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1.
Clin Rehabil ; 38(7): 898-909, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38556253

RESUMO

OBJECTIVE: This systematic review and meta-analysis aimed to analyze the published randomized controlled trials (RCTs) that investigated the effects of exercise interventions on functioning and health-related quality of life following hospital discharge for recovery from critical illness. DESIGN: Systematic review and meta-analysis of RCTs. DATA SOURCES: We searched PubMed/MEDLINE, Cochrane Central Register of Controlled Trials, PEDro data base, and SciELO (from the earliest date available to January 2023) for RCTs that evaluated the effects of physical rehabilitation interventions following hospital discharge for recovery from critical illness. REVIEW METHODS: Study quality was evaluated using the PEDro Scale. Mean differences (MDs), standard MDs (SMD), and 95% confidence intervals (CIs) were calculated. RESULTS: Fourteen studies met the study criteria, including 1259 patients. Exercise interventions improved aerobic capacity SMD 0.2 (95% CI: 0.03-0.3, I2 = 0% N = 880, nine studies, high-quality evidence), and physical component score of health-related quality of life MD 3.3 (95% CI: 1.0-5.6, I2 = 57%, six studies N = 669, moderate-quality evidence). In addition, a significant reduction in depression was observed MD -1.4 (95% CI: -2.7 to -0.1, I2 = 0% N = 148, three studies, moderate-quality evidence). No serious adverse events were reported. CONCLUSION: Exercise intervention was associated with improvement of aerobic capacity, depression, and physical component score of health-related quality of life after hospital discharge for survivors of critical illness.


Assuntos
Estado Terminal , Terapia por Exercício , Alta do Paciente , Qualidade de Vida , Ensaios Clínicos Controlados Aleatórios como Assunto , Humanos , Estado Terminal/reabilitação , Terapia por Exercício/métodos , Recuperação de Função Fisiológica
2.
Clin Rehabil ; 36(4): 449-471, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-35014892

RESUMO

OBJECTIVE: To determine the effects of neuromuscular electrical stimulation on disabilities and activity limitation of individuals affected by chronic obstructive pulmonary disease. DATA SOURCES: MEDLINE, PEDro database, Cochrane Controlled Trials Register, and SciELO, were searched from inception until October 2021. REVIEW METHODS: Inclusion criteria were patients with COPD, randomized controlled trials comparing neuromuscular electrical stimulation alone or combined conventional pulmonary rehabilitation and neuromuscular electrical stimulation versus control or sham or pulmonary rehabilitation in disabilities and activity limitation in COPD. There were no mandatory language or publication date restrictions. Two reviewers selected studies independently. Weighted mean differences and 95% confidence intervals were calculated. Results 32 studies met the study criteria, including 1.269 participants. Neuromuscular electrical stimulation improved exercise capacity (MD 1.10, 95% CI: 0.33, 1.86, N = 147), and muscle strength (0.53, 95% CI: 0.20, 0.87, N = 147) compared to sham group. Combined neuromuscular electrical stimulation and conventional rehabilitation improved exercise capacity (MD 34.28 meters, 95% CI: 6.84, 61.73, N = 262) compared to conventional rehabilitation alone. No adverse events were reported. CONCLUSIONS: Neuromuscular electrical stimulation resulted in small improvement in disabilities and activity limitation (below the MCID) in COPD. Thus, the inclusion of neuromuscular electrical stimulation in rehabilitation programs must consider the cost Because of inadequate methodological conduction and reporting of methods, some studies were of low quality.


Assuntos
Doença Pulmonar Obstrutiva Crônica , Qualidade de Vida , Estimulação Elétrica , Tolerância ao Exercício , Humanos , Força Muscular , Doença Pulmonar Obstrutiva Crônica/reabilitação
3.
Clin Rehabil ; 32(9): 1189-1202, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29480025

RESUMO

OBJECTIVE: To determine the effects of different intradialytic exercise training modalities on physical functioning and health-related quality of life of maintenance hemodialysis patients. METHODS: We searched MEDLINE, Cochrane Trials Register and CINAHL for controlled trials that evaluated the effects of intradialytic exercise training for maintenance hemodialysis patients and published from the earliest available date to December 2017. Weighted mean difference and 95% confidence interval (CI) were calculated, and heterogeneity was assessed using the I2 test. RESULTS: Fifty-six studies met the study criteria, comprising a total of 2586 patients. Compared with no exercise, combined aerobic and resistance exercise resulted in significant improvement in peak VO2 weighted mean difference (5.1 mL kg-1 min-1; 95% CI: 3.4, 6.8 mL kg-1 min-1), depression symptoms (-7.32; 95% CI -9.31, -5.33) and both physical function (10.67 points; 95% CI 1.08, 20.25 points) and vitality (10.01 points; 95% CI 4.30, 15.72 points) domains of health-related quality of life. Resistance exercise alone was significantly associated with improvement in the 6-minute walk test distance (30.2 m; 95% CI 24.6, 35.9 m), knee extensor strength (0.6 N; 95% CI 0.1, 1.0 N) and Physical Component Score of health-related quality of life (9.53 points; 95% CI -3.09, 22.15 points) when compared with control group. Aerobic exercise alone was not significantly associated with aerobic capacity and quality of life improvement. CONCLUSION: The results provide support to interventions that combine intradialytic aerobic and resistance exercises to improve physical functioning and quality of life in end-stage renal disease patients undergoing hemodialysis.


