Book ReviewThe Clinical Physics and Physiology of Chronic Lung Disease, Inhalation Therapy and Pulmonary Function Testing.

1974 ◽  
Vol 290 (2) ◽  
pp. 115-115
Author(s):  
Jere Mead
1983 ◽  
Vol 102 (4) ◽  
pp. 613-617 ◽  
Author(s):  
Steven L. Goldman ◽  
Tilo Gerhardt ◽  
Rajeswari Sonni ◽  
Rosalyn Feller ◽  
Dorothy Hehre ◽  
...  

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Lucy Parker ◽  
Fotini Soliotis

Abstract Introduction Head drop is an unusual clinical manifestation of myositis or neuromuscular weakness, and typically requires extensive investigation to identify the underlying pathology. Case report data are limited on this topic. Case description A 72-year-old man with a background of extractable nuclear antigen (ENA) negative mixed connective tissue disease, trigeminal neuralgia, interstitial nephritis and ischaemic heart disease presented with an isolated head drop. On further prompting, he confirmed mild shortness of breath on exertion. He had sclerodactyly but no features of mechanic’s hands. Serum creatinine kinase was 1398 IU/L. Electromyography was myelopathic. Muscle biopsy taken from the neck was inconclusive. He had a strongly positive anti-nuclear antibody (ANA) test, and borderline myositis ENA panel result with borderline positive anti-EJ antibody. The myositis panel result prompted further investigation for underlying interstitial lung disease. Pulmonary function testing revealed a restrictive picture, with KCO of 82%. High resolution computed tomography showed areas of fine interstitial fibrotic change in all lobes. He was treated with a reducing course of oral prednisolone and 15mg weekly oral methotrexate with an excellent clinical response, with resolution of the head drop and normalisation of serum CK value. Repeat pulmonary function testing remains stable after 5 months. Discussion This is an unusual presentation of presumed anti-synthetase syndrome. As methotrexate had already been prescribed before the underlying lung pathology was identified with resulting excellent clinical response and stable respiratory symptoms, a multi-disciplinary decision was made to continue with this choice of disease modifying agent. The decision to use methotrexate in the presence of interstitial fibrosis is always difficult, and requires close liaison between rheumatology and respiratory colleagues. Key learning points Positive anti-synthetase antibodies should prompt further investigation for underlying interstitial lung disease. Head drop can be a first symptom of autoimmune myositis and warrants further investigation. Conflicts of interest The authors have declared no conflicts of interest.


Rheumatology ◽  
2014 ◽  
Vol 53 (suppl_1) ◽  
pp. i104-i104
Author(s):  
Riwa Meshaka ◽  
Emma Helm ◽  
Alec Price-Forbes ◽  
Shirish Dubey ◽  
Felix Woodhead

2021 ◽  
Vol 96 (3) ◽  
pp. 209-217
Author(s):  
Sung Yoon Lim ◽  
Ho Il Yoon

Spirometry, also called office-based pulmonary function testing, is a useful tool for diagnosis and classification of lung disease. Here, we outline a simple stepwise approach for interpretation of spirometry results. The first step is to determine the forced expiratory volume in a one second/forced vital capacity (FEV1/FVC) ratio. If airflow is limited, a bronchodilator is administered followed by reassessment. The next step is to determine whether FVC is low; an observed decrease in FVC indicates a restrictive patten. For patients with obstructive disease, inhalation medication is needed. Therefore, this review also describes the most appropriate inhalation device for each patient and the correct use of the device to maximize inhalation therapy benefits.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Charlene S. Stahr ◽  
Chaminda R. Samarage ◽  
Martin Donnelley ◽  
Nigel Farrow ◽  
Kaye S. Morgan ◽  
...  

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