Kimi L. Kondo
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Kimi L. Kondo has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
Charles Ray
1 shared publicationCharles Wiltrout
1 shared publicationGiustino Albanese
Department of Radiology, University of Colorado Denver School of Medicine, Aurora, Colorado
1 shared publicationJason Oppenheimer
1 shared publicationMathew Swerdlow
1 shared publication
Latest Publications
- 1 March 2013
- Published by Elsevier in Academic Radiology
- Vol. 20 (3) , 263-271
Medical Student Radiology Curriculum
- 1 March 2013
- Published by Elsevier in Academic Radiology
- Vol. 20 (3) , 263-271
Medical Student Radiology Curriculum
- 19 November 2010
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 27 (04) , 338-347
Correction of Coagulopathy for Percutaneous Interventions
Due to medical illness or pharmacotherapy, patients undergoing percutaneous interventions often have abnormal hemostasis. Its etiology may include alterations in the protein-based coagulation system, thrombocytopenia, deficient platelet function, or mixed deficits such as disseminated intravascular coagulation. In this article, the authors review the basic science of each of these etiologies, as well as their available methods of correction. They also review the evidence and guidelines regarding the assessment and treatment of coagulopathy in image-guided procedures. The periprocedural bleeding risk and the urgency of a given procedure guide the management of abnormal hemostasis in this patient population.
- 19 November 2010
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 27 (04) , 338-347
Correction of Coagulopathy for Percutaneous Interventions
Due to medical illness or pharmacotherapy, patients undergoing percutaneous interventions often have abnormal hemostasis. Its etiology may include alterations in the protein-based coagulation system, thrombocytopenia, deficient platelet function, or mixed deficits such as disseminated intravascular coagulation. In this article, the authors review the basic science of each of these etiologies, as well as their available methods of correction. They also review the evidence and guidelines regarding the assessment and treatment of coagulopathy in image-guided procedures. The periprocedural bleeding risk and the urgency of a given procedure guide the management of abnormal hemostasis in this patient population.
- 19 November 2010
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 27 (04) , 422-430
Miscellaneous Pharmaceutical Agents in Interventional Radiology
Interventional radiologists employ a wide variety of drugs on a daily basis to improve patient experiences and outcomes during interventional procedures. The expectation is for the interventionalist to be well-versed in all pharmaceuticals used in the interventional suite. In this article, the authors review the following classes of common miscellaneous pharmaceutical agents used in interventional radiology: vasodilators, vasoconstrictors, antiemetics, bowel antiperistalsis agents, and prothrombotics.
- 19 November 2010
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 27 (04) , 422-430
Miscellaneous Pharmaceutical Agents in Interventional Radiology
Interventional radiologists employ a wide variety of drugs on a daily basis to improve patient experiences and outcomes during interventional procedures. The expectation is for the interventionalist to be well-versed in all pharmaceuticals used in the interventional suite. In this article, the authors review the following classes of common miscellaneous pharmaceutical agents used in interventional radiology: vasodilators, vasoconstrictors, antiemetics, bowel antiperistalsis agents, and prothrombotics.
- 19 November 2010
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 27 (04) , 391-399
Pharmacology of Sclerotherapy
Sclerotherapy is the therapeutic use of sclerosants in the controlled destruction of undesired target tissues. Sclerosants have been used in vascular and nonvascular settings, both as primary and adjunctive therapy. Effective sclerotherapy requires a conceptual understanding of key questions about the process being treated, including the method of delivery, the presence of flow, and the required contact time to initiate sclerosis. However, beyond technique and delivery, practical and safe application of sclerotherapy requires an understanding of the uses, limitations, dosing, and side effects of sclerosants used during interventional radiology procedures. Agents discussed here include detergents and surfactants [ethanol, Sotradecol® (Bioniche Pharma, Pointe Claire, Quebec and Angiodynamics, Latham, NY), ethanolamine oleate], hypertonics (saline, glucose), and a review of several other types that are used less frequently.
- 19 November 2010
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 27 (04) , 391-399
Pharmacology of Sclerotherapy
Sclerotherapy is the therapeutic use of sclerosants in the controlled destruction of undesired target tissues. Sclerosants have been used in vascular and nonvascular settings, both as primary and adjunctive therapy. Effective sclerotherapy requires a conceptual understanding of key questions about the process being treated, including the method of delivery, the presence of flow, and the required contact time to initiate sclerosis. However, beyond technique and delivery, practical and safe application of sclerotherapy requires an understanding of the uses, limitations, dosing, and side effects of sclerosants used during interventional radiology procedures. Agents discussed here include detergents and surfactants [ethanol, Sotradecol® (Bioniche Pharma, Pointe Claire, Quebec and Angiodynamics, Latham, NY), ethanolamine oleate], hypertonics (saline, glucose), and a review of several other types that are used less frequently.
- 15 December 2008
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 25 (04) , 413-424
Osteoporotic Vertebral Compression Fractures and Vertebral Augmentation
Vertebral fractures account for ~27% of all osteoporotic fractures in both men and women. The economic burden is substantial and growing: osteoporosis is expected to affect 14 million people by the year 2020. There is substantial morbidity associated with osteoporotic vertebral compression fractures (VCFs) including decreased quality of life, reduced pulmonary function, and increased mortality. Relatively recent additions to the treatment armamentarium include vertebral augmentation using vertebroplasty and kyphoplasty. Numerous retrospective and case studies demonstrate short-term efficacy and low complication rates of vertebroplasty and kyphoplasty in the treatment of osteoporotic VCFs, but controlled trials are needed for validation. The pathophysiology, risk factors, consequences, characteristics, and imaging of osteoporotic VCFs are presented in detail along with a discussion of treatment options and patient selection. Vertebral augmentation is comprehensively reviewed, including the technical aspects of the procedures, contraindications, complications, and clinical outcomes.
- 15 December 2008
- Published by Georg Thieme Verlag KG in Seminars in Interventional Radiology
- Vol. 25 (04) , 413-424
Osteoporotic Vertebral Compression Fractures and Vertebral Augmentation
Vertebral fractures account for ~27% of all osteoporotic fractures in both men and women. The economic burden is substantial and growing: osteoporosis is expected to affect 14 million people by the year 2020. There is substantial morbidity associated with osteoporotic vertebral compression fractures (VCFs) including decreased quality of life, reduced pulmonary function, and increased mortality. Relatively recent additions to the treatment armamentarium include vertebral augmentation using vertebroplasty and kyphoplasty. Numerous retrospective and case studies demonstrate short-term efficacy and low complication rates of vertebroplasty and kyphoplasty in the treatment of osteoporotic VCFs, but controlled trials are needed for validation. The pathophysiology, risk factors, consequences, characteristics, and imaging of osteoporotic VCFs are presented in detail along with a discussion of treatment options and patient selection. Vertebral augmentation is comprehensively reviewed, including the technical aspects of the procedures, contraindications, complications, and clinical outcomes.