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1.
Clin Nutr ; 40(11): 5430-5437, 2021 11.
Article in English | MEDLINE | ID: mdl-34653819

ABSTRACT

Up to half of ICU survivors, many of whom were premorbidly well, will have residual functional and/or cognitive impairment and be vulnerable to future health problems. Frailty describes vulnerability to poor resolution of homeostasis after a stressor event but it is not clear whether the vulnerability seen after ICU correlates with clinical measures of frailty. In clinical practice, the scales most commonly used in critically ill patients are based on the assessment of severity and survival. Identification and monitoring of frailty in the ICU may be an alternative or complimentary approach, particularly if it helps explain vulnerability during the recovery and rehabilitation period. The purpose of this review is to discuss the use of tools to assess frailty status in the critically ill, and consider their importance in clinical practice. Amongst these, we consider biomarkers with potential to identify patients at greater or lesser risk of developing post-ICU vulnerability.


Subject(s)
Critical Illness , Frailty/diagnosis , Patient Acuity , Biomarkers/analysis , Humans
4.
J Nutr Health Aging ; 24(8): 817-820, 2020.
Article in English | MEDLINE | ID: mdl-33009530

ABSTRACT

BACKGROUND/OBJECTIVES: Frailty is common in nursing homes. However, few studies reported longitudinal validation for death prediction or cut-off scores with the FRAIL-NH, which is designed to be used in nursing homes. Moreover, no studies came from Latin America, where frailty is highly prevalent. Our objectives were to evaluate (1) the prevalence of frailty according to the FRAIL-NH scale, and (2) its association to and the best cut-off score for predicting death after 12 months. DESIGN: longitudinal study with 12-month follow-up. SETTING: 6 nursing homes in southwest of Brazil. PARTICIPANTS: 293 residents with 60 years old or more. METHODS: Frailty was evaluated through the FRAIL-NH scale. Logistic regression was used to estimate the associated between frailty and mortality adjusted for age and sex. ROC curve was used to evaluate the accuracy of the scale for mortality prediction. RESULTS: Frailty was prevalent (47.4%) and was associated with death (odds ratio=1.31, 95% confidence interval [CI]=1.18-1.48, p<0.001). The area under the curve was 0.741 (95%CI=0.68-0.79). The sensitivity and specificity of the FRAIL-NH scale according to the best value of the Youden Index was 72.9% and 66.5%, respectively, for a cut-off > 8 points. CONCLUSIONS: Frailty is prevalent in nursing homes according to the FRAIL-NH and it was associated with one-year prediction of death for a cut-off > 8 points.


Subject(s)
Frail Elderly/statistics & numerical data , Frailty/mortality , Geriatric Assessment/methods , Mortality/trends , Aged , Aged, 80 and over , Brazil , Female , Humans , Longitudinal Studies , Male , Middle Aged , Nursing Homes , Prevalence
5.
Actas dermo-sifiliogr. (Ed. impr.) ; 110(6): 469-473, jul.-ago. 2019. tab
Article in Spanish | IBECS | ID: ibc-185274

ABSTRACT

Introducción: La cirugía dermatológica ambulatoria es una práctica clínica cada vez más habitual, basada en la extirpación de tumores cutáneos mediante anestesia local y con un tiempo quirúrgico reducido. Tradicionalmente, la valoración preoperatoria se ha realizado con el fin de detectar alguna alteración o proceso patológico desconocido que pudiera modificar el plan anestésico y/o quirúrgico. Existe una gran variabilidad entre centros y especialistas sobre las pruebas a solicitar en aquellos pacientes que van a ser sometidos a una intervención quirúrgica dermatológica ambulatoria, teniendo en cuenta que, por el perfil de esta cirugía, prácticamente ningún hallazgo podría modificar o contraindicar la intervención. El objetivo es ofrecer una referencia de actuación para la petición de pruebas preoperatorias en cirugía dermatológica ambulatoria. Métodos: En 2017 se desarrolló en nuestro centro un protocolo para intentar unificar la petición de pruebas preoperatorias en cirugía dermatológica ambulatoria. Se realizó un estudio observacional, descriptivo y retrospectivo analizando las pruebas solicitadas a pacientes sometidos a este tipo de cirugía, comparando antes y después de la aplicación del protocolo. Resultados: Tras la instauración del protocolo se solicitó menor número de pruebas complementarias, sin diferencias estadísticamente significativas en el tipo de cirugía ni complicaciones postoperatorias. Conclusiones: Los pacientes que vayan a ser sometidos, bajo anestesia local, a cirugía dermatológica ambulatoria, y que se encuentren en su estado de salud habitual, podrían no tener indicación de realización de pruebas complementarias preoperatorias


