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1.
Crit Care Med ; 36(4): 1119-24, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18379236

RESUMO

OBJECTIVE: Ambulation of patients with acute respiratory failure may be unnecessarily limited in the acute intensive care setting. We hypothesized that ambulation of patients with acute respiratory failure would increase with transfer to an intensive care unit where activity is a key component of patient care. DESIGN: Pre-post cohort study of respiratory failure patients. SETTING: Adult intensive care units at LDS Hospital. PATIENTS: Respiratory failure patients requiring >4 days of mechanical ventilation who were transferred from other LDS Hospital intensive care units to the respiratory intensive care unit. INTERVENTIONS: We prospectively applied an early activity protocol to all consecutive respiratory failure patients transferred to the respiratory intensive care unit. MEASUREMENTS AND MAIN RESULTS: We studied 104 respiratory failure patients who required mechanical ventilation for >4 days. Transferring a patient to the respiratory intensive care unit substantially increased the probability of ambulation (p < .0001). After 2 days in the respiratory intensive care unit, the number of patients ambulating had increased three-fold compared with pretransfer rates. Female gender (p = .019), the absence of sedatives (p = .009), and lower Acute Physiology and Chronic Health Evaluation II scores (p = .017) also predicted an increased probability of ambulation. Improvements in ambulation with transfer to the respiratory intensive care unit remained significant after adjustment for Acute Physiology and Chronic Health Evaluation II scores and other covariates. CONCLUSIONS: Transfer of acute respiratory failure patients to the respiratory intensive care unit substantially improved ambulation, independent of the underlying pathophysiology. The intensive care environment may contribute unnecessary immobilization throughout the course of acute respiratory failure. Sedatives, even given intermittently, substantially reduce the likelihood of ambulation. Controlled studies are needed to determine whether intensive care unit immobilization contributes to long-term neuromuscular dysfunction or whether early intensive care unit activity improves outcomes.


Assuntos
Cuidados Críticos/métodos , Unidades de Terapia Intensiva/estatística & dados numéricos , Atividade Motora , Síndrome do Desconforto Respiratório/terapia , Caminhada , APACHE , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Mortalidade Hospitalar , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Transferência de Pacientes , Estudos Prospectivos , Respiração Artificial , Síndrome do Desconforto Respiratório/classificação , Resultado do Tratamento
2.
Crit Care Clin ; 23(1): 81-96, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17307118

RESUMO

Growing interest in reducing costs for patients requiring long-term mechanical ventilation has led to development of different care delivery models. This article describes the development and implementation a respiratory care process model focusing on best practices and improvement in care, including early mobility. To implement the care process model, the authors had to make significant changes in the respiratory ICU (RICU), which included changes in how the RICU staff worked together. ICU culture was transformed in a way that resulted in improved and consistent care, including early mobility, while stabilizing or even decreasing cost. Involvement of front-line staff in early mobility and other components of the care process model resulted in the development of a culture of safety and teamwork.


Assuntos
Protocolos Clínicos , Cuidados Críticos/organização & administração , Estado Terminal/reabilitação , Deambulação Precoce , Unidades de Terapia Intensiva/organização & administração , Insuficiência Respiratória/terapia , Deambulação Precoce/enfermagem , Humanos , Cultura Organizacional , Equipe de Assistência ao Paciente , Qualidade da Assistência à Saúde , Respiração Artificial/enfermagem , Insuficiência Respiratória/enfermagem , Insuficiência Respiratória/reabilitação , Sono , Traqueostomia/estatística & dados numéricos , Utah
3.
AACN Adv Crit Care ; 27(2): 187-203, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27153308

RESUMO

Immobility in the intensive care unit (ICU) is associated with neuromuscular weakness, post-intensive care syndrome, functional limitations, and high costs. Early mobility-based rehabilitation in the ICU is feasible and safe. Mobility-based rehabilitation varied widely across 5 ICUs in 1 health care system, suggesting a need for continuous training and evaluation to maintain a strong mobility-based rehabilitation program. Early mobility-based rehabilitation shortens ICU and hospital stays, reduces delirium, and increases muscle strength and the ability to ambulate. Long-term effects include increased ability for self-care, faster return to independent functioning, improved physical function, and reduced hospital readmission and death. Factors that influence early mobility-based rehabilitation include having an interdisciplinary team; strong unit leadership; access to physical, occupational, and respiratory therapists; a culture focused on patient safety and quality improvement; a champion of early mobility; and a focus on measuring performance and outcomes.


