RESUMEN
Background. The effective use of ICU care after lung resections has not been completely studied. The aims of this study were to identify predictive factors for effective use of ICU admission after lung resection and to develop a risk composite measure to predict its effective use. Methods. 120 adult patients undergoing elective lung resection were enrolled in an observational prospective cohort study. Preoperative evaluation and intraoperative assessment were recorded. In the postoperative period, patients were stratified into two groups according to the effective and ineffective use of ICU. The use of ICU care was considered effective if a patient experienced one or more of the following: maintenance of controlled ventilation or reintubation; acute respiratory failure; hemodynamic instability or shock; and presence of intraoperative or postanesthesia complications. Results. Thirty patients met the criteria for effective use of ICU care. Logistic regression analysis identified three independent predictors of effective use of ICU care: surgery for bronchiectasis, pneumonectomy, and age ≥ 57 years. In the absence of any predictors the risk of effective need of ICU care was 6%. Risk increased to 25-30%, 66-71%, and 93% with the presence of one, two, or three predictors, respectively. Conclusion. ICU care is not routinely necessary for all patients undergoing lung resection.
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Unidades de Cuidados Intensivos , Neumonectomía/rehabilitación , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Medición de RiesgoRESUMEN
OBJECTIVE: To determine whether the use of a set of preoperative variables can predict the need for postoperative ICU admission. METHODS: This was a prospective observational cohort study of 120 patients undergoing elective pulmonary resection between July of 2009 and April of 2012. Prediction of ICU admission was based on the presence of one or more of the following preoperative characteristics: predicted pneumonectomy; severe/very severe COPD; severe restrictive lung disease; FEV1 or DLCO predicted to be < 40% postoperatively; SpO2 on room air at rest < 90%; need for cardiac monitoring as a precautionary measure; or American Society of Anesthesiologists physical status ≥ 3. The gold standard for mandatory admission to the ICU was based on the presence of one or more of the following postoperative characteristics: maintenance of mechanical ventilation or reintubation; acute respiratory failure or need for noninvasive ventilation; hemodynamic instability or shock; intraoperative or immediate postoperative complications (clinical or surgical); or a recommendation by the anesthesiologist or surgeon to continue treatment in the ICU. RESULTS: Among the 120 patients evaluated, 24 (20.0%) were predicted to require ICU admission, and ICU admission was considered mandatory in 16 (66.6%) of those 24. In contrast, among the 96 patients for whom ICU admission was not predicted, it was required in 14 (14.5%). The use of the criteria for predicting ICU admission showed good accuracy (81.6%), sensitivity of 53.3%, specificity of 91%, positive predictive value of 66.6%, and negative predictive value of 85.4%. CONCLUSIONS: The use of preoperative criteria for predicting the need for ICU admission after elective pulmonary resection is feasible and can reduce the number of patients staying in the ICU only for monitoring.
OBJETIVO: Avaliar se a utilização de um conjunto de variáveis pré-operatórias é capaz de antever a necessidade de internação em UTI no pós-operatório. MÉTODOS: Estudo de coorte observacional prospectivo, com 120 pacientes submetidos à ressecção pulmonar eletiva entre julho de 2009 e abril de 2012. A previsão de indicação de internação em UTI indicação foi baseada na presença de uma ou mais das seguintes condições pré-operatórias: previsão de pneumonectomia; DPOC grave/muito grave; doença restritiva grave; VEF1 ou DLCO previstos para o pós-operatório < 40% do previsto; SpO2 em repouso e ar ambiente < 90%; necessidade de monitorização cardíaca profilática; classificação da American Society of Anesthesiologists ≥ 3. O padrão ouro para internação justificada em UTI foi baseado na presença de uma ou mais das seguintes condições pós-operatórias: manutenção de ventilação mecânica ou reintubação; insuficiência respiratória aguda ou necessidade de ventilação não invasiva; instabilidade hemodinâmica ou choque; intercorrências intraoperatórias ou no pós-operatório imediato (cirúrgicas ou clínicas); indicação do anestesiologista ou cirurgião para a manutenção de tratamento na UTI. RESULTADOS: Dos 120 pacientes avaliados, houve previsão de necessidade de internação em UTI em 24 (20,0%), sendo essa considerada justificada em 16 deles (66,6%) desses 24, ao passo que dos 96 pacientes sem previsão de necessidade de internação em UTI, essa foi necessária em 14 (14,5%). A utilização dos critérios preditivos para a internação em UTI mostrou boa acurácia (81,6%), sensibilidade de 53,3%, especificidade de 91%, valor preditivo positivo de 66,6% e valor preditivo negativo de 85,4%. CONCLUSÕES: A utilização de critérios pré-operatórios para a indicação de internação em UTI após ressecção pulmonar eletiva é factível e é capaz de reduzir o número de pacientes que aí permanecem apenas para vigilância.
