Relación entre la enfermedad periodontal y la enfermedad pulmonar obstructiva crónica: revisión bibliográfica / Relationship between periodontal disease and chronic obstructive pulmonary disease: a bibliographic review

Introducción: la enfermedad periodontal y la enfermedad pulmonar obstructiva crónica son patologías de origen inflamatorio crónico y progresivo que afectan a pacientes de edad avanzada, fumadores con mal estado de salud oral, encontrándose una correlación por el grado de severidad en la enfermedad periodontal sobre aquellos individuos con presencia de enfermedad pulmonar obstructiva crónica (EPOC) y exacerbaciones. Objetivos: determinar la relación de la enfermedad periodontal y la enfermedad pulmonar obstructiva crónica, explicando los factores de riesgo que intervienen en estas enfermedades. Material y métodos: se realizó una búsqueda en los principales buscadores de datos digitales: PubMed, SciELO, Science Direct, BMC, Journal of Periodontology, Web of Science y Scopus. Se escogieron artículos publicados en los últimos cinco años; se excluyeron artículos incompletos y que no se relacionan al tema. En el resultado de la búsqueda, 45 artículos cumplieron con el propósito de la revisión bibliográfica. Resultados: en esta revisión bibliográfica, se obtuvo que 18 artículos comprueban la relación de la enfermedad periodontal y la enfermedad pulmonar obstructiva crónica. Conclusiones: se ha comprobado la relación entre la enfermedad periodontal y enfermedad pulmonar obstructiva crónica. Se requiere el análisis de más estudios para determinar una relación directa entre estas dos enfermedades e incluir variables como la edad y el tratamiento (AU)

Introduction: periodontal disease and chronic obstructive pulmonary disease are diseases of chronic and progressive inflammatory origin that affect elderly patients, smokers with poor oral health, finding a correlation by the degree of severity in periodontal disease on those individuals with the presence of chronic obstructive pulmonary disease (COPD) and exacerbations. Objectives: to determine the relationship between periodontal disease and chronic obstructive pulmonary disease explaining the risk factors involved in these diseases. Material and methods: a search was carried out in the main digital data search engines: PubMed, SciELO, Science Direct, BMC, Journal of Periodontology, Web of Science, and Scopus, articles published in the last 5 years were chosen, incomplete articles and those not related to the subject were excluded, in the result of the search 45 articles fulfilled the purpose of the bibliographic review. Results: in this literature review it was obtained that 18 articles, prove the relationship between periodontal disease and chronic obstructive pulmonary disease. Conclusions: the relationship between periodontal disease and chronic obstructive pulmonary disease has been proved. More studies are needed to determine a direct relationship between these two diseases and to include variables such as age and treatment (AU)

Neumomediastino espontáneo. Reporte de un caso / Spontaneouspneumomediastinum. Case report

RESUMEN El neumomediastino espontáneo se caracteriza por la presencia de aire en el mediastino. Es una enfermedad generalmente benigna, que evoluciona de forma satisfactoria entre 2 y 15 días, no asociada a causa directa conocida. Es infrecuente en la tercera edad. Se presenta principalmente con dolor torácico, disnea y enfisema subcutáneo. El diagnóstico se realiza sobre la base del cuadro clínico, la radiografía de tórax y la tomografía axial computarizada de tórax, siendo esta última importante, además, para establecer el diagnóstico diferencial con el síndrome de Boerhaave de manera oportuna. Se presentó el caso de un paciente masculino de 67 años de edad, fumador con antecedente de enfermedad pulmonar obstructiva crónica, que acude al cuerpo de guardia por dolor torácico, disnea y enfisema subcutáneo después de un episodio de tos intensa. Se le realizaron radiografías de tórax posteroanterior y lateral, en las que se observan la presencia de aire en el mediastino, se descartan otras enfermedades agudas, y se corrobora el diagnóstico de neumomediastino mediante tomografía axial computarizada de tórax. Recibió tratamiento con oxígeno, broncodilatadores, esteroides y antibióticoterapia, obteniéndose una mejoría evidente. La literatura reporta que no es habitual la presencia de este cuadro en pacientes de la tercera edad, y que debe sospecharse en aquellos que presenten una exacerbación de la enfermedad pulmonar obstructiva crónica, fundamentalmente después de un episodio de tos.

ABSTRACT The spontaneous pneumomediastinum is characterized by the air presence in the mediastinum. It is a generally benign disease which evolves in a satisfactory way between 2 and 15 days, that is not associated to any directly known cause. It is infrequent in the old age. It mainly presents with chest pain, dyspnea and subcutaneous emphysema. Diagnosis realizes on the base of clinical characteristics, thorax radiography and thorax axial computed tomography, being the last one also important to establish the differential diagnosis with Boerhaave syndrome in an opportune way. The case presented is the case of a male patient aged 67 years, who smokes and has antecedents of chronic obstructive pulmonary disease. He assisted to the consultation due to thoracic pain, dyspnea and subcutaneous emphysema after an episode of intense cough. Posteroanterior and lateral thorax radiography were done, finding air presence in the mediastinum; other acute diseases were discarded and the diagnosis of pneumomediastinum was corroborated through thorax computed tomography scan. He was treated with oxygen, bronchodilators, steroids and antibiotics therapy, obtaining an evident improvement. The literature reports that the presence of these characteristics in old-aged patients is not common and that it must be suspected in those presenting an aggravation of the chronic obstructive pulmonary disease, mainly after a cough episode.

