Criteria
Shionoya clinical criteria of diagnosis[31]
All 5 criteria must be met:
Smoking history
Onset before the age of 50 years
Infrapopliteal arterial occlusive lesions
Upper limb involvement of phlebitis migrans (also known as thrombophlebitis migrans)
Absence of atherosclerotic risk factors aside from smoking.
These criteria were described in 1998 to make the diagnosis of Buerger's disease.[31] However, patients >50 years of age have been given the diagnosis. Probable Buerger's disease is considered when all but the fourth criterion are met.
Point scoring system of diagnosis (Papa criteria)[32]
Positive points:
Age at onset: less than 30 years (+2) / 30-40 years (+1)
Foot intermittent claudication: present (+2) / by history (+1)
Upper extremity: symptomatic (+) / asymptomatic (+1)
Migrating superficial vein thrombosis: present (+2) / by history only (+1)
Raynaud colour changes: present (+2) / by history only (+1)
Angiography; Biopsy: if typical, both (+2) / either (+1)
Negative points:
Age at onset: 45-50 years (-1) / >50 years (-2)
Sex, smoking: female (-1) / non-smoker (-2)
Location: single limb (-1) / no lower extremity involved (-2)
Absent pulses: brachial (-1) / femoral (-2)
Arteriosclerosis, diabetes mellitus, hypertension, hypercholesterolaemia: discovered after diagnosis 5.1-10 years (-1) / 2.1-5 years (-2)
Total of points defines the probability of the diagnosis:
0-1 points: Diagnosis excluded
2-3 points: Suspected, low probability
4-5 points: Probable, medium probability
≥6 points: Definite, high probability
International Consensus of VAS[33]
The three main features for definitive diagnosis:
History of smoking
Typical angiographic features (normal proximal arterial structure, absence of atherosclerotic plaque, lack of microaneurysm, infra-popliteal arterial occlusion, corkscrew collaterals, and skip lesion)
Typical histopathological features (particularly, intact internal elastic lamina, Infiltration of polymorphonuclear inflammatory cells in all small and medium-sized vessels’ wall layers)
Suspected Buerger’s disease if one major feature listed above plus four or more of the following minor criteria are present:
Disease onset before the age of 45 years
Ischaemic involvement of lower limbs (absent DP or PT, ABPI <0.9 or TBI <0.75)
Ischaemic involvement of one or both upper limbs (positive Allen’s test, absence of radial artery pulse, or Raynaud’s phenomenon)
Thrombophlebitis migrans
Red-blue shade of purple discolouration on oedematous toes or fingers
Olin criteria[34]
Age under 45 years
Current or recent history of tobacco use
Presence of distal-extremity ischaemia indicated by claudication, pain at rest, ischaemic ulcers or gangrenes and documented by non-invasive vascular testing
Exclusion of autoimmune diseases, hypercoagulable states and diabetes mellitus
Exclusion of a proximal source of emboli by echocardiography or arteriography
Consistent arteriographic findings in the clinically involved and non-involved limbs
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