Assuntos
Exercício Físico , Falência Renal Crônica/terapia , Qualidade de Vida , Diálise Renal , Depressão/terapia , Humanos , Falência Renal Crônica/fisiopatologia , Força Muscular/fisiologia , Consumo de Oxigênio/fisiologia , Teste de Caminhada
4.
BMC Musculoskelet Disord ; 16: 108, 2015 May 06.
Artigo em Inglês | MEDLINE | ID: mdl-25943762

RESUMO

BACKGROUND: Sarcopenia is an important public health problem that affects mainly elders, and has negative consequences, such as disability and even death. Due to the lack of studies evaluating sarcopenia in elderly persons hospitalized in Brazil, the aim of the present study was to describe the frequency of sarcopenia and associated factors among elders in a hospital in the city of Salvador-Brazil. METHODS: This cross-sectional study included 110 hospitalized elderly patients in a multi-specialty hospital in Salvador-BA, Brazil. Inclusion criteria: were elders aged ≥60 years between the first and fifth day of hospitalization; who were able to walk without external assistance; with medical permission to walk, and who did not take vasoactive and inotropic drugs. The diagnosis of sarcopenia was determined by combining the reduction in skeletal muscle mass with muscle weakness (women, <20 kg; men, <30 kg) and/or poor physical performance (gait speed ≤0.8 m/s). To obtain reduced skeletal muscle mass, the skeletal muscle mass index ≤6.37 kg/m(2) for women and ≤8.90 kg/m(2) for men was used. Cognitive function, Charlson index, admission profile (clinical and surgical), smoking, falls suffered in the last year and physical inactivity prior to admission were also evaluated. The frequency of sarcopenia was described in percentages with their respective confidence intervals and logistic regression was performed for multivariate analysis of factors associated with sarcopenia. RESULTS: Among the 110 patients included, the frequency of sarcopenia was 21.8%, with 10.0% being of the severe type. There was a predominance of clinical profile (59.1%), such as heart disease (20.0%), pneumonia (13.6%) and skin infections (9.1%), with a Charlson index of 5.4 ± 1.8. The factors associated with sarcopenia were age (OR = 1.14; 95% CI = 1.06 to 1.23), clinical profile on admission (OR = 5.15; 95% CI = 1.16-22.9) and smoking (OR = 7.8; 95% CI = 1.53-39.9). CONCLUSIONS: The frequency of sarcopenia in elderly hospitalized patients was high (1 in 5 elderly) and anthropometric equation can be a viable and inexpensive alternative to screening and programming intervention in this population.


Assuntos
Hospitalização , Sarcopenia/diagnóstico , Idoso , Idoso de 80 Anos ou mais , Brasil , Estudos Transversais , Feminino , Força da Mão , Humanos , Masculino , Pessoa de Meia-Idade , Debilidade Muscular/etiologia , Músculo Esquelético/patologia , Sarcopenia/complicações , Sarcopenia/patologia
5.
Braz J Phys Ther ; 28(2): 101047, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38522390

RESUMO

BACKGROUND: Existing mobility scales for hospitalized patients do not include assessment of tasks for the right and left side, ability to transfer from sitting to lying and from standing to sitting, ability to climbing steps and pick up an object from the floor in the same instrument. OBJECTIVE: Evaluate the reliability and validity of the hospital mobility assessment scale (HMob) according to the Consensus-based standards for the selection of health measurement instruments (COSMIN). METHODS: Study conducted in three inpatient units (cardiology, neurology, and gastrohepatology) and one adult intensive care unit in a hospital. Patients of both sexes were included; age >18 years; collaborative and who obeyed commands, with different medical diagnoses and clinical release to leave their bed (provided by the doctor). Special populations such as those with burns and orthopedics were excluded. RESULTS: The sample consisted of 130 patients; 20 from the pilot study and 110 to assess the clinimetric properties of the HMob. Cronbach alpha coefficient was 0.949. Relative intra- (A1-A2) and inter-rater (A1-B; A2-B) reliability was excellent (A1-A2: ICC = 0.982, p-value < 0.0001; A1-B: ICC = 0.993, p-value < 0.0001; A2-B: ICC = 0.986, p-value < 0.0001.) The convergent criterion validity of HMob in relation to the ICU Functional Status Score was 0.967 (p-value < 0.0001) and for Functional Independence measure (MIF) was 0.926 (p-value < 0.0001). CONCLUSION: The HMob scale showed excellent internal consistency, intra- and inter-rater reliability, and concurrent validity in the motor domain, which suggests that it can be used in daily practice to measure mobility in hospitalized patients.


Assuntos
Hospitalização , Humanos , Reprodutibilidade dos Testes , Unidades de Terapia Intensiva , Pacientes Internados
6.
Braz J Phys Ther ; 28(3): 101066, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38870596

RESUMO

BACKGROUND: The Brazilian Classification of Physical Therapy Diagnosis, developed by the Federal Council of Physiotherapy and Occupational Therapy (COFFITO), has the constitutional objectives of standardizing ethical, scientific and social aspects of the Physical Therapy profession. OBJECTIVE: To describe the work process, rationale and proposal for standardization of a physical therapy diagnosis classification system in Brazil. METHODS: A working group was created to propose a standardized classification for the description and codification of physical therapy diagnoses. Some terminologies common to the International Classification of Functioning (ICF) were used to make the nomenclature of diagnoses compatible with the outcomes inherent in the field of physical therapy. RESULTS: The Brazilian Classification of Physical Therapy Diagnosis project culminated in a physical therapy diagnosis model consisting of terms grouped by organic systems and identifying codes. In addition, an application was developed to allow professionals to use the standardized diagnostic classification in an online system. CONCLUSION: The diagnostic classification system is expected to advance the Physical Therapy profession allowing the identification of structural and/or functional alterations in a simplified and standardised manner. From a physical therapy perspective, this classification may help to consolidate the autonomy of the Brazilian physical therapists by establishing a clearer pathway between the diagnosis and interventions.