Treatments used by chronic obstructive pulmonary disease patients in Brazil: National Survey of Health, 2013 / Tratamentos utilizados por portadores de DPOC no Brasil: Pesquisa Nacional de Saúde, 2013

ABSTRACT OBJECTIVE To estimate the prevalence of treatments used for the management of chronic obstructive pulmonary disease (COPD) in the Brazilian adult population. METHODS A population-based cross-sectional study with data from the 2013 Brazilian National Survey of Health, including individuals aged 40 years or older, with a self-reported medical diagnosis of COPD, chronic bronchitis and/or emphysema, who were asked about treatments used for disease management. RESULTS A total of 60,202 adults were interviewed, of which 636 were 40 years of age or older and had reported a medical diagnosis of COPD, emphysema, or chronic bronchitis. Less than half (49.4%) of the diagnosed population reported using some type of treatment, with differences regarding the macro-region of the country (South 53.8% - Northeast 41.2%, p = 0.007). Pharmacological treatment was the most reported, and emphysema patients had the highest proportion of those undergoing more than one type of treatment. Among the individuals who reported having only chronic bronchitis, 55.1% (95%CI: 48.7-61.4) used medication, 4.7% (95%CI: 2.6-8.3) underwent physical therapy, and 6.0% (95%CI: 3.6-9.9) oxygen therapy. On the other hand, among the emphysema patients, 44.1% (95%CI: 36.8-51.7) underwent drug treatment, 8.8% (95%CI: 5.4-14.2) physical therapy, and 10.0% (95%CI: 6.3-15.6) oxygen therapy. CONCLUSION The prevalence of treatments for COPD management was below ideal in 2013. The pharmacological treatment was the main type of treatment, followed by oxygen therapy and physical therapy.

RESUMO OBJETIVO Estimar a prevalência dos tratamentos utilizados para o manejo da doença pulmonar obstrutiva crônica (DPOC) na população adulta brasileira. MÉTODOS Estudo transversal de base populacional com dados oriundos da Pesquisa Nacional de Saúde de 2013, incluindo indivíduos com 40 anos ou mais, com diagnóstico médico autorreferido de DPOC, bronquite crônica e/ou enfisema, os quais foram questionados sobre tratamentos utilizados para o manejo da doença. RESULTADOS Foram entrevistados 60.202 adultos, dos quais 636 tinham 40 ou mais anos de idade e haviam referido diagnóstico médico de DPOC, enfisema ou bronquite crônica. Menos da metade (49,4%) da população diagnosticada relatou utilizar algum tipo de tratamento, havendo diferenças quanto à macrorregião do país (Sul 53,8% - Nordeste 41,2%, p = 0,007). O tratamento medicamentoso foi o mais referido e portadores de enfisema apresentaram a maior proporção de mais de um tipo de tratamento utilizado. Entre os indivíduos que declararam ter apenas bronquite crônica, 55,1% (IC95% 48,7-61,4) usavam medicamento, 4,7% (IC95% 2,6-8,3) realizavam fisioterapia e 6,0% (IC95% 3,6-9,9) oxigenoterapia. Por outro lado, entre os enfisematosos, 44,1% (IC95% 36,8-51,7) realizavam tratamento medicamentoso, 8,8% (IC95% 5,4-14,2) fisioterapia e 10,0% (IC95% 6,3-15,6) oxigenoterapia. CONCLUSÕES As prevalências de tratamentos para o manejo da DPOC estavam aquém do ideal em 2013. O medicamentoso foi o principal tipo de tratamento, seguido de oxigenoterapia e fisioterapia.

Pulmonary Hypertension in General Cardiology Practice / Hipertensão Pulmonar na Prática do Cardiologista

Abstract The finding of pulmonary hypertension (PH) by echocardiography is common and of concern. However, echocardiography is just a suggestive and non-diagnostic assessment of PH. When direct involvement of pulmonary circulation is suspected, invasive hemodynamic monitoring is recommended to establish the diagnosis. This assessent provides, in addition to the diagnostic confirmation, the correct identification of the vascular territory predominantly involved (arterial pulmonary or postcapillary). Treatment with specific medication for PH (phosphodiesterase type 5 inhibitors, endothelin receptor antagonists and prostacyclin analogues) has been proven effective in patients with pulmonary arterial hypertension, but its use in patients with PH due to left heart disease can even be damaging. In this review, we discuss the diagnosis criteria, how etiological investigation should be carried out, the clinical classification and, finally, the therapeutic recommendations for PH.

Resumo O achado de hipertensão pulmonar (HP) em avaliação ecocardiográfica é frequente e preocupante. No entanto, o ecocardiograma é apenas um exame sugestivo e não diagnóstico de HP. Quando se suspeita de acometimento direto da circulação pulmonar, está indicada medida hemodinâmica invasiva para estabelecer o diagnóstico. Essa avaliação permite, além da confirmação diagnóstica, a correta identificação do território vascular predominantemente acometido (arterial pulmonar ou pós-capilar). O tratamento com as medicações específicas de HP (inibidores da fosfodiestarese 5, antagonistas do receptor de endotelina, análogos da prostaciclina e estimulador da guanilil ciclase solúvel) é comprovadamente eficaz para pacientes com hipertensão arterial pulmonar, mas seu uso em pacientes com HP decorrente de doença cardíaca de câmaras esquerdas pode até mesmo ser prejudicial. Discutiremos nesta revisão o critério diagnóstico, a maneira de proceder a investigação etiológica, a classificação clínica e, finalmente, as recomendações terapêuticas na HP.

Resultados del tratamiento con pleurostomía en pacientes con neumotórax espontáneo / Outcomes of Pleurostomy Treatment in Patients with Spontaneous Pneumothorax

RESUMEN Introducción: La presencia de aire dentro de la cavidad pleural es definida como neumotórax. El tratamiento quirúrgico inicial es la pleurostomía, que puede acarrear complicaciones, relacionadas con varios factores, entre los cuales se encuentra el diámetro de la sonda intratorácica utilizada. Objetivo: Evaluar los resultados del tratamiento con pleurostomía en pacientes con neumotórax espontáneo en el Hospital Universitario Manuel Ascunce Domenech. Método: Se realizó un estudio descriptivo longitudinal retrospectivo desde septiembre de 2012 hasta septiembre de 2017. Se estudiaron 63 pacientes afectos de neumotórax espontáneos que recibieron pleurostomía como tratamiento inicial. Resultados: Los neumotórax espontáneos primarios representaron 56 por ciento de los casos. Del total de pacientes, 82 por ciento eran fumadores. En todos los pacientes el síntoma predominante fue el dolor. Las complicaciones fueron más frecuentes con el uso de sondas pleurales de menor diámetro (86 por ciento). Conclusiones: El neumotórax espontáneo primario fue el de mayor frecuencia. Las causas predominantes en el neumotórax secundario fueron las bulas de enfisema y la enfermedad pulmonar obstructiva crónica. En la totalidad de los casos, estuvo presente algunos de los síntomas del síndrome pleural con predominancia absoluta del dolor. El mayor número de complicaciones se presentó en pacientes fumadores(AU)

