Respiratory Equipment Not Labeled or Stored Properly
Summary
The facility failed to ensure that respiratory equipment was handled and stored according to infection control measures for residents receiving O2 and nebulizer treatments. For one resident with chronic respiratory failure with hypercapnia, COPD, interstitial pulmonary disease, obstructive sleep apnea, morbid obesity with alveolar hypoventilation, and chronic diastolic CHF, surveyors observed O2 via nasal cannula at 2 LPM, but the O2 tubing had no date or label. The resident’s neb tubing and neb mask were lying loose on the bedside table without a date or label and were not stored in a bag. The resident’s BiPAP mask was also lying loose on the bedside table and was not stored in a bag. The resident’s record showed orders for continuous O2, weekly tubing changes with labeling of each component, and BiPAP use at night if the resident agreed. For a second resident with diagnoses including multiple sclerosis and atelectasis, surveyors observed an O2 concentrator with nasal cannula tubing connected and lying on the floor. The tubing was not dated and was not stored in a plastic bag. The resident stated that O2 had not been used for two weeks. Surveyors also observed the resident’s nebulizer mask lying on top of a plastic bag on the dresser rather than stored in a bag, and there was no cautionary sign on the door indicating O2 use. The resident’s May 2026 medication record included an order for O2 at 2 LPM via nasal cannula for shortness of breath or O2 saturation below 92%, and a short course of ipratropium-albuterol inhalation treatment that had been discontinued. Staff interviews confirmed the expected practice for respiratory equipment storage and labeling. An LPN/UM, RN, DON, and other nursing staff stated that O2 tubing should be labeled with the date changed and that neb and BiPAP masks should generally be stored in a plastic bag. The DON also stated that O2 tubing should have a label indicating when it was changed. The facility’s respiratory equipment policies stated that O2 delivery devices and tubing were to be changed every 7 days or as needed, that O2 tubing was to be labeled with the date changed, and that respiratory equipment was to be stored appropriately to prevent contamination. The nebulizer policy stated that the treatment bag was to be labeled with the patient name and date.
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