Pennsylvania Department of Health
LUTHERAN HOME AT KANE
Patient Care Inspection Results

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LUTHERAN HOME AT KANE
Inspection Results For:

There are  85 surveys for this facility. Please select a date to view the survey results.

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LUTHERAN HOME AT KANE - 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 completed on November 19, 2025, it was determined that Lutheran Home at Kane 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:


483.15(c)(2)(iii)(3)-(6)(8)(d)(1)(2); 483.21(c)(2)(i)-(iii) REQUIREMENT Discharge Process:This is a less serious (but not lowest level) deficiency and affects more than a limited 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. This deficiency was not found to be throughout this facility.
§483.15(c)(2) Documentation.
When the facility transfers or discharges a resident under any of the circumstances specified in paragraphs (c)(1)(i)(A) through (F) of this section, the facility must ensure that the transfer or discharge is documented in the resident's medical record and appropriate information is communicated to the receiving health care institution or provider.
(iii) Information provided to the receiving provider must include a minimum of the following:
(A) Contact information of the practitioner responsible for the care of the resident.
(B) Resident representative information including contact information
(C) Advance Directive information
(D) All special instructions or precautions for ongoing care, as appropriate.
(E) Comprehensive care plan goals;
(F) All other necessary information, including a copy of the resident's discharge summary, consistent with §483.21(c)(2) as applicable, and any other documentation, as applicable, to ensure a safe and effective transition of care.

§483.15(c)(3) Notice before transfer.
Before a facility transfers or discharges a resident, the facility must-
(i) Notify the resident and the resident's representative(s) of the transfer or discharge and the reasons for the move in writing and in a language and manner they understand. The facility must send a copy of the notice to a representative of the Office of the State Long-Term Care Ombudsman.
(ii) Record the reasons for the transfer or discharge in the resident's medical record in accordance with paragraph (c)(2) of this section; and
(iii) Include in the notice the items described in paragraph (c)(5) of this section.

§483.15(c)(4) Timing of the notice.
(i) Except as specified in paragraphs (c)(4)(ii) and (c)(8) of this section, the notice of transfer or discharge required under this section must be made by the facility at least 30 days before the resident is transferred or discharged.
(ii) Notice must be made as soon as practicable before transfer or discharge when-
(A) The safety of individuals in the facility would be endangered under paragraph (c)(1)(i)(C) of this section;
(B) The health of individuals in the facility would be endangered, under paragraph (c)(1)(i)(D) of this section;
(C) The resident's health improves sufficiently to allow a more immediate transfer or discharge, under paragraph (c)(1)(i)(B) of this section;
(D) An immediate transfer or discharge is required by the resident's urgent medical needs, under paragraph (c)(1)(i)(A) of this section; or
(E) A resident has not resided in the facility for 30 days.

§483.15(c)(5) Contents of the notice. The written notice specified in paragraph (c)(3) of this section must include the following:

(i) The reason for transfer or discharge;
(ii) The effective date of transfer or discharge;
(iii) The location to which the resident is transferred or discharged;
(iv) A statement of the resident's appeal rights, including the name, address (mailing and email), and telephone number of the entity which receives such requests; and information on how to obtain an appeal form and assistance in completing the form and submitting the appeal hearing request;
(v) The name, address (mailing and email) and telephone number of the Office of the State Long-Term Care Ombudsman;
(vi) For nursing facility residents with intellectual and developmental disabilities or related disabilities, the mailing and email address and telephone number of the agency responsible for the protection and advocacy of individuals with developmental disabilities established under Part C of the Developmental Disabilities Assistance and Bill of Rights Act of 2000 (Pub. L. 106-402, codified at 42 U.S.C. 15001 et seq.); and
(vii) For nursing facility residents with a mental disorder or related disabilities, the mailing and email address and telephone number of the agency responsible for the protection and advocacy of individuals with a mental disorder established under the Protection and Advocacy for Mentally Ill Individuals Act.

§483.15(c)(6) Changes to the notice.
If the information in the notice changes prior to effecting the transfer or discharge, the facility must update the recipients of the notice as soon as practicable once the updated information becomes available.

§483.15(c)(8) Notice in advance of facility closure
In the case of facility closure, the individual who is the administrator of the facility must provide written notification prior to the impending closure to the State Survey Agency, the Office of the State Long-Term Care Ombudsman, residents of the facility, and the resident representatives, as well as the plan for the transfer and adequate relocation of the residents, as required at § 483.70(l).

