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1.
Acta Ortop Mex ; 38(3): 155-163, 2024.
Article in Spanish | MEDLINE | ID: mdl-38862145

ABSTRACT

INTRODUCTION: metatarsophalangeal resection arthroplasty is considered a salvage surgical procedure able to improve the quality of life of patients with major forefoot deformities. MATERIAL AND METHODS: a retrospective observational study of 31 patients (36 feet) with major forefoot deformities operated at our institution was performed. Thirty two feet required additional surgery involving the first ray, most of them (72.2%) through MTP joint fusion. The mean follow-up period was 10.3 ± 4.6 years. Most patients were women (87.1%), the mean age was 74.2 ± 11.5 years. RESULTS: at the final follow-up, mean AOFAS score was 77.9 ± 10.2 points and mean MOxFQ score was 18.3 ± 8.3 points. Visual analog scale (VAS) for pain improved significantly from 7.5 ± 1.2 points to 3.4 ± 2.1 points on average. Good clinical results were also reported on ability to put on shoes comfortably. The mean resection arthroplasty spaces at the end of the study were 1.3, 1.8, 2.5 and 4.4 mm, for second to fifth rays, respectively. The mean sizes of remodeling osteophytes at the end of the study were 1.6, 1.4, 1.1 and 0.7 mm, respectively. Significant improvement was also achieved in the hallux valgus angle (HVA) and intermetatarsal angle (IMA) at the end of the study. CONCLUSION: in our experience, metatarsophalangeal resection arthroplasty continues to be a valid choice in patients with major forefoot deformities, with satisfactory long-term clinical and radiographic results.


INTRODUCCIÓN: la artroplastía de resección metatarsofalángica se considera un procedimiento quirúrgico de salvamento capaz de mejorar la calidad de vida de pacientes con deformidades importantes en el antepié. MATERIAL Y MÉTODOS: se realizó un estudio observacional retrospectivo de 31 pacientes (36 pies) con deformidades importantes en el antepié operados en nuestra institución. Treinta y dos pies requirieron cirugía adicional que involucró el primer metatarsiano, la mayoría de ellos (72.2%) a través de la fusión de la articulación metatarsofalángica. El período de seguimiento promedio fue 10.3 ± 4.6 años. La mayoría de los pacientes fueron mujeres (87.1%), con una edad promedio de 74.2 ± 11.5 años. RESULTADOS: en la última visita de seguimiento, la puntuación AOFAS promedio fue de 77.9 ± 10.2 puntos y la puntuación MOxFQ promedio fue de 18.3 ± 8.3 puntos. La escala visual analógica (EVA) para el dolor mejoró significativamente, pasando de 7.5 ± 1.2 puntos a 3.4 ± 2.1 puntos de media. También se constataron buenos resultados clínicos en cuanto a la capacidad de calzarse con comodidad. Los espacios de resección promedio al final del estudio fueron 1.3, 1.8, 2.5 y 4.4 mm para el segundo al quinto radio, respectivamente. Los tamaños promedio de los osteofitos por remodelación al final del estudio fueron de 1.6, 1.4, 1.1 y 0.7 mm, respectivamente. También se logró una mejora significativa en el ángulo de hallux valgus (AHV) y en el ángulo intermetatarsiano (IMA) al final del estudio. CONCLUSIÓN: en nuestra experiencia, la artroplastía de resección metatarsofalángica sigue siendo una opción válida en pacientes con deformidades graves del antepié, con resultados clínicos y radiográficos satisfactorios a largo plazo.


Subject(s)
Arthroplasty , Humans , Female , Retrospective Studies , Male , Aged , Middle Aged , Arthroplasty/methods , Aged, 80 and over , Time Factors , Metatarsophalangeal Joint/surgery , Metatarsophalangeal Joint/diagnostic imaging , Follow-Up Studies , Radiography , Treatment Outcome , Foot Deformities/surgery , Foot Deformities/diagnostic imaging
2.
Eur J Orthop Surg Traumatol ; 34(1): 201-208, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37402889

