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1.
Pacing Clin Electrophysiol ; 44(9): 1607-1615, 2021 09.
Artículo en Inglés | MEDLINE | ID: mdl-34219243

RESUMEN

Several cardiovascular diseases and arrhythmic disorders have been described in COVID-19 era as likely related to SARS-CoV-2 infection. The prognostic relevance of bradyarrhythmias during the infection has not been yet described and no data are available about long-term heart conduction disorders. A review of literature concerning the association between hypokinetic arrhythmias and COVID-19 from January 2020 to February 2021 was performed. The key-words used for the research were: "sinus node disfunction," "sick sinus syndrome (SSS)," "sino-atrial block," "atrio-ventricular block (AVB)," "bradyarrhythmias," and "COVID-19″ or "SARS-CoV-2.″ Excluding "relative bradycardia," a total of 38 cases of bradyarrhythmia related to SARS-CoV-2 infection have been described, even in very young people, requiring in many cases a definitive pacemaker implantation. Furthermore, we report a case of non-hospitalized 47-years old man with a SSS developed as a consequence of mild SARS-CoV-2 infection. While in all described cases heart conduction disorders were found at presentation of the infection or during hospitalization for COVID-19, in our case the diagnosis of SSS was made after the resolution of the infection. Although rarely, heart conduction disorders may occur during COVID-19 and the present case highlights that a cardiological follow up may be desirable even after the resolution of infection, especially in the presence of symptoms suggesting a possible heart involvement.


Asunto(s)
Bradicardia/virología , COVID-19/complicaciones , Síndrome del Seno Enfermo/virología , Bradicardia/fisiopatología , Bradicardia/terapia , Electrocardiografía , Humanos , Masculino , Persona de Mediana Edad , Marcapaso Artificial , Pronóstico , SARS-CoV-2 , Síndrome del Seno Enfermo/fisiopatología , Síndrome del Seno Enfermo/terapia
2.
J Cell Physiol ; 233(3): 2572-2580, 2018 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-28777459

RESUMEN

To assess the safety profile of iso-osmolar contrast medium (CM) versus low osmolar CM in cancer patients with an estimated glomerular filtration rate (eGFR) >60 ml/min. In this multicenter, blind trial of patients seeking a chest-abdomen-pelvis contrast enhanced computed tomography (CT) with iodated CM, participants were centrally randomized to iodixanol or iopromide. Contrast induced nephropathy (CIN) at 24 and/or 72 hr were our primary outcomes. We further considered irreversible CIN, average eGFR percentage variation (%Δ), and adverse events (AEs). Overall, 607 patients were enrolled. Among them, 497 eligible patients were randomized to iodixanol (N: 247) or iopromide (N: 250). No differences emerged by descriptive characteristics. Seven and 3 CIN at 24 hr (p = 0.34) and 8 and 2 CIN at 72 hr (p = 0.11) occurred in the iopromide and iodixanol group, respectively. Within the subgroup of individual patients who developed CIN (N: 17), the event rate was higher in the iopromide arm (p = 0.045). No cases of permanent CIN or significant differences in terms of AEs or GFR %Δ were observed. Our results suggest a more favorable safety profile of iodixanol versus iopromide. Adequately sized trials with similar design are warranted to confirm our findings and clarify the underlying biological mechanisms.


Asunto(s)
Medios de Contraste/efectos adversos , Yohexol/análogos & derivados , Enfermedades Renales/inducido químicamente , Riñón/efectos de los fármacos , Neoplasias/diagnóstico por imagen , Tomografía Computarizada por Rayos X , Ácidos Triyodobenzoicos/efectos adversos , Adolescente , Adulto , Anciano , Medios de Contraste/administración & dosificación , Femenino , Tasa de Filtración Glomerular/efectos de los fármacos , Humanos , Yohexol/administración & dosificación , Yohexol/efectos adversos , Italia , Riñón/fisiopatología , Enfermedades Renales/diagnóstico , Enfermedades Renales/fisiopatología , Masculino , Persona de Mediana Edad , Neoplasias/patología , Seguridad del Paciente , Valor Predictivo de las Pruebas , Factores de Riesgo , Factores de Tiempo , Tomografía Computarizada por Rayos X/efectos adversos , Ácidos Triyodobenzoicos/administración & dosificación , Adulto Joven
3.
Radiol Med ; 122(3): 186-193, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-27943097

