143 research outputs found
The Risk of Stroke after Percutaneous Vertebroplasty for Osteoporosis: A Population-Based Cohort Study
PURPOSE: To investigate the incidence and risk of stroke after percutaneous vertebroplasty in patients with osteoporosis. METHODS: A group of 334 patients with osteoporosis, and who underwent percutaneous vertebroplasty during the study period, was compared to 1,655 age-, sex- and propensity score-matched patients who did not undergo vertebroplasty. All demographic covariates and co-morbidities were deliberately matched between the two groups to avoid selection bias. Every subject was followed-up for up to five years for stroke. Adjustments using a Cox regression model and Kaplan-Meier analyses were conducted. RESULTS: A total of 1,989 osteoporotic patients were followed up for 3,760.13 person-years. Overall, the incidence rates of any stroke, hemorrhagic stroke and ischemic stroke were 22.6, 4.2 and 19.6 per 1,000 person-years, respectively. Patients who underwent vertebroplasty were not more likely to have any stroke (crude hazard ratio = 1.13, p = 0.693), hemorrhagic stroke (HR = 2.21, p = 0.170), or ischemic stroke (HR = 0.96, p = 0.90). After adjusting for demographics, co-morbidities and medications, the vertebroplasty group had no significant difference with the comparison group in terms of any, hemorrhagic and ischemic strokes (adjusted HR = 1.22, 3.17, and 0.96, p = 0.518, 0.055, and 0.91, respectively). CONCLUSIONS: Osteoporotic patients who undergo percutaneous vertebroplasty are not at higher risk of any stroke in the next five years after the procedure
The allogeneic effect. M-locus differences substitute for differences in the h-2 major histocompatibility complex.
Secondary in vitro cytotoxic allograft responses. No requirement for the mlc gene product.
Induction of Secondary Cytotoxic T-Lymphocytes in Vitro Does Not Require Cell Proliferation
Induction of secondary cytotoxic t-lymphocytes in vitro does not require cell proliferation.
Specificity of In Vivo Tumor Rejection Assessed by Mixing Immune Spleen Cells with Target and Unrelated Tumor Cells
T-t-cell interactions during in vitro cytotoxic allograft responses. I. Soluble products from activated ly1+ t cells trigger autonomously antigen-primed ly23+ t cells to cell proliferation and cytolytic activity.
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