Survival rates in TAK according to specific disease features
Study identification | N | Studied groups (follow-up duration) | Survival rates | P value | RoB QUIPS tool |
Ishikawa and Maetani18 | 120 | According to prognostic score classification. Stage 1 vs 2 vs 3. (median 13 years and 2 months) | 100% vs 83.6% vs 43% | <0.001 | Moderate |
Ishikawa15 | 81 | I+IIa vs IIb+III†. At 5 years and 10 years. (mean 7.4±5.8 years) | 100% vs 74.2% | <0.005 | Moderate |
Soto et al 22 | 94 | Patients with coronary disease developing between 10 and 19 years vs between 20 and 39 years at 2, 5 and 10 years. | 50% at each time point vs 88% at each time point | – | High |
Patients with hypertension developing between 10 and 19 years vs between 20 and 39 years at 2, 5 and 10 years. (mean 75±83 months) | 65% vs 87% 57% vs 87% 48% vs 87% | – |
*Stages defined according to the presence or absence of three predictors, major complications, progressive disease course or low ESR (<20 mm/hour): stage 1 (0 predictor or only progressive disease or only low ESR), stage 2 (only major complication or progressive disease course and low ESR or major complication and low ESR) and stage 3 (major complication and progressive course or the 3 predictors).
†(I) with or without involvement of the pulmonary artery, but all patients had narrowing or occlusion in some region of the aorta or its main branches, or both; (II) one of the following: Takayasu’s retinopathy, secondary hypertension, aortic regurgitation, or aortic or arterial aneurysm; if mild or moderate complications (IIa), if severe complications (IIb); (III) two or more of the four complications mentioned above.
ESR, erythrocyte sedimentation rate; QUIPS, Quality in Prognosis Studies tool; RoB, risk of bias; TAK, Takayasu arteritis.