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1.
Zhonghua Wai Ke Za Zhi ; 53(3): 189-92, 2015 Mar.
Artículo en Zh | MEDLINE | ID: mdl-26269013

RESUMEN

OBJECTIVE: To provide a theoretical basis for designing of lumbar intervertebral disc prosthesis by collecting the data of the lumbar endplate morphology. METHODS: A total of 100 healthy adults were measured about the following parameters: lumbar lordosis, the Cobb angle of each segment, the concavity depth (ECD) of the endplate, the location of concavity apex (ECA) of the endplate. And a correlation analysis on lumbar lordosis and ECD, ECA was made, respectively. RESULTS: In total, 100 volunteers were measured. The mean age of the volunteer was 40 years (range 20 - 50 years); the average depth of ECD was (2. 37 ± 1. 42) mm, the average location of ECA was (52. 21 ± 9. 70) %; the average depth of ECD of inferior endplate (IEP) was (2. 81 ± 1. 52) mm (0. 54 - 7. 60 mm), and the parameter of the superior endplate (SEP) was (1. 94 ± 1. 16)mm(0. 39 - 6. 10 mm). The average depth of ECD of the IEP was bigger than of the SEP for each lumbar vertebral body. Most of the location of ECA was at the back of the intervertebral body, the average location of ECA of IEP was (49. 60 ± 8. 78) % (22. 57% - 75. 58%), and the parameter of the SEP was (55. 03 ± 9. 90) % (16. 03% -75. 58%); the mean angle of lumbar lordosis was 39. 760 11. 25°(13. 8° - 72. 00°). There was no obvious correlation between the lumbar lordosis and the ECD (r -0. 193, P =0. 195), neither was the location of ECA(r =0. 080, P =0. 592). CONCLUSION: Most of the location of ECA is at the back of the intervertebral body, the average depth of ECD is 2. 37 mm, the average location of ECA is 52. 21%.


Asunto(s)
Vértebras Lumbares/anatomía & histología , Columna Vertebral/anatomía & histología , Adulto , Humanos , Disco Intervertebral , Región Lumbosacra/anatomía & histología , Persona de Mediana Edad , Prótesis e Implantes , Estándares de Referencia , Adulto Joven
2.
J Int Med Res ; 48(4): 300060519895868, 2020 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-31884849

RESUMEN

OBJECTIVE: A systematic review and meta-analysis was carried out to evaluate the efficacy and safety of Botulinum Toxin Type A in painful knee osteoarthritis. METHODS: The EMBASE and MEDLINE databases were searched to identify randomized controlled trials (RCTs) of Botulinum Toxin Type A in the treatment of painful knee osteoarthritis. The references of included literature were also searched. RESULTS: Five articles involving 5 RCTs including 314 patients were included in this analysis. There was a significant difference between Botulinum Toxin Type A and placebo in the visual analog scale (VAS) pain scale and Western Ontario & McMaster Universities Osteoarthritis Index (WOMAC) questionnaire score in both the short-term (≤4 weeks) and long-term (≥8 weeks) treatment period. There were no serious adverse events in the Botulinum Toxin Type A groups. CONCLUSIONS: This meta-analysis suggests that Botulinum Toxin Type A is effective and safe in the painful knee OA treatment. However, high-quality randomized controlled studies are still needed to further confirm our findings.


Asunto(s)
Toxinas Botulínicas Tipo A , Osteoartritis de la Rodilla , Toxinas Botulínicas Tipo A/uso terapéutico , Humanos , Articulación de la Rodilla , Osteoartritis de la Rodilla/tratamiento farmacológico , Dolor/tratamiento farmacológico , Dimensión del Dolor , Resultado del Tratamiento
3.
Medicine (Baltimore) ; 99(19): e20143, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-32384498

RESUMEN

STUDY DESIGN: The present study was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) statement. OBJECTIVE: The present study aimed to conduct a systematic review of overlapping meta-analyses comparing ACDR with fusion for treating CDDD in order to assist decision makers in their selection among conflicting meta-analyses and to provide treatment recommendations based on the best available evidence. SUMMARY OF BACKGROUND DATA: Although several meta-analyses have been performed to compare total disc replacement (TDR) and fusion for treating cervical degenerative disc disease (CDDD), their findings are inconsistent. METHODS: Multiple databases were comprehensively searched for meta-analyses comparing TDR with fusion for treating CDDD. The meta-analyses that comprised only randomized controlled trials (RCTs) were included. Two authors independently assessed the meta-analysis study quality and extracted the data. The Jadad decision algorithm was used to ascertain which meta-analysis studies represented the best evidence. RESULTS: A total of 14 meta-analysis studies were included. All these studies only included RCTs and were determined as Level-II evidence. CONCLUSIONS: Cervical disc arthroplasty was superior compared to anterior discectomy and fusion for the treatment of symptomatic cervical disc disease.


Asunto(s)
Vértebras Cervicales/cirugía , Discectomía/métodos , Degeneración del Disco Intervertebral/cirugía , Fusión Vertebral/métodos , Reeemplazo Total de Disco/métodos , Algoritmos , Discectomía/efectos adversos , Humanos , Metaanálisis como Asunto , Tempo Operativo , Ensayos Clínicos Controlados Aleatorios como Asunto , Rango del Movimiento Articular , Reoperación , Fusión Vertebral/efectos adversos , Reeemplazo Total de Disco/efectos adversos
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