Pennsylvania Department of Health
TITUSVILLE HEALTHCARE AND REHABILITATION CENTER
Patient Care Inspection Results

Note: If you need to change the font size, click the "View" menu at the top of the page, place the mouse over the "Text Size" menu item, and select the desired font size.

Severity Designations

Click here for definitions Click here for definitions Click here for definitions Click here for definitions
Minimal Citation - No Harm Minimal Harm Actual Harm Serious Harm
TITUSVILLE HEALTHCARE AND REHABILITATION CENTER
Inspection Results For:

There are  66 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.
TITUSVILLE HEALTHCARE AND REHABILITATION CENTER - Inspection Results Scope of Citation
Number of Residents Affected
By Deficient Practice
Initial comments:

Based on a Medicare/Medicaid Recertification, State Licensure, and Civil Rights Compliance Survey, and an Abbreviated Complaint Survey completed on July 25, 2024, it was determined that Titusville Healthcare and Rehabilitation Center was not in compliance with the following requirements of 42 CFR Part 483, Subpart B, Requirements for Long Term Care Facilities and the 28 PA Code, Commonwealth of Pennsylvania Long Term Care Licensure Regulations.



 Plan of Correction:


483.25 REQUIREMENT Quality of Care:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§ 483.25 Quality of care
Quality of care is a fundamental principle that applies to all treatment and care provided to facility residents. Based on the comprehensive assessment of a resident, the facility must ensure that residents receive treatment and care in accordance with professional standards of practice, the comprehensive person-centered care plan, and the residents' choices.
Observations:

Based on observations, review of facility policy and clinical records, and staff interviews, it was determined that the facility failed to notify the physician and begin treatment timely related to a change in a resident's condition, and obtain a physician's order/clarification for the use of an assistive device for two of 17 residents reviewed (Residents R4 and R25).

Findings include:

Review of facility policy entitled, "Change in a Resident's Condition or Status" dated 3/28/24, indicated, "The nurse will notify the resident's Attending Physician or physician on call when there has been a(an): significant change in the resident's physical/emotional/mental condition."

Resident R4's admission record revealed an admission date of 4/1/22, with diagnoses that included dementia (condition with symptoms that affect memory and thinking), atrial fibrillation (irregular heart rate), and type II diabetes (condition of insufficient production of insulin).

Review of a nursing note dated 7/20/24, at 6:01 p.m. indicated that the physician was faxed information regarding white patches in Resident R4's mouth.

Continued review of Resident R4's clinical record revealed a nursing note dated 7/22/24, at 11:40 a.m. indicating that the physician's office was contacted regarding white patches on Resident R4's tongue and mouth. A nursing note dated 7/23/24, at 12:03 p.m. indicated an order was received for Nystatin Mouth/Throat Suspension (a medication used to treat a fungal infection in the mouth) Give 5 milliliters by mouth three times a day (8:00 a.m., 1:00 p.m., and 5:00 p.m.) for thrush swish and spit. Nursing notes dated 7/23/24, at 1:31 p.m. and 7/23/24, at 4:18 p.m. revealed that Resident R4 did not receive the Nystatin Mouth/Throat Suspension as ordered due to it not being delivered to the facility.

Review of Resident R4's July 2024 Medication Administration Record revealed Resident R4 received his/her first dose of Nystatin Mouth/Throat Suspension on 7/24/24, during the 8:00 a.m. medication pass, this was approximately 86 hours after the white patches on his/her mouth and tongue were observed.

During an interview with the Director of Nursing (DON) on 7/24/24, at 12:20 p.m. it was confirmed that there was a delay in treatment regarding Resident R4's change in condition and that nursing staff should have called the physician on Saturday 7/20/24, rather than faxing the physician with the resident condition concerns.


Resident R25's clinical record revealed an admission date of 1/16/24, with diagnoses that included status post right hip fracture and repair, heart failure, and right leg blood clots. The clinical record lacked of evidence of physician's orders, care plan interventions, nurse aide tasks, or progress notes regarding application of an abductor pillow (soft but firm foam pillow that is placed between the thighs and strapped onto the patient's legs while they are in a resting position to aid in keeping the body stable and prevents an abducting motion that could cause pain or further injury post-surgery).

During an interview on 7/24/24, at 11:45 a.m. Licensed Practical Nurse (LPN) Employee E1 confirmed that Resident R25 came back from an orthopedic appointment with the pillow and that there was no physician's order for it in the clinical record.