Assuntos
Cuidados Críticos/psicologia , Estado Terminal/psicologia , Estado Terminal/reabilitação , Limitação da Mobilidade , Pacientes/psicologia , Estresse Psicológico/terapia , Sobreviventes/psicologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Educação Continuada , Feminino , Humanos , Unidades de Terapia Intensiva , Masculino , Pessoa de Meia-Idade , Alta do Paciente , Síndrome
4.
J Am Med Inform Assoc ; 12(6): 589-95, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16049226

RESUMO

Mechanical ventilators are designed to generate alarms when patients become disconnected or experience other critical ventilator events. However, these alarms can blend in with other accustomed sounds of the intensive care unit. Ventilator alarms that go unnoticed for extended periods of time often result in permanent patient harm or death. We developed a system to monitor critical ventilator events through our existing hospital network. Whenever an event is identified, the new system takes control of every computer in the patient's intensive care unit and generates an enhanced audio and visual alert indicating that there is a critical ventilator event and identifies the room number. Once the alert is acknowledged or the event is corrected, all the computers are restored back to the pre-alert status and/or application. This paper describes the development and implementation of this system and reports the initial results, user acceptance, and the increase in valuable information and patient safety.


Assuntos
Sistemas de Informação Hospitalar , Monitorização Fisiológica/instrumentação , Ventiladores Mecânicos , Sistemas Computacionais , Falha de Equipamento , Humanos , Unidades de Terapia Intensiva , Projetos Piloto
5.
Transplantation ; 99(6): 1216-9, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25539461

RESUMO

BACKGROUND: Lactic acidosis (LA) frequently occurs after heart transplantation (HTx). It is hypothesized to be related to inotropic support or metabolic derangements from chronic heart failure. As such, restoring hemodynamic stability with mechanical circulatory support before HTx should mitigate this problem. Our aim was to evaluate the incidence and outcomes of LA after HTx. METHODS: We evaluated HTx recipients January 2000 to May 2011. Post-HTx outcomes included graft dysfunction, length of intensive care unit stay, length of hospital stay, inotropic support, and survival. RESULTS: Of 143 eligible patients, 98.6% had LA, 67% severe, after HTx. Data were analyzed based on the severity of LA. Time to peak lactate, intensive care unit stay, length of hospital stay, peak glucose, inotropic dose, graft dysfunction, and survival after HTx were similar between groups. Statistically significant differences included pretransplant support (25.6% mechanical circulatory support in nonsevere vs. 44.9% severe LA), hospitalization at the time of HTx (37.2% vs. 21.4%), glucose at the time of peak lactate (182.88 ± 69.80 vs. 221.31 ± 56.91), ischemic time (187.4 ± 63.1 vs. 215.5 ± 68.1), and duration of inotrope. CONCLUSION: Severe LA is common after HTx, though it appears to be transient and benign. Mechanical circulatory support after HTx does not prevent LA. High lactate levels are associated with longer ischemic times, longer duration of inotrope, and correspond with higher glucose levels. The underlying mechanism is yet to be satisfactorily elucidated.


