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1.
Orthop Rev (Pavia) ; 12(1): 8359, 2020 Apr 22.
Article in English | MEDLINE | ID: mdl-32391132

ABSTRACT

Poly-ether-ether-ketone (PEEK) cages have lower modulus of elasticity when compared with Titanium (TTN) cages. This suggests that PEEK-cages could show a lower rate of subsidence after anterior cervical discectomy-fusion (ACDF) and might lead to a lower loss of correction. We investigated the one to five year-results of standalone PEEK-TTN-porous coated cages in a patient cohort from 2014 to 2017. The patients underwent single-level ACDF for disc herniation and degenerative discopathy. Clinical and radiological outcome were assessed in 50 eligible patients after a mean of 27 months. Results: Solid arthrodesis was found in 84%. Neck disability index (NDI), and visual analogue scale (VAS) of neck and arm show comparable results to the literature. Conclusions: Clinical and radiological outcomes of ACDF with PEEK-body-cages with a porous coated surface show good bony integration. The modulus of elasticity, design, shape, size, cage surface architecture, as well as bone density, endplate preparation, radical microdiscectomy and distraction during surgery should be considered as important factors influencing the clinical results. One main advantage, over titanium cages, is the absence of MRI artifacts, allowing an excellent postoperative follow-up.

2.
Rev. esp. med. legal ; 46(1): 20-27, ene.-mar. 2020. tab
Article in Spanish | IBECS | ID: ibc-193986

ABSTRACT

El objetivo de la monitorización neurofisiológica intraoperatoria es la detección de daño o alteración funcional en el sistema nervioso lo más precozmente posible, asegurando la funcionalidad medular, evitando las complicaciones neurológicas. Sin embargo, la falta de estandarización en la metodología, junto con cierta inconsistencia en los estudios sobre su utilidad, limita el establecimiento de unas recomendaciones universales para su utilización. El presente trabajo pretende revisar los procedimientos de monitorización neurofisiológica, sus fortalezas y debilidades, así como la conveniencia de su empleo en cirugía espinal. Concluimos que, con carácter general, su falta de uso en dicha cirugía no contraviene la «lex artis», pues no existe evidencia de que pueda ayudar en revertir el daño neurológico. Sin embargo, puede emplearse como elemento de prueba tanto para detectar el momento y el tipo de daño neurológico como para aumentar la defensibilidad. Se requieren protocolos de uso, bien por las sociedades científicas o por los propios centros hospitalarios


The purpose of neurophysiological monitoring during surgery is to identify damage or functional neurological disturbances as soon as possible, ensuring spinal cord functionality and avoiding neurological complications. However, the lack of standardisation of the methodology, together with some inconsistencies in the studies on its usefulness, limit the establishment of universal recommendations for its use. The present paper intends to review neurophysiological monitoring procedures during surgery, including their strength and weaknesses, as well as to assess the convenience of their use during spinal surgery. It is concluded that, in general, the lack of its use in this surgery does not legally contravene the standard of care, as there is no evidence it could result in reverting neurological damage. Nevertheless, it can be used as evidence both in detecting the time and kind of neurological injury, and for increasing the defensibility. Protocols of use, provided either by scientific societies or hospitals themselves, are required


Subject(s)
Humans , Intraoperative Neurophysiological Monitoring/methods , Malpractice/legislation & jurisprudence , Surgical Procedures, Operative/legislation & jurisprudence , Intraoperative Complications/diagnostic imaging , Insurance, Liability/trends , Spinal Cord/surgery
3.
Rev. Fac. Cienc. Méd. Univ. Cuenca ; 38(1): 43-51, 2020. ilus, tab
Article in Spanish | LILACS | ID: biblio-1100678