During an interview on 7/24/24, at 11:57 a.m. Nurse Aide (NA) Employee E2 confirmed that he/she has inconsistently discovered the abductor pillow between Resident R25's legs upon entering the room and removed the pillow and placed at the top of his/her closet in an effort to prevent others from using it because there was no physician's order for it.

During an interview on 7/24/24, at 1:21 p.m. the DON confirmed Resident R25 did not have a physician's order for the use of an abductor pillow and the Therapy Director confirmed that the abductor pillow present in Resident R25's room was not an the appropriate size for he/she to use.

During an interview on 7/24/24, at 1:35 p.m. Registered Nurse (RN) Employee E3 confirmed he/she had only seen the pillow once prior on 7/19/24.

During an interview on 7/24/24, at 2:20 p.m. LPN Employee E4 confirmed he/she had only seen the pillow once prior on 7/19/24, and did not know where it came from.

During an interview on 7/24/24, at 2:28 p.m. NA Employee E5 confirmed he/she was not sure how often the pillow was placed between Resident R25's legs and that if used, it was painful for the resident.

During an interview on 7/24/24, at 2:35 p.m. NA Employee E6 confirmed that when he/she comes over to that hall to help the pillow is already in there, it is removed to provide care and Resident R25 doesn't like it in there.

During an interview on 7/25/24, at 10:00 a.m. the Corporate Nurse Consultant confirmed there was no care plan or nurse aide tasks for the use of the abductor pillow.

Observation on 7/25/24, at 10:26 a.m. revealed a pink, foam abductor pillow remained laying in Resident R25's closet.

During an interview at that time, LPN Employee E1 confirmed the abductor pillow was laying in Resident R25's closet and that there was no physician's order for the pillow.

During an interview on 7/25/24, at 1:00 p.m. NA Employee E7 confirmed that he/she has discovered the pillow already in place between Resident R25's legs upon entering the room.


28 Pa. Code 211.10(c) Resident care policies

28 Pa. Code 211.12(d)(1) Nursing services

28 Pa. Code 211.12 (d)(2)(3) Nursing services


 Plan of Correction - To be completed: 08/29/2024

F 0684
Resident R4 received Nystatin Mouth/Throat suspension 5ml by mouth three times a day for 7 days. Family/responsible party notified of new orders.
Resident R25's orders have been updated. The abductor pillow was discontinued. Family/responsible party notified of new orders.
The Director of Nursing/or designee will complete an audit of the past 2 weeks resident notes and verify if residents had a change of condition, it was addressed timely, and physician notification was documented. The audit will also include a review to ensure other residents with medical devices have physician orders and of timely notification. Any orders that are missed will be completed and notifications made.
The Director of Nursing/or designee will re-educate all Licensed staff on Change of condition policy and medical devices without orders when a resident has a change in condition or medical device if we are updating the physician and looking for treatment.
Licensed staff need to call physician do not fax physician for change of condition including clarification of devices with no orders. If the physician is unavailable, then nursing needs to follow up with on call physician until response is received.
Director of Nursing or designee will audit nurses' notes, and daily report for changes in condition and medical device orders to ensure physician notification of change of condition/consult summary for medical device orders follow up daily during morning meeting to ensure that follow up was completed. Audits will be completed 5 times weekly for 2 weeks then 3 times weekly for 2 weeks then monthly until compliance is met. Audits will be reviewed at monthly QAPI meeting.


483.45(g)(h)(1)(2) REQUIREMENT Label/Store Drugs and Biologicals:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.45(g) Labeling of Drugs and Biologicals
Drugs and biologicals used in the facility must be labeled in accordance with currently accepted professional principles, and include the appropriate accessory and cautionary instructions, and the expiration date when applicable.

§483.45(h) Storage of Drugs and Biologicals

§483.45(h)(1) In accordance with State and Federal laws, the facility must store all drugs and biologicals in locked compartments under proper temperature controls, and permit only authorized personnel to have access to the keys.

§483.45(h)(2) The facility must provide separately locked, permanently affixed compartments for storage of controlled drugs listed in Schedule II of the Comprehensive Drug Abuse Prevention and Control Act of 1976 and other drugs subject to abuse, except when the facility uses single unit package drug distribution systems in which the quantity stored is minimal and a missing dose can be readily detected.
Observations:


Based on review of facility policies, observations, and staff interview, it was determined that the facility failed to ensure that keys to the medication cart and medication room were secured on one of five units reviewed (Unit B).

