Anaesthetic Management of Women With Heart Disease For Labor and Delivery
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|ClinicalTrials.gov Identifier: NCT00403871|
Recruitment Status : Completed
First Posted : November 27, 2006
Last Update Posted : March 2, 2007
|Condition or disease|
|Heart Diseases Pregnancy|
Heart disease among pregnant women is increasing in incidence. The cardiovascular changes associated with pregnancy may be particularly hazardous for both mother and fetus in a subset of these patients. The period of greatest risk is peripartum while these patients are under the care of the obstetrician and anesthesiologist. Exposing a compromised patient to general anesthesia is further complicated by the cardiovascular stress response to intubation and surgery, the cardiorespiratory implications of mechanical ventilation, the cardiac depression and vasodilation from general anesthetics, residual post-operative respiratory depression from general anesthetics and narcotics and the stress of weaning from mechanical ventilation and post-operative pain.
In the Adult Congenital Heart Program, obstetric patients are followed the by a specialized team of cardiologists, obstetricians and anesthesiologists who also follow all pregnant women referred with acquired cardiac disease. From this referral practice approximately 100 patients per year are now followed during their pregnancy and delivery. In conjunction with the ongoing system we intend to identify all parturients who delivered at the University Health Network (Toronto General Hospital) or Mount Sinai Hospital between the years 1986 and 2001. We will evaluate the anesthetic management of all women with heart disease whose pregnancies were followed at the University Health Network and/or Mount Sinai Hospital between 1986 and 2001.
|Study Type :||Observational|
|Estimated Enrollment :||700 participants|
|Observational Model:||Defined Population|
|Official Title:||Anaesthetic Management of Women With Heart Disease For Labor and Delivery|
|Study Start Date :||November 2002|
|Estimated Study Completion Date :||June 2005|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00403871
|Mount Sinai Hospital|
|Toronto, Ontario, Canada, M5G 1X5|
|Univeristy Health Network|
|Toronto, Ontario, Canada, M5G 1Z5|
|Principal Investigator:||Eric Goldszmidt, MD||Mount Sinai Hosiptal|