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Cranial defects secondary to trauma, surgery or pathological causes, result in large cranial imperfection, which affects the appearance of the patient as well as results in sinking flap syndrome. Rehabilitation of such a defect can be done using prosthetic options like custom-made polymethyl methacrylate (PMMA) cranial prosthesis or surgical options like outer table calvarial graft segments. It is usually observed that the conventional moulage impression of the defective site is the most difficult task. The accuracy of the prosthesis is affected by conventional moulage impression, a moulage cast of the defect and techniques of fabricating wax pattern. Orthodox method is to mark the tentative outline of the defect and make a conventional moulage impression of the site. However, this is an arbitrary method which offers challenges to accurate replication of the borders of the defect. Recently, medical imaging and digital modeling in dentistry have paved the way for digital dental practice and additive manufacturing replacing most manual or subtractive procedures. The use of computerized tomography scan to obtain a 3 D digital image of cranial defect for fabricating a replica with rapid prototyping has markedly improved the accuracy at the margin of the defect/prosthesis interface, resulting in a better fit and optimal contour lending itself to the improved esthetic outcome. It is a more reliable method of fabricating a cranial implant prosthesis, which requires minimum adjustment when the patient is on the OT table. These case reports compare rehabilitation of cranial defect with custom-made PMMA cranial prosthesis using the conventional methods as well as rapid prototyping technique. It is seen that the rapid prototyping method is expensive but accurate and gives a better esthetic outcome.
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OBJECTIVES: To prospectively study the effectiveness and safety of clobazam as an add-on therapy in patients with epilepsy whose seizures are not adequately controlled with antiseizure medicine (ASM) monotherapy. METHODS: We conducted a prospective, observational study at 28 neurology outpatient clinics in India from June 2017 to October 2019. Consecutive patients with epilepsy (older than 3â¯years) with inadequate seizure control with ASM monotherapy were initiated on clobazam. Patients were followed up at 1, 3, 6, 9, and 12â¯months. Seizure control and adverse events were assessed through personal interviews and seizure diaries. RESULTS: Out of 475 eligible patients, data of 429 patients (men: 65.5%) were evaluated (46 excluded due to protocol deviations). The median age was 25 (range, 3-80â¯years) years and the median duration of epilepsy was 3 (0.1-30) years. The majority of patients had focal epilepsy (55.0%) and genetic generalized epilepsy (40.1%). The one-year follow-up was completed by 380 (88.5%) patients. At one-year follow-up, 317 (83.4%; Nâ¯=â¯380) patients in the study remained seizure free. These 317 patients who were seizure free at 12â¯months comprised 73.9% of the evaluable population (Nâ¯=â¯429). In 98.8% of patients, the primary reason for adding clobazam was inadequate control of seizures with treatment. During one-year follow-up, a total of 113 (22.6%) patients experienced at least one adverse event which included 103 (20.6%) patients who experienced 386 episodes of seizures. CONCLUSION: The study provides preliminary evidence that clobazam is effective and well-tolerated as add-on therapy for a period of one year among patients with epilepsy inadequately stabilized with monotherapy. TRIAL REGISTRATION NUMBER: CTRI/2017/12/010906.
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Anticonvulsivantes , Epilepsia , Adulto , Anticonvulsivantes/efectos adversos , Benzodiazepinas , Clobazam/uso terapéutico , Epilepsia/inducido químicamente , Epilepsia/tratamiento farmacológico , Humanos , Masculino , Estudios Prospectivos , Convulsiones/inducido químicamente , Convulsiones/tratamiento farmacológicoRESUMEN
RATIONALE: Maxillofacial defect is of great concern physically, emotionally, and psychologically for a patient. However, it is an even bigger challenge for a team attempting rehabilitation, as a crucial decision has to be made between surgical approach and/or prosthetic rehabilitation. However, if both are combined, it will result in best of esthetics and function with ease of maintainance, resulting in a sucessful rehabilitation. This case report represents a case of auricular defect rehabilitated with a combination of implants and bar-retained silicone prosthesis. PATIENT CONCERN: A 38-year-old male patient with right auricular defect reported with the main concern of esthetic rehabilitation of a lost part of the external ear. DIAGNOSIS: With through evaluation and examination, a diagnosis of acquired partial auricular defect of the right side secondary to trauma was established. TREATMENT: An implant-retained auricular prosthesis was planned for this case. Surgically, three intraoral implants were placed in the mastoid bone, and after healing, bar framework was fabricated and attached. Finally, silicone prosthesis was fabricated and delivered to the patient. OUTCOME: A successful rehabilitation was carried out in this case using implants and bar attachment for retention of the silicone prosthesis. This prosthesis provided excellent retention and restored the appearance and confidence of the patient. TAKE-AWAY LESSONS: Rehabilitation of the auricular defect can be carried out with surgical approach, which involves multiple surgeries, and still, the results may not be esthetically favorable. Prosthetic rehabilitation is an option, but retention is generally a hindrance. However, implant-retained prosthesis has really paved a way for rehabilitation of the maxillofacial defect esthetically and more reliably. Cone-beam computerized tomography (CT) can be used for planning and evaluation instead of CT, which will save the patient from a lot of radiation exposure. Hence, in the maxillofacial defect, attempts should be made to explore the option of implant-retained prosthesis.