RESUMEN

Significant advances in medical imaging have been made in the past decades, enabling physicians to reach high precision in diagnosing patients' diseases by means of sophisticated imaging tools. However, the use of sophisticated tools is limited by the high costs and, in some cases, by the utilization of ionizing radiation, which have both great impact on the economy of a nation and on citizens' health, respectively. Guidelines have been published among countries to provide physicians with structured rules to be followed to suggest the correct imaging technique, suiting better the diagnostic question and avoiding inappropriate imaging requests. The COLLABORADI is a research project that addressed the phenomenon of inappropriate imaging prescriptions in Sicily (Italy) and proposed the design and implementation of a clinical decision support system to help physicians to set up the most appropriate diagnostic route for their patients. The aim of this paper is to describe the characteristics of the COLLABORADI software and its potential impact in diminishing inappropriate imaging.


Asunto(s)
Sistemas de Apoyo a Decisiones Clínicas , Medicina General/normas , Guías de Práctica Clínica como Asunto , Prescripciones/normas , Radiografía/normas , Programas Informáticos , Procedimientos Innecesarios , Algoritmos , Humanos , Sicilia , Diseño de Software
4.
Tumori ; 101 Suppl 1: S51-4, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-27096274

RESUMEN

The accreditation process is, on the one hand, a tool used to homogenize procedures, rendering comparable and standardized processes of care, and on the other, a methodology employed to develop a culture of quality improvement. Although not yet proven by evidence-based studies that health outcomes improve as a result of an accreditation to excellence, it is undeniable that better control of healthcare processes results in better quality and safety of diagnostic and therapeutic pathways. The Regina Elena National Cancer Institute underwent the accreditation process in accordance with the standards criteria set by the Organisation of European Cancer Institutes (OECI), and it has recently completed the process, acquiring its designation as a Comprehensive Cancer Center (CCC). This was an invaluable opportunity for the Regina Elena Institute to create a more cohesive environment, to widely establish a culture of quality, to implement an institutional information system, and to accelerate the process of patient involvement in strategic decisions. The steps of the process allowed us to evaluate the performance and the organization of the institute and put amendments in place designed to be adopted through 26 improvement actions. These actions regarded several aspects of the institute, including quality culture, information communication technology system, care, clinical trials unit, disease management team, nursing, and patient empowerment and involvement. Each area has a timeline. We chose to present the following 3 improvement actions: clinical trial center, computerized ambulatory medical record, and centrality of patient and humanization of clinical pathway.


Asunto(s)
Acreditación , Instituciones Oncológicas/normas , Vías Clínicas/normas , Oncología Médica/normas , Calidad de la Atención de Salud , Acreditación/métodos , Atención Ambulatoria/normas , Ensayos Clínicos como Asunto/normas , Vías Clínicas/organización & administración , Europa (Continente) , Humanos , Cooperación Internacional , Italia , Oncología Médica/organización & administración , Garantía de la Calidad de Atención de Salud , Mejoramiento de la Calidad
5.
Tumori ; 99(6): 293e-8e, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24503807

RESUMEN

A panel of experts from Italian Comprehensive Cancer Centers defines the recommendations for external quality control programs aimed to accreditation to excellence of these institutes. After definition of the process as a systematic, periodic evaluation performed by an external agency to verify whether a health organization possesses certain prerequisites regarding structural, organizational and operational conditions that are thought to affect health care quality, the panel reviews models internationally available and makes final recommendations on aspects considered of main interest. This position paper has been produced within a special project of the Ministry of Health of the Italian Government aimed to accredit, according to OECI model, 11 Italian cancer centers in the period 2012-2014. The Project represents the effort undertaken by this network of Comprehensive Cancer Centers to find a common denominator for the experience of all Institutes in external quality control programs. Fourteen shared "statements" are put forth, designed to offer some indications on the main aspects of this subject, based on literature evidence or expert opinions. They deal with the need for "accountability" and involvement of the entire organization, the effectiveness of self-evaluation, the temporal continuity and the educational value of the experience, the use of indicators and measurement tools, additionally for intra- and inter-organization comparison, the system of evaluation models used, the provision for specific requisites for oncology, and the opportunity for mutual exchange of evaluation experiences.