§483.15(d) Notice of bed-hold policy and return-

§483.15(d)(1) Notice before transfer. Before a nursing facility transfers a resident to a hospital or the resident goes on therapeutic leave, the nursing facility must provide written information to the resident or resident representative that specifies-
(i) The duration of the state bed-hold policy, if any, during which the resident is permitted to return and resume residence in the nursing facility;
(ii) The reserve bed payment policy in the state plan, under § 447.40 of this chapter, if any;
(iii) The nursing facility's policies regarding bed-hold periods, which must be consistent with paragraph (e)(1 ) of this section, permitting a resident to return; and
(iv) The information specified in paragraph (e)(1) of this section.

§483.15(d)(2) Bed-hold notice upon transfer. At the time of transfer of a resident for hospitalization or therapeutic leave, a nursing facility must provide to the resident and the resident representative written notice which specifies the duration of the bed-hold policy described in paragraph (d)(1) of this section.

§483.21(c)(2) Discharge Summary
When the facility anticipates discharge, a resident must have a discharge summary that includes, but is not limited to, the following:
(i) A recapitulation of the resident's stay that includes, but is not limited to, diagnoses, course of illness/treatment or therapy, and pertinent lab, radiology, and consultation results.
(ii) A final summary of the resident's status to include items in paragraph (b)(1) of §483.20, at the time of the discharge that is available for release to authorized persons and agencies, with the consent of the resident or resident's representative.
(iii) Reconciliation of all pre-discharge medications with the resident's post-discharge medications (both prescribed and over-the-counter).
Observations:

Based on review of facility policy, clinical records, and staff interview it was determined that the facility failed to make certain that the necessary resident information was communicated to the receiving health care provider upon transfer to the hospital for three of 18 residents reviewed (Residents R1, R3, and R77).


Findings include:

Review of facility policy entitled "Transfer or Discharge, Emergency" dated 11/3/25, indicated "Should it become necessary to make emergency transfer or discharge to a hospital or other related institution, our facility will prepare a transfer packet to send with the resident that includes; face sheet, administration record, order summary, bed hold policy, immunization report, recent weight and vitals, copy of advance directives, and complete e-interact form."

Resident R1's clinical record revealed an admission date of 8/27/25, with diagnoses that included diabetes (a health condition caused by the body's inability to produce enough insulin), atrial fibrillation (A-Fib irregular and often rapid heartbeat that can lead to stroke, heart failure, and other complications), and chronic obstructive pulmonary disease (COPD a condition that prevents airflow to the lungs resulting in difficulty breathing).

Resident R1's progress notes revealed a note dated 8/29/25,indicating transfer to the hospital. The clinical record lacked evidence that his/her necessary clinical information was communicated to the receiving health care provider.

Resident R3's clinical record revealed an admission date of 12/30/24, with diagnoses that included hypertension (high blood pressure), hyperlipidemia (high cholesterol), and heart failure (a condition where the heart cannot supply the body with enough blood).

Resident R3's progress notes revealed notes dated 5/18/25,8/11/25, and 8/14/25, indicating transfers to the hospital. The clinical record lacked evidence that his/her necessary clinical information was communicated to the receiving health care provider.

Review of Resident R77's clinical record revealed an admission date of 8/25/25, with diagnoses that included weakness, dysphagia (difficulty swallowing), and chronic respiratory failure.

Resident R77's progress notes revealed a note dated 9/5/25,indicating transfer to the hospital. The clinical record lacked evidence that his/her necessary clinical information was communicated to the receiving health care provider.

During an interview on 11/19/25, at 9:09 a.m. the Director of Nursing confirmed that Residents R1, R3, and R77s clinical records lacked evidence that the necessary clinical information was provided to the receiving healthcare provider upon transfer and when the transfers occurred clinical information should have been provided to the receiving healthcare provider.

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

28 Pa. Code 201.29(c.3) (2) Resident rights






 Plan of Correction - To be completed: 01/05/2026

1. Corrective Action Taken for Residents Found to Be Affected
- The Director of Nursing and Assistant Director of Nursing immediately reviewed the clinical records of Residents R1, R3, and R77. For each resident, the Director of Nursing reconstructed the complete transfer packet in accordance with §483.15(c)(2)(iii), including practitioner contact information, resident representative information, advance directives, special instructions, current care plan goals, current clinical summaries, and all other necessary documentation.
- Involved nursing staff were counseled and re-educated on correct transfer packet procedures.