Assuntos
Acidose Láctica/etiologia , Transplante de Coração/efeitos adversos , Acidose Láctica/epidemiologia , Acidose Láctica/terapia , Adulto , Circulação Assistida , Cardiotônicos/uso terapêutico , Feminino , Sobrevivência de Enxerto , Humanos , Incidência , Ácido Láctico/sangue , Masculino , Pessoa de Meia-Idade , Preservação de Órgãos , Fatores de Risco , Resultado do Tratamento , Utah/epidemiologia
6.
Cardiovasc Pathol ; 24(2): 71-5, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25483742

RESUMO

BACKGROUND: Driveline exit site (DLES) infection is a major complication of ventricular assist devices (VADs). Differences in the sheath material interfacing with exit site tissue appear to affect healing time and infection risk more than site hygiene, but the mechanistic basis for this is not clear. METHODS: Health record data from Utah Artificial Heart Program patients with HeartMate II (HMII) devices implanted from 2008 to 2012 were retrospectively reviewed, with particular attention to interface type, incorporation (healing) time, and infections. Tissue samples from the DLES were collected at the time of VAD removal in a small subset. These samples were examined by routine histology and environmental scanning electron microscopy (ESEM). RESULTS: Among 57 patients with sufficient data, 15 had velour interfaces and 42 had silicone. Indications for and duration of support were similar between the groups. The silicone group had shorter incorporation time (45 ±22 vs. 56 ±34 days, P=.17) and fewer DLES infections (20% vs. 1.7%, P=.026, for patient infections and 0.0340 vs. 0.166, P=.16, for infections per patient-year). Tissues from five patients, three with velour, were examined. Velour interfaces demonstrated more hyperkeratosis, hypergranulosis, and dermal inflammation. By ESEM, the silicone driveline tracts appeared relatively smooth and flat, whereas the velour interface samples were irregular with deep fissures and globular material adhering to the surface. CONCLUSIONS: Using the silicone portion of the HMII driveline at the DLES was associated with fewer infections and a trend toward faster healing in this small retrospective series. Whether the intriguing microscopic differences directly account for this needs further study on a larger scale.


Assuntos
Coração Auxiliar/efeitos adversos , Poliésteres/efeitos adversos , Infecções Relacionadas à Prótese/etiologia , Silicones/efeitos adversos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Infecções Relacionadas à Prótese/epidemiologia
7.
Crit Care Nurse ; 32(6): 25-34, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23203952

RESUMO

BACKGROUND: Many critically ill patients have severe volume overload due to vigorous fluid resuscitation. Optimal fluid management strategies to clear tissue edema are unclear. OBJECTIVE: To assess safety and effectiveness of a clinical application of a furosemide infusion protocol in edematous critically ill patients. METHODS: A prospective, cohort study of consecutive adult critically ill patients who received furosemide infusion by protocol from June 2003 to July 2004. RESULTS: The mean total dose of furosemide was 2240 mg. The mean cumulative fluid balance therapy was -3376 mL. Electrolyte values in the critical laboratory range were 3.3% for potassium, 0.2% for sodium, and no critical values for magnesium. The mean change in creatinine level was +0.2 mg/dL during furosemide infusion therapy, but the mean creatinine level returned to baseline by 3 days after the furosemide infusion. A minimum mean arterial pressure less than 55 mm Hg occurred 12% of the time during the furosemide infusion. CONCLUSIONS: Furosemide infusion therapy was associated with moderately negative cumulative fluid balances, electrolyte shifts, and mild transient worsening of renal function.


Assuntos
Diuréticos/administração & dosagem , Edema/tratamento farmacológico , Furosemida/administração & dosagem , Unidades de Terapia Intensiva , Desequilíbrio Hidroeletrolítico/tratamento farmacológico , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Cuidados Críticos , Estado Terminal/mortalidade , Estado Terminal/terapia , Diuréticos/efeitos adversos , Relação Dose-Resposta a Droga , Edema/diagnóstico , Feminino , Seguimentos , Furosemida/efeitos adversos , Taxa de Filtração Glomerular/efeitos dos fármacos , Humanos , Infusões Intravenosas , Testes de Função Renal , Masculino , Pessoa de Meia-Idade , Segurança do Paciente , Estudos Prospectivos , Medição de Risco , Taxa de Sobrevida , Resultado do Tratamento , Desequilíbrio Hidroeletrolítico/fisiopatologia
8.
Phys Ther ; 92(12): 1518-23, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22491481