Asunto(s)
Hospitalización/estadística & datos numéricos , Unidades de Cuidados Intensivos/estadística & datos numéricos , Neumonectomía , Complicaciones Posoperatorias/prevención & control , Cuidados Preoperatorios , Estudios de Cohortes , Femenino , Humanos , Masculino , Persona de Mediana Edad , Periodo Posoperatorio , Estudios Prospectivos , Factores de Riesgo , Sensibilidad y Especificidad , Índice de Severidad de la EnfermedadRESUMEN
BACKGROUND: Cough impairment is often described as part of the pathophysiological basis of postoperative pulmonary complications (PPCs). However, there have been few studies examining cough effectiveness and its relationship with PPCs following open upper abdominal surgery. The goal of this study was to estimate (1) changes in cough efficacy after upper abdominal surgery through the assessment of peak cough flow and (2) the extent to which cough impairment is associated with postoperative pain, FVC, and risk of PPCs. METHODS: This prospective cohort study assessed 101 subjects (45% male, 56 ± 16 y old) admitted for elective upper abdominal surgery. Measurements of peak cough flow and FVC were performed on the day before surgery and repeated on postoperative days 1, 3, and 5. PPCs were assessed daily by a pulmonologist blinded to the cough measurement results. RESULTS: Peak cough flow dropped to 54% of the preoperative value on postoperative day 1 and gradually increased on postoperative days 3 (65%) and 5 (72%) (P < .05). On all postoperative days, peak cough flow was strongly correlated with FVC (P < .001) and weakly correlated with pain (P = .006). Six subjects (6%) developed PPCs. The association between peak cough flow and risk of PPCs was not statistically significant (unadjusted odds ratio of 0.80, 95% CI 0.45-1.40, P = .44; adjusted odds ratio of 0.66, 95% CI 0.32-1.38, P = .41). CONCLUSIONS: Cough effectiveness is impaired after upper abdominal surgery. Postoperative restrictive lung dysfunction seems to be associated with this impairment. There is no significant association between peak cough flow and PPCs; however, cough impairment might result in clinically important consequences in a high-risk population.
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Abdomen/cirugía , Tos/fisiopatología , Procedimientos Quirúrgicos del Sistema Digestivo/efectos adversos , Enfermedades Pulmonares/epidemiología , Complicaciones Posoperatorias/epidemiología , Adulto , Anciano , Estudios de Cohortes , Tos/etiología , Femenino , Humanos , Enfermedades Pulmonares/etiología , Masculino , Persona de Mediana Edad , Oportunidad Relativa , Ápice del Flujo Espiratorio , Complicaciones Posoperatorias/etiología , Estudios Prospectivos , Factores de Riesgo , Capacidad VitalRESUMEN
Objective: To determine whether the use of a set of preoperative variables can predict the need for postoperative ICU admission. Methods: This was a prospective observational cohort study of 120 patients undergoing elective pulmonary resection between July of 2009 and April of 2012. Prediction of ICU admission was based on the presence of one or more of the following preoperative characteristics: predicted pneumonectomy; severe/very severe COPD; severe restrictive lung disease; FEV1 or DLCO predicted to be < 40% postoperatively; SpO2 on room air at rest < 90%; need for cardiac monitoring as a precautionary measure; or American Society of Anesthesiologists physical status ≥ 3. The gold standard for mandatory admission to the ICU was based on the presence of one or more of the following postoperative characteristics: maintenance of mechanical ventilation or reintubation; acute respiratory failure or need for noninvasive ventilation; hemodynamic instability or shock; intraoperative or immediate postoperative complications (clinical or surgical); or a recommendation by the anesthesiologist or surgeon to continue treatment in the ICU. Results: Among the 120 patients evaluated, 24 (20.0%) were predicted to require ICU admission, and ICU admission was considered mandatory in 16 (66.6%) of those 24. In contrast, among the 96 patients for whom ICU admission was not predicted, it was required in 14 (14.5%). The use of the criteria for predicting ICU admission showed good accuracy (81.6%), sensitivity of 53.3%, specificity of 91%, positive predictive value of 66.6%, and negative predictive value of 85.4%. Conclusions: The use of preoperative criteria for predicting the need for ICU admission after elective pulmonary resection is feasible and can reduce the number of patients staying in the ICU only for monitoring. .
Objetivo: Avaliar se a utilização de um conjunto de variáveis pré-operatórias é capaz de antever a necessidade de internação em UTI no pós-operatório. Métodos: Estudo de coorte observacional prospectivo, com 120 pacientes submetidos à ressecção pulmonar eletiva entre julho de 2009 e abril de 2012. A previsão de indicação de internação em UTI indicação foi baseada na presença de uma ou mais das seguintes condições pré-operatórias: previsão de pneumonectomia; DPOC grave/muito grave; doença restritiva grave; VEF1 ou DLCO previstos para o pós-operatório < 40% do previsto; SpO2 em repouso e ar ambiente < 90%; necessidade de monitorização cardíaca profilática; classificação da American Society of Anesthesiologists ≥ 3. O padrão ouro para internação justificada em UTI foi baseado na presença de uma ou mais das seguintes condições pós-operatórias: manutenção de ventilação mecânica ou reintubação; insuficiência respiratória aguda ou necessidade de ventilação não invasiva; instabilidade hemodinâmica ou choque; intercorrências intraoperatórias ou no pós-operatório imediato (cirúrgicas ou clínicas); indicação do anestesiologista ou cirurgião para a manutenção de tratamento na UTI. Resultados: Dos 120 pacientes avaliados, houve previsão de necessidade de internação em UTI em 24 (20,0%), sendo essa considerada justificada em 16 deles (66,6%) desses 24, ao passo que dos 96 pacientes sem previsão de necessidade de internação em UTI, essa foi necessária em 14 (14,5%). A utilização dos critérios preditivos para a internação em UTI mostrou boa acurácia (81,6%), sensibilidade de 53,3%, especificidade de 91%, valor preditivo positivo de 66,6% e valor preditivo negativo de 85,4%. Conclusões: A utilização de critérios pré-operatórios para a indicação de internação em UTI após ressecção pulmonar eletiva é factível e é capaz de reduzir o número de pacientes que aí permanecem apenas para vigilância. .