Assuntos
Modalidades de Fisioterapia , Brasil , Humanos , Especialidade de Fisioterapia , Fisioterapeutas
7.
Phys Ther ; 103(5)2023 05 04.
Artigo em Inglês | MEDLINE | ID: mdl-37249533

RESUMO

OBJECTIVE: The purpose of this study was to compare high-intensity interval training (HIIT) with moderate-intensity continuous training (MICT) for feasibility, safety, adherence, and short- and long-term efficacy in improving functioning and health-related quality of life in survivors of coronavirus disease 2019 (COVID-19). METHODS: COVIDEX is a two-pronged, parallel-group, randomized controlled trial with an 8-week training intervention. The study participants will be 94 patients aged >18 years, admitted to a specialized post-COVID center. Participants will be randomized to HIIT (4 × 4 minutes of high-intensity work periods at 85% to 90% of peak heart rate) and MICT (47 minutes at 70% to 75% peak heart rate) groups for biweekly sessions for 8 weeks. The participants will undergo 2 phases of supervised training (phases 1 and 2) of 4 weeks each, in a public, specialized, post-COVID center. In phase 1, we will assess and compare the feasibility, acceptability, and short-term efficacy of HIIT and MICT intervention. In phase 2, the long-term efficacy of HIIT and MICT will be assessed and compared regarding function and health-related quality of life. To prevent any expectation bias, all study participants and assessors will be blinded to the study hypotheses. Group allocation will be masked during the analysis. All statistical analyses will be conducted following intention-to-treat principles. IMPACT: This study is the first randomized controlled trial that will compare the feasibility, safety, adherence, and efficacy of the HIIT and MICT intervention programs in this population. The findings will potentially provide important information and assist in clinical decision making on exercise to optimize the benefits of clinical health care in survivors of COVID-19.


Assuntos
COVID-19 , Treinamento Intervalado de Alta Intensidade , Humanos , Treinamento Intervalado de Alta Intensidade/métodos , Qualidade de Vida , Exercício Físico/fisiologia , Sobreviventes , Ensaios Clínicos Controlados Aleatórios como Assunto
8.
Heart Lung ; 56: 8-23, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35649308

RESUMO

INTRODUCTION: It is important to clarify the effect of ventilator hyperinflation(VHI) on pulmonary function and secretion clearance in adults receiving mechanical ventilation(MV). There is no published meta-analysis on the effects VHI on pulmonary function and secretion clearance in adults receiving MV. Objective Analyze the published randomized clinical trials(RCTs) that investigated the effects of VHI on pulmonary function and secretion clearance in adults receiving MV, comparing VHI with isolated aspiration, VHI with manual hyperinflation(MHI), VHI +vibrocompression(VB) versus VB and VHI+VB versus isolated aspiration. METHODS: The following databases PubMed, LILACS, EMBASE, SciELO, PEDro database and Cochrane Central Register of Controlled Trials (CENTRAL) were consulted up to December 2021. Secretion clearance, static and dynamic compliance of the respiratory system(Cstat and Cdyn), airway resistance(Raw) and oxygenation outcomes were evaluated. RESULTS: Thirteen studies met the study criteria, but only 12 studies were included on meta-analysis. There was no difference between VHI versus isolated aspiration for amount of secretions removed(0.41 SMD; 95% CI: -0.08 to 0.89; n=270), VHI versus MHI(0.51 grams; 95% CI: -0.08 to 1.11; n=256), VHI+VB versus VB(0.31 grams; 95% CI: -0.42 to 1.05; n=130) and VHI+VB versus isolated aspiration(0.54 grams; 95% CI: -0.06 to 1.14; n=132). There was difference for VHI versus isolated aspiration to Cstat (4.77 ml/cm H2O; 95% CI: 2.41 to 7.14; n= 136). CONCLUSION: Taking into account all studies included in meta-analysis, no evidences was found that VHI was effective in increasing the amount of secretions removed, Cdyn and oxygenation, but VHI seems to show a slight improvement in Cstat when compared to isolated aspiration. No evidence was found that VHI was effective in increasing the amount of secretions removed, Cdyn and oxygenation, but VHI seems to show a slight improvement in Cstat when compared to isolated aspiration.


Assuntos
Respiração Artificial , Ventiladores Mecânicos , Adulto , Humanos , Respiração Artificial/efeitos adversos , Pulmão
9.
Phys Ther ; 101(7)2021 07 01.
Artigo em Inglês | MEDLINE | ID: mdl-33704496

RESUMO

OBJECTIVE: Exercise is a recommended component of care for people living with HIV/AIDS; however, it is unclear which type of exercise is most effective. The purpose of this study was to investigate the relative effects of different types of exercise interventions on aerobic capacity measured by peak oxygen consumption (peak VO2) and health-related quality of life (HRQoL) in this population. METHODS: For this systematic review and indirect-comparisons meta-analysis (network meta-analysis), different electronic databases were searched up to February 2020 for randomized controlled trials that evaluated the effects of different types of exercise interventions on peak VO2 and HRQoL of people living with HIV/AIDS. Mean differences, standardized mean difference (SMD), and 95% CI were calculated. Fixed- and random-effects Bayesian network meta-analysis were used to compare the relative effectiveness of the different exercise interventions. RESULTS: Forty studies met the study criteria, reporting on a total of 1518 patients. When comparing the exercise interventions with usual care (control group) for the peak VO2 outcome, combined aerobic and resistance exercise was the highest ranked exercise intervention with an SMD of 4.2 (95% CI = 2.5 to 5.9), followed by aerobic exercise (SMD = 3.1; 95% CI = 1.4 to 5.1). Compared with aerobic exercise, resistance training, and yoga, combined aerobic and resistance exercise was the best exercise intervention to promote improvement on physical function, general health, mental health, and energy/vitality domains HRQoL. CONCLUSION: The combined aerobic and resistance exercise was the highest ranked exercise intervention to improve peak VO2 and HRQoL. Combined aerobic and resistance exercise should be considered as a component of care for people living with HIV/AIDS.