ABSTRACT

INTRODUCTION: The therapeutic management of calcaneal fractures is currently a major source of controversy in the literature. There is no consensus on the need to treat these injuries conservatively or surgically, nor on the criteria for deciding one option or the other. Although the gold standard has classically been the open approach and osteosynthesis, there are currently minimally invasive techniques that also report good results. Our objective is to present our results and experience with the MBA® Orthofix external fixator in a series of cases of calcaneal fractures. METHODS: We performed a retrospective observational study in our center, between the years 2019 and 2021, of Sanders types II-IV calcaneal fractures operated with MBA® Orthofix external fixator. We recorded a total of 38 patients, 42 fractures. We registered demographic information, intraoperative, postoperative, radiological and functional parameters, using the American Orthopedic Foot and Ankle Society (AOFAS), Manchester-Oxford Foot Questionnaire (MOXFQ), EQ-5D and VAS scales. RESULTS: A total of 26 men and 12 women were included, and the median age was 38 years. Mean follow-up was 24,4 months (6, 8-40, 1). The average time to surgery was 7 days and partial loading was started at 2.5 weeks after external fixation, which was removed at 9.2 weeks. The average Böhler angle correction was 7, 4°, Gissane - 12,2°, length 2 mm and calcaneal width was reduced by 5 mm. We recorded two superficial infections, one peroneal entrapment and three subtalar arthrodesis due to post-traumatic osteoarthritis. The AOFAS obtained was 79.1 + / - 15.7 points, MOXFQ 20.1 + / - 16.1 points, EQ-5D 0.84 + / - 0.2 and VAS 3.3 + / - 1.9. CONCLUSION: The external fixator is an excellent surgical alternative for complex articular fractures of the calcaneus, obtaining clinical and radiological results comparable to other osteosynthesis techniques and significantly reducing soft tissue complications.


Subject(s)
Ankle Injuries , Calcaneus , Foot Injuries , Fractures, Bone , Intra-Articular Fractures , Knee Injuries , Male , Humans , Female , Adult , Intra-Articular Fractures/diagnostic imaging , Intra-Articular Fractures/surgery , Calcaneus/diagnostic imaging , Calcaneus/surgery , Calcaneus/injuries , External Fixators , Fracture Fixation , Treatment Outcome , Fractures, Bone/diagnostic imaging , Fractures, Bone/surgery , Fracture Fixation, Internal/methods , Retrospective Studies
3.
Acta Ortop Mex ; 36(2): 85-91, 2022.
Article in Spanish | MEDLINE | ID: mdl-36481548

ABSTRACT

INTRODUCTION: in March 2020, lockdown was established in Spain because of the COVID-19 pandemic. The aim of this study is to assess its impact on pain and quality of life in patients with musculoskeletal pain. MATERIAL AND METHODS: prospective study including 490 individuals grouped in: 140 people without pain, 140 people with musculoskeletal pain but without any related pathology diagnosed, 140 patients diagnosed for a musculoskeletal condition and 70 patients in surgical waiting list (SWL) for a musculoskeletal condition. Data regarding pain, physical activity and quality of life (EuroQol-5D) was collected at the beginning of lockdown and one year after (March 2021). RESULTS: mean age was 53 ± 17.5 years old (18-88) and 51.3% were women. Patients in SWL referred significantly more pain than the rest of groups (p < 0.001), with a score in the visual analogue scale of 6.3 ± 1.9. Groups 3 and 4 suffered a significant increase of their pain from 2020 to 2021 (p < 0.001), while decreasing in group 2 (p < 0.001). Analgesics intake grew from 2020 to 2021 (39.9% versus 44.3%, p = 0.007). 70.2% experienced a worsening of at least one dimension of EuroQol-5D over last year, with patients in SWL being the most affected (p < 0.001). CONCLUSION: lockdown has caused in patients with musculoskeletal conditions a greater aggravation of pain and deterioration of quality of life than in the general population, especially in patients in SWL, translating in an increase in analgesics intake.


INTRODUCCIÓN: en Marzo de 2020 se estableció el confinamiento en España debido a la pandemia por COVID-19. El objetivo de este estudio es determinar su impacto en el dolor y la calidad de vida de personas con dolor osteomuscular. MATERIAL Y MÉTODOS: estudio prospectivo que incluyó 490 personas agrupadas en: 140 personas sin dolor (grupo 1), 140 personas con dolor osteomuscular, pero sin patología diagnosticada (grupo 2), 140 pacientes con patología musculoesquelética (grupo 3) y 70 pacientes en lista de espera quirúrgica (LEQ) por patología musculoesquelética (grupo 4). Se recogieron datos sobre el dolor, la actividad física y la calidad de vida (EuroQol-5D) al inicio del confinamiento y un año después. RESULTADOS: la edad media fue de 53 ± 17.5 años (18-88) y 51.3% fueron mujeres. Las personas en LEQ refirieron un dolor significativamente mayor que el resto de grupos (p < 0.001) con una puntuación en la escala visual analógica del dolor de 6.3 ± 1.9. Los grupos 3 y 4 sufrieron un aumento significativo de su dolor desde 2020 hasta 2021 (p < 0.001), mientras que en el grupo 2 disminuyó (p < 0.001). El consumo de analgésicos creció de 2020 a 2021 (39.9% versus 44.3%, p = 0.007); 70.2% sufrió un empeoramiento en alguna de las dimensiones del EuroQol-5D, siendo el grupo en LEQ el más afectado (p < 0.001). CONCLUSIONES: el confinamiento ha producido en pacientes con patología musculoesquelética un empeoramiento del dolor y de calidad de vida mayor que en el resto de personas, especialmente en aquéllas en espera de cirugía, traduciéndose en un aumento del consumo de analgésicos.