Asunto(s)
Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Autoanticuerpos/sangre , Diabetes Mellitus Tipo 1/diagnóstico , /diagnóstico , Glutamato Descarboxilasa/inmunología , Edad de Inicio , Anticolesterolemiantes/uso terapéutico , Método Doble Ciego , Diabetes Mellitus Tipo 1/tratamiento farmacológico , Diabetes Mellitus Tipo 1/inmunología , /tratamiento farmacológico , /inmunología , Intolerancia a la Glucosa , Alemania/epidemiología , Ácidos Heptanoicos/uso terapéutico , Hipoglucemiantes/uso terapéutico , Insulina/uso terapéutico , Síndrome Metabólico/diagnóstico , Síndrome Metabólico/tratamiento farmacológico , Fenotipo , Prevalencia , Estudios Prospectivos , Pirroles/uso terapéutico , Factores de RiesgoRESUMEN
A avaliação pulmonar pré-operatória é realizada para estimar o risco de ocorrência de complicações pulmonares no pós-operatório. Esse risco varia na dependência do sítio operatório, da anestesia utilizada e do estado clínico dos doentes, sendo que a presença de pneumopatia crônica pode elevá-lo. Os testes de função pulmonar durante a avaliação pré-operatória têm múltiplas finalidades: diagnosticar e graduar a intensidade dos distúrbios, indicar o melhor tratamento, otimizando-o, fornecer valores de corte que podem diferenciar risco aceitável de risco alto para complicações e eventualmente induzir a mudança de estratégia operatória ou descartar essa modalidade de tratamento. Inicialmente espirometria e gasometria arterial eram os únicos exames disponíveis para tal, mas, atualmente, podemos contar com outros exames como a medida da capacidade de difusão pulmonar para o monóxido de carbono, pressões respiratórias máximas, teste de exercício cardiopulmonar e testes de exercício de campo. O objetivo desta revisão é apresentar os testes de função pulmonar utilizados rotineiramente na avaliação pré-operatória e como eles são capazes de contribuir com essa avaliação.
Preoperative pulmonary evaluation is performed to estimate risk of postoperative pulmonary complications. Risk depends on the operative site, type of anesthesia and clinical status of patient. Chronic lung disease may increase this risk. Pulmonary function testing during the preoperative evaluation has multiple purposes: establish the diagnosis and severity of disorders, indicate the most appropriate treatment, provide cutoff values that can establish high risk for complications. In this case it is possible to change operative strategy or offer another treatment option. Initially spirometry and blood gases analysis were the only tests available for that, but now we can rely on other tests such as measurement of diffusing capacity for carbon monoxide, respiratory muscle strength, cardiopulmonary exercise testing and field testing. The aim of this review is to present the pulmonary function tests usually used in preoperative evaluation and how they are able to contribute in this field.
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Humanos , Masculino , Femenino , Cuidados Preoperatorios , Pruebas de Función Respiratoria , Procedimientos Quirúrgicos Operativos , Técnicas y Procedimientos DiagnósticosRESUMEN
OBJECTIVE: To determine morbidity and mortality rates by risk category in accordance with the American College of Chest Physicians guidelines, to determine what role pulmonary function tests play in this categorization process, and to identify risk factors for perioperative complications (PCs). METHODS: This was a historical cohort study based on preoperative and postoperative data collected for cases of lung cancer diagnosed or suspected between 2001 and 2010. RESULTS: Of the 239 patients evaluated, only 13 (5.4%) were classified as being at high risk of PCs. Predicted postoperative FEV1 (FEV1ppo) was sufficient to define the risk level in 156 patients (65.3%); however, cardiopulmonary exercise testing (CPET) was necessary for identifying those at high risk. Lung resection was performed in 145 patients. Overall morbidity and mortality rates were similar to those reported in other studies. However, morbidity and mortality rates for patients at an acceptable risk of PCs were 31.6% and 4.3%, respectively, whereas those for patients at high risk were 83.3% and 33.3%. Advanced age, COPD, lobe resection, and lower FEV1ppo were correlated with PCs. CONCLUSIONS: Although spirometry was sufficient for risk assessment in the majority of the population studied, CPET played a key role in the identification of high-risk patients, among whom the mortality rate was seven times higher than was that observed for those at an acceptable risk of PCs. The risk factors related to PCs coincided with those reported in previous studies.
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Neoplasias Pulmonares/mortalidad , Complicaciones Posoperatorias/mortalidad , Adulto , Anciano , Algoritmos , Estudios de Cohortes , Humanos , Neoplasias Pulmonares/cirugía , Persona de Mediana Edad , Morbilidad , Pruebas de Función Respiratoria , Factores de RiesgoRESUMEN
BACKGROUND AND OBJECTIVES: In daily clinical practice, pulmonary complications related to surgical procedure are common, increasing the morbidity and mortality of patients. Assessment of the risk of pulmonary complications is an important step in the preoperative evaluation. Thus, we review the most relevant aspects of preoperative assessment of the patient with lung disease. CONTENT: Pulmonary risk stratification depends on clinical symptoms and patient's physical status. Age, preexisting respiratory diseases, nutritional status, and continued medical treatment are usually more important than additional tests. Pulmonary function tests are of great relevance when high abdominal or thoracic procedures are scheduled, particularly when lung resection are considered. CONCLUSION: Understanding the perioperative evaluation of the potential risk for developing pulmonary complication allows the medical team to choose the adequate anesthetic technique and surgical and clinical care required by each patient, thereby reducing adverse respiratory outcomes.