Assuntos
Síndrome da Imunodeficiência Adquirida/reabilitação , Terapia por Exercício/métodos , Tolerância ao Exercício/fisiologia , Consumo de Oxigênio/fisiologia , Qualidade de Vida , Humanos , Ensaios Clínicos Controlados Aleatórios como Assunto
10.
Ultrasound Med Biol ; 47(11): 3041-3067, 2021 11.
Artigo em Inglês | MEDLINE | ID: mdl-34417065

RESUMO

This study aims to review published studies that use protocols and ultrasound measurements to evaluate skeletal and diaphragmatic muscles in patients who are critically ill. We searched for references on databases through September 2020 and included in our systematic review studies that used muscular ultrasound to assess skeletal or diaphragm muscles in patients who are critically ill. Seventy-six studies were included, 32 (1720 patients) using skeletal-muscle ultrasound and 44 (2946 patients) using diaphragmatic-muscle ultrasound, with a total of 4666 patients. The population is predominantly adult men. As for designs, most studies (n = 62) were cohort studies. B-mode B was dominant in the evaluations. Medium-to-high frequency bands were used in the analysis of peripheral muscles and medium-to-low frequency bands for diaphragmatic muscles. Evaluation of the echogenicity, muscle thickness and pennation angle of the muscle was also reported. These variables are important in the composition of the diagnosis of muscle loss. Studies demonstrate great variability in their protocols, and sparse description of the important variables that can directly interfere with the quality and validity of these measures. Therefore, a document is needed that standardizes these parameters for ultrasound assessment in patients who are critically ill.


Assuntos
Estado Terminal , Diafragma , Adulto , Diafragma/diagnóstico por imagem , Humanos , Masculino , Músculo Esquelético/diagnóstico por imagem , Tórax , Ultrassonografia
11.
PLoS One ; 15(9): e0238352, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32881921

RESUMO

The dose of progressive active mobilization is still uncertain. The purpose of this study is to identify if the addition of a protocol of progressive active mobilization with dose and training load control to usual care is effective in reducing the length of stay in intensive care unit (ICU) and the improvement of the functioning, incidence of ICU-acquired weakness (ICUAW), mechanical ventilation duration and mortality rate in patients hospitalized in ICU. It is Double-blind randomised clinical trial. The setting for this trial will be medical and surgical ICU of a university hospital. The study participants will be 118 patients aged> 18 years admitted to ICU for less than 72 hours. Participants will be randomized to either an experimental or control group. The experimental group will undertake addition of a protocol of progressive active mobilization with dose and training load control to usual care, while the control group will undertake only usual care. The primary outcome will be length of ICU stay. The secondary outcomes will be Cross-sectional area and muscle thickness of the rectus femoris and biceps brachii, Change in muscle strength from the baseline, Functional Status, incidence of ICUAW, Days with mechanical ventilation and Mortality. All statistical analyses will be conducted following intention-to-treat principles. It has a detailed description of the dose of exercise, was designed with the strictest methodological criteria. These characteristics allow to investigate with greater certainty the results progressive active mobilization in critical patients, allowing replication and future combinations in meta-analyzes.


Assuntos
Estado Terminal/terapia , Adulto , Protocolos Clínicos , Estado Terminal/mortalidade , Método Duplo-Cego , Exercício Físico , Músculos Isquiossurais/fisiologia , Humanos , Unidades de Terapia Intensiva , Estimativa de Kaplan-Meier , Tempo de Internação , Força Muscular , Músculo Quadríceps/fisiologia , Ensaios Clínicos Controlados Aleatórios como Assunto , Respiração Artificial , Adulto Jovem
12.
Rev Bras Ter Intensiva ; 32(3): 398-404, 2020.
Artigo em Português, Inglês | MEDLINE | ID: mdl-33053029

