Adjunctive Nitrous Oxide During ED Incision and Drainage of Abscess

This study will be a prospective, randomized, double-blinded clinical trial of patients undergoing incision and drainage of abscesses in the ED of an urban, tertiary, academic medical center. Subjects will be randomized to one of two groups: 100% oxygen or 50/50 O2/Nitrous oxide while undergoing standard incision and drainage of cutaneous abscess.

Recruitment Methods

The research associates as well as the heath care team (both residents and attending physicians) will screen patients who may need incision and drainage of abscesses in the ED and may qualify for the study. Research associates will use the Cerner/AeCIS System for screening, and they will be in charge of informed consent, enrollment, placement of the capnography monitor, as well as data collection. The health care team will be in charge of the local anesthesia and incision and drainage of abscess and all other management.

Procedures Involved in the Research

Initial medical assessment will be made in accordance with established clinical procedures, including the history, physical examination, and vital signs. If by clinical assessment the patient meets eligibility criteria, then they will be approached by a research associate for enrollment in the study. After informed consent is obtained and prior to starting the procedure, standard vital sign monitoring will be placed on the patient (electrocardiogram, non-invasive blood pressure monitoring, pulse oximetry, and capnography). The Capnostream 20 ETCO2 monitor will be used as the primary device to measure ETCO2, with a nasal cannula capable of delivering supplemental oxygen and measuring ETCO2 (Oridion Medical, Needham, MA).

The SEDARA gas mixer system [Linde Gas North America LLC] will be used as our primary nitrous oxide delivery device. It will mix and deliver nitrous oxide and oxygen in a 1:1 ratio, at a fixed concentration of 50%/50%. It uses a patient driven demand valve system that is hand held. This device provides a consistent, fixed 50%/50% blend of nitrous oxide (N2O) and oxygen (O2), eliminates the need to titrate, and provides fixed concentrations for controlled and consistent dosing. The device comparator detects dosing imbalance to protect against hypoxic mixtures, it cannot deliver nitrous gas without concurrent oxygen, and the device has an anti-asphyxia valve override. The on demand valve requires patient inspiration to trigger dosing and also allows option for 100% oxygen delivery through same delivery mask. This portable device scavenges exhaled waste gases for environmental safety, as well as a key mechanism that renders the system inoperable without it for security.

After informed consent, the patient will fill out a pre procedure questionnaire and a 100 mm VAS baseline pain scale. The patient will be randomized to either the control group (100% oxygen) or treatment group (50/50) by using a randomization scheme generated using the web site Randomization.com (http://www.randomization.com). The treating physician will measure erythema and induration using a measuring tape, estimate the amount of fluctuance as small, moderate, or large, and note the location of the abscess. Once randomized, subjects will be given the mask for delivery of inhaled gas and instructed on its use, and the research associate will mark the time the patient began using the device. The SEDARA Gas Mixer will be only facing the research associate as to ensure blinding of study arm by provider and subject. The subject will be given nitrous oxide or oxygen for a minimum of 10 minutes prior to incision and drainage. The treating physician will then clean the abscess with chlorhexidine solution. The abscess will be incised with a single linear incision using a No. 11 surgical scalpel, and a cotton tipped applicator will be used to break up loculations within the abscess cavity. The method of I\&D, and decision to probe to break-up loculations will be standardized, but the degree of probing, depth, and decision to pack will be left to the discretion of the treating physician. Subjects pain will be assessed using the VAS at ten minutes after NO administration but before beginning I\&D, immediately post I\&D procedure, and ten minutes after procedure completion.

The subject's clinical data (refer to data management) will be entered into a standardized data collection form. Study will end when the subjects recovers back to baseline. Vital signs will be flagged electronically when a physician intervenes for clinical respiratory depression. Respiratory depression will be defined as peripheral SaO2 below 92%, ETCO2 level above 50, a rise or decrease of 10% above or below baseline, the loss of the ETCO2 waveform for more than 15 seconds. Once the procedure is complete, and the patient is deemed back to their mental status baseline, they will fill out a post procedure satisfaction questionnaire. The physician will also fill out a post procedure questionnaire.