Asunto(s)
Enfermedades Pulmonares/prevención & control , Complicaciones Posoperatorias/prevención & control , Cuidados Preoperatorios , Volumen Espiratorio Forzado , Humanos , NeumonectomíaRESUMEN
INTRODUCTION: The goal of this study is to determine whether bronchodilator (BD) response can be used as a reliable measure of asthma control by analyzing the effects of a short course of oral corticosteroids (OC) or placebo (P) on spirometry, sputum cytology and BD response in controlled asthma patients scoring less than 1.5 on the ACQ5. METHODS: Seventy patients with moderate to severe asthma who were undergoing combination therapy and were considered to be controlled based on ACQ5 scores, but who exhibited persistent positive BD response, were randomly assigned to two groups, one receiving OC and the other P. Patients were evaluated before and after 2 weeks of treatment. Intervention response (comparison of FEV(1) before and after OC or P treatment) was used as a measure of intervention efficacy, with values equal to or greater than 200 mL considered positive. RESULTS: Patients who received OC showed significant improvement in FEV(1), and no longer exhibited a positive BD response. Those in the P group showed no change. In addition, sputum eosinophil counts significantly decreased in the OC group. CONCLUSIONS: BD response can be used as a reliable measure of asthma control. This study suggests that ACQ5 scores alone are not sufficient to fully assess asthma control, and that BD response should be included as an essential measurement in any algorithm of asthma control evaluation.
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Corticoesteroides/administración & dosificación , Asma/diagnóstico , Asma/tratamiento farmacológico , Broncodilatadores/administración & dosificación , Administración Oral , Adolescente , Adulto , Anciano , Relación Dosis-Respuesta a Droga , Método Doble Ciego , Esquema de Medicación , Femenino , Estudios de Seguimiento , Humanos , Modelos Lineales , Masculino , Persona de Mediana Edad , Valores de Referencia , Pruebas de Función Respiratoria , Índice de Severidad de la Enfermedad , Espirometría/métodos , Esputo/citología , Resultado del Tratamiento , Adulto JovenRESUMEN
OBJECTIVE: To determine morbidity and mortality rates by risk category in accordance with the American College of Chest Physicians guidelines, to determine what role pulmonary function tests play in this categorization process, and to identify risk factors for perioperative complications (PCs). METHODS: This was a historical cohort study based on preoperative and postoperative data collected for cases of lung cancer diagnosed or suspected between 2001 and 2010. RESULTS: Of the 239 patients evaluated, only 13 (5.4%) were classified as being at high risk of PCs. Predicted postoperative FEV1 (FEV1ppo) was sufficient to define the risk level in 156 patients (65.3%); however, cardiopulmonary exercise testing (CPET) was necessary for identifying those at high risk. Lung resection was performed in 145 patients. Overall morbidity and mortality rates were similar to those reported in other studies. However, morbidity and mortality rates for patients at an acceptable risk of PCs were 31.6% and 4.3%, respectively, whereas those for patients at high risk were 83.3% and 33.3%. Advanced age, COPD, lobe resection, and lower FEV1ppo were correlated with PCs. CONCLUSIONS: Although spirometry was sufficient for risk assessment in the majority of the population studied, CPET played a key role in the identification of high-risk patients, among whom the mortality rate was seven times higher than was that observed for those at an acceptable risk of PCs. The risk factors related to PCs coincided with those reported in previous studies. .
OBJETIVO: Determinar as taxas de morbidade e mortalidade por categoria de risco conforme as diretrizes do American College of Chest Physicians, verificar como exames funcionais participaram dessa categorização e identificar fatores de risco para complicações perioperatórias (CPOs). MÉTODOS: Estudo de coorte histórica a partir de avaliações pré e pós-operatórias de casos diagnosticados ou suspeitos de câncer de pulmão avaliados entre 2001 e 2010. RESULTADOS: Dos 239 pacientes avaliados, apenas 13 (5,4%) foram considerados como de alto risco para CPOs. O cálculo do VEF1 previsto para o pós-operatório (VEF1ppo) foi suficiente para a estratificação do risco em 156 pacientes (65,3%); entretanto, o teste de exercício cardiopulmonar (TECP) foi necessário para a identificação de alto risco. Foram operados 145 pacientes, e as taxas globais de morbidade e mortalidade encontradas foram semelhantes às de outros estudos. Entretanto, as taxas de morbidade e mortalidade para aqueles com risco aceitável foram de 31,6% e 4,3%, respectivamente, enquanto as taxas para aqueles com alto risco foram de 83,3% e 33,3%. Idade mais avançada, presença da DPOC, ressecção de um ou mais lobos e VEF1ppo mais baixo estiveram relacionados à ocorrência de CPOs. CONCLUSÕES: Embora a espirometria tenha sido suficiente para a determinação de risco na maioria da população estudada, o TECP teve papel fundamental na identificação de pacientes com risco alto, que apresentaram uma taxa de mortalidade sete vezes maior que os de risco aceitável. Os fatores de risco relacionados a CPOs coincidiram aos relatados em outros estudos. .
Asunto(s)
Adulto , Anciano , Humanos , Persona de Mediana Edad , Neoplasias Pulmonares/mortalidad , Complicaciones Posoperatorias/mortalidad , Algoritmos , Estudios de Cohortes , Neoplasias Pulmonares/cirugía , Morbilidad , Pruebas de Función Respiratoria , Factores de RiesgoRESUMEN
BACKGROUND: Despite numerous studies on endotracheal tube cuff pressure (CP) management, the literature has yet to establish a technique capable of adequately filling the cuff with an appropriate volume of air while generating low CP in a less subjective way. The purpose of this prospective study was to evaluate and compare the CP levels and air volume required to fill the endotracheal tubes cuff using 2 different techniques (volume-time curve versus minimal occlusive volume) in the immediate postoperative period after coronary artery bypass grafting. METHODS: A total of 267 subjects were analyzed. After the surgery, the lungs were ventilated using pressure controlled continuous mandatory ventilation, and the same ventilatory parameters were adjusted. Upon arrival in the ICU, the cuff was completely deflated and re-inflated, and at this point the volume of air to fill the cuff was adjusted using one of 2 randomly selected techniques: volume-time curve and minimal occlusive volume. We measured the volume of air injected into the cuff, the CP, and the expired tidal volume of the mechanical ventilation after the application of each technique. RESULTS: The volume-time curve technique demonstrated a significantly lower CP and a lower volume of air injected into the cuff, compared to the minimal occlusive volume technique (P < .001). No significant difference was observed in the expired tidal volume between the 2 techniques (P = .052). However, when the subjects were submitted to the minimal occlusive volume technique, 17% (n = 47) experienced air leakage as observed by the volume-time graph. CONCLUSIONS: The volume-time curve technique was associated with a lower CP and a lower volume of air injected into the cuff, when compared to the minimal occlusive volume technique in the immediate postoperative period after coronary artery bypass grafting. Therefore, the volume-time curve may be a more reliable alternative for endotracheal tube cuff management.