ABSTRACT Introduction: The presence of air within the pleural cavity is defined as pneumothorax. The initial surgical treatment is pleurostomy, which can lead to complications associated with several factors, among which is the diameter of the intrathoracic probe that is used. Objective: To evaluate the outcomes of the treatment with pleurostomy in patients with spontaneous pneumothorax at Manuel Ascunce Domenech University Hospital. Method: A retrospective, longitudinal, descriptive study was conducted from September 2012 to September 2017. We studied 63 patients affected by spontaneous pneumothorax who received pleurostomy as initial treatment. Results: Primary spontaneous pneumothorax accounted for 56 percent of the cases. From the total amount of patients, 82 percent were smokers. In all patients, the predominant symptom was pain. Complications were more frequent with the use of pleural probes of smaller diameter (86 percent). The primary spontaneous pneumothorax was the most frequent. The predominant causes of secondary pneumothorax were bullous emphysema and chronic obstructive pulmonary disease. In all the cases, some of the symptoms of pleural syndrome with absolute predominance of pain were present. The greatest number of complications occurred in smoking patients. Conclusions: Pleurostomy, with the use of the drainage catheter, is the initial treatment for all patients with spontaneous pneumothorax in our hospital, regardless of the diameter of the probe to be used according to the type of pneumothorax (primary or secondary)(AU)

Interrelationship between Emphysema and Left Ventricular Diastolic Dysfunction: our experience in the Hospital Privado Centro Médico de Córdoba

Introduction: The hemodynamic consequences of hyperinflation and emphysema are produced by cardiac compression due to high intrathoracic pressures, which could produce subclinical left ventricular diastolic dysfunction. Our purpose is to correlate the percentage of emphysema with lung function parameters and cardiac chamber sizes, the global ventricular systolic function and the left ventricular diastolic function, in cases of chronic obstructive pulmonary disease. Materials and Methods: The participants were patients with moderate and severe chronic obstructive pulmonary disease treated in the Pulmonology Service of the Hospital Privado Centro Médico de Córdoba from January 1st to October 13th, 2014. We quantified the volume and percentage of emphysema by high resolution computed tomography and carried out a spirometry, a Six Minute Walk Test, measurement of pulmonary volumes and color Doppler echocardiography. Results: We found a significant negative correlation between the percentage of emphysema and the percentage of the post-bronchodilator FEV1 theoretical value (p = 0.005) and the post-bronchodilator FEV1/FVC (Forced Expiratory Volume in First Second/Forced Vital Capacity) quotient (p = 0.004), and, also, between the post-bronchodilator FEV1/FVC quotient and the emphysema volume in cm3 (p = 0.000). Out of a sub-group of 20 patients, seven patients (35%) were diagnosed with grade I left ventricular diastolic dysfunction. We found negative, but not significant correlations between the percentage of emphysema and global ventricular systolic function and cardiac chamber sizes. Conclusions: We should emphasize the usefulness of the echocardiography in reducing sub-diagnoses of left ventricular diastolic dysfunction. We should also stress on the importance hyperinflation and emphysema would have in the impairment of the left ventricular diastolic filling pattern and in the decrease in cardiac chamber sizes, with a decrease in exercise tolerance.

Eficacia de la budesonida/formoterol comparado con la fluticasona/salmeterol en la mejoría de la capacidad pulmonar de personas mayores con Enfermedad Pulmonar Obstructiva Crónica: revisión sistemática de literatura / Effectiveness of budesonide/formoterol compared to fluticasone / salmeterol in improving the lung capacity of older people with Chronic Obstructive Pulmonary Disease: systematic literature review / Eficiência da budesonida/formoterol comparado com fluticasona/salmeterol na melhora da capacidade pulmonar de idosos com Doença Pulmonar Obstrutiva Crônica: revisão sistemática da literatura

Introducción. La Enfermedad Pulmonar Obstructiva Crónica (EPOC) es una patología no transmisible, caracterizada por una limitación de flujo de aire en las vías respiratorias debido a una respuesta inmunológica anormal frente a partículas. Objetivo. Conocer la eficacia que tiene la budesonida/formoterol comparado con la fluticasona/salmeterol en la mejoría de la capacidad pulmonar en personas mayores de 40 años con Enfermedad Pulmonar Obstructiva Crónica. Materiales y métodos. Se realizó una revisión sistemática de documentos producidos entre el año 2000 y 2018 en distintas bases de datos, donde se incluyeron ensayos clínicos. Se identificaron cuatro artículos para el análisis final. Resultados. Durante la evaluación comparativa de budesonida con formoterol, los artículos muestran un total de 709 personas evaluadas, con un promedio de edad de 53,5 años. El 65,4 % eran varones, el 21 % manifestaba no haber consumido tabaco, todos con diagnóstico de Enfermedad Pulmonar Obstructiva Crónica moderada-severa, según la escala GOLD (Global Initiative For Chronic Obstrutive Lung Disease). Los estudios determinaron que al administrar budesonida/formoterol de 400/12 mcg y 320/9 mcg, los pacientes tuvieron una leve mejoría en el Volumen Espiratorio Forzado del primer segundo (VEF1). Solo dos pacientes presentaron efectos adversos. No obstante, para los resultados mencionados anteriormente no se encontró diferencias significativas. Conclusiones. El uso de budesonida/formoterol es eficaz al mejorar la capacidad ventilatoria pulmonar, disminuye el número de exacerbaciones anuales y genera un adecuado control de los síntomas, sin embargo, es igual de efectivo a la fluticasona/salmeterol.