Asunto(s)
Acreditación , Benchmarking , Investigación Biomédica , Instituciones Oncológicas/normas , Calidad de la Atención de Salud , Investigación Biomédica/organización & administración , Investigación Biomédica/normas , Investigación Biomédica/tendencias , Competencia Clínica , Vías Clínicas , Agencias Gubernamentales , Personal de Salud , Humanos , Capacitación en Servicio , Internacionalidad , Italia , Revisión por Pares , Control de Calidad , Investigadores , Responsabilidad Social
6.
Med Phys ; 35(11): 4793-9, 2008 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19070211

RESUMEN

PURPOSE: The aim was to correlate the color Doppler flow activity pre- and postradiotherapy, using transrectal color Doppler ultrasonography (CDUS) and the 2 year positive biopsy rate after radiotherapy in patients with prostate cancer. METHODS AND MATERIALS: Analysis was carried out in 69 out of 160 patients who had undergone treatment with 3D-conformal radiotherapy (3D-CRT) to prostate and seminal vesicles. Patients were randomized to receive 80 Gy in 40 fractions in 8 weeks (arm A) and 62 Gy in 20 fractions in 5 weeks, 4 fractions per week (arm B). Color Doppler flow activity (CDFA) was evaluated calculating the vascularization index (VI), defined as the ratio between the colored and total pixels in the whole and peripheral prostate, delineated by a radiation oncologist on CDUS images, using EcoVasc a home-made software. The difference between the 2 year post- and pre-3D-CRT maximum VI (VImax), named deltaVImax, was calculated in the whole and peripheral prostate for each patient. Then, deltaVImax and the detected 2 year biopsy outcome were analyzed using the receiver operating characteristics (ROC) technique. RESULTS: The VImax increased or decreased in patients with positive or negative biopsies, respectively, compared to the value before RT in both arms. The area under the ROC curve for deltaVImax in the whole and peripheral prostate is equal to 0.790 and 0.884, respectively. CONCLUSION: The AVImax index, comparing CDFA at 2 years compared to that before RT, allows the 2 year postradiotherapy positive biopsy rate to be predicted.


Asunto(s)
Neoplasias de la Próstata/diagnóstico por imagen , Neoplasias de la Próstata/patología , Biopsia , Humanos , Masculino , Neovascularización Patológica/diagnóstico por imagen , Neoplasias de la Próstata/irrigación sanguínea , Neoplasias de la Próstata/radioterapia , Reproducibilidad de los Resultados , Programas Informáticos , Ultrasonografía Doppler en Color
7.
Spine (Phila Pa 1976) ; 27(23): E499-502, 2002 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-12461406

RESUMEN

STUDY DESIGN: This report documents a case of asymptomatic esophageal perforation, secondary to a dislocated and then migrated cervical screw after anterior plating, and reviews the relevant Western literature. OBJECTIVES: To report a rare and potentially dangerous complication and suggest mechanisms of asymptomatic esophageal perforation and healing. SUMMARY OF BACKGROUND DATA: Anterior surgical approaches to the cervical spine have become popular and safer during the past decade. Materials and devices for anterior stabilization have improved in quality and safety. Nevertheless, failure of the devices may occur either because of technical mistakes or rupture. Reoperation is not always necessary, as spontaneous recovery is possible. METHODS: Our patient was operated on for severe cervical spondylotic myelopathy. One year after surgery, one of the screws migrated and was found anteriorly to the spine. Six months later, the screw could no longer be identified, and we concluded that an esophageal perforation had occurred and that the screw had been eliminated through the intestinal tract. The results of esophagoscopy were normal. RESULTS: The neurologic conditions of our patient improved constantly, and his spine alignment was maintained despite the missing screw. CONCLUSIONS: This case demonstrates that a serious complication may not need any treatment. Each case of screw displacement in anterior cervical spine surgery should be evaluated separately in conjunction with the clinical symptoms of the patient, as spontaneous resolution is possible.


Asunto(s)
Tornillos Óseos/efectos adversos , Vértebras Cervicales/cirugía , Perforación del Esófago/etiología , Migración de Cuerpo Extraño/diagnóstico , Falla de Prótesis , Fusión Vertebral/efectos adversos , Perforación del Esófago/diagnóstico , Humanos , Remisión Espontánea , Fusión Vertebral/instrumentación , Osteofitosis Vertebral/cirugía , Tiempo
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