RESUMO

OBJECTIVE: To evaluate the intra- and interexaminer reproducibility of measurements of the resistance and static and dynamic compliance of the respiratory system in patients on mechanical ventilation. METHODS: This was an analytical study conducted with individuals aged ≥ 18 years who were on invasive mechanical ventilation and had no clinical diagnosis of respiratory system disease and/or chest abnormality. Three measurements of respiratory mechanics were performed with a 1-minute interval between them. The first and third measurements were performed by examiner A, the second by examiner B. The values for the resistance and static and dynamic compliance of the respiratory system were compared using the intraclass correlation coefficient. RESULTS: A total of 198 measurements of respiratory mechanics were performed for 66 patients on mechanical ventilation. The patients had a mean age of 52.6 ± 18.6 years and a mean body mass index of 21.6 ± 2.1kg/m2; a surgical profile (61.5%) and female sex (53.8%) were predominant. Mean values were obtained for the three measurements of respiratory system resistance (A1: 15.7 ± 6.8cmH2O/L/s; B1: 15.7 ± 6.4cmH2O/L/s and A2: 15.9 ± 6.2cmH2O/L/s), respiratory system static compliance (A1: 42.1 ± 13.7mL/cmH2O; B1: 42.4 ± 14.6mL/cmH2O and A2: 42.2 ± 14.5mL/cmH2O) and respiratory system dynamic compliance (A1: 21.3 ± 7.3mL/cmH2O; B1: 21.4 ± 7.5mL/cmH2O and A2: 21.3 ± 6.2mL/cmH2O). The intraclass correlation coefficient was also calculated for respiratory system resistance (R = 0.882 and p = 0.001; R = 0.949 and p = 0.001 - interexaminer A1 versus B and B versus A2, respectively; R = 0.932 and p = 0.001 - intraexaminer); respiratory system static compliance (R = 0.951 and p = 0.001; R = 0.958 and p = 0.001 - interexaminer A1 versus B and B versus A2, respectively; R = 0.965 and p = 0.001 - intraexaminer) and respiratory system dynamic compliance (R = 0.957 and p = 0.001; R = 0.946 and p = 0.001 - interexaminer A1 versus B and B versus A2, respectively; R = 0.926 and p = 0.001 - intraexaminer). CONCLUSION: The measurements of resistance and static and dynamic compliance of the respiratory system show good intra- and interexaminer reproducibility for ventilated patients.


OBJETIVO: Avaliar a reprodutibilidade intra e interexaminador das mensurações da resistência e das complacências estática e dinâmica do sistema respiratório em pacientes sob ventilação mecânica. MÉTODOS: Trata-se de estudo analítico realizado com indivíduos com idade ≥ 18 anos, em ventilação mecânica invasiva, que não tinham diagnóstico clínico de doença do aparelho respiratório e/ou anormalidade de caixa torácica. Foram realizadas três aferições da mecânica respiratória com intervalo de 1 minuto entre elas. A primeira e a terceira aferições foram realizadas pelo avaliador A e a segunda aferição, pelo avaliador B. A comparação dos valores de resistência e complacências estática e dinâmica do sistema respiratório foi calculada por meio do coeficiente de correlação intraclasse. RESULTADOS: Foram realizadas 198 aferições da mecânica respiratória em 66 pacientes sob ventilação mecânica, com idade média de 52,6 ± 18,6 anos, índice de massa corporal médio de 21,6 ± 2,1kg/m2, predomínio do perfil cirúrgico (61,5%) e sexo feminino (53,8%). Foram obtidos valores médios das três aferições para resistência do sistema respiratório (A1: 15,7 ± 6,8cmH2O/L/s; B1: 15,7 ± 6,4cmH2O/L/s e A2: 15,9 ± 6,2cmH2O/L/s), para complacência estática do sistema respiratório (A1: 42,1 ± 13,7mL/cmH2O; B1: 42,4 ± 14,6mL/cmH2O e A2: 42,2 ± 14,5mL/cmH2O) e para complacência dinâmica do sistema respiratório (A1: 21,3 ± 7,3mL/cmH2O; B1: 21,4 ± 7,5mL/cmH2O e A2: 21,3 ± 6,2mL/cmH2O). Também foram encontrados valores do coeficiente de correlação intraclasse para resistência do sistema respiratório (R = 0,882 e p = 0,001; R = 0,949 e p = 0,001 - interexaminadores A1 versus B e B versus A2, respectivamente; R = 0,932 e p = 0,001 - intraexaminador); complacência estática do sistema respiratório (R = 0,951 e p = 0,001; R = 0,958 e p = 0,001 - interexaminadores A1 versus B e B versus A2, respectivamente; R = 0,965 e p = 0,001 - intraexaminador) e complacência dinâmica do sistema respiratório (R = 0,957 e p = 0,001; R = 0,946 e p = 0,001 - interexaminadores A1 versus B e B versus A2 respectivamente; R = 0,926 e p = 0,001 - intraexaminador). CONCLUSÃO: A mensuração de mecânica respiratória apresenta boa reprodutibilidade intra e interexaminador para as aferições de resistência e complacências estática e dinâmica do sistema respiratório em pacientes ventilados.


Assuntos
Resistência das Vias Respiratórias/fisiologia , Complacência Pulmonar/fisiologia , Respiração Artificial/métodos , Mecânica Respiratória/fisiologia , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes
13.
Rev Bras Ter Intensiva ; 31(4): 521-528, 2019.
Artigo em Português, Inglês | MEDLINE | ID: mdl-31967227

RESUMO

OBJECTIVE: To compare the measurement properties (internal consistency, intra and interrater reliability, construct validity, and ceiling and floor effects) of the Functional Status Score for the ICU (FSS-ICU) and the Functional Independence Measure (FIM-motor domain). METHODS: In this study of measurement properties, the FSS-ICU and FIM were applied to 100 patients (72.1 ± 15.9 years; 53% male; Sequential Organ Failure Assessment = 11.0 ± 3.5 points, Simplified Acute Physiology Score 3 = 50.2 ± 16.8 points) in an intensive care unit at baseline and after 2 hours by physiotherapist 1 (test and retest) and 30 minutes after baseline by physiotherapist 2. The measurement properties evaluated were internal consistency (Cronbach's alpha), intra- and interrater reliability (intraclass correlation coefficient), agreement (standard error of measurement) and minimum detectable change at a 90% confidence level, ceiling and floor effects (frequency of maximum and minimum scores) and construct validity (Pearson's correlation). RESULTS: The FSS-ICU and FIM presented adequate internal consistency (Cronbach's alpha, FSS-ICU = 0.95 and FIM = 0.86), intra-and interrater reliability for overall FSS-ICU and FIM score (ICC > 0.75), agreement (minimum detectable change at a 90% confidence level: FSS-ICU and FIM = 1.0 point; standard error of measurement: FSS-ICU = 2% and FIM = 1%) and construct validity (r = 0.94; p < 0.001). However, the FSS-ICU and FIM presented ceiling effects (maximum score for 16% of patients for the FSS-ICU and 18% for the FIM). CONCLUSION: The FSS-ICU and FIM present adequate measurement properties to assess functionality in critically ill patients, although they present ceiling effects.


