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1.
J Cardiovasc Pharmacol Ther ; 13(1): 13-31, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18287587

ABSTRACT

A large number of heart transplants are performed annually in different transplant centers in the United States. This is partly because of the improved survival of patients who undergo cardiac transplantation, thus making it a more viable option in the management of end-stage heart failure. The survival benefit after heart transplantation is a result of newer immunosuppressive drug regimens and a better understanding of their effects and interactions. Several studies, mostly involving a small number of patients, describe use and comparison of the many distinct immunosuppressive drugs available to date. Interestingly, many transplant centers perform in-house typical induction treatment regimens because of their own experience and intra-institutional preference. This review summarizes current practices of immunosuppressive drug therapy in the first year post-heart transplant based on the available clinical evidence and discusses future options of heart transplant immunosuppressive drug therapies.


Subject(s)
Graft Rejection/prevention & control , Heart Transplantation/immunology , Immunosuppressive Agents/therapeutic use , Comorbidity , Drug Monitoring , Graft Rejection/classification , Graft Rejection/diagnosis , Hospitals, Special/methods , Humans , Immunosuppressive Agents/pharmacology , Survival Analysis , Time Factors , United States
2.
J Gravit Physiol ; 14(1): P9-13, 2007 Jul.
Article in English | MEDLINE | ID: mdl-18372685

ABSTRACT

The NASA artificial gravity-bed rest pilot study (AGPS) was designed to investigate the efficacy of daily exposure to a +Gz acceleration gradient for counteracting the physiologic decrements induced by prolonged bed rest. Test subjects were continuously monitored by a physician for signs and symptoms of pre-syncope, motion sickness, and arrhythmias while on the centrifuge. In this article, we have summarized the medical monitoring observations that were made during the AGPS and included an assessment of the relative usefulness of the information provided by the various monitoring tools in making a decision to terminate a centrifuge spin.


Subject(s)
Bed Rest/adverse effects , Centrifugation , Gravity, Altered , Monitoring, Physiologic , Weightlessness Countermeasures , Adult , Arrhythmias, Cardiac/etiology , Centrifugation/adverse effects , Equipment Design , Equipment Failure Analysis , Gravity, Altered/adverse effects , Head-Down Tilt , Humans , Male , Monitoring, Physiologic/instrumentation , Motion Sickness/etiology , Patient Selection , Pilot Projects , Reproducibility of Results , Space Flight , Syncope/etiology , Time Factors , United States , United States National Aeronautics and Space Administration , Weightlessness Simulation
3.
Aviat Space Environ Med ; 77(5): 475-84, 2006 May.
Article in English | MEDLINE | ID: mdl-16708526

ABSTRACT

BACKGROUND: Candidates for commercial spaceflight may be older than the typical astronaut and more likely to have medical problems that place them at risk during flight. Since the effects of microgravity on many medical conditions are unknown, physicians have little guidance when evaluating and certifying commercial spaceflight participants. This dynamic new era in space exploration may provide important data for evaluating medical conditions, creating appropriate medical standards, and optimizing treatment alternatives for long-duration spaceflight. CASE: A 57-yr-old spaceflight participant for an ISS mission presented with medical conditions that included moderately severe bullous emphysema, previous spontaneous pneumothorax with talc pleurodesis, a lung parenchymal mass, and ventricular and atrial ectopy. The medical evaluation required for certification was extensive and included medical studies and monitoring conducted in analogue spaceflight environments including altitude chambers, high altitude mixed-gas simulation, zero-G aircraft, and high-G centrifuge. To prevent recurrence of pneumothorax, we performed video-assisted thoracoscopic pleurodesis, and to assess lung masses, several percutaneous or direct biopsies. The candidate's 10-d mission was without incident. CONCLUSION: Non-career astronauts applying for commercial suborbital and orbital spaceflight will, at least in the near future, challenge aerospace physicians with unknowns regarding safety during training and flight, and highlight important ethical and risk-assessment problems. The information obtained from this new group of space travelers will provide important data for the evaluation and in-flight treatment of medical problems that space programs have not yet addressed systematically, and may improve the medical preparedness of exploration-class missions.


Subject(s)
Aerospace Medicine/standards , Physical Examination , Space Flight/standards , Cysts/diagnosis , Exercise Test , Humans , Kidney Diseases/diagnosis , Lung Diseases, Interstitial/diagnosis , Male , Middle Aged , Monitoring, Ambulatory , Pleurodesis , Pneumothorax/diagnosis , Pneumothorax/therapy , Pulmonary Atelectasis/diagnosis , Pulmonary Disease, Chronic Obstructive/diagnosis , Pulmonary Emphysema/diagnosis , Respiratory Function Tests , Thoracic Surgery, Video-Assisted , Ventricular Premature Complexes/diagnosis
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