RESUMO

BACKGROUND: Weakness and debilitation are common following critical illness. Studies that assess whether early physical activity initiated in the intensive care unit (ICU) continues after a patient is transferred to a ward are lacking. OBJECTIVE: The purpose of this study was to assess whether physical activity and mobility initiated during ICU treatment were maintained after patients were discharged from a single ICU to a ward. DESIGN: This was a cohort study. METHODS: Consecutive patients who were diagnosed with respiratory failure and admitted to the respiratory ICU (RICU) at LDS Hospital underwent early physical activity and mobility as part of usual care. Medical data, the number of requests for a physical therapy consultation or nursing assistance with ambulation at ICU discharge, and mobility data were collected during the first 2 full days on the ward. RESULTS: Of the 72 patients who participated in the study, 65 had either a physical therapy consultation or a request for nursing assistance with ambulation at ward transfer. Activity level decreased in 40 participants (55%) on the first full ward day. Of the 61 participants who ambulated 100 ft (30.48 m) or more on the last full RICU day, 14 did not ambulate, 22 ambulated less than 100 ft, and 25 ambulated 100 ft or more on the first ward day. LIMITATIONS: Limitations include lack of data regarding why activity was not performed on the ward, lack of longitudinal follow-up to assess effects of activity, and lack of generalizability to patients not transferred to a ward or not treated in an ICU with an early mobility program. CONCLUSIONS: Despite the majority of participants having a physical therapy consultation or a request for nursing assistance with ambulation at the time of transfer to the medical ward, physical activity levels decreased in over half of participants on the first full ward day. The data suggest a need for education of ward staff regarding ICU debilitation, enhanced communication among care providers, and focus on the importance of patient-centered outcomes during and following ICU treatment.


Assuntos
Continuidade da Assistência ao Paciente/estatística & dados numéricos , Estado Terminal/reabilitação , Unidades de Terapia Intensiva , Atividade Motora , Transferência de Pacientes , Modalidades de Fisioterapia/estatística & dados numéricos , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Estado Terminal/enfermagem , Deambulação Precoce , Humanos , Pessoa de Meia-Idade , Limitação da Mobilidade , Debilidade Muscular/etiologia , Debilidade Muscular/enfermagem , Debilidade Muscular/reabilitação , Alta do Paciente , Respiração Artificial , Insuficiência Respiratória/terapia , Caminhada
9.
Crit Care Med ; 35(1): 139-45, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17133183

RESUMO

OBJECTIVE: To determine whether early activity is feasible and safe in respiratory failure patients. DESIGN: Prospective cohort study. SETTING: From June 1, 2003, through December 31, 2003, we assessed safety and feasibility of early activity in all consecutive respiratory failure patients who required mechanical ventilation for >4 days admitted to our respiratory intensive care unit (RICU). A majority of patients were treated in another intensive care unit (ICU) before RICU admission. We excluded patients who required mechanical ventilation for < or =4 days. PATIENTS: Eight-bed RICU at LDS Hospital. INTERVENTIONS: We assessed patients for early activity as part of routine respiratory ICU care. We prospectively recorded activity events and adverse events. We defined three activity events as sit on bed, sit in chair, and ambulate. We defined six activity-related adverse events as fall to knees, tube removal, systolic blood pressure >200 mm Hg, systolic blood pressure <90 mm Hg, oxygen desaturation <80%, and extubation. MEASUREMENTS AND MAIN RESULTS: During the study period, we conducted a total of 1,449 activity events in 103 patients. The activity events included 233 (16%) sit on bed, 454 (31%) sit in chair, and 762 (53%) ambulate. In patients with an endotracheal tube in place, there were a total of 593 activity events, of which 249 (42%) were ambulation. There were <1% activity-related adverse events, including fall to the knees without injury, feeding tube removal, systolic blood pressure >200 mm Hg, systolic blood pressure <90 mm Hg, and desaturation <80%. No patient was extubated during activity. CONCLUSIONS: We conclude that early activity is feasible and safe in respiratory failure patients. A majority of survivors (69%) were able to ambulate >100 feet at RICU discharge. Early activity is a candidate therapy to prevent or treat the neuromuscular complications of critical illness.


