Inspection Reports for
Mary Anna Nursing Home
125 TURNER STREET, WISNER, LA, 71378
Back to Facility Profile3 Reports
Inspection Report — Jan 28, 2025
Annual Inspection CMS
Date: Jan 28, 2025
Visit Reason
The inspection was conducted as a standard annual survey of Mary Anna Nursing Home to assess compliance with regulatory requirements related to resident care, use of restraints, accident hazards, and bed rail safety.
Findings
The facility failed to ensure residents were free from physical restraints without proper consent, physician orders, and assessments prior to use of bed bolsters. The facility also failed to ensure appropriate interventions after falls and did not assess residents for entrapment risks prior to installing bed rails for several residents.
Deficiencies (3)
F 0604: The facility failed to ensure residents were free from physical restraints without obtaining consent, physician orders, and appropriate assessments prior to placing bolsters on beds for 4 of 5 residents reviewed.
F 0689: The facility failed to ensure a resident was free from accident hazards by not providing appropriate interventions after each fall for 1 resident sampled for falls.
F 0700: The facility failed to assess residents for the risk of entrapment prior to installing bed rails for 3 of 4 residents reviewed for accident hazards.
Report Facts
Residents reviewed for restraints: 5
Residents affected by restraint deficiency: 4
Residents reviewed for accident hazards: 4
Residents affected by entrapment risk assessment deficiency: 3
Employees mentioned
| Name | Title | Context |
|---|---|---|
| S1 Administrator | Confirmed failures to obtain consent, physician orders, and assessments for restraints and bed rails | |
| S2 Director of Nursing (DON) | Confirmed interventions for falls were not appropriate for resident #11 |
Inspection Report — Dec 13, 2023
Annual Inspection CMS
Date: Dec 13, 2023
Visit Reason
The inspection was conducted to evaluate compliance with nursing care competencies, medication administration, drug regimen appropriateness, and medication storage standards at Mary Anna Nursing Home.
Findings
The facility failed to ensure nurses documented insulin injection sites and followed sliding scale insulin parameters for residents #14 and #33. The facility also failed to document justification or parameters for as needed medications for resident #17. Additionally, multiple opened medications and biologicals were not labeled with opened dates and some medications were improperly stored.
Deficiencies (3)
F 0726: Nurses and nurse aides failed to document insulin injection sites and did not follow parameters for insulin sliding scale for residents #14 and #33, risking resident safety.
F 0757: The facility failed to ensure resident #17's drug regimen was free from unnecessary drugs due to lack of documented parameters or justification for as needed medications administered.
F 0761: Drugs and biologicals were not labeled with opened dates and were improperly stored, including medications belonging to discharged residents still available for use.
Report Facts
Times blood sugar >400 not reported: 13
Humalog insulin administrations documented: 56
Humalog insulin administrations documented: 30
As needed medication administrations: 4
Opened Lidocaine vials observed: 4
Opened insulin pens observed: 6
Employees mentioned
| Name | Title | Context |
|---|---|---|
| S3LPN | Licensed Practical Nurse | Failed to document insulin injection sites and notify physician of blood sugar >400 for residents #14 and #33. |
| S2DON | Director of Nursing | Confirmed failures in documentation and notification related to insulin administration and medication parameters. |
| S6Registered Nurse | Registered Nurse | Reported lack of documentation for as needed medication parameters for resident #17. |
| S5LPN | Licensed Practical Nurse | Confirmed opened insulin pens and Lidocaine vials were unlabeled and improperly stored. |
| S4LPN | Licensed Practical Nurse | Confirmed opened Humalog KwikPens were unlabeled. |
| S1Administrator | Administrator | Notified of findings related to medication storage and documentation failures. |
Inspection Report — Nov 2, 2022
Annual Inspection CMS
Date: Nov 2, 2022
Visit Reason
The inspection was conducted to assess compliance with professional standards of care related to respiratory care, medication regimen reviews, and monitoring of residents receiving anticoagulant medications.
Findings
The facility failed to properly change, label, and store oxygen and nebulizer equipment for residents #4 and #9. Additionally, the pharmacist failed to identify and report irregularities in monitoring resident #5 who was receiving an anticoagulant medication, resulting in inadequate monitoring for signs and symptoms of bleeding.
Deficiencies (3)
F 0695: The facility failed to properly change, label, and store oxygen tubing and nebulizer facemasks for residents #4 and #9 as required by facility policy.
F 0756: The pharmacist failed to perform a monthly drug regimen review and did not identify or report irregularities in monitoring resident #5 receiving an anticoagulant medication.
F 0757: The facility failed to ensure resident #5's drug regimen was free from unnecessary drugs by not adequately monitoring for signs and symptoms of bleeding while on anticoagulant therapy.
Report Facts
Residents reviewed for respiratory care: 2
Residents reviewed for unnecessary medications: 5
Residents affected by respiratory care deficiency: 2
Residents affected by medication monitoring deficiency: 1
Employees mentioned
| Name | Title | Context |
|---|---|---|
| S2DON | Director of Nursing | Notified and confirmed findings regarding oxygen tubing and anticoagulant monitoring deficiencies |
| S1Administrator | Administrator | Notified of oxygen tubing and nebulizer storage deficiencies |
| S5LPN | Licensed Practical Nurse | Confirmed oxygen tubing was not dated, labeled, or stored per policy |
| S6LPN | Licensed Practical Nurse | In charge of changing oxygen tubing monthly and confirmed improper storage and labeling |
| S4LPN | Licensed Practical Nurse | Confirmed oxygen tubing and nebulizer were not dated and not stored properly |
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