Findings include:

Facility policy entitled, "Security of Medication Cart" dated 3/28/24, indicated, "The nurse must secure the medication cart during the medication pass to prevent unauthorized entry."

Facility policy entitled, "Medication Storage in The Facility" dated 3/28/24, indicated, "Medication rooms, carts, and medication supplies are locked or attended by persons with authorized access."

Observations on 7/22/24, at 1:30 p.m. in room 200 on Unit B revealed the nurse's medication cart and medication room keys were on the resident's bed and were unsecured.

At that time, the Director of Nursing (DON) was called to room 200 on Unit B. The DON confirmed that the unsecured keys were for the medication cart on Unit B and the medication room. The DON confirmed that medication cart keys and medication room keys should be secured at all times and should never be left in a resident's room.

28 Pa. Code 211.9(a)(1) Pharmacy services

28 Pa. Code 211.12(d)(1)(2) Nursing services









 Plan of Correction - To be completed: 08/29/2024

F0761
Medication Cart keys were immediately removed from room 200. Licensed Practical Nurse was given written education on the importance of not setting med cart keys down and need to be kept secured at all times.

On 07/22/2024 the Director of Nursing immediately went to all medication carts and ensured that carts were locked and licensed staff had medication keys on them.

The Director of Nursing/or designee will re-educate Licensed staff on the Medication storage and security policy and that they must have the medication cart always keys on them during their shift.

Audits of medication storage will be conducted by the Director of Nursing or designee to ensure all medications and keys are properly secured. Audits will be conducted on random shifts 4 times a week for 2 weeks and twice a week for 3 weeks until compliance is achieved. Results of the audits will be reviewed at monthly QAPI meetings.

483.45(c)(3)(e)(1)-(5) REQUIREMENT Free from Unnec Psychotropic Meds/PRN Use:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§483.45(e) Psychotropic Drugs.
§483.45(c)(3) A psychotropic drug is any drug that affects brain activities associated with mental processes and behavior. These drugs include, but are not limited to, drugs in the following categories:
(i) Anti-psychotic;
(ii) Anti-depressant;
(iii) Anti-anxiety; and
(iv) Hypnotic

Based on a comprehensive assessment of a resident, the facility must ensure that---

§483.45(e)(1) Residents who have not used psychotropic drugs are not given these drugs unless the medication is necessary to treat a specific condition as diagnosed and documented in the clinical record;

§483.45(e)(2) Residents who use psychotropic drugs receive gradual dose reductions, and behavioral interventions, unless clinically contraindicated, in an effort to discontinue these drugs;

§483.45(e)(3) Residents do not receive psychotropic drugs pursuant to a PRN order unless that medication is necessary to treat a diagnosed specific condition that is documented in the clinical record; and

§483.45(e)(4) PRN orders for psychotropic drugs are limited to 14 days. Except as provided in §483.45(e)(5), if the attending physician or prescribing practitioner believes that it is appropriate for the PRN order to be extended beyond 14 days, he or she should document their rationale in the resident's medical record and indicate the duration for the PRN order.

§483.45(e)(5) PRN orders for anti-psychotic drugs are limited to 14 days and cannot be renewed unless the attending physician or prescribing practitioner evaluates the resident for the appropriateness of that medication.
Observations:

Based on review of facility policy and clinical records, and staff interviews, it was determined that the facility failed to provide a clinical rationale and duration for the continued use of a PRN (as needed) psychotropic (affecting the mind) medication beyond 14 days for one of five residents reviewed for psychotropic medications (Resident R6).

Findings include:

A facility policy entitled " Antipsychotic Medication Use" dated 3/28/2024, indicated that "PRN orders for psychotropic medications are limited to 14 days" and "If the prescriber or attending physician believes it is appropriate to extend the PRN order beyond 14 days, he or she will document the rationale for extending the use and include the duration for the PRN order."

Resident R6's clinical record revealed an admission date of 5/18/17, with diagnoses that included chronic obstructive pulmonary disease (when your lungs do not have adequate air flow), anxiety (a condition that causes a person to be nervous, uneasy, or worried about something or someone), and heart failure (a condition where the heart cannot supply the body with enough blood).

