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2.
J Sleep Res ; 27(3): e12607, 2018 06.
Artigo em Inglês | MEDLINE | ID: mdl-28944590

RESUMO

Intensive care unit (ICU) environment has a very strong and unavoidable negative impact on patients' sleep. Sleep deprivation in ICU patients has been already studied and negative effects on their outcome (prolonged ICU stay, decreased recovery) and complication rates (incidence of delirium, neuropsychological sequels of critical illness) discussed. Several interventions potentially improving the sleep disturbance in ICU (sleep-promotion strategies) have been assumed and tested for clinical practice. We present a review of recent literature focused on chosen types of non-pharmacological interventions (earplugs and eye mask) analysing their effect on sleep quality/quantity. From the total amount of 82 papers found in biomedical databases (CINAHL, PubMed and SCOPUS) we included the 19 most eligible studies meeting defined inclusion/exclusion criteria involving 1 379 participants. Both experimental and clinical trials, either ICU and non-ICU patient populations were analysed in the review. Most of the reviewed studies showed a significant improvement of subjective sleep quality when using described non-pharmacological interventions (objective parameters were not significantly validated). Measuring the sleep quality is a major concern limiting the objective comparison of the studies' results since non-standardised (and mainly individual) tools for sleep quality assessment were used. Despite the heterogeneity of analysed studies and some common methodological issues (sample size, design, outcome parameters choice and comparison) earplugs and eye mask showed potential positive effects on sleep quality and the incidence of delirium in ICU patients.


Assuntos
Cuidados Críticos/métodos , Dispositivos de Proteção das Orelhas , Dispositivos de Proteção dos Olhos , Unidades de Terapia Intensiva , Privação do Sono/prevenção & controle , Sono/fisiologia , Cuidados Críticos/tendências , Delírio/epidemiologia , Delírio/fisiopatologia , Delírio/terapia , Dispositivos de Proteção das Orelhas/tendências , Dispositivos de Proteção dos Olhos/tendências , Humanos , Unidades de Terapia Intensiva/tendências , Ensaios Clínicos Controlados Aleatórios como Assunto/métodos , Privação do Sono/epidemiologia , Privação do Sono/fisiopatologia , Transtornos do Sono-Vigília/epidemiologia , Transtornos do Sono-Vigília/fisiopatologia , Transtornos do Sono-Vigília/prevenção & controle
4.
US Army Med Dep J ; (2-16): 135-9, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27215881

RESUMO

Appreciation for combat eye protection steadily increased following World War II. Products derived from experiences in World War I, World War II, Korea, Vietnam, and the Iran/Iraq war drove technical improvements throughout the 1980s and 1990s. Dismal wear compliance prior to 2004 indicates Soldiers and their leaders did not appreciate these improvements and found little value in the bulky, ugly, and uncomfortable products. In 2003, the 10th Mountain Division requested enhanced eye protection. Program Executive Office Soldier, the optometry consultant to the Army Surgeon General, members of the Tri-Service Vision Conservation and Readiness Program, and other subject matter experts selected and tested commercial off-the-shelf eye protection against military ballistic impact standards. Optical devices that met ballistic standards formed the first Authorized Protective Eyewear List and were fielded beginning in 2004. Wear compliance rose dramatically for the stylish protective eyewear, reaching 85% to 95% and eye injuries decreased across the Department of Defense even as the incidence of attacks in Iraq increased. Researchers continue to evaluate new materials and designs to increase the capabilities, features and level of protection of future ballistic eyewear.


Assuntos
Desenho de Equipamento/normas , Dispositivos de Proteção dos Olhos/tendências , Militares/educação , Dispositivos de Proteção dos Olhos/normas , Humanos , Incidência , Estados Unidos , Guerra
7.
Br J Sports Med ; 36(6): 442-5, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12453839