Introduction. Chronic Obstructive Pulmonary Disease (COPD) is a not transmissible disease, characterized by a limitation of airflow in the respiratory tract, due to an abnormal immune response to particles. Objective. This article aims to show that the application of budesonide / formoterol improves lung capacity in people over 40 years with Chronic Obstructive Pulmonary Disease. Materials and methods. A systematic review was conducted in the period between 2000 and 2018 in different databases where clinical trials were included. Four articles were identified for the final analysis. Results. During the comparative evaluation of budesonide with formoterol, a total of 709 people were evaluated, with an average age of 53.5 years, 65.4% were male, 21% reported not having used tobacco, all with a diagnosis of moderate-severe Chronic Obstructive Pulmonary Disease according to the GOLD scale (Global Initiative For Chronic Obstrutive Lung Disease). The studies determined that when budesonide / formoterol of 400/12 mcg and 320/9 mcg was administered, the patients had a slight improvement in the Forced Expiratory Volume of the first second (FEV1). Only two patients presented adverse effects. However, for the results mentioned above no significant differences were found. Conclusions. The use of budesonide / formoterol is effective in improving pulmonary ventilatory capacity, decreases the number of annual exacerbations and generates adequate control of symptoms, however, it is equally effective in fluticasone / salmeterol.

Introdução. A Doença Pulmonar Obstrutiva Crônica (DPOC) é uma patologia não transmissível, caraterizada por uma limitação do fluxo de ar nas vias aéreas devido a uma resposta imune anormal contra partículas. Objetivo. Conhecer a eficiência que apresenta a budesonida/formoterol comparado com fluticasona/salmeterol na melhora da capacidade pulmonar em pessoas com mais de 40 anos com Doença Pulmonar Obstrutiva Crônica. Materiais e métodos. Foi realizada uma revisão sistemática dos documentos produzidos entre 2000 e 2018 em diferentes bancos de dados, onde foram incluídos ensaios clínicos. Quatro artigos foram identificados para a análise final. Resultados. Durante a avaliação comparativa de budesonida com formoterol, os artículos mostram um total de 709 pessoas avaliadas, com uma idade média de 53,5 anos. O 65,4 % eram do sexo masculino, o 21 % disseram que não usavam tabaco, todos diagnosticados com Doença Pulmonar Obstrutiva Crônica moderada a grave, de acordo com a escala GOLD (Global Initiative For Chronic Obstrutive Lung Disease). Os estudos determinaram que administrar budesonida/formoterol de 400/12 mcg e 320/9 mcg, os pacientes apresentaram uma leve melhora no Volume Expiratório Forçado no primeiro segundo (VEF1). Apenas dois pacientes tiveram efeitos adversos. No entanto, não foram encontradas diferenças significativas para os resultados mencionados acima. Conclusões. O uso de budesonida/formoterol é eficaz na melhora da capacidade ventilatória pulmonar, diminui o numero de exacerbações anuais e gera controle adequado dos sintomas, no entanto, é igualmente eficaz para a fluticasona/salmeterol.

The patient profile of individuals with Alpha-1 antitrypsine gene mutations at a referral center in Brazil / Perfil dos pacientes com mutação no gene da alfa-1 antitripsina em um centro de referência no Brasil

ABSTRACT Objective: The clinical, functional, radiological and genotypic descriptions of patients with an alpha-1 antitrypsin (A1AT) gene mutation in a referral center for COPD in Brazil. Methods: A cross-sectional study of patients with an A1AT gene mutation compatible with deficiency. We evaluated the A1AT dosage and genotypic, demographic, clinical, tomographic, and functional characteristics of these patients. Results: Among the 43 patients suspected of A1AT deficiency (A1ATD), the disease was confirmed by genotyping in 27 of them. The A1AT median dosage was 45 mg/dL, and 4 patients (15%) had a normal dosage. Median age was 54, 63% of the patients were male, and the respiratory symptoms started at the age of 40. The median FEV1 was 1.37L (43% predicted). Tomographic emphysema was found in 77.8% of the individuals. The emphysema was panlobular in 76% of them and 48% had lower lobe predominance. The frequency of bronchiectasis was 52% and the frequency of bronchial thickening was 81.5%. The most common genotype was Pi*ZZ in 40.7% of participants. The other genotypes found were: Pi*SZ (18.5%), PiM1Z (14.8%), Pi*M1S (7.4%), Pi*M2Z (3.7%), Pi*M1I (3.7%), Pi*ZMnichinan (3.7%), Pi*M3Plowell (3.7%), and Pi*SF (3.7%). We did not find any significant difference in age, smoking load, FEV1, or the presence of bronchiectasis between the groups with a normal and a reduced A1AT dosage, neither for 1 nor 2-allele mutation for A1ATD. Conclusions: Our patients presented a high frequency of emphysema, bronchiectasis and bronchial thickening, and early-beginning respiratory symptoms. The most frequent genotype was Pi*ZZ. Heterozygous genotypes and normal levels of A1AT also manifested significant lung disease.