2. Identification of Other Residents Potentially Affected
- Director of Nursing/Assistant Director of Nursing did an audit of all resident transfers that occurred within the past 60 days to determine whether all required clinical information was provided at the time of transfer.
- Where missing documentation was identified, it was immediately corrected and communicated to the receiving provider.
- No negative outcomes were identified for any residents.

3. Systemic Changes Implemented to Prevent Recurrence

The Lutheran Home at Kane has implemented the following corrective systems:

A. Revised Transfer Packet and Checklist
The facility's Emergency Transfer/Discharge Packet was revised to include a standardized checklist encompassing all required elements under:

- §483.15(c)(2)(iii)(A)–(F)
- §483.15(c)(3)–(6) and (d)(1)–(2)
- §483.21(c)(2)
The checklist must be completed and signed by the charge nurse before transfer.

B. EHR Workflow Enhancements
- The electronic health record was updated to include a required transfer packet prompt, preventing completion of a transfer note until all required documents are uploaded or verified.

C. Staff Education
Director of Nursing and Assistant Director of Nursing educated all licensed nursing staff, unit clerks, admissions staff, and nursing supervisors re-educated on:
- Regulatory requirements for resident transfer and discharge documentation
- Required content to be communicated to receiving facilities
- Documentation of reasons for transfer
- Bed-hold notice requirements under §483.15(d)(1)–(2)
- Discharge summary requirements under §483.21(c)(2)
- Staff unable to attend the initial session will receive education prior to their next shift.

D. DON Oversight Process
The Director of Nursing or designee will review all transfer packets within 24 hours of any resident transfer to ensure accuracy and completeness.

4. Monitoring to Ensure Ongoing Compliance

The DON or designee will conduct audits as follows:
- 100% of all transfers weekly × 4 weeks
- 50% of transfers weekly × 8 weeks

Audits will verify that all required information under §483.15(c)(2)(iii) was transmitted, including care plan goals, advance directives, practitioner contact information, representative information, special instructions, and clinical summaries.
Audit findings will be reviewed monthly during Quality Assurance Performance Improvement meeting.
Any identified non-compliance will result in immediate re-education and repeated focused audits until sustained compliance is demonstrated.

5. Completion Date

The facility will be in full compliance on or before: 1/5/2026



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 promote cleanliness and help prevent the spread of infection regarding respiratory care equipment for two of four residents reviewed for respiratory care (Residents R4 and R49).

Findings include:

Review of facility policy entitled "Oxygen Administration" dated 11/3/25, indicated "Concentrator filters cleaned weekly on night shift."

Review of resident R4's clinical record revealed an admission date of 8/8/25, with diagnoses that included chronic obstructive pulmonary disease (COPD) (a disease that obstructs air flow from the lungs), heart failure (a condition where the heart cannot supply the body with enough blood), and diabetes (a health condition that is caused by the body's inability to produce enough insulin).

Review of Resident R4's physician's orders revealed an order dated 8/8/25, for oxygen between two and four liters 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) continuously.

Review of Resident R4's care plan for COPD revealed an intervention of oxygen between two and four liters continuously.

Review of Resident R4's tasks (an area in the clinical record where nursing assistant document) revealed a task for oxygen tubing/cannula change/concentrator filter cleaned.

Observations on 11/17/25, at 1:55 p.m. and again at 2:25 p.m. revealed Resident R4 lying in his/her bed with oxygen being administered. Further observations revealed a filter on the back of his/her oxygen concentrator that had a large amount of a fluffy white substance covering the filter.

Review of Resident R49's clinical record revealed an admission date of 12/5/25, with diagnoses that included COPD, congestive heart failure (the inability of the heart to maintain an adequate supply of blood to organs and tissues), and chronic respiratory failure (a condition where your lungs don't exchange air properly).

Review of Resident R49's physician's orders revealed an order dated 4/15/19, for oxygen at two liters via nasal cannula every evening and night shift.

Review of Resident R49's care plan for congestive heart failure revealed an intervention of oxygen at two liters per minute at hour of sleep.

Review of Resident R49's tasks revealed a task for oxygen tubing/cannula change/concentrator filter cleaned.

Observations on 11/17/25, at 1:08 p.m. and again at 2:25 p.m. revealed Resident R4's oxygen concentrator sitting in his/her room with the nasal cannula lying over the concentrator and the nasal cannula touching the floor. Further observations revealed a filter on the back of his/her oxygen concentrator that had a large amount of a fluffy white substance covering the filter.