OBJETIVO: Comparar as propriedades de medida (consistência interna, confiabilidade intra e interavaliadores, validade do construto, e efeitos teto e piso) da Escala de Estado Funcional para UTI (FSS-ICU - Functional Status Score for the ICU) e da Medida de Independência Funcional (MIF)-domínio motor). MÉTODOS: Neste estudo de propriedades de medida, a FSS-ICU e a MIF foram aplicadas em 100 pacientes (72,1 ± 15,9 anos; 53% masculino; Sequential Organ Failure Assessment = 11,0 ± 3,5 pontos; Simplified Acute Physiology Score 3 = 50,2 ± 16,8 pontos) na unidade de terapia intensiva na linha de base e após 2 horas pelo fisioterapeuta 1 (teste e reteste) e 30 minutos após a linha de base pelo fisioterapeuta 2. As propriedades de medidas avaliadas foram a consistência interna (alfa de Cronbach), as confiabilidades intra e interavaliadores (coeficiente de correlação intraclasse), a concordância (erro padrão de medida), a diferença mínima detectável com confiança de 90%, os efeitos teto e piso (frequência de pontuação máxima e mínima) e a validade do construto (correlação de Pearson). RESULTADOS: Para a FSS-ICU e a MIF, foram encontradas adequadas consistência interna (alfa de Cronbach: FSS-ICU = 0,95 e MIF = 0,86), confiabilidades intra e interavaliadores para pontuação geral da FSS-ICU e MIF (coeficiente de correlação intraclasse > 0,75), concordância (diferença mínima detectável com confiança de 90% e MIF = 1,0 ponto; erro padrão de medida: FSS-ICU = 2% e MIF = 1%) e validade do construto (r = 0,94; p < 0,001). A FSS-ICU apresentou efeito teto de 16% e a MIF de 18%. CONCLUSÃO: As escalas FSS-ICU e MIF têm adequadas propriedades de medida para avaliarem funcionalidade em pacientes críticos, embora apresentem efeito teto.


Assuntos
Estado Terminal/terapia , Unidades de Terapia Intensiva , Desempenho Físico Funcional , Atividades Cotidianas , Idoso , Idoso de 80 Anos ou mais , Brasil , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Índice de Gravidade de Doença
14.
Rev. bras. geriatr. gerontol. (Online) ; 27: e230227, 2024. tab, graf
Artigo em Português | LILACS-Express | LILACS | ID: biblio-1559526

RESUMO

Resumo Objetivo Identificar na literatura, intervenções que auxiliam na promoção da funcionalidade da pessoa idosa durante a transição hospital domicílio. Método Revisão integrativa de literatura com buscas entre outubro e novembro de 2022, nas bases de dados: MEDLINE, Lilacs, IBECS, BDENF, WoS, SCOPUS, CINAHL e PEDro, com os MeSh: Aged, Transitional Care e Functional Status, em qualquer idioma, sem recorte temporal, com operador booleano OR e AND. Resultado: Identificou-se 2.123 artigos, nove atenderam aos critérios de inclusão, emergindo quatro categorias: Educação em saúde; Envolvimento ativo das pessoas idosas e cuidadores familiares; Atuação de equipe multidisciplinar; Acompanhamento após alta hospitalar. Conclusão A continuidade dos cuidados após alta hospitalar através de intervenções para manter e recuperar a funcionalidade é uma estratégia que fortalece a autonomia e a independência das pessoas idosas.


Abstract Objective To identify interventions in the literature that assist in promoting functionality in older adults during the hospital-to-home transition. Method Integrative literature review with searches conducted between October and November 2022, in the following databases: MEDLINE, Lilacs, IBECS, BDENF, WoS, SCOPUS, CINAHL, and PEDro, using the MeSH terms: Aged, Transitional Care, and Functional Status, in any language, without temporal restriction, employing boolean operators OR and AND. Result A total of 2,123 papers were identified, with nine meeting the inclusion criteria, resulting in four categories: Health education; Active involvement of older adults and family caregivers; Multidisciplinary team involvement; Follow-up care post-hospital discharge. Conclusion The continuity of care post-hospital discharge through interventions aimed at maintaining and restoring functionality is a strategy that strengthens the autonomy and independence of older adults.

15.
Rev Bras Med Trab ; 16(2): 225-235, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-32270086

RESUMO

BACKGROUND: The prevalence of low back pain is high among the economically active population. Low back pain reduces productivity and causes absenteeism, impaired quality of life and leaves of absence. Several measures were suggested to reduce the occurrence of this occupational condition, among which physical exercise at the workplace stands out. AIM: To analyze studies which assessed physical exercise at the workplace for treatment of low back pain. METHODS: The present study consisted of a systematic review with meta-analysis. An electronic search was conducted on database MEDLINE using keywords "workplace," "low back pain" and "exercise," synonyms and headings located on Health Sciences Descriptors and Medical Subject Headings. We considered all the studies that included physical exercise at the workplace and defined low back pain as outcome. RESULTS: We located 499 potential studies and finally included 15 for review. The duration of treatment varied from 3 weeks to 18 months, and the main interventions were strength and stretching exercises and muscle relaxation. CONCLUSIONS: The meta-analysis showed that physical exercise at the workplace did not reduce the occurrence of low back pain (difference of means=0.62, 95%CI -0.8-2.04, p<0.4). The present systematic review was registered in database PROSPERO, registration number CRD42017071563.


