نتایج جستجو برای: nsip

تعداد نتایج: 277  

2015
Hironao Hozumi Noriyuki Enomoto Masato Kono Tomoyuki Fujisawa Naoki Inui Yutaro Nakamura Hiromitsu Sumikawa Takeshi Johkoh Ran Nakashima Yoshitaka Imura Tsuneyo Mimori Takafumi Suda

BACKGROUND In polymyositis/dermatomyositis (PM/DM), anti-aminoacyl-tRNA synthetase (ARS) antibodies are closely associated with interstitial lung disease (ILD), a frequent pulmonary complication. However, the clinical significance of anti-ARS antibodies is not well established. OBJECTIVE We aimed to evaluate the clinical significance of anti-ARS antibodies in PM/DM-ILD patients. METHODS For...

Journal: :Annals of the Rheumatic Diseases 2023

Background Interstitial lung disease (ILD) is a critical manifestation of connective tissue diseases (CTDs) that may cause morbidity and mortality. Objectives This study aimed to evaluate the clinical demographic characteristics treatment patients who had CTD-related ILD. Methods retrospective observational includes followed up with ILD in tertiary rheumatology outpatient clinic between January...

Journal: :American journal of respiratory and critical care medicine 1998
J A Bjoraker J H Ryu M K Edwin J L Myers H D Tazelaar D R Schroeder K P Offord

Idiopathic pulmonary fibrosis (IPF) is a generally fatal disorder with a reported median survival of 3 to 6 yr. This has been based on relatively few studies with diagnoses inconsistently confirmed by adequate lung biopsy. Retrospective analysis of 104 patients with IPF who had open lung biopsy (OLB) at Mayo Medical Center from 1976 to 1985 was performed to establish the overall survival rate, ...

2014
Stefano Aliberti Grazia Messinesi Silvia Gamberini Sveva Maggiolini Dina Visca Vanni Galavotti Fabio Giuliani Roberto Cosentini Anna Maria Brambilla Francesco Blasi Raffaele Scala Mauro Carone Francesca Luisi Sergio Harari Antonio Voza Antonio Esquinas Alberto Pesci

BACKGROUND To evaluate noninvasive ventilation (NIV) in diffuse interstitial lung diseases (DILD) patients with acute respiratory failure (ARF) according to baseline radiological patterns and the etiology of ARF. METHODS In a multicenter, observational, retrospective study, consecutive DILD patients undergoing NIV because of an episode of ARF were evaluated in six Italian high dependency unit...

2017
Sven Jungmann Wolf-Dieter Ludwig Nicolas Schönfeld Torsten-Gerriet Blum Claudia Großwendt Christian Boch Beate Rehbock Sergej Griff Alexander Schmittel Torsten T Bauer

We present a 74-year-old male with nonspecific interstitial pneumonia (NSIP) during treatment with ibrutinib for mantle cell lymphoma. Previously, the patient had received six cycles of bendamustine and rituximab and six cycles of R-CHOP, followed by rituximab maintenance therapy. Respiratory tract complications of ibrutinib other than infectious pneumonia have not been mentioned in larger tria...

1992
Mattias Johannesson Anders Åström Per-Erik Danielsson

Range image acquisition can be made in many different ways. In this paper the range data are acquired by using a sheet-of-light to illuminate the scene 121, [31. Our image sensor design incorporates the concept of Near-Sensor Image Processing (NSIP) where the individual sensor operation is an integrated part of the signal processing algorithm [I]. This architecture can provide range images with...

Journal: :Thorax 2004
W E Lawson S W Grant V Ambrosini K E Womble E P Dawson K B Lane C Markin E Renzoni P Lympany A Q Thomas J Roldan T A Scott T S Blackwell J A Phillips J E Loyd R M du Bois

BACKGROUND While idiopathic pulmonary fibrosis (IPF) is one of the most common forms of interstitial lung disease, the aetiology of IPF is poorly understood. Familial cases of pulmonary fibrosis suggest a genetic basis for some forms of the disease. Recent reports have linked genetic mutations in surfactant protein C (SFTPC) with familial forms of pulmonary fibrosis, including one large family ...

2011
Katerina D. Samara George Margaritopoulos Athol U. Wells Nikolaos M. Siafakas Katerina M. Antoniou

The relationship between smoking and pulmonary fibrosis is under debate and intense investigation. The aim of this paper is to review the existing literature and identify further areas of research interest. Recently the negative influence of cigarette smoking on IPF outcome was highlighted, as non-smokers exhibit a better survival than ex-smokers and combined current- and ex-smokers. In patient...

Journal: :The European respiratory journal 2009
H Chen A Gomez A Shum H R Collard

In a recent article, PARK et al. [1] described the clinical course and changes in lung function of 83 patients classified as idiopathic nonspecific interstitial pneumonia (NSIP). PARK et al. [1] found that 81% of patients with fibrotic NSIP had improved or stable lung function over time after initial treatment. Specifically, the authors showed an increase in the percentage of patients with an i...

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