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BACKGROUND: In the emerging field of nanotechnology, copper oxide (CuO) nanomaterials are considered to be one of the most important transition metal oxides owing to its fascinating properties. Its synthesis from green chemistry principles is gaining importance as next-generation antibiotics due to its simplicity, eco-friendliness, and cost-effectiveness. In the present study, CuO nanorods (CuO NRs) were synthesized from the aqueous fruit extract of Momordica charantia and characterized using different analytical techniques. Further, the biomedical therapeutic potential was evaluated against multi-drug resistant microbial strains. MATERIALS AND METHODS: To synthesize CuO NRs, 0.1M of CuSO4.5H2O solution was added to aqueous extract of Momordica charantia in a 1:3 (v/v) ratio (pH=11) and heated at 50°C followed by washing and drying. The synthesized CuO NRs were subjected to characterization using different analytical techniques such as UV visible spectroscopy, zeta sizer equipped with zeta potential, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) equipped with energy-dispersive X-ray spectroscopy (EDS) and transmission electron microscopy (TEM). Further, the application as a biomedical therapeutic potential was evaluated in vitro using well diffusion method against eleven multidrug-resistant clinical bacterial strains, a fungus- Trichophyton rubrum and in ovo against the R2B virus using haemagglutination (HA) test. RESULTS: Characterization was preliminarily done by the spectral study that confirms the absorbance band at 245nm. FTIR analysis at 628 cm-1 peak identified copper oxide vibration. SEM analysis revealed agglomerated particle clusters. However, with TEM clear nanorods of average diameter of 61.48 ± 2 nm were observed. EDAX confirmed CuO formation while XRD showed a typical monoclinic structure with 6 nm crystallite size. Biological screening of CuO NRs showed significant results against both in vitro and in ovo methods. Significant inhibitory activity (p<0.0001) was noted against most of the resistant human pathogenic strains including both Gram-positive and Gram-negative bacteria. The highest efficacy was observed against Bacillus cereus with a 31.66 mm zone of inhibition. Besides, the therapeutic potential of CuO NRs against Corynebacterium xerosis, Streptococcus viridians and R2B strain of Newcastle disease is reported for the first time. CONCLUSION: Based on the present results, it could be expected that green synthesized CuO NRs would find potential applications in the field of nanomedicine.
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Antibacterianos/farmacología , Cobre/farmacología , Tecnología Química Verde , Momordica charantia/química , Nanoestructuras/química , Animales , Antifúngicos/farmacología , Bacterias/efectos de los fármacos , Pollos , Hongos/efectos de los fármacos , Pruebas de Hemaglutinación , Humanos , Nanopartículas del Metal/química , Nanopartículas del Metal/ultraestructura , Pruebas de Sensibilidad Microbiana , Nanoestructuras/ultraestructura , Nanotubos/química , Nanotubos/ultraestructura , Tamaño de la Partícula , Espectrometría por Rayos X , Espectrofotometría Ultravioleta , Espectroscopía Infrarroja por Transformada de Fourier , Electricidad Estática , Difracción de Rayos XRESUMEN
Microstomia is a clinical condition of reduced mouth opening that can be acquired or congenital in origin. Problems associated with microstomia can be related to function, esthetics, or both. Management of microstomia due to facial burns is complex due to the presence of hypertrophic and contracture scars. Available treatment options can be broadly classified as surgical, nonsurgical, or both. Splints can be used to prevent the contraction of perioral musculature or to recuperate lost mouth opening. Various intraoral or extraoral, tooth-borne or tissue-borne, and static or dynamic appliances are in clinical use, but their designs are case specific. This case report explains the management of microstomia secondary to facial burns by using a dynamic splint in combination with intralesional injections of triamcinolone acetonide and hyaluronidase.
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Quemaduras , Contractura , Microstomía , Estética Dental , Humanos , Férulas (Fijadores)RESUMEN
Cranial vault defects may be acquired or congenital in origin. Rehabilitation of these patients often poses challenge to the operating team and prosthodontist. Polymethylmethacrylate is a commonly used alloplastic graft material which is used for the fabrication of cranial prosthesis. Nowadays, with the advancement in the bioengineering, custom-made template and cranial prosthesis can be made by rapid prototyping technology (RPT) by patient three-dimensional (3D) computed tomography (CT) scan images. This series of two cases explained two different techniques for the rehabilitation of the patient with frontotemporoparietal cranial defect. Case 1 had a history of cerebrovascular accident, followed by decompression craniotomy which led to frontotemporoparietal defect of the left side. This defect area was associated with the cerebrospinal fluid accumulation which made delineation of underlying bony margins difficult and interfered with conventional impression procedures. Case 2 had a road traffic accident which led to intracerebral hemorrhage followed by decompression craniotomy which resulted in frontotemporoparietal defect of the right side. The patient had a poor neuromuscular control which impedes with the upright posture of the head during impression making of the defect area. Therefore, these cases were planned to rehabilitate by RPT. In these techniques, the prosthesis was made using custom-made skull template produced by RPT, using the data of 3D-CT scan images. This technique resulted in the prosthesis with good esthetics and better fit of the prosthesis. The contours of the prosthesis were replicated in the same manner as compared to the contralateral side. RPT is an additive manufacturing technology which is now used in the field of dentistry too. This technique is easy to use; fabricate prosthesis with high precision is less time-consuming and has fewer chances of error.
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Osteochondroma or exostosis is the most common primary bone tumor containing both bone and cartilage. Soft tissue osteochondromas have been described at various locations, however, to the best of our knowledge, there is only a single case report of a soft tissue osteochondroma around the femoral neck. We, hereby report second such case. CASE REPORT: A forty year old female presented with swelling on medial aspect of left thigh since four years. Radiographs showed a large mass at the inferior surface of the left femoral neck. CT scan revealed a well defined lobulated mass lesion involving muscles of adductor compartment of thigh. MRI showed lobulated periarticular, intramuscular, non enhancing lesion isointense to the bone, but without any continuity to the adjacent femur. Histopathology of the excised lesion turned out to be osteochondroma with origin from soft tissue. This case highlights an important differential diagnosis to be considered whenever an ossified mass is located in soft tissue.