Review of Resident R6's Medication Administration Record (MAR) revealed a physician's order dated 7/9/24, to administer Vistaril (anti-anxiety medication) 25 milligrams (mg) every eight hours as needed (PRN) for 14 days. Further review of Resident R6's MAR revealed PRN Vistaril order was revised on 7/16/24, 7/17/24, and 7/18/24. After the revision on 7/18/24, the PRN Vistaril order lacked evidence of a specified duration. Resident R6 received PRN Vistaril on 7/16/24, 7/17/24, 7/18/24, 7/19/24, 7/23/24 and 7/24/24, which was beyond 14 days from the original order date. Resident R6's Vistaril order lacked the required stop date within 14 days and a clinical rationale for continued use beyond 14 days.

During interview on 7/25/24, at 9:25 a.m. the Director of Nursing revealed he/she was provided information that the PRN Vistaril did not need a duration to continue use, he/she confirmed that the information was incorrect. He/she also confirmed that the PRN Vistaril lacked the required stop date within 14 days and a clinical rationale for continued use beyond 14 days.

28 Pa. Code 211.10(d) Resident care policies

28 Pa. Code 211.12(d)(1)(3)(5) Nursing services


 Plan of Correction - To be completed: 08/29/2024

F0758
Resident R6's physician order was updated to include a fourteen (14) day stop date and Nonpharmacological Interventions.

A14 day look back audit was conducted on 07/26/2024 to identify other residents receiving psychotropic medications to ensure proper orders are in place.

The Director of Nursing/or designee will reeducate Licensed staff on psychotropic medications requiring a fourteen (14) day stop date and Non pharmacological interventions.

Audits will be conducted by the Social Worker or designee on all residents currently on psychotropic medications and new orders received for the categories under the classification of medications to ensure proper diagnosis and, fourteen (14) stop date orders and Non pharmacological Interventions are in place. Audits will be completed daily for 2 weeks and twice a week until compliance is achieved. Results of the audits will be reviewed at monthly QAPI meetings.

483.25(i) REQUIREMENT Respiratory/Tracheostomy Care and Suctioning:This is a less serious (but not lowest level) deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency is one that results in minimal discomfort to the resident or has the potential (not yet realized) to negatively affect the resident's ability to achieve his/her highest functional status.
§ 483.25(i) Respiratory care, including tracheostomy care and tracheal suctioning.
The facility must ensure that a resident who needs respiratory care, including tracheostomy care and tracheal suctioning, is provided such care, consistent with professional standards of practice, the comprehensive person-centered care plan, the residents' goals and preferences, and 483.65 of this subpart.
Observations:

Based on review of facility policy and clinical records, observations, and staff interview, it was determined that the facility failed to maintain proper care of respiratory equipment for one resident reviewed for respiratory care (Resident R210).

Findings include:

Facility policy entitled "Departmental (Respiratory Therapy) - Prevention of Infection" dated 3/28/24, indicated "Infection Control Considerations Related to Oxygen Administration ... Keep the oxygen cannula and tubing used PRN in a plastic bag when not in use."

Resident R210's clinical record revealed an admission date of 7/10/24, with diagnoses that included fracture of right femur (broken bone of the upper leg), hypertension (high blood pressure), and diabetes (a health condition that causes by the body's inability to produce enough insulin).

Resident R210's physician orders dated 7/12/24, revealed an order indicating to provide oxygen at 2 liters per minute via nasal cannula (oxygen tubing that has prongs that go into the nostrils and loops around the ears to secure in place to ensure adequate oxygen delivery).

Observation on 7/22/24, at 11:45 a.m. revealed Resident R210's nasal cannula had a piece of tape wrapped around the oxygen tubing dated 7/17/24. The oxygen tubing was connected to the oxygen concentrator and the prongs that go into the nostrils was laying on the floor. Observation on 7/22/24, at 4:10 p.m. revealed that the oxygen tubing remained with the prongs that go into the nostrils laying on the floor. Observation on 7/23/24, at 8:28 a.m. revealed Resident R210's nasal cannula had a piece of tape wrapped around the oxygen tubing dated 7/17/24, the oxygen tubing was connected to the oxygen concentrator and the prongs that go into the nostrils was laying on the floor.