Assuntos
Cuidados Críticos/métodos , Deambulação Precoce/métodos , Respiração Artificial , Insuficiência Respiratória/terapia , Acidentes por Quedas/estatística & dados numéricos , Atividades Cotidianas , Fatores Etários , Idoso , Repouso em Cama/efeitos adversos , Comorbidade , Estado Terminal/terapia , Deambulação Precoce/efeitos adversos , Estudos de Viabilidade , Feminino , Humanos , Hipotensão/etiologia , Hipóxia/etiologia , Tempo de Internação/estatística & dados numéricos , Masculino , Pessoa de Meia-Idade , Avaliação em Enfermagem , Seleção de Pacientes , Estudos Prospectivos , Segurança , Fatores de Tempo , Utah
10.
AMIA Annu Symp Proc ; : 951, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16779238

RESUMO

The alarms generated by mechanical ventilators when patients become disconnected can blend in with other typical sounds of the intensive care unit. Ventilator alarms that go unnoticed for extended periods of time often result in permanent patient harm or death. We developed a unit-wide system to monitor ventilator disconnection alarms. When a disconnection is identified, the system takes control of every computer in the patient's intensive care unit and generates an enhanced audio and visual alert. This system was tested in four ICUs at LDS Hospital. Acceptance by medical personnel was very high and patient safety was improved through early intervention that avoided prolonged hypoxia. In addition, the system facilitated root cause analyses and new safety strategies.


Assuntos
Ventiladores Mecânicos , Falha de Equipamento , Humanos , Unidades de Terapia Intensiva , Microcomputadores
11.
Am J Respir Crit Care Med ; 167(5): 690-4, 2003 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-12493646

RESUMO

Although survival rates for acute respiratory distress syndrome have increased, there is only limited information regarding the quality of life and the relationship between quality of life and pulmonary function after survival. We prospectively measured pulmonary function, emotional function, and health-related quality of life in a cohort of acute respiratory distress syndrome survivors recruited from patients who were enrolled in a randomized clinical trial of high versus low tidal volume mechanical ventilation at 1 year after their recovery. No significant differences were found between the patients treated with high and low tidal volumes on any pulmonary function measure. Approximately 80% of the patients in both groups demonstrated reduced diffusing capacity; 20% had airflow obstruction, and 20% had chest restriction. Scores on measures of depression and anxiety were within the normal ranges, suggesting that they did not have significant affective symptoms. However, both groups reported decreased health-related quality of life in physical functioning, physical ability to maintain their roles (role-physical), bodily pain, general health, and vitality (energy) on the Medical Outcome Study Short Form Health Survey with similar physical limitations reported on the Sickness Impact Profile questionnaire. The pulmonary function abnormalities correlated with decreased health-related quality of life for domains reflecting physical function. Acute respiratory distress syndrome survivors treated with high and low tidal volumes have abnormal pulmonary function that was related to decreased health-related quality of life 1 year after hospital discharge.


Assuntos
Qualidade de Vida , Síndrome do Desconforto Respiratório , APACHE , Adulto , Ansiedade , Distribuição de Qui-Quadrado , Estudos de Coortes , Interpretação Estatística de Dados , Depressão/diagnóstico , Feminino , Seguimentos , Inquéritos Epidemiológicos , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Capacidade de Difusão Pulmonar , Respiração Artificial , Síndrome do Desconforto Respiratório/psicologia , Síndrome do Desconforto Respiratório/terapia , Testes de Função Respiratória , Fatores de Risco , Inquéritos e Questionários , Volume de Ventilação Pulmonar , Fatores de Tempo
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