During an interview on 11/17/25, at 2:32 p.m. Registered Nurse (RN) Employee E1 confirmed that Resident's R4 and R49's oxygen concentrator filters were covered in a large amount of a white fluffy substance and that Resident R49's nasal cannula was touching the floor. RN Employee E1 also confirmed that the oxygen concentrator filters should be clean, and the nasal cannula should not be on the floor.

28 Pa. Code 211.10(c) Resident care policies

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







 Plan of Correction - To be completed: 01/05/2026

1. Corrective Action for Residents Identified as Affected
Resident R4 and R49
The oxygen concentrator filters were immediately removed, cleaned, and replaced per manufacturer guidelines.
The cannula and tubing were replaced with new supplies
The residents' oxygen concentrators were inspected for function and cleanliness.
The nurse aide task list was reviewed to ensure proper tracking of tubing changes and filter cleaning and encouragement of as needed (PRN) cleaning/changes.

Director of Nursing and Assistant Director of Nursing provided Nurse aide staff re-education on proper handling and storage of oxygen tubing.

2. Identification of Other Residents Who May Have Been Affected
Director of Nursing/Assistant Director of Nursing conducted a facility-wide audit on all residents receiving oxygen therapy
The audit included:
Inspection of all oxygen concentrator filters
Review of tubing placement to ensure it is not touching the floor
Verification of tubing and cannula change dates
Verification that Nurse Aide task lists correctly included tubing changes and filter cleaning
Any resident found with unclean filters or improperly stored tubing received immediate corrective action and new supplies.

3. Systemic Changes to Prevent Recurrence
A. Policy Review and Revision
The "Oxygen Administration policy was reviewed by the Director of Nursing to ensure it contains the following elements:
Required weekly filter cleaning responsibilities, times, and documentation steps.
Clear instructions prohibiting tubing/cannulas from touching the floor.
Requirement that staff visually inspect concentrators and tubing each shift.
Infection-control expectations consistent with professional standards of practice and §483.25(i).
B. Staff Education
Director of Nursing and Assistant Director of Nursing educated all nursing staff (Registered Nurses, License Practical Nurse, and Nurse Aides) were in-serviced on:
Proper oxygen concentrator maintenance
Weekly and PRN filter cleaning protocol and documentation
Correct storage/placement of cannulas and tubing
Infection prevention related to respiratory equipment
Consequences of improper handling (infection risk, equipment failure, compromised oxygen delivery)
C. Environmental & Equipment Management Improvements
- Each concentrator now includes a labeling tag showing:
Date filter last cleaned
Next cleaning due date
Staff initials
The night shift supervisor will ensure filter cleaning per policy.
Hooks installed in all rooms to hang oxygen tubing when not in use

4. Monitoring & Quality Assurance to Ensure Ongoing Compliance
To maintain compliance:
Short-Term Monitoring
The DON or designee will audit 100% of residents on oxygen weekly for 4 weeks, checking:
Cleanliness of concentrator filters
Proper placement of tubing/cannula
Documentation of filter cleaning and tubing changes
Functionality and safety of respiratory equipment
Long-Term Monitoring
After the initial 4 weeks, audits will be conducted monthly for 3 months.
Any identified non-compliance will result in immediate corrective action and re-education.
QAPI Oversight
All audit findings will be reviewed at monthly Quality Assurance Performance Improvement meetings.

5. Date the Facility Will Achieve Full Compliance
The Lutheran Home at Kane will be in full compliance with F695 by:
January 5, 2026.

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 appropriately discard outdated medications for one of two medication carts reviewed (300 hall medication cart).

Findings include:

Review of facility policy entitled "Storage of Medications" dated 11/3/25, indicated "Discontinued, outdated, or deteriorated drugs or biologicals are returned to the dispensing pharmacy or destroyed.

Review of manufacturer's guidelines revealed that an open pen of Lispro Insulin must be used within 28 days after opening or be discarded, even if the vial still contains insulin.

Observation of drug storage on 11/17/25, at 12:55 p.m. of the 300-hall medication cart revealed an open Lispro Insulin pen with an open date of 10/3/25, and an expiration date of 10/31/25.

During an interview on 11/17/25, at the time of observation Licensed Practical Nurse Employee E2 confirmed that the open Lispro insulin pen was beyond the expiration date and also confirmed that the insulin pen should have been discarded.