Asunto(s)
Intubación Intratraqueal , Volumen de Ventilación Pulmonar , Anciano , Puente de Arteria Coronaria , Femenino , Humanos , Masculino , Persona de Mediana Edad , Presión , Estudios ProspectivosRESUMEN
BACKGROUND AND OBJECTIVE: Field exercise tests have been increasingly used for pulmonary risk assessment. The 6-min walking distance (6MWD) is a field test commonly employed in clinical practice; however, there is limited evidence supporting its use as a risk assessment method in abdominal surgery. The aim was to assess if the 6MWD can predict the development of post-operative pulmonary complications (PPCs) in patients having upper abdominal surgery (UAS). METHODS: This prospective cohort study included 137 consecutive subjects undergoing elective UAS. Subjects performed the 6MWD on the day prior to surgery, and their performance were compared with predicted values of 6MWD (p6MWD) using a previously validated formula. PPCs (including pneumonia, tracheobronchitis, atelectasis with clinical repercussions, bronchospasm and acute respiratory failure) were assessed daily by a pulmonologist blinded to the 6MWD results. 6MWD and p6MWD were compared between subjects who developed PPC (PPC group) and those who did not (no PPC group) using Student's t-test. RESULTS: Ten subjects experienced PPC (7.2%) and no significant difference was observed between the 6MWD obtained in the PPC group and no PPC group (466.0 ± 97.0 m vs. 485.3 ± 107.1 m; P = 0.57, respectively). There was also no significant difference observed between groups for the p6MWD (100.7 ± 29.1% vs. 90.6 ± 20.9%; P > 0.05). CONCLUSIONS: The results of the present study suggest that the 6-min walking test is not a useful tool to identify subjects with increased risk of developing PPC following UAS.
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Abdomen/cirugía , Procedimientos Quirúrgicos del Sistema Digestivo/efectos adversos , Procedimientos Quirúrgicos Electivos/efectos adversos , Prueba de Esfuerzo/métodos , Enfermedades Pulmonares/etiología , Complicaciones Posoperatorias/epidemiología , Cuidados Preoperatorios/métodos , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Prevalencia , Estudios Prospectivos , CaminataRESUMEN
Os clínicos reconhecem bem a importância e os fatores de risco para a ocorrência de complicações cardíacas no período pós-operatório, mas subestiman as complicações pulmonares pós-operatórias. Elas são muito importantes na análise do risco cirúrgico de doentes que serão submetidos a cirurgias não-cardiotorácicas, porque, além de não prevalentes quanto as complicações cardíacas, aumentam a morbidade e a mortalidade, o tempo de permanência hospitalar e, consequentemente, os custos. Fatores de risco relacionados ao procedimento operatório são mais importantes que os relacionados ao doente em predizer eventos pulmonares pós-operatórios, mas os clínicos devem avaliar ambos. O reconhecimento desses fatores é essencial para a prescrição de estratégias com reconhecida capacidade de reduzir a ocorrência dessas complicações pulmonares. As estrategias incluem otimização das doenças pulmonares crônicas...
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Humanos , Persona de Mediana Edad , Complicaciones Posoperatorias , Medición de Riesgo , Factores de RiesgoRESUMEN
OBJECTIVE: To evaluate the capacity of the criteria described in Complementary Directive SAS/MS 12, issued on November 12, 2002, to identify patients with severe asthma, describing and comparing clinical, functional and treatment data of such patients. METHODS: This was a nested case-control study using a structured database for adult asthma outpatients. We defined cases as asthma patients who met the inclusion criteria described in the directive, defining controls as those who did not. We collected and compared data related to the following: demographic characteristics; history of asthma; medications in use; comorbidities; history of tobacco use; number of exacerbations within the last 12 months, asthma-related hospitalizations and intensive care unit admissions within the last 12 months; spirometry; and sputum cytology. RESULTS: The case and control groups consisted of 29 and 31 patients, respectively. The number of asthma exacerbations and emergence room visits within the last 12 months, as well as the number of patients that received at least one pulse of oral corticosteroids, was significantly higher in the case group than in the control group. In addition, prebronchodilator FVC was lower among the cases than among the controls. Furthermore, cytology revealed that eosinophil counts were significantly higher in the induced sputum of cases than in that of controls. CONCLUSIONS: The criteria described in the directive are suited to stratifying patients with severe asthma.