During an interview on 7/23/24, at 8:41 a.m. the Director of Nursing confirmed that the nasal cannula was laying on the floor. He/she also confirmed that the nasal cannula should not be on the floor and the nasal cannula should be placed in a bag when the resident is not using it.

28 Pa. Code 211.12(d)(1)(5) Nursing services

28 Pa. Code 211.10(d) Resident care policies


 Plan of Correction - To be completed: 08/29/2024

F 0695
Resident R210's O2 tubing was thrown away and replaced with new O2 tubing. This Resident was supplied with a plastic bag to keep Oxygen tubing in when not in use.

Residents with Oxygen orders were reviewed to ensure that they had orders for O2 cleaning and tube replacement /storage bag in place weekly.

Audit completed of all oxygen orders on 07/23/2024 to ensure that residents with oxygen orders have plastic bags attached to oxygen concentrators to place oxygen tubing in when not in use.

The Director of Nursing/or designee will re-educate Licensed staff on Respiratory Prevention of Infection Oxygen Policy to include they must keep oxygen tubing in plastic bag when not in use and stored appropriately.

Director of Nursing or designee will audit residents with oxygen orders on all 3 shifts to ensure that they have plastic bag to put oxygen tubing in when not in use and that oxygen tubing is in plastic bag when not in use.

Audits will be completed 5 times weekly for 2 weeks then 3 times weekly for 2 weeks then monthly until compliance is met.

Audits will be reviewed at monthly QAPI meeting.

483.75(g)(1)(i)-(iii)(2)(i); 483.80(c) REQUIREMENT QAA Committee:Least serious deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents. This deficiency has the potential for causing no more than a minor negative impact on the resident.
§483.75(g) Quality assessment and assurance.
§483.75(g) Quality assessment and assurance.
§483.75(g)(1) A facility must maintain a quality assessment and assurance committee consisting at a minimum of:
(i) The director of nursing services;
(ii) The Medical Director or his/her designee;
(iii) At least three other members of the facility's staff, at least one of who must be the administrator, owner, a board member or other individual in a leadership role; and
(iv) The infection preventionist.

§483.75(g)(2) The quality assessment and assurance committee reports to the facility's governing body, or designated person(s) functioning as a governing body regarding its activities, including implementation of the QAPI program required under paragraphs (a) through (e) of this section. The committee must:
(i) Meet at least quarterly and as needed to coordinate and evaluate activities under the QAPI program, such as identifying issues with respect to which quality assessment and assurance activities, including performance improvement projects required under the QAPI program, are necessary.

§483.80(c) Infection preventionist participation on quality assessment and assurance committee.
The individual designated as the IP, or at least one of the individuals if there is more than one IP, must be a member of the facility's quality assessment and assurance committee and report to the committee on the IPCP on a regular basis.
Observations:

Based on review of facility records and staff interview, it was determined that the facility failed to assure required attendance of the Infection Preventionist to Quality Assurance and Performance Improvement (QAPI) Committee meetings for two of four quarterly QAPI Committee meetings (July 2023 through December 2023).

Findings include:

A facility policy entitled "Guardian Elder Care Quality Assurance and Process Improvement Committee" dated 3/28/24, indicated "the following individuals will serve on the committee ... j. Infection Control Representative ..." and "The committee will meet monthly at an appointed time."

Review of the QAPI Committee Attendance Records from July 2023 through December 2023 revealed no evidence on the attendance sign-in sheets for the required QAPI meetings that the Infection Preventionist was in attendance.

During an interview on 7/25/24, at 11:00 a.m. the Nursing Home Administrator confirmed the facility lacked evidence that an Infection Preventionist attended the quarterly QAPI Committee meetings as required in the quarters between July 2023 through December 2023. He/she also confirmed that the Infection Preventionist should be in attendance for the QAPI meetings as required.

28 Pa. Code 201.18(e)(1)(3) Management

28 Pa. Code 211.10(d) Resident care policies


 Plan of Correction - To be completed: 08/29/2024

F 0868
The facility is unable to correct the absences of the Infection Control Preventionist as they occurred in the past. This has been corrected moving forward. An Infection Preventionist was hired and has been attending monthly Quality Assurance meetings per facility policy.

The facility Administrator or designee will monitor monthly to ensure the Infection Preventionist participates in monthly Quality Assurance meetings and signs an attendance sheet as verification.

Sign in sheets will serve as an audit and reviewed at Quality Assurance meetings monthly.