CONTEXTO: A dor lombar apresenta alta prevalência na população economicamente ativa, promovendo a diminuição da capacidade produtiva, absenteísmo, prejuízos à qualidade de vida e afastamento previdenciário. Medidas diversas têm sido adotadas no intuito de diminuir esse infortúnio laboral, destacando-se a prática de exercício físico no ambiente de trabalho. OBJETIVO: O objetivo desta revisão foi identificar estudos que utilizaram o exercício físico realizado no ambiente laboral para tratamento da dor lombar. MÉTODOS: Trata-se de uma revisão sistemática com metanálise. Foi realizada busca eletrônica na base de dados MEDLINE utilizando os descritores "workplace"; "low back pain" e "exercise" e os respectivos sinônimos e palavras-chaves identificados nos Descritores em Ciências da Saúde e no Medical Subject Headings. RESULTADOS: Foram considerados todos os estudos que adotaram exercício físico no ambiente de trabalho e possuíam desfechos relacionados à dor lombar. Foram encontrados 499 estudos em potencial, resultando na inclusão final de 15 artigos. O tempo de tratamento variou de 3 semanas a 18 meses, e as principais intervenções foram exercícios de força, alongamentos e relaxamento muscular. CONCLUSÃO: A metanálise demonstrou que não há efeito do exercício físico no ambiente de trabalho na redução da percepção da dor lombar (diferença entre médias=0.62, CI95%, -0.8,2.04; p<0.4). Esta revisão sistemática foi registrada no PROSPERO, sob protocolo CRD42017071563.

16.
Heart Lung ; 47(3): 253-260, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29609834

RESUMO

BACKGROUND: The complete description of exercise interventions is essential to allow for the replication of clinical trials and to the correct application in clinical practice. OBJECTIVES: The aim of this review was to evaluate of the description of the active mobilisation protocols in patients on invasive mechanical ventilation at intensive care units (ICU). METHODS: Systematic review of randomised controlled trials (RCTs) using the Consensus on Exercise Reporting Template. RESULTS: We identified 16 RCTs (n = 1,850). None sufficiently described the intervention for all items required for replication. The frequency, intensity, time, volume, and progression of active mobilisation as well as other important components of the intervention such as the instructor's qualifications/expertise, the types and incidence of adverse events, and the adherence to the exercise intervention were not adequately reported. CONCLUSION: Active mobilisation interventions were only incompletely described in RCTs, which can compromise replication in both, clinical and research settings. REGISTRATION: PROSPRERO (CRD42017068762).


Assuntos
Unidades de Terapia Intensiva , Respiração Artificial , Humanos , Ensaios Clínicos Controlados Aleatórios como Assunto
18.
J Crit Care ; 42: 218-222, 2017 12.
Artigo em Inglês | MEDLINE | ID: mdl-28780488

RESUMO

PURPOSE: To identify predictors and develop a risk score for the prediction of extubation failure in TBI patients. MATERIALS AND METHODS: We prospectively evaluated 311 TBI adults receiving mechanical ventilation for >48h in the intensive care unit. Epidemiological, ventilatory, airway protective, laboratory, and hemodynamic predictors were evaluated. A multiple logistic regression model was developed to predict the extubation failure risk. A score was developed using the arithmetic sum of the points for each independent predictor, whose scores were proportional to the regression coefficient. The accuracy of the model was determined using the C statistic. RESULTS: Extubation failure occurred in 43 patients (13.8%). Five independent predictors were identified: female sex (4 points) Glasgow Coma Scale motor score≤5 (4 points), moderate-to-large secretion volume (4 points), absent or weak cough (3 points), and mechanical ventilation≥10days (2 points). We calculated the risk score for patients and three risk categories were defined: low (0-3 points), moderate (4-7 points), high (8-17 points). The extubation failure rates in the three groups were 3.5%, 21.2%, and 42.9%, respectively. CONCLUSION: The score developed to predict extubation failure in TBI patients can identify three risk categories and can be easily applied in the ICU.


Assuntos
Extubação/estatística & dados numéricos , Lesões Encefálicas Traumáticas/terapia , Adulto , Tosse/etiologia , Cuidados Críticos , Feminino , Escala de Coma de Glasgow , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Respiração Artificial/estatística & dados numéricos , Medição de Risco , Desmame do Respirador/estatística & dados numéricos
19.
Rev. Pesqui. Fisioter ; 12(1)jan., 2022. ilus, tab
Artigo em Inglês, Português | LILACS | ID: biblio-1373645

