULTS: The main indication for surgery was rotator cuff arthropathy (52.2%), followed by massive rotator cuff tear (28.3%), osteoarthritis (8.7%), fractures (6.5%), and rheumatoid arthritis (4.3%). Also, 65.2% of the cases were referred by general practitioners, 26% of the cases were referred by other consultants, and 8.8% of the cases were already under the care of a shoulder surgeon. The average preoperative Constant score was 23.5 (range, 8 to 59). The average Constant score at the final follow-up was 56 (range, 22 to 83). On average, there was an improvement of 33 points in the Constant score. The improvement in the Constant score was significant (p < 0.001). We observed complications in four patients (8.6%). Three of four patients (6.5%) needed reoperation. The first complication was pulmonary embolism in the early postoperative period. The other complications included dissociation of the glenosphere from the metaglene, deltoid detachment, and stitch abscess. CONCLUSIONS: This is a single-surgeon, single-approach series of 46 cases with a minimum follow-up of 2 years. At this stage, the results are encouraging with no cases of loosening, dislocation, or nerve injury.


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Young Adult , Arthroplasty, Replacement/adverse effects , Follow-Up Studies , Postoperative Complications/epidemiology , Reoperation/statistics & numerical data , Retrospective Studies , Shoulder Joint/surgery
6.
Clinics in Orthopedic Surgery ; : 196-202, 2010.
Article in English | WPRIM | ID: wpr-46906

ABSTRACT

Rotator cuff deficient arthritis of the glenohumeral joint, especially cuff tear arthropathy, has proved a challenging clinical entity for orthopaedic surgeons ever since Charles Neer originally detailed the problem in 1983. Understanding has improved regarding the pathophysiology and pathomechanics underlying cuff tear arthropathy. Surgical reconstruction options can lead to excellent outcomes for patients afflicted with these painful and functionally limited shoulders. Humeral hemiarthroplasty and reverse total shoulder arthroplasty have jumped to the forefront in the treatment of cuff tear arthropathy. As studies continue to look at the results of these procedures in cuff tear arthropathy, existing indications and treatment algorithms will be further refined. In this article the history and pathophysiology of cuff tear arthropathy are reviewed. Additionally, the clinical findings and results of surgical reconstruction are discussed.


Subject(s)
Humans , Arthritis/diagnosis , Arthroplasty, Replacement/adverse effects , Magnetic Resonance Imaging , Rotator Cuff/injuries , Shoulder Joint/diagnostic imaging , Tomography, X-Ray Computed
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