Subject(s)
COVID-19 , Musculoskeletal Pain , Humans , Female , Adult , Middle Aged , Aged , Male , Musculoskeletal Pain/epidemiology , Musculoskeletal Pain/etiology , Quality of Life , COVID-19/epidemiology , Prospective Studies , Pandemics , Communicable Disease Control
4.
Acta ortop. mex ; 36(2): 85-91, mar.-abr. 2022. tab, graf
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1505515

ABSTRACT

Resumen: Introducción: En Marzo de 2020 se estableció el confinamiento en España debido a la pandemia por COVID-19. El objetivo de este estudio es determinar su impacto en el dolor y la calidad de vida de personas con dolor osteomuscular. Material y métodos: Estudio prospectivo que incluyó 490 personas agrupadas en: 140 personas sin dolor (grupo 1), 140 personas con dolor osteomuscular, pero sin patología diagnosticada (grupo 2), 140 pacientes con patología musculoesquelética (grupo 3) y 70 pacientes en lista de espera quirúrgica (LEQ) por patología musculoesquelética (grupo 4). Se recogieron datos sobre el dolor, la actividad física y la calidad de vida (EuroQol-5D) al inicio del confinamiento y un año después. Resultados: La edad media fue de 53 ± 17.5 años (18-88) y 51.3% fueron mujeres. Las personas en LEQ refirieron un dolor significativamente mayor que el resto de grupos (p < 0.001) con una puntuación en la escala visual analógica del dolor de 6.3 ± 1.9. Los grupos 3 y 4 sufrieron un aumento significativo de su dolor desde 2020 hasta 2021 (p < 0.001), mientras que en el grupo 2 disminuyó (p < 0.001). El consumo de analgésicos creció de 2020 a 2021 (39.9% versus 44.3%, p = 0.007); 70.2% sufrió un empeoramiento en alguna de las dimensiones del EuroQol-5D, siendo el grupo en LEQ el más afectado (p < 0.001). Conclusiones: El confinamiento ha producido en pacientes con patología musculoesquelética un empeoramiento del dolor y de calidad de vida mayor que en el resto de personas, especialmente en aquéllas en espera de cirugía, traduciéndose en un aumento del consumo de analgésicos.


Abstract: Introduction: In March 2020, lockdown was established in Spain because of the COVID-19 pandemic. The aim of this study is to assess its impact on pain and quality of life in patients with musculoskeletal pain. Material and methods: Prospective study including 490 individuals grouped in: 140 people without pain, 140 people with musculoskeletal pain but without any related pathology diagnosed, 140 patients diagnosed for a musculoskeletal condition and 70 patients in surgical waiting list (SWL) for a musculoskeletal condition. Data regarding pain, physical activity and quality of life (EuroQol-5D) was collected at the beginning of lockdown and one year after (March 2021). Results: Mean age was 53 ± 17.5 years old (18-88) and 51.3% were women. Patients in SWL referred significantly more pain than the rest of groups (p < 0.001), with a score in the visual analogue scale of 6.3 ± 1.9. Groups 3 and 4 suffered a significant increase of their pain from 2020 to 2021 (p < 0.001), while decreasing in group 2 (p < 0.001). Analgesics intake grew from 2020 to 2021 (39.9% versus 44.3%, p = 0.007). 70.2% experienced a worsening of at least one dimension of EuroQol-5D over last year, with patients in SWL being the most affected (p < 0.001). Conclusion: Lockdown has caused in patients with musculoskeletal conditions a greater aggravation of pain and deterioration of quality of life than in the general population, especially in patients in SWL, translating in an increase in analgesics intake.

5.
Rev Esp Anestesiol Reanim ; 59(9): 511-4, 2012 Nov.
Article in Spanish | MEDLINE | ID: mdl-22683272

ABSTRACT

Spinal cord stimulation is increasingly used to manage chronic pain syndromes, such as complex regional pain syndrome, chronic back pain, refractory angina pectoris or peripheral vascular diseases, which are unresponsive to other common less aggressive treatment methods. The early use of this technique in the aforementioned diseases makes it suitable in young women of childbearing age and who wish to become pregnant. We report the case of a 33-year-old woman who became pregnant 4 months after having undergone posterior cord stimulation, and we review the approach to this situation and the perioperative management during the perinatal period.


