scholarly journals Response to: A Rebuttal of the Holistic 8-Point Protocol to Eliminate Deep Venous Thromboses After Abdominoplasty

Author(s):  
Marcos Sforza ◽  
Rodwan Husein ◽  
Reyan Saghir ◽  
Norman Saghir ◽  
Renee Okhiria ◽  
...  
Keyword(s):  
2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Gina Elhammady ◽  
Andrew T. Schubeck ◽  
Vicky El-Najjar ◽  
Morton J. Robinson

Periprostatic or paravaginal venous thromboses are rarely considered clinically as sites of clot origin in patients with pulmonary thromboembolism. The majority of emboli have been demonstrated to originate in the veins of the legs. This report raises awareness of pelvic vein thrombosis as a potential source of pulmonary embolism that is rarely considered or detected clinically, and which usually requires postmortem examination for recognition. It also reviews the possible routes emboli may take to reach the lungs.


2021 ◽  
pp. 026835552097728
Author(s):  
Kirtan D Patel ◽  
Alison YY Tang ◽  
Ashik DJ Zala ◽  
Rakesh Patel ◽  
Kishan R Parmar ◽  
...  

Objectives Post thrombotic syndrome (PTS) is a serious complication of deep venous thromboses (DVTs). PTS occurs more frequently and severely following iliofemoral DVT compared to distal DVTs. Catheter directed thrombolysis (CDT) of iliofemoral DVTs may reduce PTS incidence and severity. We aimed to determine the rate of iliofemoral DVT within our institution, their subsequent management, and compliance with NICE guidelines. Methods Retrospective review of all DVTs diagnosed over a 3-year period was conducted. Cases of iliofemoral DVT were identified using ICD-10 codes from patient notes, and radiology reports of Duplex scans. Further details were retrieved, such as patient demographics and referrals to vascular services. NICE guidance was applied to determine if patients would have been suitable for CDT. A survey was sent to clinicians within medicine to identify awareness of CDT and local guidelines for iliofemoral DVT management. Results 225 patients with lower limb DVTs were identified. Of these, 96 were radiographically confirmed as iliofemoral DVTs. The median age was 77. 67.7% of iliofemoral DVTs affected the left leg. Right leg DVTs made up 30.2% and 2.1% were bilateral DVTs. Of the 96 iliofemoral DVTs, 21 were deemed eligible for CDT. Only 3 patients (14.3%) were referred to vascular services, and 3 received thrombolysis. From our survey, 95.5% of respondents suggested anticoagulation alone as management for iliofemoral DVT. Only one respondent recommended referral to vascular services. There was a knowledge deficiency regarding venous anatomy, including superficial versus deep veins. Conclusions CDT and other mechanochemical procedures have been shown to improve outcomes of patients post-iliofemoral DVT, however a lack of awareness regarding CDT as a management option results in under-referral to vascular services. We suggest closer relations between vascular services and their “tributary” DVT clinics, development of guidelines and robust care pathways in the management of iliofemoral DVT.


2014 ◽  
Vol 32 (2) ◽  
pp. 126-128
Author(s):  
Nurdan Dinlen Fettah ◽  
Dilek Dilli ◽  
Berna Uçan ◽  
Murat Koç ◽  
Elif Özyazıcı ◽  
...  

2003 ◽  
Vol 29 (5) ◽  
pp. S210 ◽  
Author(s):  
Y. Kono ◽  
K. Alton ◽  
S.C. Rose ◽  
T.I. Hassanein ◽  
S. Choi ◽  
...  

Angiology ◽  
2009 ◽  
Vol 61 (1) ◽  
pp. 78-81 ◽  
Author(s):  
Alfried Germing ◽  
Mahmud Schakrouf ◽  
Michael Lindstaedt ◽  
Peter Grewe ◽  
Renate Meindl ◽  
...  

2016 ◽  
Vol 27 (3) ◽  
pp. 605-608 ◽  
Author(s):  
Marianna Fabi ◽  
Francesca Lami ◽  
Maurizio Zompatori

AbstractA 12-year-old boy with a right atrium endocardial mass was initially diagnosed as having Lemierre’s syndrome on the basis of previous mastoiditis and jugular vein and cerebral venous thrombosis. Lack of response to antibiotics, persistent high fever with chills, acute-phase reactants, and peripheral arterial pseudoaneurysms made us reconsider the diagnosis. Only after the late appearance of radiological pulmonary lesions and recognition of pulmonary artery aneurysms, Hughes–Stovin syndrome was diagnosed. Hughes–Stovin syndrome is an exceedingly rare vasculitis, especially in childhood, consisting of multiple pulmonary artery aneurysms and deep venous thromboses. The lack of formal diagnostic criteria and the rarity of the disease make the diagnosis very challenging, especially when respiratory complaints are not present at onset, as in the presented case. The treatment aims to reduce inflammation, although there is debate about anticoagulation therapy because of the risk of pulmonary haemorrhage.


2018 ◽  
Vol 53 ◽  
pp. 25
Author(s):  
Tom Le Corvec ◽  
Olivier Espitia ◽  
Philippe Chaillou ◽  
Jérôme Connault ◽  
Marc Antoine Pistorius ◽  
...  

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