Upper extremity deep venous thrombosis prevalence in the NHS Grampian Medical Ambulatory clinic: diagnostic, therapeutic, and prognostic considerations in oncology patients

被引:4
作者
Kastora, Stavroula Lila [1 ]
Oduyoye, Olusegun [1 ,2 ]
Mahmood, Shafaq [2 ]
机构
[1] Univ Aberdeen, Med Sci & Nutr, Sch Med, Aberdeen, Scotland
[2] Aberdeen Royal Infirm, Emergency Care Ctr, Foresterhill Campus, Aberdeen AB25 2ZN, Scotland
关键词
Bioinformatics; Oncology; Prevalence; Survival analysis; Upper extremity deep venous thrombosis; VEIN THROMBOSIS; RISK-FACTORS; ULTRASONOGRAPHY; CANCER;
D O I
10.1007/s11845-021-02775-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Whilst upper extremity deep vein thromboses (UEDVT) account for approximately 5 to 10% of all cases of DVT, rigorous guidelines regarding diagnosis and management of presenting patients remain to be developed. The association of UEDVT with concurrent asymptomatic pulmonary embolism as well as the first presentation of malignancy deems essential rigorous research and clinical guideline development to ensure optimal patient care. Methods This retrospective audit study is the first to provide estimates of UEDVT prevalence in the North-East Deanery main hospital centre, Aberdeen Royal Infirmary (ARI). Results Of the 605 patients attending the ARI Ambulatory Emergency Care (AEC) clinic with clinical suspicion of UEDVT, 38 (6.2%) had a confirmatory diagnosis. Underlying malignancy, presence of PICC line, and cardiovascular co-morbidities were identified as common confounding factors. Subclavian vein with concurrent extension to primarily the cephalic vein thrombosis was identified as the most commonly thrombosed venous territories. Importantly, oncology patients were found to have poorer survival outcomes following an UEDVT, in comparison to patients with other significant co-morbidities (cardiovascular, chronic renal disease, inflammatory bowel disease): HR 5.814 (95%CI 1.15, 29.25), p 0.012. Lastly, genetic associations were drawn between patient genetic status as tested for other co-morbidities and prothrombotic cellular cascades, suggesting rigorous VTE assessment in patients identified with congenital or acquired mutations, namely, in CALR, JAK, MSH 2/6, MYC, and FXN. Conclusions Overall, this study offers the first report of UEDVT presentations in the UK with no restrictions of patient performance status or underlying co-morbidities and provides a rounded clinical picture of patient characteristics, diagnosis, management, and prognostic associations in view of rigorous guideline development.
引用
收藏
页码:1569 / 1575
页数:7
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