Introduction: Short-duration ambulatory surgery for the removal of skin tumors under local anesthesia is increasingly common in dermatology. Preoperative assessment has traditionally targeted the identification of any unknown diseases or other health conditions that might lead to changes in plans for anesthesia or surgery. Hospitals and specialists differ greatly in the tests they order in patients about to undergo outpatient dermatologic surgery given that hardly any finding would be likely to contraindicate or lead to changes in the procedure. This study aimed to provide guidance for those ordering tests before outpatient dermatologic surgery. Methods: In 2017 our hospital developed a protocol to standardize preoperative testing for outpatient dermatologic surgery. We designed an observational, descriptive, retrospective analysis of tests ordered for patients scheduled for such surgery before and after the protocol was applied. Results: Fewer tests were ordered after the protocol was introduced. We detected no statistically significant differences in relation to type of surgery planned or postoperative complications. Conclusions: Patients about to undergo outpatient dermatologic surgery under local anesthesia who have no unusual health risks may not require preoperative testing


Subject(s)
Humans , Male , Female , Adolescent , Young Adult , Adult , Middle Aged , Aged , Aged, 80 and over , Ambulatory Surgical Procedures , Dermatologic Surgical Procedures , Preoperative Care/standards , Anesthesia, Local , Hospitals, University , Preoperative Care/methods , Retrospective Studies , Risk Assessment , Spain
6.
Actas Dermosifiliogr (Engl Ed) ; 110(6): 469-473, 2019.
Article in English, Spanish | MEDLINE | ID: mdl-31023483

ABSTRACT

INTRODUCTION: Short-duration ambulatory surgery for the removal of skin tumors under local anesthesia is increasingly common in dermatology. Preoperative assessment has traditionally targeted the identification of any unknown diseases or other health conditions that might lead to changes in plans for anesthesia or surgery. Hospitals and specialists differ greatly in the tests they order in patients about to undergo outpatient dermatologic surgery given that hardly any finding would be likely to contraindicate or lead to changes in the procedure. This study aimed to provide guidance for those ordering tests before outpatient dermatologic surgery. METHODS: In 2017 our hospital developed a protocol to standardize preoperative testing for outpatient dermatologic surgery. We designed an observational, descriptive, retrospective analysis of tests ordered for patients scheduled for such surgery before and after the protocol was applied. RESULTS: Fewer tests were ordered after the protocol was introduced. We detected no statistically significant differences in relation to type of surgery planned or postoperative complications. CONCLUSIONS: Patients about to undergo outpatient dermatologic surgery under local anesthesia who have no unusual health risks may not require preoperative testing.


Subject(s)
Ambulatory Surgical Procedures , Dermatologic Surgical Procedures , Practice Guidelines as Topic , Preoperative Care/standards , Adolescent , Adult , Aged , Aged, 80 and over , Anesthesia, Local , Female , Hospitals, University , Humans , Male , Middle Aged , Preoperative Care/methods , Retrospective Studies , Risk Assessment , Spain , Young Adult
14.
Cardiovasc Intervent Radiol ; 40(4): 510-519, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27999918