RESUMO Objetivo: Caracterização clínica, funcional, radiológica e genotípica dos pacientes portadores de mutações do gene da alfa-1 antitripsina (A1AT) em um centro de referência em doença pulmonar obstrutiva crônica (DPOC) no Brasil. Métodos: Estudo transversal de pacientes com mutação no gene da A1AT compatível com deficiência. Foram avaliadas características genotípicas, demográficas, clínicas, tomográficas, de função pulmonar, e dosagem de A1AT. Resultados: De 43 pacientes suspeitos para deficiência de alfa-1 antitripsina (DA1AT), a doença foi confirmada por genotipagem em 27. A mediana da dosagem de A1AT foi de 45 mg/dL, e 4 pacientes (15%) apresentavam dosagens normais. A idade mediana foi de 54 anos, 63% dos participantes eram do sexo masculino e a idade do início dos sintomas prevalente foi aos 40 anos. A mediana do volume expiratório forçado no primeiro segundo (VEF1) foi de 1,37 L (43% do previsto). Enfisema tomográfico foi encontrado em 77,8% dos indivíduos, sendo panlobular em 76% e de predomínio em lobos inferiores em 48%. A frequência de bronquiectasias foi de 52%, e a de espessamento brônquico, de 81,5%. O genótipo mais encontrado foi Pi*ZZ (40,7%). Os demais genótipos foram: Pi*SZ (18,5%), Pi*M1Z (14,8%), Pi*M1S (7,4%), Pi*M2Z (3,7%), Pi*M1I (3,7%), Pi*ZMnichinan (3,7%), Pi*M3Plowell (3,7%) e Pi*SF (3,7%). Não encontramos diferença significativa para idade, carga tabágica, VEF1 e presença de bronquiectasias entre os grupos com dosagem de A1AT normal versus alterada, nem entre 1 alelo versus 2 alelos com mutação para DA1AT. Conclusões: Nossos pacientes apresentaram alta frequência de enfisema, bronquiectasias e espessamento brônquico, com início precoce dos sintomas respiratórios. O genótipo mais frequente foi Pi*ZZ, embora genótipos heterozigotos e níveis normais de A1AT também tenham se manifestado com doença pulmonar significativa.

Enfermedad Pulmonar Obstructiva Crónica en el Siglo XXI - Optimismo basado en evidencia / Chronic Obstructive Pulmonary Disease in the 21st Century - Evidence-based optimism

There are increasingly more data on the prevalence and distribution of Chronic Obstructive Pulmonary Disease (COPD) from around the world. COPD is predicted to be the third most frequent cause of death in the world by 2020. COPD is mainly caused by chronic tobacco smoking, which induces important changes in both the airways and lung parenchyma. COPD is a progressive, disabling condition that ultimately ends in respiratory failure and death. Is a multicomponent disease, there is evidence that systemic inflammation and extrapulmonary effects are also common in COPD, although the association between systemic inflammation and systemic manifestations of COPD is still not entirely clear. COPD has been associated with a nihilistic attitude. On the basis of current evidence, this nihilistic attitude is totally unjustified. The disease must be viewed through the lens of a new paradigm: COPD is not only preventable but also treatable. The past decade has witnessed great progress in COPD research. New drugs have been developed and tested and a growing base of scientific evidence now documents the efficacy of various therapies for symptoms and exacerbations. It is clear that many patients with COPD can benefit from aggressive management, with a decrease in the frequency of hospitalizations and improvements in symptoms and quality of life. In addition, basic and clinical scientists have now identified cells, mechanisms, and molecules that appear to play key roles in disease pathogenesis. Additional novel treatments are on the horizon and the advent of newer and more effective therapies will lead to a decline in the contribution of this disease to poor world health. The good news about COPD is to increase awareness of the disease. COPD is now viewed under a new paradigm as preventable and treatable.

Pulmonary placental transmogrification associated with adenocarcinoma of the lung: a case report with a comprehensive review of the literature

Pulmonary placental transmogrification (PT) is a rare entity with less than 40 cases reported in the literature. Most reported cases are associated with either bullous emphysema or with pulmonary fibrochondromatous hamartomas. We present only the second case of PT associated with adenocarcinoma of the lung. A 67-year-old female with multiple chronic medical ailments presented with shortness of breath and was found to have a 6-cm mass in the upper lobe of her right lung. A computed tomography (CT) guided core biopsy was performed that showed a well-differentiated adenocarcinoma. Interestingly the normal lung tissue showed placental villous architecture. A unique feature of our case is that the diagnosis was made on a needle core biopsy, unlike all the other cases in the literature. We also provide a comprehensive review of this rare entity.

Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers

In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity, which comprised centrilobular or paraseptal emphysema in the upper pulmonary lobes, and fibrosis in the lower lobes accompanied by reduced diffused capacity of the lungs for carbon monoxide (DLCO). Recently, the fibrosis associated with the connective tissue disease was also included in the diagnosis of CPFE, although the exposure to tobacco, coal, welding, agrochemical compounds, and tire manufacturing are the most frequent causative agents. This entity characteristically presents reduced DLCO with preserved lung volumes and severe pulmonary hypertension, which is not observed in emphysema and fibrosis alone. We present the case of a 63-year-old woman with a history of heavy tobacco smoking abuse, who developed progressive dyspnea, severe pulmonary hypertension, and cor pulmonale over a 2-year period. She attended the emergency facility several times complaining of worsening dyspnea that was treated as decompensate chronic obstructive pulmonary disease (COPD). The imaging examination showed paraseptal emphysema in the upper pulmonary lobes and fibrosis in the middle and lower lobes. The echo Doppler cardiogram revealed the dilation of the right cardiac chambers and pulmonary hypertension, which was confirmed by pulmonary trunk artery pressure measurement by catheterization. During this period, she was progressively restricted to the minimal activities of daily life and dependent on caregivers. She was brought to the hospital neurologically obtunded, presenting anasarca, and respiratory failure, which led her to death. The autopsy showed signs of pulmonary hypertension and findings of fibrosis and emphysema in the histological examination of the lungs. The authors highlight the importance of the recognition of this entity in case of COPD associated with severe pulmonary hypertension of unknown cause.

Reducción de volumen pulmonar endoscópica en enfisema pulmonar avanzado: Casos clínicos / Endoscopic lung volume reduction in advanced pulmonary emphysema: initial experience in Chile

Chronic obstructive pulmonary disease (COPD) has no curative treatment, and in moderate to advanced stages, functional parameters and quality of life are affected. Lung volume reduction improves respiratory parameters and quality of life of these patients. Endoscopic lung volume reduction is a minimally invasive procedure that uses endobronchial valves or coils. Valves are unidirectional, blocking the air from entering the target lobe during inspiration, allowing the exit of air and secretions during expiration. Complete fissure and absence of collateral ventilation are needed for an adequate functioning of endobronchial valves. Endobronchial coils cause mechanical retraction of the lung parenchyma. We report two patients who underwent endoscopic lung volume reduction by endobronchial valves. One patient was on continuous positive pressure non-invasive ventilation due to his severe emphysema.