483.80(b)(1)-(4) REQUIREMENT Infection Preventionist Qualifications/Role:Least serious deficiency but was found to be widespread throughout the facility and/or has the potential to affect a large portion or all the residents. This deficiency has the potential for causing no more than a minor negative impact on the resident.
§483.80(b) Infection preventionist
The facility must designate one or more individual(s) as the infection preventionist(s) (IP)(s) who are responsible for the facility's IPCP. The IP must:

§483.80(b)(1) Have primary professional training in nursing, medical technology, microbiology, epidemiology, or other related field;

§483.80(b)(2) Be qualified by education, training, experience or certification;

§483.80(b)(3) Work at least part-time at the facility; and

§483.80(b)(4) Have completed specialized training in infection prevention and control.
Observations:

Based on review of facility records and staff interviews, it was determined that the facility failed to ensure the designated Infection Preventionist (IP) attended the Infection Control Committee meetings and works at the facility focusing only on infection control at least part-time as required.

Findings include:

Review of facility documentation identified that the Director of Nursing (DON) fulfilled the job of the IP from November 2023 through May 2024. The DON works full-time and was unable to provide proof that additional part-time hours focusing only on infection control were completed in addition to his/her full-time DON duties.

Review of Infection Control committee meetings from July 2023 through December 2023 revealed there was not anyone who attended the meetings and signed in as the IP.

During an interview on 7/25/24, at 11:00 a.m. the Nursing Home Administrator confirmed the facility lacked evidence that an IP attended the meetings from July 2023-December 2023, and the DON confirmed that he/she could not provide proof that he/she completed additional part-time hours focusing only on infection control in addition to his/her full-time DON duties.


28 Pa. Code 201.18(e)(1)(3) Management

28 Pa. Code 211.10(d) Resident care policies

28 Pa. Code 211.12(d)(1)(5) Nursing services



 Plan of Correction - To be completed: 08/29/2024

F 0882
The facility is unable to correct the absences of the Infection Control Preventionist as they occurred in the past. This has been corrected moving forward. An Infection Preventionist was hired and has been attending monthly Infection Control meetings per facility policy.

The facility Administrator or designee will monitor monthly to ensure the Infection Preventionist participates in monthly Infection Control meetings and signs an attendance sheet as verification.

Sign in sheets will serve as an audit and reviewed at Quality Assurance meetings monthly.



483.20(g) REQUIREMENT Accuracy of Assessments:Least serious deficiency and is isolated to the fewest number of residents, staff, or occurrences. This deficiency has the potential for causing no more than a minor negative impact on the resident.
§483.20(g) Accuracy of Assessments.
The assessment must accurately reflect the resident's status.
Observations:

Based on review of clinical records and facility documentation, and staff interview, it was determined that the facility failed to complete the Minimum Data Set (MDS-periodic assessment of resident care needs) to accurately reflect the resident's status at the time discharge for one of 17 residents reviewed (Resident CR59).

Findings include:

Resident CR59's admission record revealed an admission date of 5/12/2024, with diagnoses that included weakness, anxiety, and pain.

Resident CR59's clinical record revealed that he/she had a planned discharge home on 6/1/2024.

The Nursing Home Discharge MDS dated 6/1/2024, Section A - Identification Information category A2105. Discharge Status was marked "04 Short-Term General Hospital" indicating Resident CR59 was discharged to the hospital.

During an interview on 7/25/2024, at 11:49 a.m. the Registered Nurse Assessment Coordinator confirmed that Section A - Identification Information category A2105. Discharge Status of the Nursing Home Discharge MDS dated 6/1/2024, was incorrectly coded for Resident CR59 regarding their discharge status.

28 Pa. Code 211.5(xi) Medical records



 Plan of Correction - To be completed: 08/07/2024

I hereby acknowledge the CMS 2567-A, issued to TITUSVILLE HEALTHCARE AND REHABILITATION CENTER for the survey ending 07/25/2024, AND attest that all deficiencies listed on the form will be corrected in a timely manner.

Back to County Map


  
Home : Press Releases : Administration
Health Planning and Assessment : Office of the Secretary
Health Promotion and Disease Prevention : Quality Assurance



Copyright © 2001 Commonwealth of Pennsylvania. All Rights Reserved.
Commonwealth of PA Privacy Statement

Visit the PA Power Port