28. Pa. Code 201.18(b)(1) Management

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

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




 Plan of Correction - To be completed: 01/05/2026

1. Immediate Corrective Action for Identified Deficiency
- The expired Lispro insulin pen on the 300 Hall medication cart (open date 10/3/25, expiration 10/31/25) was immediately removed and discarded according to facility policy and manufacturer guidelines.
- The medication cart was inspected, and all other medications were reviewed to ensure none were expired or beyond manufacturer-recommended use dates.
2. Facility-Wide Identification Audit:
- The Director of Nursing/Assistant Director of Nursing completed a facility-wide audit of all medication carts and medication rooms was conducted to identify any expired, discontinued, or deteriorated medications or biologicals.

Audit included:
Verification of expiration dates on all medications, including multi-dose vials and insulin pens.
Verification that multi-dose vials and pens were labeled with the date opened and expiration per manufacturer guidelines.
Documentation of all audit findings and corrective actions was completed.

3. Systemic Changes to Prevent Recurrence
A. Policy Review
The facility's "Storage of Medications" policy was reviewed by the Director of Nursing to ensure the following are included:
Explicit requirement to discard medications or biologicals beyond expiration, including manufacturer-specific use guidelines for multi-dose vials or insulin pens.
Requirement to label multi-dose medications and insulin pens with date opened.
B. Staff Education
All licensed nursing staff (Registered Nurse, Licensed Practical Nurses) and medication administration staff were in-serviced on:
Facility policy on medication expiration, labeling, and discard requirements.
Manufacturer guidelines for multi-dose vials and insulin pens.
Proper storage of medications and controlled substances.
Documentation and audit procedures for medication safety.

4. Ongoing Monitoring & Quality Assurance
Registered Nurses (who do not typically pass medications) will conduct ongoing weekly audits of all medication carts and medication storage areas, including:
Expiration and open-date verification
Proper labeling
Compliance with locked storage requirements
Any deficiencies will result in immediate corrective action and staff re-education.
Audit results will be reported to the Quality Assurance Performance Improvement meetings for review and trending.
Recurrent non-compliance will trigger escalation of corrective action, including retraining and potential disciplinary measures.
Audits will continue weekly ongoing to ensure compliance.

5. Date the Facility Will Be in Full Compliance
The Lutheran Home at Kane will achieve full compliance with F761 by: January 5, 2026.

483.20(g)(h)(i)(j) 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.

§483.20(h) Coordination. A registered nurse must conduct or coordinate each assessment with the appropriate participation of health professionals.

§483.20(i) Certification.
§483.20(i)(1) A registered nurse must sign and certify that the assessment is completed.
§483.20(i)(2) Each individual who completes a portion of the assessment must sign and certify the accuracy of that portion of the assessment.

§483.20(j) Penalty for Falsification.
§483.20(j)(1) Under Medicare and Medicaid, an individual who willfully and knowingly-
(i) Certifies a material and false statement in a resident assessment is subject to a civil money penalty of not more than $1,000 for each assessment; or
(ii) Causes another individual to certify a material and false statement in a resident assessment is subject to a civil money penalty or not more than $5,000 for each assessment.
§483.20(j)(2) Clinical disagreement does not constitute a material and false statement.
Observations:

Based on review of clinical records and staff interviews, it was determined that the facility failed to accurately code the Minimum Data Set (MDS-periodic assessment of resident care needs) for one of 18 residents reviewed (Resident R3).

Findings include:

Resident R3's clinical record revealed an admission date of 12/30/24, with diagnoses that included hypertension (high blood pressure), hyperlipidemia (high cholesterol), and heart failure (a condition where the heart cannot supply the body with enough blood).

Review of Resident R3's MDS dated 10/2/25, Section P Restraints and Alarms under P0100 physical restraints revealed documentation under used in bed A. Bed rail was coded 1. Used less than daily.

Review of Resident R3's clinical record lacked evidence that any type of physical restraint was being utilized.

During an interview on 11/18/25, at 1:15 p.m. the Registered Nurse Assessment Coordinator confirmed that Resident R3 was not currently utilizing a restraint and also confirmed that Section P0100 of the MDS dated 10/2/25, was incorrectly coded for Resident R3 regarding use of a physical restraint.

28 Pa. Code 211.5(ix) Medical records

28 Pa. Code 201.14 (a) Responsibility of Licensee






 Plan of Correction - To be completed: 01/05/2026

I hereby acknowledge the CMS 2567-A, issued to The Lutheran Home at Kane for the survey ending 11/19/2025, AND attest that all deficiencies listed on the form will be corrected in a timely manner.

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