Deficiência de alfa-1 antitripsina: uma condição subdiagnosticada / Alpha-1 antitrypsin deficiency: an underdiagnosed condition

A deficiência de alfa-1-antitripsina (AAT) é associada ao desenvolvimento de doenças hepáticas graves e enfisema pulmonar precoce. Em todo o mundo, considera-se que apenas 2% dos casos estimados da deficiência de AAT tenham sido diagnosticados. A disciplina de Pneumologia da Universidade do Estado do Rio de Janeiro vem realizando testes de varredura para deficiência de AAT através da técnica de nefelometria em papel filtro em todos os pacientes com diagnóstico de DPOC. A prevalência de mutações graves encontradas nos genes da AAT em pacientes com DPOC foi de 2,4% e não difere dos dados existentes previamente na literatura, mas o número de outros pacientes com mutações leves é bastante elevado (4%). As autoras sugerem que a dosagem sistemática de AAT em todos os pacientes com DPOC possa ser uma estratégia eficiente para captura dos pacientes com deficiência enzimática, permitindo que medidas preventivas como a suspensão do fumo e o aconselhamento genético seja efetivadas.

Alpha-1-antitrypsin deficiency (AAT) is associated with the development of severe liver disease and early pulmonary emphysema. Around the world, only 2% of the estimated cases of AAT deficiency are believed to have been diagnosed. The discipline of Pulmonology of the University of the State of Rio de Janeiro has been conducting tests for AAT deficiency by filter nephelometry technique in all patients diagnosed with COPD. The prevalence of severe mutations found in AAT genes in patients with COPD was 2.4% and does not differ from previous data in the literature, but the number of other patients with mild mutations is quite high (4%). The authors suggest that the systematic dosing of AAT in all patients with COPD may be an effective strategy to capture patients with enzyme deficiency, allowing preventive measures such as smoking cessation and genetic counseling to be effective.

Tratamento Endoscópico com Válvulas Endobrônquicas nos Pacientes com Enfisema Pulmonar / Endoscopic treatment with endobronchial valves in patients with pulmonary emphysema

A doença pulmonar obstrutiva crônica (DPOC) é uma patologia de grande prevalência na sociedade contemporânea, causando grande morbimortalidade e consumo de recursos em saúde. Apesar de flagrante melhora no entendimento de sua fisiopatologia e acréscimo no arsenal terapêutico experimentado nas últimas duas décadas, ainda existe grande parcela de doentes que convivem com limitação funcional extrema a despeito de tratamento clínico otimizado, reabilitação cardiopulmonar e oxigenoterapia suplementar. Tratam-se dos pacientes com doença em estágio avançado, que até pouco tempo só tinham como alternativa terapêutica o transplante pulmonar ou cardiopulmonar. Porém, nos últimos dez anos, esse panorama sombrio vem ganhando mais uma alternativa viável e factível, mesmo em pacientes com comorbidades limitantes e em países como o nosso, onde a realização de transplante pulmonar em larga escala não é uma realidade. Trata-se do tratamento endoscópico do enfisema pulmonar. Dentre as modalidades de terapia disponíveis atualmente, discutiremos o uso de válvulas endobrônquicas, método dos mais estudados, já com diversas publicações importantes e recentemente incluído no documento GOLD como opção terapêutica nos pacientes com doença pulmonar obstrutiva crônica.

Chronic obstructive pulmonary disease is a highly prevalent pathology in contemporary society, causing great morbidity, mortality and consumption of health resources. Despite a striking improvement in the understanding of its pathophysiology and increase in the therapeutic arsenal experienced in the last two decades, there is still a large number of patients living with extreme functional limitation despite optimal clinical treatment, cardiopulmonary rehabilitation and supplemental oxygen therapy. They are those patients with advanced disease that until recently had only as a therapeutic alternative the lung or cardiopulmonary transplantation. However, in the last ten years, this bleak picture has been gaining yet another viable and feasible alternative, even in patients with limiting comorbidities and in countries such as ours, where large-scale lung transplantation is not a reality. It is the endoscopic treatment of pulmonary emphysema. Among the modalities of therapy currently available, we will discuss the use of endobronchial valves, a method most studied, already with several important publications and recently included in the GOLD document as a therapeutic possibility in patients with chronic obstructive pulmonary disease.

Nuevos procedimientos broncoscópicos en Argentina: Reducción volumétrica pulmonar endoscópica con válvulas endobronquiales / Bronchoscopic lung volume reduction. New bronchoscopic procedures in Argentina

La Enfermedad Pulmonar Obstructiva Crónica (EPOC) es una enfermedad caracterizada por limitación del flujo aéreo espiratorio donde el atrapamiento aéreo y la hiperinsuflación dinámica conducen a la producción de disnea que muchas veces incapacita al paciente a pesar de un correcto tratamiento farmacológico y de rehabilitación. Los tratamientos quirúrgicos destinados a paliar esta situación como la cirugía de reducción de volumen pulmonar (CRVP) presentan una morbimortalidad que limita su uso. La búsqueda de formas menos invasivas para conseguir el mismo propósito dieron origen a una serie de procedimientos broncoscópicos para la reducción de volumen pulmonar dentro de los cuales, las válvulas endobronquiales (VEB), son las que acumulan mayor desarrollo y experiencia. Si bien los estudios con VEB son heterogéneos y en su conjunto, muestran modestos beneficios en los test de función pulmonar, ejercicio y calidad de vida relacionada con la salud, existe un grupo de pacientes con enfisema pulmonar heterogéneo, cisura interlobar intacta, atrapamiento aéreo severo y baja tolerancia al ejercicio que muestra beneficios estadística y clínicamente significativos. Nuevos estudios se encuentran en desarrollo para dar más peso de evidencia a la acumulada en la actualidad.