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Asma/diagnóstico , Broncodilatadores/provisión & distribución , Budesonida/provisión & distribución , Programas Nacionales de Salud/normas , Selección de Paciente , Administración por Inhalación , Adulto , Asma/tratamiento farmacológico , Asma/patología , Brasil , Broncodilatadores/uso terapéutico , Budesonida/uso terapéutico , Estudios de Casos y Controles , Eosinófilos , Hospitalización , Humanos , Índice de Severidad de la Enfermedad , Espirometría , Esputo/citologíaRESUMEN
OBJETIVO: Avaliar a capacidade dos critérios descritos na Portaria Complementar SAS/MS nº12, de 12 de novembro de 2002, em identificar pacientes asmáticos graves, bem como descrever e comparar dados clínicos, funcionais e de tratamento destes pacientes. MÉTODOS: Estudo caso-controle aninhado em um banco de dados estruturado de atendimento ambulatorial de asmáticos. Foram considerados casos os pacientes asmáticos que preencheram os critérios de inclusão determinados na portaria e considerados controles os que não preencheram os mesmos critérios. Foram coletados e comparados dados demográficos; história pregressa da asma; medicamentos em uso; presença de comorbidades; história de tabagismo; presença, no último ano, de exacerbações, de hospitalizações e de admissões em unidades de terapia intensiva devido à asma; e resultados de espirometria e de citologia de escarro. RESULTADOS: Foram incluídos 29 e 31 pacientes, respectivamente, nos grupos caso e controle. O grupo caso apresentou maior número de exacerbações e maior número de visitas ao pronto-socorro no último ano, maior porcentagem de pacientes que receberam pelo menos um pulso de corticosteroide oral, assim como menores valores de CVF pré-broncodilatador em relação ao grupo controle. O grupo caso também apresentou um aumento significante de eosinófilos na citologia do escarro induzido. CONCLUSÕES: Os critérios de inclusão descritos na portaria são adequados para estratificar pacientes com asma grave.
OBJECTIVE: To evaluate the capacity of the criteria described in Complementary Directive SAS/MS 12, issued on November 12, 2002, to identify patients with severe asthma, describing and comparing clinical, functional and treatment data of such patients. METHODS: This was a nested case-control study using a structured database for adult asthma outpatients. We defined cases as asthma patients who met the inclusion criteria described in the directive, defining controls as those who did not. We collected and compared data related to the following: demographic characteristics; history of asthma; medications in use; comorbidities; history of tobacco use; number of exacerbations within the last 12 months, asthma-related hospitalizations and intensive care unit admissions within the last 12 months; spirometry; and sputum cytology. RESULTS: The case and control groups consisted of 29 and 31 patients, respectively. The number of asthma exacerbations and emergence room visits within the last 12 months, as well as the number of patients that received at least one pulse of oral corticosteroids, was significantly higher in the case group than in the control group. In addition, prebronchodilator FVC was lower among the cases than among the controls. Furthermore, cytology revealed that eosinophil counts were significantly higher in the induced sputum of cases than in that of controls. CONCLUSIONS: The criteria described in the directive are suited to stratifying patients with severe asthma.
Asunto(s)
Adulto , Humanos , Asma/diagnóstico , Broncodilatadores/provisión & distribución , Budesonida/provisión & distribución , Programas Nacionales de Salud/normas , Selección de Paciente , Administración por Inhalación , Asma/tratamiento farmacológico , Asma/patología , Brasil , Broncodilatadores/uso terapéutico , Budesonida/uso terapéutico , Estudios de Casos y Controles , Eosinófilos , Hospitalización , Índice de Severidad de la Enfermedad , Espirometría , Esputo/citologíaRESUMEN
OBJETIVO: Avaliar a influência do dreno pleural sobre a distância percorrida no teste de caminhada de seis minutos, da intensidade da dor e da capacidade vital de pacientes submetidos à ressecção pulmonar. MÉTODOS: Foram avaliados treze pacientes consecutivos, internados na Enfermaria da Cirurgia de Tórax do Hospital São Paulo, submetidos à drenagem pleural fechada (dreno tubular multiperfurado de 0,5 polegada), no período pós-operatório de ressecção pulmonar (lobectomia, segmentectomia e nodulectomia). A opção pela retirada do dreno seguiu critérios clínicos definidos por médicos da equipe cirúrgica alheios ao estudo. A determinação da capacidade vital, da intensidade da dor através da escala visual analógica de dor e da distância percorrida no teste de caminhada de seis minutos foram realizadas 30 min antes da retirada do dreno e 30 min após. A análise estatística dos dados foi realizada através do teste t pareado, com nível de significância estabelecido em 0,05. RESULTADOS: Após a retirada do dreno, os valores obtidos na avaliação da escala visual analógica de dor foram significativamente menores (3,46 cm vs. 1,77 cm; p = 0,001), e a distância percorrida no teste de caminhada de seis minutos foi significativamente maior (374,34 m vs. 444,62 m; p = 0,03). A capacidade vital antes e após a retirada do dreno não foi alterada de forma significativa (2,15 L vs. 2,25 L, respectivamente; p = 0,540). CONCLUSÕES: Os resultados deste estudo sugerem que a presença do dreno pleural é um importante fator associado à dor pós-operatória e à limitação funcional em pacientes submetidos à ressecção pulmonar.
OBJECTIVE: To evaluate the influence of pleural drainage on the distance covered on the six-minute walk test, pain intensity and vital capacity in patients submitted to pulmonary resection. METHODS: Thirteen consecutive patients from the Thoracic Surgery Infirmary of Hospital São Paulo, Brazil, submitted to closed pleural drainage (0.5-in multiperforated chest tube) in the postoperative period following pulmonary resection (lobectomy, segmentectomy and pulmonary nodule resection) were evaluated. The decision for chest tube removal followed clinical criteria defined by the surgical team, who did not participate in the study. Vital capacity, pain intensity (using a visual analog pain scale) and the distance covered on the six-minute walk test were determined 30 min prior to and 30 min after the removal of the chest tube. The statistical analysis was performed using paired t-tests, and the level of significance was set at 0.05. RESULTS: After the removal of the chest tube, the visual analog scale pain scores were significantly lower (3.46 cm vs. 1.77 cm; p = 0.001) and the distance covered on the six-minute walk test was significantly higher (374.34 m vs. 444.62 m; p = 0.03). Vital capacity prior to and after chest tube removal was not significantly affected (2.15 L and 2.25 L, respectively; p = 0.540). CONCLUSIONS: The results of the present study suggest that the presence of a chest tube is a factor significantly associated with postoperative pain and functional limitation in patients submitted to pulmonary resection.
