Vascular Medicine
Showing 21 of 21 topics
A
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Primary acrocyanosis is benign distal cyanosis; Achenbach syndrome causes sudden painful finger bruising. Rule out serious mimics (Raynaud, emboli, vasculitis) and reassure.
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Recognize the six Ps, start systemic anticoagulation promptly, classify severity, and obtain urgent vascular consultation for revascularization.
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Identify the agent and timing, control bleeding source, reverse anticoagulation with targeted antidotes or prothrombin complex concentrate, and restart thoughtfully after hemostasis.
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Choose antithrombotic therapy by PAD phenotype and bleeding risk: single antiplatelet for most; consider dual pathway inhibition (rivaroxaban 2.5 mg BID + aspirin) in symptomatic PAD and post‑revascularization.
B
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Thromboangiitis obliterans (Buerger disease) is a non‑atherosclerotic, segmental vasculitis in young tobacco users causing distal ischemia. Absolute tobacco cessation is the only disease‑modifying therapy.
C
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Look for livedo reticularis/blue toe, eosinophilia, AKI after vascular procedures. Management is supportive: stop anticoagulation if suspected procedure‑related plaque disruption, control BP, statins, and renal support.
D
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Stable patients without high risk features can start outpatient anticoagulation; choose a direct oral anticoagulant for most and consider low molecular weight heparin in active cancer or pregnancy.
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Use pretest probability and D dimer to guide imaging; compression ultrasound is first line and repeat imaging is needed in selected high risk patients with negative initial study.
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Deep vein thrombosis is diagnosed by integrating clinical probability, D-dimer when appropriate, and compression ultrasonography. Proximal DVT generally requires anticoagulation unless bleeding risk is prohibitive. Distal calf DVT can be anticoagulated or followed with serial imaging in carefully selected lower-risk patients. Treatment choice depends on renal function, pregnancy, cancer, drug interactions, bleeding risk, and the likelihood that the patient can adhere safely to outpatient therapy.
E
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After initial 3–6 months, extend anticoagulation in unprovoked VTE or persistent risk factors if bleeding risk is acceptable; use reduced‑dose DOACs for long‑term prevention.
H
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Heparin-induced thrombocytopenia is an immune prothrombotic disorder caused by antibodies to PF4-heparin complexes, typically producing a platelet fall beginning 5 to 10 days after heparin exposure and a high risk of new venous or arterial thrombosis. Use the 4Ts score to estimate pretest probability. With intermediate or high probability, stop all heparin and begin an appropriate non-heparin anticoagulant while laboratory testing proceeds; do not start warfarin until platelet recovery.
I
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Reserve IVC filters for acute VTE with absolute contraindication to anticoagulation or recurrent VTE despite adequate anticoagulation. Plan retrieval early to reduce complications.
L
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Inflammatory panniculitis from chronic venous insufficiency. Treat with compression, ambulation, weight management, and address reflux; topical steroids for acute phase; pentoxifylline as adjunct.
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Differentiate lymphedema (non‑pitting, Stemmer sign) from venous edema (pitting, worse at day’s end). Treatments differ: CDT for lymphedema vs compression/elevation for venous disease.
P
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Lower-extremity peripheral artery disease is systemic atherosclerotic disease with high risk of myocardial infarction, stroke, limb ischemia, and amputation. Core therapy includes high-intensity statin treatment, antiplatelet therapy for symptomatic disease, aggressive blood-pressure and diabetes management, smoking cessation, structured exercise, and preventive foot care. Low-dose rivaroxaban 2.5 mg twice daily plus low-dose aspirin reduces cardiovascular and limb events in selected patients without high b
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Chronic symptoms after DVT (pain, swelling, heaviness, ulcers). Prevent with appropriate anticoagulation and early mobilization; manage with compression, exercise, and ulcer care.
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Use validated tools with clinical judgment to identify low risk patients for outpatient care and high risk features for admission and escalation.
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Intermediate-risk pulmonary embolism describes a normotensive patient with evidence of right-ventricular strain, myocardial injury, or other features associated with early deterioration. Anticoagulation is the foundation. Routine systemic thrombolysis is not recommended for a stable intermediate-risk patient because major bleeding and intracranial hemorrhage offset benefit, but rapid escalation to systemic thrombolysis, catheter-based therapy, surgery, or mechanical support is appropriate when hemodynamic d
S
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Superficial venous thrombosis is not always benign. Duplex ultrasound should define clot length, proximity to the deep venous junctions, and concomitant DVT. Anticoagulation is recommended for many lower-extremity SVTs that are extensive, close to the saphenofemoral or saphenopopliteal junction, or associated with high-risk features. Fondaparinux 2.5 mg daily for 45 days is a well-established regimen for eligible higher-risk SVT away from the deep junction; clot within roughly 3 cm of a deep junction is com
U
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Upper-extremity DVT commonly involves the axillary or subclavian veins and may be catheter-associated, cancer-associated, or effort-related. Duplex ultrasound is first-line diagnosis. Proximal UEDVT is treated with therapeutic anticoagulation, usually for at least 3 months. A functioning needed central catheter can often remain in place during anticoagulation; remove it when infected, malfunctioning, no longer needed, or when anticoagulation cannot be given safely.
V
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Use compression US for DVT; V/Q or CTPA for suspected PE with pregnancy‑adapted protocols. Treat with LMWH throughout pregnancy and 6 weeks postpartum; avoid warfarin and most DOACs.
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