ABSTRACT

Introducción: la obesidad afecta al 22.1% de la población ecuatoriana y su prevalencia continúa en aumento. La cirugía bariátrica constituye una opción efectiva para su tratamiento, pero alcanza apenas al 1% de la población afectada. Objetivo: describir la experiencia en la implementación del programa de cirugía bariátrica en el Hospital de Especialidades de las Fuerzas Armadas N°1. Metodología: estudio descriptivo, retrospectivo, desde febrero del 2016 hasta febrero del 2019; se reportó características demográficas, seguimiento prequirúrgico, evolución del peso antes y después del procedimiento a corto, mediano y largo plazo. Resultados: se incluyeron 39 individuos, 74.4% mujeres y 25.6% hombres. La edad media fue 45.9 años (DS ±9.9 años); el índice de masa corporal medio en la primera valoración fue 41.04 kg/m2 (DS ±5.1), al primer mes se logró un porcentaje de reducción del exceso de peso del 21.7 % (DS ±14.7), al tercer mes del 42.8 % (DS ±18.27) y al año del 66.3 % (DS ±12.6), sin embargo, 13 pacientes abandonaron el seguimiento. Conclusión: a pesar de la dificultad técnica y operativa para implementar un programa de cirugía bariátrica, queda demostrado su beneficio.


Introduction: the obesity affects about 22.1% of the Ecuadorian population and its prevalence continues to increase. Bariatric surgery is an effective option for its treatment, but it reaches only 1% of the affected population. Objective: to describe the experience in the implementation of bariatric surgery program at the Hospital de Especialidades de las Fuerzas N° 1. Methodology: It is a descriptive and retrospective study, it was conducted from February 2016 to February 2019; demographic characteristics, presurgical follow-up, weight evolution before and after the procedure was measured at short, medium and long term. Results: A total of 39 individuals were included, 74.4% women and 25.6% men. The average age was 45.9 years (SD ± 9.9 years); the mean body mass index at the first evaluation was 41.04 kg / m2 (DS ± 5.1), at the first month a percentage reduction of excess weight of 21.7% (DS ± 14.7) was achieved, at the third month 42.8% ( SD ± 18.27) and one year after 66.3% (DS ± 12.6), however, 13 patients abandoned follow-up. Conclusion: despite the technical and operational difficulties in implementing a bariatric surgery program, its benefit has been demonstrated.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Bariatric Surgery , Obesity/surgery , Gastric Bypass , Weight Loss , Body Mass Index , Retrospective Studies , Follow-Up Studies , Treatment Outcome , Bariatric Surgery/methods
4.
Rev. esp. med. legal ; 45(4): 147-154, oct.-dic. 2019. ilus, graf
Article in Spanish | IBECS | ID: ibc-188619

ABSTRACT

La donación corporal es la base de los programas de trasplantes, cuya regulación se fundamenta en los derechos del donante y receptor. Sin embargo, si su objetivo no es asistencial, la normativa difiere tanto en vivos como en fallecidos. Las llamadas «técnicas de imagen» permiten obtener ficheros digitales con el cuerpo virtual del paciente, lo que brinda una nueva posibilidad: la donación corporal virtual, no regulada en España y tampoco ajustada a la normativa del resto de las donaciones. Presentamos un programa de donación corporal, analizando sus características, aspectos médico-legales, clínicos, de organización y funcionamiento. Contar con un número ilimitado de especímenes virtuales impulsa una nueva forma de docencia e investigación. Tiene, además, ventajas para la formación de los profesionales en técnicas de autopsia virtual. Creemos que este programa, pionero en España, puede servir para extender iniciativas similares de utilidad ilimitada en docencia e investigación en ciencias forenses, morfológicas y afines


Body donation is in the basis of transplantation programs, founded on receptor and donor rights. Nevertheless, if the purpose is not directed to healthcare, the regulation is different both in live or deceased individuals. "Imaging techniques" generates digital files containing the «virtual body» of the patient, raising a new possibility: virtual body donation, which is not regulated in Spain and would not be compliant with legal requirements for other ways of donation. A pioneer program for virtual body donation is presented, analysing its characteristics, medico-legal issues, organisation and functioning. Having an unlimited number of virtual specimens (normal and pathological) could support a new way for teaching and research. These resources would also have the advantage of learning virtual biopsy (virtopsy). It is thought that these programs, pioneers in Spain, could be useful for introducing similar initiatives that would have unlimited applications in teaching and research both in forensic and morphological sciences


Subject(s)
Humans , Tissue Donors/legislation & jurisprudence , Living Donors/legislation & jurisprudence , Bioethical Issues , Virtual Reality , Informed Consent/legislation & jurisprudence , Informed Consent/standards
5.
Orthop Rev (Pavia) ; 11(2): 7774, 2019 May 23.
Article in English | MEDLINE | ID: mdl-31210909