Subject(s)
Failed Back Surgery Syndrome/therapy , Pregnancy Complications/therapy , Spinal Cord Stimulation , Adult , Analgesia, Epidural , Analgesia, Obstetrical , Anesthesia, General , Anesthesia, Obstetrical/methods , Cesarean Section , Contraindications , Dystocia/surgery , Electrodes, Implanted/adverse effects , Equipment Failure , Female , Humans , Pregnancy , Recurrence , Spinal Cord Stimulation/adverse effects , Spinal Cord Stimulation/instrumentation
6.
Rev Esp Anestesiol Reanim ; 58(10): 589-94, 2011 Dec.
Article in Spanish | MEDLINE | ID: mdl-22263403

ABSTRACT

BACKGROUND AND OBJECTIVE: Headache has a great impact on patients' quality of life and in industrialized countries there is economic impact as well. One of the pathophysiologic theories to explain headache is activation of afferent C2-C3 nerve fibers. Afferent peripheral nerve stimulation by occipital nerve provocation at C2-C3 seems to alleviate headache by acting on the trigeminocervical complex, which would largely explain the effectiveness of this modality. The aim of this study was to describe peripheral nerve stimulation as an alternative therapy in patients who do not respond to other headache treatments. MATERIAL AND METHODS: Multicenter retrospective study between April 2005 and May 2009, analyzing cases of patients treated with nerve stimulation for severe chronic headache. In all patients the medical history included type of headache, intensity of pain on a numerical scale, medical treatment used, and number of headache episodes. We recorded the percentage of patients with negative tests. Patients implanted with a generator assessed effectiveness on the numerical scale; we analyzed the percentage of perceived improvement at 1, 3, 6, and 12 months. We also analyzed the extent of coverage provided by the electrodes, patient satisfaction, reduction in the number of episodes and medication, and complications. RESULTS: Of 31 patients, 87% had positive results, with a significant decrease in pain from baseline (P < .001); 85.2% reported sustained improvement of > 50%, and 96.3% reported a decrease of > 2 points on the pain scale. All patients expressed satisfaction during the period of follow-up. Fifty-six percent had no headaches after a year and 47% had stopped taking medication. The most frequent complication was electrode migration.


Subject(s)
Electric Stimulation Therapy/methods , Headache/therapy , Female , Humans , Implantable Neurostimulators , Male , Middle Aged , Retrospective Studies
7.
Rev Esp Anestesiol Reanim ; 56(6): 380-4, 2009.
Article in Spanish | MEDLINE | ID: mdl-19725346

ABSTRACT

Patients treated with long-term spinal infusion of high doses of morphine develop a granuloma at the location of the catheter tip. Diagnosis is based on a steady increase in intrathecal morphine dosage after a relatively prolonged period of stability, on the gradual development of neurologic signs and symptoms suggesting radicular or spinal cord compression, and on magnetic resonance images. We describe a man with central neuropathic pain after removal of a tumor. The presence of all 3 of the aforementioned diagnostic criteria led to suspicion of a spinal granuloma.


Subject(s)
Analgesia, Epidural/instrumentation , Analgesics, Opioid/therapeutic use , Back Pain/etiology , Catheterization/adverse effects , Clonidine/therapeutic use , Granuloma, Foreign-Body/etiology , Infusion Pumps, Implantable/adverse effects , Morphine/therapeutic use , Muscle Relaxants, Central/therapeutic use , Neuralgia/etiology , Postoperative Complications/etiology , Spinal Cord Compression/etiology , Analgesics, Opioid/administration & dosage , Clonidine/administration & dosage , Drug Therapy, Combination , Emergencies , Granuloma, Foreign-Body/surgery , Hemangioma, Cavernous, Central Nervous System/surgery , Humans , Infusions, Parenteral/instrumentation , Laminectomy , Male , Middle Aged , Morphine/administration & dosage , Muscle Relaxants, Central/administration & dosage , Postoperative Complications/drug therapy , Postoperative Complications/surgery , Spinal Cord Compression/surgery , Spinal Cord Diseases/surgery
8.
Rev Esp Anestesiol Reanim ; 56(5): 292-8, 2009 May.
Article in Spanish | MEDLINE | ID: mdl-19580132