RESUMO

OBJECTIVE: To assess indicative trends in the use of protective eyewear by Australian squash players and their attitudes towards its use since 1989. METHODS: Data were extracted from three Australian surveys of squash players conducted in 1989, 1995, and 2000. Responses to directly similar attitudinal questions relating to protective eyewear use from each survey were compared. The proportion of players giving each response was calculated for each survey, along with 95% confidence intervals for the differences between the 2000 survey and those from the earlier surveys. RESULTS: Self reported use of protective eyewear ranged from 10.0% in 1989, to 8.6% in 1995, and 18.8% in 2000. However, only 8.9% of the players surveyed in 2000 actually wore appropriate standards approved/polycarbonate lens eyewear. This can be compared with 8.0% and 2.0% of players who reported wearing appropriate polycarbonate lens eyewear in the 1989 and 1995 surveys respectively. Compared with the 1995 survey, significantly more players in 2000 believed that more players should wear protective eyewear (95% confidence interval (CI) for difference 1 to 18). A significantly higher proportion of players also supported the compulsory use of protective eyewear by juniors in 2000 than in both 1989 (95% CI for difference 6 to 24) and 1995 (95% CI for difference 5 to 22). No other attitudes had significantly changed over the decade. CONCLUSION: These data suggest that self reported use of protective eyewear has probably increased over the past decade. However, many players report wearing inappropriate eyewear. A transition from positive attitudes to appropriate eyewear behaviours is required before mandatory protective eyewear use can be effectively introduced.


Assuntos
Atitude Frente a Saúde , Traumatismos Oculares/prevenção & controle , Dispositivos de Proteção dos Olhos/tendências , Esportes com Raquete/lesões , Esportes com Raquete/psicologia , Adulto , Austrália , Feminino , Humanos , Masculino , Esportes com Raquete/tendências
8.
Surg Endosc ; 16(7): 1050-4, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12165821

RESUMO

BACKGROUND: Intraoperative hypothermia is a common event during laparoscopic operations. An external warming blanket has been shown to be effective in preventing hypothermia. It has now been proposed that using heated and humidified insufflation gas can prevent hypothermia and decrease postoperative pain. Therefore, we examined the extent of intraoperative hypothermia in patients undergoing laparoscopic Nissen fundoplication using an upper body warming blanket. We also attempted to determine whether using heated and humidified insufflation gas in addition to an external warming blanket would help to maintain intraoperative core temperature or decrease postoperative pain. METHODS: Twenty patients were randomized to receive either standard carbon dioxide (CO2) gas (control, n = 10) or heated and humidified gas (heated and humidified, n = 10). After the induction of anesthesia, an external warming blanket was placed on all patients in both groups. Intraoperative core temperature and intraabdominal temperature were measured at 15-min intervals. Postoperative pain intensity was assessed using a visual analogue pain scale, and the amount of analgesic consumption was recorded. Volume of gas delivered, number of lens-fogging episodes, intraoperative urine output, and hemodynamic data were also recorded. RESULTS: There was no significant difference between the two groups in age, length of operation, or volume of CO2 gas delivered. Compared with baseline value, mean core temperature increased by 0.4 degrees C in the heated and humidified group and by 0.3 degrees C in the control group at 1.5 h after surgical incision. Intraabdominal temperature increased by 0.2 degrees C in the heated and humidified group but decreased by 0.5 degrees C in the control group at 1.5 h after abdominal insufflation. There was no significant difference between the two groups in visual analog pain scale (5.4 +/- 1.6 control vs 4.5 +/- 2.8 heated and humidified), morphine consumed (27 +/- 26 mg control vs 32 +/- 19 mg heated and humidified), urine output, lens-fogging episodes, or hemodynamic parameters. CONCLUSION: Heated and humidified gas, when used in addition to an external warming blanket, minimized the reduction of intraabdominal temperature but did not alter core temperature or reduce postoperative pain.


Assuntos
Temperatura Corporal/fisiologia , Dióxido de Carbono/uso terapêutico , Temperatura Alta/uso terapêutico , Umidade , Dor Pós-Operatória/prevenção & controle , Adulto , Dispositivos de Proteção dos Olhos/tendências , Feminino , Fundoplicatura/métodos , Refluxo Gastroesofágico/cirurgia , Hemodinâmica/efeitos dos fármacos , Hemodinâmica/fisiologia , Humanos , Umidade/efeitos adversos , Hipotermia/prevenção & controle , Insuflação/métodos , Laparoscopia/métodos , Tempo de Internação , Masculino , Morfina/uso terapêutico , Medição da Dor/métodos , Dor Pós-Operatória/tratamento farmacológico , Espaço Retroperitoneal/fisiologia , Fatores de Tempo , Micção/fisiologia
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