Asunto(s)
Adolescente , Adulto , Femenino , Humanos , Masculino , Adulto Joven , Tubos Torácicos , Drenaje , Dolor Postoperatorio/etiología , Neumonectomía/efectos adversos , Capacidad Vital/fisiología , Caminata/fisiología , Drenaje/instrumentación , Drenaje/métodos , Prueba de Esfuerzo , Dimensión del Dolor , Periodo Posoperatorio , Estudios Prospectivos , Dolor Postoperatorio/fisiopatología , Factores de Tiempo , Adulto JovenRESUMEN
OBJECT: It has been shown that craniotomy may lead to a decrease in lung volumes and arterial blood gas tensions as well as a change in the respiratory pattern. The purpose of this study was to determine the incidence of postoperative pulmonary complications (PPCs) and the mortality rate in patients who have undergone elective craniotomy and to evaluate the associations between preoperative and postoperative variables and PPCs in this population. METHODS: Two hundred thirty-six patients were followed up based on a protocol including a clinical questionnaire, physical examination and observation of clinical characteristics in the preoperative period, type of surgery performed, duration of surgery, time spent in the intensive care unit (ICU) and hospital, and the occurrence of any PPCs. RESULTS: Postoperative pulmonary complications occurred in 58 patients (24.6%) and 23 other patients (10%) died. Predicting factors for PPCs according to multivariate analyses were as follows: type of surgery performed (p < 0.0001), prolonged mechanical ventilation >or= 48 hours (p < 0.0001), time spent in the ICU > 3 days (p < 0.0001), decrease in level of consciousness (p < 0.002), duration of surgery >or= 300 minutes (p < 0.01), and previous chronic lung disease (p < 0.04). CONCLUSIONS: The incidence from March 2003 to March 2005 of PPCs in patients who had undergone craniotomy was 25% and death occurred in 10%. Some risk factors for PPCs may be predicted such as the type of surgery performed, prolonged mechanical ventilation, a longer time in the ICU, a decreased level of consciousness, duration of surgery, and previous chronic lung disease.
Asunto(s)
Encefalopatías/mortalidad , Encefalopatías/cirugía , Craneotomía/efectos adversos , Craneotomía/estadística & datos numéricos , Enfermedades Pulmonares/mortalidad , Complicaciones Posoperatorias/mortalidad , Adulto , Procedimientos Quirúrgicos Electivos/efectos adversos , Procedimientos Quirúrgicos Electivos/estadística & datos numéricos , Femenino , Humanos , Incidencia , Tiempo de Internación/estadística & datos numéricos , Masculino , Persona de Mediana Edad , Análisis Multivariante , Estudios Prospectivos , Factores de Riesgo , Tasa de SupervivenciaRESUMEN
CONTEXT AND OBJECTIVE: Changes in pulmonary function commonly occur after general surgery. The aims were to evaluate vital capacity, tidal volume and respiratory frequency among patients undergoing elective craniotomy and to determine possible correlations of these parameters with surgery duration and etiology for neurosurgery. DESIGN AND SETTING: Prospective, open study at a tertiary university hospital. METHODS: Twenty-six patients underwent elective craniotomy for aneurysm clipping (11) or tumor resection (15). Vital capacity (VC), tidal volume (TV), minute volume (VE) and respiratory rate were determined before the operation and on the first to fourth postoperative days. RESULTS: There were significant decreases of 25% in VC, 22% in TV and 12% in VE (p < 0.05) and no significant increase in respiratory frequency (5%) on the first postoperative day. VE returned to baseline on the second postoperative day and TV on the third postoperative day, while VC was 8% lower on the fourth postoperative day, compared with before the operation (p < 0.05). VC reduction was significantly greater in patients undergoing aneurysm clipping (43%) than in patients undergoing tumor resection (14%) when surgery duration was more than four hours (p < 0.05), with no significant change when surgery duration was less than four hours. CONCLUSION: Reductions in VC, TV and VE were observed during the postoperative period in patients undergoing aneurysm clipping or tumor resection. The reductions in VC and TV were greater in patients undergoing craniotomy due to aneurysm and with longer surgery duration.
Asunto(s)
Craneotomía/efectos adversos , Enfermedades Pulmonares/etiología , Pulmón/fisiopatología , Ventilación Pulmonar , Capacidad Vital , Adulto , Neoplasias Encefálicas/cirugía , Craneotomía/normas , Femenino , Hospitales Universitarios , Humanos , Aneurisma Intracraneal/cirugía , Enfermedades Pulmonares/fisiopatología , Masculino , Complicaciones Posoperatorias/prevención & control , Periodo Posoperatorio , Cuidados Preoperatorios , Estudios Prospectivos , Volumen de Ventilación Pulmonar , Factores de TiempoRESUMEN
CONTEXT AND OBJECTIVE: Changes in pulmonary function commonly occur after general surgery. The aims were to evaluate vital capacity, tidal volume and respiratory frequency among patients undergoing elective craniotomy and to determine possible correlations of these parameters with surgery duration and etiology for neurosurgery. DESIGN AND SETTING: Prospective, open study at a tertiary university hospital. METHODS: Twenty-six patients underwent elective craniotomy for aneurysm clipping (11) or tumor resection (15). Vital capacity (VC), tidal volume (TV), minute volume (VE) and respiratory rate were determined before the operation and on the first to fourth postoperative days. RESULTS: There were significant decreases of 25 percent in VC, 22 percent in TV and 12 percent in VE (p < 0.05) and no significant increase in respiratory frequency (5 percent) on the first postoperative day. VE returned to baseline on the second postoperative day and TV on the third postoperative day, while VC was 8 percent lower on the fourth postoperative day, compared with before the operation (p < 0.05). VC reduction was significantly greater in patients undergoing aneurysm clipping (43 percent) than in patients undergoing tumor resection (14 percent) when surgery duration was more than four hours (p < 0.05), with no significant change when surgery duration was less than four hours. CONCLUSION: Reductions in VC, TV and VE were observed during the postoperative period in patients undergoing aneurysm clipping or tumor resection. The reductions in VC and TV were greater in patients undergoing craniotomy due to aneurysm and with longer surgery duration.