Chronic Obstructive Pulmonary Disease (COPD) is characterized by airflow limitation, air trapping and dynamic hyperinflation that lead to disabling dyspnea despite appropriate pharmacologic treatment and pulmonary rehabilitation. Though surgical treatments such as lung transplant surgery and lung volume reduction (LVRS) are available, their high morbidity and mortality limit their use. To avoid these complications multiple procedures for bronchoscopic lung volume reduction have been developed, among which endobronchial valves (EBV) have accumulated the largest amount of evidence. While studies with EBV are heterogeneous and show modest benefits in pulmonary function tests, exercise capacity and quality of life, there is a group of patients with heterogeneous emphysema, intact interlobar fissure, severe air trapping and low exercise tolerance that show a statistically and clinically significant benefits. New studies are under way to further support the growing evidence.

Resultados tempranos y alejados del trasplante pulmonar en el enfisema avanzado / Early and Late Results of Lung Transplantation in Advanced Emphysema

Introducción y objetivos: El enfisema constituye la indicación más frecuente de trasplante pulmonar (TP). El propósito del presente trabajo fue evaluar las características demográficas y funcionales de pacientes con enfisema y analizar la supervivencia. Métodos: Estudio observacional analítico de 84 pacientes con enfisema que recibieron TP entre junio 1994 y marzo 2012. Se utilizó el método de Kaplan-Meier para analizar la supervivencia. Resultados: Se realizaron 84 TP en 84 pacientes con enfermedad pulmonar obstructiva crónica (EPOC) por enfisema avanzado, todos fumadores, 11 (13%) padecían déficit de alfa-1 antitripsina (DA1AT); 70 trasplantes unipulmonares (TUP) (83%) y 14 trasplantes bipulmonares (TBP) (17%); 69 en situación electiva (82%) y 15 en emergencia/urgencia (18%). Edad promedio: 54,95 ± 6,10 años, 54 hombres (64%). Volumen espiratorio forzado en el primer segundo (VEF1) 0,60 ± 0,28 L (20 ± 9%); capacidad vital forzada (CVF) 1,78 ± 0,62 L (46 ± 16%); presión arterial pulmonar media (PAPm) 21,08 ± 5,79 mmHg; presión parcial de oxígeno arterial (PaO2) 67,54 ± 12,27 mmHg; presión parcial de dióxido de carbono arterial (PaCO2) 46,40 ± 8,04 mmHg; distancia recorrida en prueba de marcha de 6 minutos (PM6M) 225,59 ± 113,67 m. La mortalidad hospitalaria (MH) fue 16% (13/84). La supervivencia global a 1, 3, 5, 7 y 10 años: 67%, 53%, 40%, 27% y 13%. Supervivencia condicional a 3, 5, 7 y 10 años: 79%, 59%, 41% y 20%. Conclusiones: El TP es una opción terapéutica en enfisema avanzado. Este trabajo muestra características y supervivencia de pacientes con EPOC trasplantados en Hospital Universitario Fundación Favaloro (HUFF).

Introduction and objectives: Emphysema is the most frequent indication of lung transplantation (LT)). The aim of this paper is to evaluate the demographic and functional characteristics of patients with emphysema and to analize survival. Methods: Observational and analytic study of 84 patients with emphysema who were transplanted between june 1994 and march 2012. Kaplan-Meier method was used to analyze survival. Results: 84 (40%) out of 212 transplanted patients had diagnosis of emphysema; 11 (13%) of them with diagnosis of alfa-1 antitrypsin defcit. Seventy of them (83%) were single lung transplantation and 14 (17%) double lung transplantation; 69 in elective situation (82%) and 15 in emergency/urgency situation (18%). Mean age: 54, 95 ± 6, 10 years, 54 male (64%). Baseline characteristics were: forced expiratory volume in first second (FEV1) 0,60 ± 0,28 L (20 ±9%); forced vital capacity (FVC) 1,78 ± 0,62 L (46 ± 16%); mean pulmonary artery pressure (map) 21,08 ± 5,79 mmHg; mean partial artery oxygen pressure (PaO2) 67,54 ± 12,27 mmHg; mean partial carbon dioxide pressure (PaCO2) 46,40 ± 8,04 mmHg, Six minute walk test (6MWT) distance was 225,59± 113,67 m. In-hospital mortality was 16% (13/84). Global survival at 1, 3, 5, 7 y 10 years was 67%, 53%, 40%, 27% y 13% respectively. Conditional survival at 3, 5, 7 y 10 years was 79%, 59%, 41% y 20% respectively. Conclusions: lung transplantation is a therapeutic option in advanced emphysema. This paper shows characteristics and survival of COPD patients who underwent lung transplantation in the University Hospital Foundation Favaloro.

Influence of emphysema distribution on pulmonary function parameters in COPD patients / Influência da distribuição do enfisema nos parâmetros de função pulmonar em pacientes com DPOC

ABSTRACT OBJECTIVE: To evaluate the impact that the distribution of emphysema has on clinical and functional severity in patients with COPD. METHODS: The distribution of the emphysema was analyzed in COPD patients, who were classified according to a 5-point visual classification system of lung CT findings. We assessed the influence of emphysema distribution type on the clinical and functional presentation of COPD. We also evaluated hypoxemia after the six-minute walk test (6MWT) and determined the six-minute walk distance (6MWD). RESULTS: Eighty-six patients were included. The mean age was 65.2 ± 12.2 years, 91.9% were male, and all but one were smokers (mean smoking history, 62.7 ± 38.4 pack-years). The emphysema distribution was categorized as obviously upper lung-predominant (type 1), in 36.0% of the patients; slightly upper lung-predominant (type 2), in 25.6%; homogeneous between the upper and lower lung (type 3), in 16.3%; and slightly lower lung-predominant (type 4), in 22.1%. Type 2 emphysema distribution was associated with lower FEV1, FVC, FEV1/FVC ratio, and DLCO. In comparison with the type 1 patients, the type 4 patients were more likely to have an FEV1 < 65% of the predicted value (OR = 6.91, 95% CI: 1.43-33.45; p = 0.016), a 6MWD < 350 m (OR = 6.36, 95% CI: 1.26-32.18; p = 0.025), and post-6MWT hypoxemia (OR = 32.66, 95% CI: 3.26-326.84; p = 0.003). The type 3 patients had a higher RV/TLC ratio, although the difference was not significant. CONCLUSIONS: The severity of COPD appears to be greater in type 4 patients, and type 3 patients tend to have greater hyperinflation. The distribution of emphysema could have a major impact on functional parameters and should be considered in the evaluation of COPD patients.

