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1.
Plast Reconstr Surg ; 130(3): 681-689, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22575855

ABSTRACT

BACKGROUND: The second part of the authors' study on operating room fires analyzes the construct of the nasal cannula used during facial surgery for patients under conscious sedation with supplemental oxygen. This prospective study compares two common styles of nasal cannulas with a nasopharyngeal system described in their first report. METHODS: Twenty patients underwent upper and/or lower lid blepharoplasty under conscious sedation with one of three methods of supplemental oxygen delivery: a Mac-Safe nasal cannula (Unomedical, Inc., McAllen, Texas), a Salter nasal cannula (Salter Laboratories, Arvin, Calif.), and a nasopharyngeal system with cut ends of a cannula placed into a rubber nasopharyngeal tube. Oxygen concentrations were measured at 24 locations around the face for each method at a low (3 liters/minute) and high flow rates (6 liters/minute) using a random access mass spectrometer unit. RESULTS: At both low and high oxygen flow rates, the median oxygen concentration at and above the nose was statistically lower (p < 0.001) using the nasopharyngeal system than with either the Mac-Safe or Salter nasal cannula. In addition, the oxygen concentrations measured using the two nasal cannulas were more variable than with the nasopharyngeal method, particularly at locations around and above the nose. CONCLUSIONS: This study demonstrates that mass spectrometry oxygen readings around the face are similar to room air when the cut ends of the oxygen cannulas are passed down the nasaopharyngeal tube, whereas readings are significantly higher with the nasal cannulas. The nasopharyngeal system that the authors describe represents a significantly safer means of oxygen delivery during conscious sedation.


Subject(s)
Catheters , Conscious Sedation/instrumentation , Equipment Safety , Fires/prevention & control , Intubation, Intratracheal/instrumentation , Operating Rooms , Oxygen/analysis , Administration, Intranasal , Adult , Aged , Aged, 80 and over , Blepharoplasty/instrumentation , Environmental Monitoring , Humans , Middle Aged , Oxygen/administration & dosage
2.
J Plast Reconstr Aesthet Surg ; 63(9): 1443-6, 2010 Sep.
Article in English | MEDLINE | ID: mdl-19716355

ABSTRACT

BACKGROUND: This study was performed to determine if pretreatment application of a topical anesthetic skin refrigerant reduced discomfort during botulinum toxin injection. METHODS: Twenty patients were assigned to four groups determined by side of the face pretreated with skin refrigerant and side receiving the first injection. On a Visual Analog Scale of 0-10 patients rated discomfort levels after injections in the glabellar complex with and without pretreatment. RESULTS: Mean discomfort rating for the pretreated side was 3.1, while the mean discomfort rating for the non-pretreated side was 4.5. Discomfort was not affected by the side sprayed (p=0.33) nor by administering the injection to the sprayed side first (p=0.37). The paired t-test revealed a significant difference between discomfort levels on the pretreated and non-pretreated sides (p=0.038) yielding a 95% confidence interval of (-2.71, -0.09). CONCLUSIONS: Topical anesthetic skin refrigerant significantly reduces discomfort in a cost-effective manner for reported by patients undergoing botulinum injections.


Subject(s)
Anesthetics, Local/therapeutic use , Botulinum Toxins, Type A/administration & dosage , Botulinum Toxins, Type A/adverse effects , Facial Pain/drug therapy , Hydrocarbons, Fluorinated/therapeutic use , Injections/adverse effects , Neuromuscular Agents/administration & dosage , Neuromuscular Agents/adverse effects , Administration, Topical , Aerosols , Anesthetics, Local/administration & dosage , Drug Combinations , Facial Pain/etiology , Female , Humans , Hydrocarbons, Fluorinated/administration & dosage , Male , Middle Aged , Pain Measurement , Regression Analysis , Treatment Outcome
3.
Adv Skin Wound Care ; 17 Suppl 2: 1-16, 2004.
Article in English | MEDLINE | ID: mdl-15716646

ABSTRACT

Pressure ulcers are a serious health issue, leading to clinical, financial, and emotional challenges. Numerous treatment modalities are available to promote wound healing, yet clinicians may be unsure how to incorporate these treatment options into an overall plan of care for the patient with a pressure ulcer. A consensus panel of experienced wound care clinicians convened in July 2004 to review the mechanisms of action and research basis for one such treatment modality: negative pressure wound therapy. After answering key questions about this modality, they developed an algorithm to assist the clinician in making decisions about using negative pressure wound therapy appropriately in patients with Stage III and Stage IV pressure ulcers.


Subject(s)
Pressure Ulcer/therapy , Algorithms , Humans , Practice Guidelines as Topic , Pressure Ulcer/pathology , Suction , Wound Healing
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