CONTEXTO E OBJETIVO: Após cirurgia é comum ocorrerem alterações na função pulmonar. O objetivo foi avaliar a evolução da capacidade vital, do volume corrente e da freqüência respiratória em pacientes submetidos a craniotomia eletiva e determinar uma possível correlação dessas variáveis com o tempo de cirurgia e a causa da neurocirurgia. TIPO DE ESTUDO E LOCAL: Prospectivo aberto realizado em hospital universitário terciário. MÉTODOS: Vinte e seis pacientes submetidos a craniotomia eletiva para clipagem de aneurisma (11) ou ressecção de tumor (15). A capacidade vital (CV), o volume corrente (VC), o volume minuto (VM) e a freqüência respiratória (FR) foram determinados durante o período pré-operatório e do primeiro ao quarto dia do pós-operatório (PO). RESULTADOS: Houve uma redução significante de 25 por cento no CV, 22 por cento no VC e 12 por cento no VM (p < 0,05) e aumento não significante da FR (5 por cento) no primeiro dia de PO. O VM retornou ao normal no segundo PO e o VC no terceiro PO, enquanto a CV continuou 8 por cento menor no quarto PO comparado com o período pré-operatório (p < 0,05). A redução na CV foi significantemente maior em pacientes submetidos a clipagem de aneurisma (43 por cento) do que em pacientes submetidos a ressecção de tumor (14 por cento) quando o tempo de cirurgia foi maior que quatro horas (p < 0,05), sem apresentar diferença quando o tempo cirúrgico foi menor que quatro horas. CONCLUSÕES: A redução na CV, VC e VM foi observada durante o período pós-operatório em pacientes submetidos a clipagem de aneurisma ou ressecção de tumor. A redução na CV e no VC foi maior em pacientes submetidos a craniotomia por aneurisma com tempo cirúrgico mais longo.
Asunto(s)
Adulto , Femenino , Humanos , Masculino , Craneotomía/efectos adversos , Enfermedades Pulmonares/etiología , Pulmón/fisiopatología , Ventilación Pulmonar , Capacidad Vital , Neoplasias Encefálicas/cirugía , Craneotomía/normas , Hospitales Universitarios , Aneurisma Intracraneal/cirugía , Enfermedades Pulmonares/fisiopatología , Complicaciones Posoperatorias/prevención & control , Periodo Posoperatorio , Cuidados Preoperatorios , Estudios Prospectivos , Volumen de Ventilación Pulmonar , Factores de TiempoRESUMEN
OBJECTIVE: To evaluate the influence of pleural drainage on the distance covered on the six-minute walk test, pain intensity and vital capacity in patients submitted to pulmonary resection. METHODS: Thirteen consecutive patients from the Thoracic Surgery Infirmary of Hospital São Paulo, Brazil, submitted to closed pleural drainage (0.5-in multiperforated chest tube) in the postoperative period following pulmonary resection (lobectomy, segmentectomy and pulmonary nodule resection) were evaluated. The decision for chest tube removal followed clinical criteria defined by the surgical team, who did not participate in the study. Vital capacity, pain intensity (using a visual analog pain scale) and the distance covered on the six-minute walk test were determined 30 min prior to and 30 min after the removal of the chest tube. The statistical analysis was performed using paired t-tests, and the level of significance was set at 0.05. RESULTS: After the removal of the chest tube, the visual analog scale pain scores were significantly lower (3.46 cm vs. 1.77 cm; p = 0.001) and the distance covered on the six-minute walk test was significantly higher (374.34 m vs. 444.62 m; p = 0.03). Vital capacity prior to and after chest tube removal was not significantly affected (2.15 L and 2.25 L, respectively; p = 0.540). CONCLUSIONS: The results of the present study suggest that the presence of a chest tube is a factor significantly associated with postoperative pain and functional limitation in patients submitted to pulmonary resection.
Asunto(s)
Tubos Torácicos , Drenaje , Dolor Postoperatorio/etiología , Neumonectomía/efectos adversos , Capacidad Vital/fisiología , Caminata/fisiología , Adolescente , Adulto , Drenaje/instrumentación , Drenaje/métodos , Prueba de Esfuerzo , Femenino , Humanos , Masculino , Dimensión del Dolor , Dolor Postoperatorio/fisiopatología , Periodo Posoperatorio , Estudios Prospectivos , Factores de Tiempo , Adulto JovenRESUMEN
AIM: To study any discriminative properties of SF-36 and QQL-EPM in stable and non-controlled moderate asthmatic patients. METHODS: A total of 63 asthmatic patients were assessed regarding asthma symptoms, FEV1 % predicted value, PEF, ED visits and hospitalizations, QQL-EPM and SF-36 questionnaires. RESULTS: QQL-EPM highlighted significance in all domains to distinguish stable from non-controlled patients (p = 0.0001) while SF-36 was only significant in 3 of its 7 domains (p = 0.009). CONCLUSION: The study showed that the specific quality of life questionnaire for asthma (QQL-EPM) demonstrates better discriminative properties that characterize asthma control when compared with the more generic SF-36 questionnaire.