ABSTRACT

PURPOSE: Acute hemorrhage associated with cancers of the head and neck is a life-threatening condition that requires immediate action. The aim of this study was to assess the safety and efficacy of endovascular embolization for acute hemorrhage in patients with head and neck cancers. MATERIALS AND METHODS: Data were retrospectively collected from patients with head and neck cancers who underwent endovascular embolization to treat acute hemorrhage. The primary endpoint was the rate of immediate control of hemorrhage during the first 24 h after embolization. The secondary endpoints were technical or clinical complications, rate of re-hemorrhage 24 h after the procedure, time from embolization to re-hemorrhage, hospitalization time, mortality rate, and time from embolization to death. RESULTS: Fifty-one patients underwent endovascular embolization. The primary endpoint was achieved in 94% of patients. The rate of technical complications was 5.8%, and no clinical complication was observed. Twelve patients (23.5%) had hemorrhage recurrence after an average time of 127.5 days. The average hospitalization time was 7.4 days, the mortality rate during the follow-up period was 66.6%, and the average time from embolization to death was 132.5 days. CONCLUSION: Endovascular embolization to treat acute hemorrhage in patients with head and neck cancers is a safe and effective method for the immediate control of hemorrhage and results in a high rate of hemorrhage control. Larger studies are necessary to determine which treatment strategy is best for improving patient outcomes.


Subject(s)
Embolization, Therapeutic/methods , Endovascular Procedures/methods , Head and Neck Neoplasms/complications , Hemorrhage/etiology , Hemorrhage/therapy , Adult , Aged , Aged, 80 and over , Female , Humans , Infant , Male , Middle Aged , Retrospective Studies , Treatment Outcome
15.
Osteoporos Int ; 23(12): 2847-53, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22297734

ABSTRACT

UNLABELLED: The relationship between surgical timing and hip fracture mortality is unknown in the context of developing countries where large delays to surgery are common. We observed that delay from fracture to hospital admission is associated with decreased survival after a hip fracture. INTRODUCTION: To examine the relationship between the time interval from fracture to surgery as well as its subcomponents (time from fracture to hospital admission and time from admission to surgery) and hip fracture survival. METHODS: The medical records of all patients aged 60 years and older admitted to a public university hospital in the city of Rio de Janeiro with a primary diagnosis of hip fracture between 1995 and 2000 were reviewed. Survival to hospital discharge and at 1 year were examined. RESULTS: Among 343 patients included in the study, there were 18 (5.3%) in-hospital deaths, and 297 (86.6%) patients remained alive 1 year after surgery. Very long delays from the time of fracture to hospital admission (mean 3 days) and from hospital admission to surgery (mean 13 days) were identified. Increased time from fracture to hospital admission was associated with reduced survival to hospital discharge (hazard ratio [HR] 1.09, 95% CI 1.03-1.15, p = 0.005) and reduced survival at 1 year after surgery (HR 1.07, 95% CI 1.03-1.10, p < 0.001). The interval of time from hospital admission to surgery was not associated with reduced survival to hospital discharge (HR 1.03, 95% CI 0.96-1.10, p = 0.379) or at 1 year after surgery (HR 1.03, 95% CI 0.99-1.07, p= 0.185). CONCLUSIONS: If the association estimated in our study is causal, our results provide evidence that some hip fracture-related deaths could be prevented by improved patient access to appropriate and timely hospital care in the context of a developing country.


Subject(s)
Hip Fractures/mortality , Aged , Aged, 80 and over , Brazil/epidemiology , Developing Countries , Female , Hip Fractures/surgery , Hospital Mortality , Hospitalization/statistics & numerical data , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors , Time Factors
16.
J. venom. anim. toxins incl. trop. dis ; 18(2): 244-252, 2012. graf, tab
Article in English | LILACS, VETINDEX | ID: lil-639484

ABSTRACT

Yeasts are becoming a common cause of nosocomial fungal infections in immunocompromised patients. Such infections often develop into sepsis with high mortality rates. The aim of this study was to evaluate some of the numerous factors associated with the development of candidemia. Medical records were retrospectively analyzed of 98 Candida spp. patients. Results showed that the most prevalent risk factors for developing candidemia were: antibiotics and antifungal agents (93.9% and 79.6%, respectively); the use of central venous catheter (93.9%); mechanical ventilation (73.5%); and parenteral nutrition (60.2%). The main species of Candida found were: C. parapsilosis (37.76%), C. albicans (33.67%); and others (28.57%). C. glabrata showed the highest mortality rate (75%), followed by C. tropicalis (57.1%) and C. albicans (54.5%). The elevated mortality rate found in this study indicates that preventive measures against candidemia must be emphasized in hospitals.(AU)