ABSTRACT

BACKGROUND AND OBJECTIVE: Patients being treated with spinal cord stimulation for chronic pain complain of variable paresthesias, particularly in relation to changes in posture. Such changes affect the great majority of patients with implantable pulse generators, requiring them to use the external programmer for avoidance of painful paresthesias or even to disconnect the generator, leading to loss of pain relief. The aim of this study was to determine the relationship between the pulse charge needed for stimulation and the patient's different postures. MATERIAL AND METHODS: Observational study of 70 patients treated with spinal cord stimulation in the following postures and situations: decubitus position, standing, seated, and walking. With the patients standing, we analyzed the thresholds of perception, pain, and pain relief, as well as the therapeutic range. Studies were performed in all patients. Later, data were analyzed by anatomical positioning of the stimulator (cervical, thoracic, sacral, occipital, or subcutaneous). RESULTS: In the analysis of the therapeutic range in the overall group we identified statistically significant differences between decubitus and standing positions and between decubitus position and walking. At the level of the thoracic spine differences were identified between all positions except between standing and walking and between seated and decubitus positions. At the level of the cervical spine, no significant differences were detected. Analysis of the pulse charge showed a significant difference in the decubitus position, in which less charge was needed to achieve satisfactory stimulation. When electrodes implanted at the cervical and thoracic levels were compared, differences were found between standing and seated positions (P=.04) but none between decubitus position or walking and the other positions. CONCLUSION: Stimulation systems are not currently designed to adapt to changes in distance between the electrodes and nerve fibers. Improvements are required in this respect.


Subject(s)
Electric Stimulation Therapy , Energy Metabolism , Pain Management , Posture/physiology , Spinal Cord/physiopathology , Adult , Aged , Aged, 80 and over , Chronic Disease , Electric Stimulation Therapy/adverse effects , Electric Stimulation Therapy/methods , Electrodes, Implanted , Female , Humans , Male , Middle Aged , Organ Specificity , Pain/physiopathology , Pain Threshold , Paresthesia/etiology , Supine Position/physiology , Walking , Young Adult
9.
Rev. esp. anestesiol. reanim ; 56(6): 380-384, jun.-jul. 2009. ilus, tab
Article in Spanish | IBECS | ID: ibc-77865

ABSTRACT

Los pacientes en tratamiento con infusión espinal demorfina a dosis elevadas presentan como efecto adversoa largo plazo la formación de un granuloma en la puntadel catéter intradural. La subida ininterrumpida de lasdosis de morfina intratecales tras un periodo relativamenteprolongada de estabilidad, la aparición progresivade una sintomatología neurológica característica decompresión radicular o medular, y las imágenes de resonanciamagnética llevan al diagnóstico de este fenómeno.Se presenta un caso clínico de un paciente con dolor neuropáticocentral tras exéresis tumoral, que reúne los tresprincipios mencionados que llevan al diagnóstico de sospechade granuloma intradural (AU)


Patients treated with long-term spinal infusion of highdoses of morphine develop a granuloma at the locationof the catheter tip. Diagnosis is based on a steadyincrease in intrathecal morphine dosage after arelatively prolonged period of stability, on the gradualdevelopment of neurologic signs and symptomssuggesting radicular or spinal cord compression, and onmagnetic resonance images. We describe a man withcentral neuropathic pain after removal of a tumor. Thepresence of all 3 of the aforementioned diagnosticcriteria led to suspicion of a spinal granuloma (AU)


Subject(s)
Humans , Male , Middle Aged , Infusion Pumps, Implantable/adverse effects , Granuloma, Foreign-Body/surgery , Granuloma, Foreign-Body/etiology , Back Pain/etiology , Clonidine/administration & dosage , Morphine/administration & dosage , Drug Therapy, Combination
10.
Rev Esp Anestesiol Reanim ; 54(2): 120-4, 2007 Feb.
Article in Spanish | MEDLINE | ID: mdl-17390693

ABSTRACT

The first of the 2 cases of cauda equina syndrome we report occurred following phenolization of sacral roots after a series of operations for Hirsprung disease. The second occurred after trauma from a bullet that hit the spine. Fecal and urinary incontinence and neuropathic pain in the lower extremities were present in both cases. After various treatments failed, both patients were given dual spinal stimulation for integrated treatment of both incontinence and neuropathic pain. We applied a novel approach, connecting both stimulators to a single rechargeable generator, reducing medium- and long-term costs. Fewer generator replacements (every 2-3 years with the standard approach) and fewer generator implantations (2 each time with the usual system) are required when rechargeable generators are used. Patient quality of life is thus improved. The overall cost of the implants is reduced from their second year of use.


Subject(s)
Polyradiculopathy/therapy , Transcutaneous Electric Nerve Stimulation/instrumentation , Female , Humans , Male , Middle Aged
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