Pennsylvania Department of Health
MID-ATLANTIC GASTROINTESTINAL CENTER 2
Patient Care Inspection Results

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MID-ATLANTIC GASTROINTESTINAL CENTER 2
Inspection Results For:

There are  37 surveys for this facility. Please select a date to view the survey results.

Surveys don't appear on this website until at least 41 days have elapsed since the exit date of the survey.
MID-ATLANTIC GASTROINTESTINAL CENTER 2 - Inspection Results Scope of Citation
Number of Residents Affected
By Deficient Practice
Initial comments:

This report is the result of a State licensure survey conducted on January 11, 2024, at Mid-Atlantic Gastrointestinal Center 2. It was determined the facility was not in compliance with the requirements of the Pennsylvania Department of Health's Rules and Regulations for Ambulatory Care Facilities, Annex A, Title 28, Part IV, Subparts A and F, Chapters 551-573, November 1999.










 Plan of Correction:


553.25 (1-6) LICENSURE Discharge Criteria:State only Deficiency.
553.25 Discharge Criteria

A patient may only be discharged from an ASF if the following physical status criteria are met:
(1) Vital signs. Blood pressure, heart rate, temperature and respiratory rate are within the normal range for the patient's age or at preoperative levels for that patient.
(2) Activity. The patient has regained preoperative mobility without assistance or syncope, or function at his usual level considering limitations imposed by the surgical procedure.
(3) Mental status. The patient is awake, alert or functions at his preoperative mental status.
(4) Pain. The patient's pain can be effectively controlled with medication.
(5) Bleeding. Bleeding is controlled and consistent with that expected from the surgical procedure.
(6) Nausea/vomiting. Minimal nausea or vomiting is controlled and consistent with that expected from the surgical procedure.
Observations:

Based on review of facility documents, medical records (MR), and employee (EMP) interview it was determined the facility failed to ensure patients met required discharge criteria prior to discharge in two of ten medical records reviewed (MR4 and MR9).

Findings Include:

On January 11, 2024, review of facility policy "Vital Signs" effective August 2023, revealed "Policy: Patient vital signs are monitored at designated times/intervals while being treated in the Center. Purpose: To document progress and/or change in the condition of the patient. Procedure: Post-Operative/Recovery...A Post-Operative temperature is taken at time of discharge".

On January 11, 2024, review of MR4 revealed there was no evidence of documentation that MR4 had a temperature vital sign assessed prior to discharge.

On January 11, 2024, review of MR9 revealed there was no evidence of documentation that MR9 had a temperature vital sign assessed prior to discharge.

Interview with EMP1 on January 11, 2024, EMP1 confirmed MR4 and MR9 did not have documentation that a temperature vital sign had been assessed prior to discharge.







 Plan of Correction - To be completed: 03/08/2024

We are working on establishing a Pre-Admission Testing Dept. that would be in contact with patients closer to their appointment date (some patients schedule 3 months in advance) to review an medical changes since they made their appointment.

553.25 (1-6) Discharge Criteria


S 3250
Systemic Changes:
TEMPERATURE VITAL SIGN .PRIOR TO DISCHARGE
On 1/11/2024 CA met with .available nursing staff .to .review the .Center's Vital Signs .policy, staff educated regarding .the documentation of .patient .temperature prior to discharge.

Systemic Changes:
All Nursing staff will review the .Vital Signs policy. Proof of policy review is confirmed by a signed roster and is to be completed by 1/26/2024. Any PRN staff who are not scheduled to work on or before 1/26/2024 will be sent the policy via email and will acknowledge review by replying via email.


Monitoring and Sustaining the .Plan:
The CA or DON will audit 10 .random .charts per day for 30 days, to .verify the documentation of patient .temperature before discharge. Audits will begin 1/29/2024. If .100% compliance is achieved after .the initial 30-day monitoring .period, .the facility will resume monitoring vital sign documentation on a monthly basis during the random Medical Record Review.

Responsible Party and Reporting:
The CA is responsible to implement .the changes identified in the PoC.


The CA will provide results of this .survey, the corrective actions, and .results from monitoring to the QAPI .Committee quarterly for review and .recommendations. Recommendations .will be submitted to the Governing Body for review and approval.



567.1 LICENSURE Principle:State only Deficiency.
567.1 Principle

The ASF shall have a sanitary environment, properly constructed,
equipped and maintained to protect surgical patients and ASF personnel from
cross-infection and to protect the health and safety of patients.

Observations:

Based on review of facility documents, observation, and employee (EMP) interview it was determined the facility failed to ensure instruments/equipment are being cleaned and disinfected properly to protect the health and safety of patients according to manufacture guidelines.

Findings include:

On January 12, 2024, review of facility policy "Reprocessing Endoscope" effective July 2023, revealed "Purpose: To establish for the cleaning and disinfection of endoscopes in accordance with current approved guidelines and manufacturer's recommendations by trained personnel. Background: ... The center adheres to manufacturer's recommendations, and state and federal guidelines, including but not limited to the cleaning, disinfection and sterilization of instruments, equipment, supplies and implants."

On January 11, 2024, review of facilities "Pure Enzymatic Detergent" guidelines revealed one-half ounce of the enzymatic detergent is to be used with every gallon of water.

Interview with EMP2 on January 11, 2024, EMP2 confirmed the facility uses four pumps of the Pure Enzymatic Detergent in four gallons of water totaling two ounces to adhere to manufactures guidelines.

Observation noted on January 11, 2024, EMP2 deposited four pumps of Pure Enzymatic Detergent into a measuring cup totaling three and a quarter ounces of detergent.

Interview with EMP1 on January 11, 2024, EMP1 confirmed the four pumps of Pure Enzymatic Detergent in the measuring cup totaled three and a quarter ounces and the facility was not adhering to manufacturer's guidelines or facility policy.





 Plan of Correction - To be completed: 03/01/2024

567.1 Principle
S 6701
Systemic Changes:
ENZYMATIC DETERGENT COMPLIANCE WITH MIFU
On 1/11/2024 the CA immediately instructed staff to measure enzymatic detergent with a measuring cup to verify the correct amount of enzymatic detergent is added to water per MIFU. The CA will conduct an in-service education for scope reprocessing staff on 1/19/2024.

Systemic Changes:
In-service to include the manufacturer instructions for use (MIFU) for enzymatic detergent.
Endoscope reprocessing staff attendance confirmed by a signed roster as proof of education on enzymatic dilution steps. A laminated sign with the recommended MIFU dilution was placed above the sink in the decontamination room for
visualization and compliance.

Monitoring and Sustaining the Plan:
The CA will complete a daily enzymatic verification audit, to begin 1/22/2024, that will last for 30 days. Observation that staff are using the measuring cup to verify the correct amount of enzymatic detergent will be documented. If100% compliance is achieved after the initial 30-day monitoring period,the facility will resume enzymatic monitoring on a monthly basis, during the Monthly Scope Audit.

Responsible Party and Reporting:
The CA is responsible to implement the changes identified in the PoC.

The CA will provide results of this survey, the corrective actions, and results from monitoring to the QAPI Committee quarterly for review and recommendations. Recommendations will be submitted to the Governing Body for review and approval.




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