Oxygen Saturation Monitoring During Surgery

NCT ID: NCT01098851

Last Updated: 2014-08-07

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 21 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2009-07-31
• Study Completion Date: 2009-11-30

Brief Summary

Patients with Obstructive Sleep Apnea (OSA) have cyclical patterns of lower blood oxygen during sleep because of repeated episodes of upper airway obstruction that cause their breathing to stop. When these patients have surgery, anesthetic drugs may worsen these patterns of lower blood oxygen. This study monitors ten patients at high risk for OSA and ten patients at low risk for OSA during surgery. Patterns of lower oxygen saturations should arise in the high risk group but not the low risk group.

Detailed Description

Patients with Obstructive Sleep Apnea (OSA) have episodes of upper airway obstruction during sleep which have been shown to be accompanied by multiple oxygen desaturations followed by short recovery intervals until rising PaCO2 causes sleep disruption/rescue arousal. In the postoperative and conscious sedation arena, these patterns can deteriorate from a stable pattern to a severely unstable pattern which may go unrecognized and lead to an adverse event (respiratory/cardiac arrest; death).

Anesthesia and the higher consumption of analgesics produce a profound reduction in pharyngeal tone, a dampening of both chemoreceptor sensitivity and arousal/rescue response. Thus the first 48 hours post operatively presents a vulnerable period. Respiratory disturbances are more prominent - respiratory arrest and hypopnea being the main adverse occurrences during this period.

An algorithm has been developed that monitors saturation and indicates repetitive reductions in airflow through the upper airway and into the lungs. Presence of this pattern in the procedural sedation patient population has not been tested for its prevalence. This study will monitor patients during surgery to determine if this pattern occurs in this hospital setting.

Conditions

Sleep Apnea, Obstructive

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Obstructive Sleep Apnea

Surgery patients at high risk for Obstructive Sleep Apnea

No interventions assigned to this group

Surgery Patients

Surgery patients at low risk for Obstructive Sleep Apnea

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Age greater than 21 years
• Patients scheduled for a procedure that requires analgesia and/or sedation by any route (intravenous, intramuscular, oral, epidural or intrathecal).
• Patients with an anticipated length of sedation greater than or equal to one hour.
• Patients in the ASA category I through III.
• Patients who only receive propofol, benzodiazepines, and opioids.

Exclusion Criteria

• Age less than 21 years
• Patients whose room air oxygen saturation is <90%
• Patients receiving post-operative positive airway pressure support
• Previous allergic/contact reactions to adhesives
• CHF
• Moderate or severe valvular disease
• TIA/CVA
• Carotid stenosis or endarterectomy
• Anemia (HCT if available < 30%)
• Pulmonary hypertension
• Dialysis
• Pregnancy
• Patients unable to give informed consent

• Minimum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medtronic - MITG

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Roger Mecca, MD

Role: STUDY_CHAIR

Medtronic - MITG

Locations

Avista Adventist Hospital

Louisville, Colorado, United States

Countries

United States

Other Identifiers

COV-MO-PO-1000

Identifier Type: -

Identifier Source: org_study_id