RESUMO OBJETIVO: Avaliar o impacto que a distribuição do enfisema tem na gravidade clínica e funcional em pacientes com DPOC. MÉTODOS: A distribuição do enfisema foi analisada em pacientes com DPOC, que foram classificados de acordo com um sistema de classificação visual de cinco pontos a partir de achados de TC de tórax. Avaliou-se a influência do tipo de distribuição do enfisema na apresentação funcional e clínica da DPOC. Hipoxemia após o teste da caminhada de seis minutos (TC6) foi também avaliada e a distância percorrida (DTC6) foi determinada. RESULTADOS: Foram incluídos 86 pacientes. A média de idade foi de 65,2 ± 12,2 anos, 91,9% eram homens, e todos menos um eram fumantes (média de carga tabágica, 62,7 ± 38,4 anos-maço). A distribuição do enfisema foi categorizada como obviamente predominante no pulmão superior (tipo 1), em 36,0% dos pacientes; levemente predominante no pulmão superior (tipo 2), em 25,6%; homogêneo entre o pulmão superior e inferior (tipo 3), em 16,3%; e levemente predominante no pulmão inferior (tipo 4), em 22,1%. A distribuição do enfisema do tipo 2 foi associada a menores valores de VEF1, CVF, relação VEF1/CVF e DLCO. Em comparação com os pacientes do tipo 1, os do tipo 4 apresentaram maior probabilidade de ter VEF1 < 65% do previsto (OR = 6,91, IC95%: 1,43-33,45; p = 0,016), DTC6 < 350 m (OR = 6,36, IC95%: 1,26-32,18; p = 0,025),e hipoxemia após o TC6 (OR = 32,66, IC95%: 3,26-326,84; p = 0,003). Os pacientes do tipo 3 tiveram uma relação VR/CPT maior, embora sem diferença significativa. CONCLUSÕES: A gravidade da DPOC parece ser maior nos pacientes do tipo 4, e os do tipo 3 tendem a apresentar maior hiperinsuflação. A distribuição do enfisema pode ter um impacto importante nos parâmetros funcionais e deve ser considerada na avaliação de pacientes com DPOC.

Efectores celulares de la respuesta inflamatoria en la enfermedad pulmonar obstructiva crónica / Cellular effectors of the inflammatory response in chronic obstructive pulmonary disease (COPD)

Approximately 3 million people in the world die every year as a consequence of COPD, which is associated with an abnormal inflammatory response of the lung to noxious particles and gases. This inflammatory pattern causes pathological changes leading to a narrowing of small airways and destruction of lung parenchyma, also known as emphysema. Classically, these changes were associated to macrophages and neutrophils, although T CD8+ lymphocytes were latter added to the equation to explain the origin of emphysematous lesions. However, in recent years, multiple evidences have arisen indicating that inflammatory response in COPD is much more complex. These findings point to a key role for mast cells, dendritic cells, T CD4+ and B cells. The aim of this article is to review such evidence and report what is known so far about those cells involved in the inflammatory response in COPD.

Enfisema orbitario espontáneo tras la maniobra de Valsalva / Orbital emphysema after Valsalva maneuver. Report of one case

Orbital emphysema is a rare complication of orbital and facial trauma, involving the sinuses and occasionally the nasal cavity. Most cases occur as a result of trauma but spontaneous orbital emphysema has been reported. Clinical manifestations are often delayed until the upper airway pressure increases as when blowing or coughing. Along with the fracture, the rupture of the underlying mucosa is essential for emphysema to manifest. We report a 29-years-old male who consulted in the emergency room due to eyelid swelling after a Valsalva maneuver, a couple of hours after suffering a facial injury secondary to a fall. In the presence of eyelid emphysema, the patient underwent craniofacial imaging studies, confirming an ethmoidal lamina papyracea fracture.

Tratamento do enfisema pulmonar avançado: Cirurgia redutora de volume pulmonar ou broncoscopia? / Treatment of advanced emphysema: Surgery or bronchoscopy?

A doença pulmonar obstrutiva crônica (DPOC) é uma grande causa de morbidade e mortalidade. O enfisema pulmonar, uma das formas clínicas da DPOC, se caracteriza pelo desenvolvimento progressivo de aprisionamento aéreo, alterações da arquitetura alveolar e hiperinsuflação pulmonar. Sua história natural é a evolução para a doença pulmonar terminal e necessidade de transplante pulmonar. Entretanto, sabe-se que uma redução da hiperinsuflação pulmonar é capaz de reestabelecer algumas das propriedades mecânicas do sistema respiratório e assim melhorar os volumes e a função pulmonar destes pacientes, com melhora da qualidade de vida e sobrevida. Há pelo menos duas formas de tratamento invasivo,baseadas nestes princípios fisiopatológicos, disponíveis na prática clínica: a cirurgia redutora do volume pulmonar (CRVP) e a redução volumétrica endoscópica (REV). Desta forma, este artigo abordará os aspectos relacionados ao emprego da CRVP e da RVE, de modo a discutir as evidências que sustentam o uso destas técnicas no tratamento do enfisema pulmonar avançado, bem como duas limitações.