RESUMO

INTRODUÇÃO: Os pacientes criticamente doentes podem sofrer alterações funcionais, sociais e mentais, incluindo deficiência de conhecimento, memória e concentração após a admissão na unidade de terapia intensiva (UTI) e alta hospitalar. Apesar do conhecimento sobre o impacto da internação hospitalar na funcionalidade e qualidade de vida, ainda há pouco reconhecimento na literatura sobre este impacto a longo prazo. OBJETIVO: Verificar a independência funcional e a qualidade de vida (QOL) em pacientes acima de 1 ano após a alta da Unidade de Tratamento Intensivo (UTI). MÉTODOS: Este é um estudo de coorte prospectivo, foram admitidos na UTI e sob ventilação mecânica por mais de 48 horas, até 24 horas após a alta da UTI, acima de 18 anos de idade, de ambos os sexos e que concordaram em participar do estudo. Foram excluídos aqueles com sequelas neurológicas e traumas recorrentes que impossibilitavam a avaliação funcional. As variáveis independência funcional (Medida de Independência Funcional - FIM) e QOL foram medidas utilizando o questionário do formulário curto 36 (SF-36) no momento da alta da UTI (período I), 30 dias (período II), e 1 ano após (período III). RESULTADOS: 33 pacientes foram incluídos no estudo com uma idade média de 49,13±16,3 anos, e a principal causa de hospitalização foi distúrbios neurológicos, dos quais 5(14,70%) morreram, e dois não completaram as avaliações, resultando em um total de 26 pacientes avaliados 1 ano após a alta. A duração da internação na UTI (dias) foi de 16 (7 - 22) e o tempo de ventilação mecânica (dias) foi de 8,5 (2 - 13). Dez pacientes lá foram diagnosticados com sepse. Foram encontrados os seguintes valores nesses três momentos para as variáveis IF (I-51 [47-64,5]; II-80[59,5-108]; III104[82,8-123]) e QOL(I-67,4[57,3-81,1]; II-80,2[70,1-99,2]; III-93,5[88,5-96,5]). A independência funcional e QOL aumentou significativamente entre os momentos II e III, em comparação com os momentos I (p <0,05), sem diferença na comparação do período II em relação ao III. CONCLUSÃO: Os pacientes recuperam sua funcionalidade e qualidade de vida após trinta dias de alta da UTI. Entretanto, a funcionalidade e a qualidade de vida deste paciente não mudam após 1 ano de alta da UTI em relação ao período de 30 dias após a alta da UTI.


INTRODUCTION: Critically ill patients may experience functional, social, and mental changes, including impaired cognition, memory, and concentration after admission to the intensive care unit (ICU) and hospital discharge. Despite the knowledge about the impact of the hospital stay on functionality and quality of life, there is still little recognition in the literature of this impact in the long term. OBJECTIVE: To verify functional independence and quality of life (QOL) in patients over 1 year after discharge from the Intensive Care Unit (ICU). METHODS: This is a prospective cohort study, were admitted to the ICU and under mechanical ventilation for more than 48 hours, up to 24 hours after discharge from the ICU, over 18 years of age, of both sexes and who agreed to participate in the study. Those with neurological sequelae and recurrent trauma that made functional assessment impossible were excluded. Functional independence (Functional Independence Measure-FIM) and QOL variables were measured using the Short Form 36 questionnaire (SF-36) at the time of discharge from the ICU (period I), 30 days (period II), and 1 year after (period III). RESULTS: 33 patients were included in the study with a mean age of 49.13±16.3, and the main cause of hospitalization was neurological disorders, of which 5 (14.70%) died, and two did not complete the evaluations, resulting in a total of 26 patients evaluated 1 year after discharge. The length of ICU stay (days) was 16 (7 - 22) and the Mechanical Ventilation time (days) was 8,5 (2 - 13). Ten patients there were diagnosed with sepsis. The following values over these three moments were found for the variables IF (I-51 [47­64.5]; II-80[59.5­108]; III-104[82.8-123]) and QOL(I­67.4[57.3­81.1]; II-80.2[70.1­99.2]; III­93.5[88.5­ 96.5]). Functional independence and QOL increased significantly between moments II and III compared to moments I (p <0.05), with no difference, when comparing period II in relation to III. CONCLUSION: Patients recover their functionality and quality of life after thirty days of discharge from the ICU. However, this patient's functionality and quality of life do not change after 1 year of discharge from the ICU in relation to the period of 30 days after discharge from the ICU.


Assuntos
Unidades de Terapia Intensiva , Qualidade de Vida , Modalidades de Fisioterapia
20.
J Cardiopulm Rehabil Prev ; 36(6): 395-401, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27182763

RESUMO

PURPOSE: Studies have reported the benefits of exercise and inspiratory muscle training (IMT) in patients with heart failure (HF); however, there is no meta-analysis on the effects of the combination of exercise and IMT in patients with HF. The objective of this study was to determine whether combined exercise/IMT was more effective than conventional exercise on exercise capacity, respiratory muscle strength, and quality of life in patients with HF. METHODS: This is a systematic review and meta-analysis. We searched MEDLINE, LILACS, CINAHL, EMBASE, PEDro, and the Cochrane Central Register of Controlled Trials (from the earliest date available to April 2015) for randomized controlled trials, examining effects of combined exercise/IMT versus conventional exercise on exercise capacity, respiratory muscle strength, and quality of life measurements in patients with HF. Two reviewers selected studies independently. Weighted mean differences and 95% CIs were calculated. RESULTS: Three studies met the study criteria. Combined exercise/IMT resulted in improvement in maximal inspiratory pressure weighted mean differences (20.89 cm H2O; 95% CI, 14.0-27.78) and Minnesota Living with Heart Failure Questionnaire weighted mean differences (4.43; 95% CI, 0.72-8.14). Nonsignificant difference was observed in peak (Equation is included in full-text article.)O2 for participants in the combined exercise/IMT group compared with the conventional exercise group. No serious adverse events were reported. CONCLUSIONS: Combined exercise/IMT may improve maximal inspiratory pressure and quality of life in patients with HF and should be considered for inclusion in cardiac rehabilitation programs.


Assuntos
Exercícios Respiratórios/métodos , Terapia por Exercício/métodos , Insuficiência Cardíaca/reabilitação , Força Muscular/fisiologia , Músculos Respiratórios/fisiologia , Humanos , Resultado do Tratamento
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