scholarly journals Idiopathic pulmonary fibrosis associated with pulmonary vein thrombosis: a case report

Cases Journal ◽  
2009 ◽  
Vol 2 (1) ◽  
Author(s):  
Raquel A Cavaco ◽  
Sunny Kaul ◽  
Timothy Chapman ◽  
Romina Casaretti ◽  
Barbara Philips ◽  
...  
2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Elodie Roels ◽  
Aline Fastrès ◽  
Anne-Christine Merveille ◽  
Géraldine Bolen ◽  
Erik Teske ◽  
...  

Abstract Background Pulmonary hypertension (PH) is a known co-morbidity in West Highland white terriers (WHWTs) affected with canine idiopathic pulmonary fibrosis (CIPF). The pulmonary vein-to-right pulmonary artery ratio (PV/PA) has recently been described for the detection of pre-capillary PH in dogs. The objective of the present study was to estimate the prevalence of PH at diagnostic, in WHWTs affected with CIPF, by using PV/PA, in comparison with a group of healthy breed-matched controls (CTRLs). Additional study objective was to explore whether the presence of PH at initial diagnosis of CIPF impacted survival time in dogs treated with sildenafil. Results Twenty-five client-owned WHWTs presented with CIPF and 19 CTRLs were included in the study. PV/PA in either two-dimensional mode (2D) or time-motion mode or both were measured from cineloops in each dog. Dogs were classified according to PV/PA value into non/mild PH (PV/PA measured in 2D ≥ 0.7) or moderate/severe PH (PV/PA < 0.7). Survival data of WHWTs affected with CIPF were extracted from medical record to assess association between presence of PH at diagnosis and outcome. 60 % overall prevalence for moderate/severe PH was estimated in this cohort of WHWTs presented with CIPF vs. 5 % in CTRLS (P = 0.0002). The presence of moderate/severe PH at initial presentation was not associated with survival. Conclusions Results of the present study confirm a high prevalence of PH at diagnosis in WHWTs affected with CIPF and highlight the utility of PV/PA as a non-invasive surrogate for assessment of PH in this population.


2015 ◽  
Vol 113 (05) ◽  
pp. 1151-1154 ◽  
Author(s):  
Fernando J. Vazquez ◽  
Pilar Paulin ◽  
Paz Rodriguez ◽  
Martin Lubertino ◽  
Esteban Gándara

CASE ◽  
2020 ◽  
Vol 4 (1) ◽  
pp. 39-42
Author(s):  
Mohammadbagher Sharifkazemi ◽  
Gholamreza Rezaian ◽  
Mohammadhassan Nemati ◽  
Morteza Chehrevar

2021 ◽  
Vol 8 ◽  
Author(s):  
Hisako Kushima ◽  
Hiroshi Ishii ◽  
Masaki Fujita

Ninjin'yoeito, a Kampo prescription, was administered to two patients with idiopathic pulmonary fibrosis (IPF) over a period of 12 weeks to improve loss of appetite and lassitude. In Case 1, improvements were observed in appetite, lassitude, and breathlessness, as well as increases or increasing tendencies in body weight, blood albumin level, and hemoglobin (Hb) level. Case 2 showed no changes in appetite but improvements in lassitude and no deterioration of breathlessness. His body weight and his blood albumin and Hb levels increased or showed increasing trends. In both cases, a trend for improvement of respiratory function was observed. In summary, ninjin'yoeito trended to improve the subjective symptoms and nutritional status of a patient with pulmonary fibrosis.


2020 ◽  
Vol 11 (6) ◽  
pp. 1720-1723
Author(s):  
Toshihiro Shiratori ◽  
Hisashi Tanaka ◽  
Chiori Tabe ◽  
Junichiro Tsuchiya ◽  
Yoshiko Ishioka ◽  
...  

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