ABSTRACT

The time interval between the date of trauma and the diagnosis of vertebral column fractures hinders management and increases liability. We have examined the features and implications of this delay. 585 consecutive thoracolumbar fractures (2005-2016), were considered; 382 (65.30%) were males and 203 (34.70%) females. Mean age was 51 yr. Fall from a height (187; 31.97%), simple fall (147; 25.13%) and road accidents (111; 18.97%) were the most frequent causes of trauma. Physical exertion caused 8.38% (N=49). 142 patients (24.27%) were not diagnosed on the injury day (mean = 3.2 days). Delay was longer in females (mean = 5.5 vs. 2.7 days) and shorter in falls from a height (mean = 2.3) or road accidents (2.8). Mean age of diagnosed on the injury day differed from those diagnosed in the first month (49.2 vs 60.1). Plain X-ray signs were found in 7 misdiagnosed cases (46.6%). Delay was more frequent in low mineralization cases. Diagnostic delay of spine fractures is frequent. Some risk profiles can help to reduce it. Careful emergency X-ray examination is encouraged, as well as early magnetic resonance imaging in risk profiles.

6.
J Neurosurg Spine ; 25(5): 556-565, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27258476

ABSTRACT

OBJECTIVE Recent studies have described encouraging outcomes after cervical total disc replacement (cTDR), but there are also critical debates regarding the long-term effects of heterotopic ossification (HO) and the prevalence of adjacent-level degeneration. The aim in this paper was to provide 4-year clinical and radiographic outcome results on the activ C disc prosthesis. METHODS A total of 200 subjects underwent single-level activ C (Aesculap AG) implantation between C-3 and C-7 for the treatment of symptomatic degenerative disc disease. Clinical and radiographic assessments were performed preoperatively, intraoperatively, at discharge, and again at 6 weeks, 6 months, 1 year, 2 years, and 4 years. Radiographic evaluations were done by an independent core laboratory using a specific software for quantitative motion analysis. RESULTS Neck Disability Index (NDI) and visual analog scale (VAS) score for neck and arm pain decreased significantly from baseline to the 4-year follow-up. The mean improvement for NDI was 20, for VAS severity and frequency of neck pain 26.4 and 28, and for VAS severity and frequency of arm pain 30.7 and 35.1, respectively. The neurological situation improved for the majority of patients (86.4%); 76.1% of cases were asymptomatic. Subsequent surgical interventions were reported in 7% of the cases, including device removals in 3%. In 2.5% a subsidence greater than 3 mm was recorded; 1 of these cases also had a migration greater than 3 mm. No device displacement, expulsion, disassembly, loose or fractured device, osteolysis, or facet joint degeneration at the index level was observed. Segmental lordotic alignment changed from -2.4° preoperatively to -6.2° at 4 years, and postoperative height was maintained during the follow-up. Advanced HO (Grade III and IV) was present in 27.1% of the cases; 82.4% showed segmental mobility. A progression of radiographic adjacent-segment degeneration occurred in 28.2%, but only 4.5% required surgical treatment. CONCLUSIONS The activ C is a safe and effective device for cervical disc replacement confirming the encouraging results after cTDR. Clinical trial registration no.: NCT02492724 ( clinicaltrials.gov ).


Subject(s)
Cervical Vertebrae , Intervertebral Disc Degeneration/diagnostic imaging , Intervertebral Disc Degeneration/surgery , Joint Prosthesis , Total Disc Replacement , Adult , Decompression, Surgical/methods , Disability Evaluation , Diskectomy/methods , Europe , Female , Follow-Up Studies , Humans , Intervertebral Disc Degeneration/complications , Lordosis/diagnostic imaging , Lordosis/etiology , Lordosis/surgery , Male , Neck Pain/diagnostic imaging , Neck Pain/etiology , Neck Pain/surgery , Pain Measurement , Prospective Studies , Severity of Illness Index , Software , Time Factors , Total Disc Replacement/instrumentation , Total Disc Replacement/methods , Treatment Outcome
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