Subject(s)
Candida , Risk Factors , Candidemia , Mycoses , Yeasts
17.
J. venom. anim. toxins incl. trop. dis ; 18(3): 335-339, 2012. tab
Article in English | LILACS, VETINDEX | ID: biblio-1484511

ABSTRACT

Yeasts are becoming a common cause of nosocomial fungal infections that affect immunocompromised patients. Such infections can evolve into sepsis, whose mortality rate is high. This study aimed to evaluate the viability of Candida species identification by the automated system Vitek-Biomerieux (Durham, USA). Ninety-eight medical charts referencing the Candida spp. samples available for the study were retrospectively analyzed. The system Vitek-Biomerieux with Candida identification card is recommended for laboratory routine use and presents 80.6% agreement with the reference method. By separate analysis of species, 13.5% of C. parapsilosis samples differed from the reference method, while the Vitek system wrongly identified them as C. tropicalis, C. lusitaneae or as Candida albicans. C. glabrata presented a discrepancy of only one sample (25%), and was identified by Vitek as C. parapsilosis. C. guilliermondii also differed in only one sample (33.3%), being identified as Candida spp. All C. albicans, C. tropicalis and C. lusitaneae samples were identified correctly.


Subject(s)
Humans , Candida albicans/isolation & purification , Candida glabrata/isolation & purification , Candida/isolation & purification , Reagent Kits, Diagnostic , Candidiasis
18.
São Paulo; SMS; 1; 2012. 3 p.
Non-conventional in Portuguese | Sec. Munic. Saúde SP, CRSSUL-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: sms-2030

ABSTRACT

Dentro das normas padronizadas ao bom atendimento à gestante e recém–nascido (RN), é fundamental a disponibilização pela Rede Pública de pronto acesso ao atendimento hospitalar, garantindo condições adequadas para o parto e assistência ao RN. Desta forma, é imprescindível que as referências sejam definidas baseadas em critérios de disponibilidade dos serviços e distância entre a origem de residência e os hospitais. Para a efetividade da grade de referência é importante que os serviços conheçam e divulguem adequadamente a grade entre as pacientes e que as façam cientes dos benefícios e importância de respeitá-la(AU)


Subject(s)
Humans , Public Health , Women's Health , Organization and Administration
19.
São Paulo; Secretaria Municipal de Saúde de São Paulo; 1; 2012. 3 p.
Non-conventional in Portuguese | LILACS, Coleciona SUS, CRSSUL-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-937356

ABSTRACT

Dentro das normas padronizadas ao bom atendimento à gestante e recém–nascido (RN), é fundamental a disponibilização pela Rede Pública de pronto acesso ao atendimento hospitalar, garantindo condições adequadas para o parto e assistência ao RN. Desta forma, é imprescindível que as referências sejam definidas baseadas em critérios de disponibilidade dos serviços e distância entre a origem de residência e os hospitais. Para a efetividade da grade de referência é importante que os serviços conheçam e divulguem adequadamente a grade entre as pacientes e que as façam cientes dos benefícios e importância de respeitá-la


Subject(s)
Humans , Organization and Administration , Public Health , Women's Health
20.
São Paulo; Secretaria Municipal de Saúde de São Paulo; 1; 2012. 3 p.
Non-conventional in Portuguese | LILACS, CAB-Producao, Sec. Munic. Saúde SP, CRSSUL-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: lil-642630

ABSTRACT

Dentro das normas padronizadas ao bom atendimento à gestante e recém–nascido (RN), é fundamental a disponibilização pela Rede Pública de pronto acesso ao atendimento hospitalar, garantindo condições adequadas para o parto e assistência ao RN. Desta forma, é imprescindível que as referências sejam definidas baseadas em critérios de disponibilidade dos serviços e distância entre a origem de residência e os hospitais. Para a efetividade da grade de referência é importante que os serviços conheçam e divulguem adequadamente a grade entre as pacientes e que as façam cientes dos benefícios e importância de respeitá-la.


Subject(s)
Humans , Organization and Administration , Public Health , Women's Health
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