Summers County Arh Hospital Laboratory

CLIA Laboratory Citation Details

3
Total Citations
22
Total Deficiencyies
11
Unique D-Tags
CMS Certification Number 51D0661760
Address 115 Summers Hospital Road, Hinton, WV, 25951
City Hinton
State WV
Zip Code25951
Phone(304) 466-1000

Citation History (3 surveys)

Survey - May 1, 2024

Survey Type: Standard

Survey Event ID: 7EEW11

Deficiency Tags: D0000 D2093 D5403 D5411 D5545 D2093 D5403 D5411 D5545 D5775 D5775

Summary:

Summary Statement of Deficiencies D0000 A routine recertification survey was performed at Summers County ARH Hospital Laboratory, April 30 and May 1, 2024, by the West Virginia Office of Laboratory Services. The laboratory was assessed for compliance with the Federal Clinical Laboratory Improvement Amendments (CLIA) regulations under 42 CFR 493. Specific deficiencies are explained below. D2093 ROUTINE CHEMISTRY CFR(s): 493.841(d) Failure to return proficiency testing results to the proficiency testing program within the time frame specified by the program is unsatisfactory performance and results in a score of 0 for the testing event. This STANDARD is not met as evidenced by: Based on record review and interview the laboratory failed to return proficiency testing (PT) results to the American Proficiency Institute (API) program by the submission date for one of three routine chemistry events in 2023. Findings: 1. Review of API records revealed unsatisfactory scores for the Routine Chemistry 2nd event of 2023: 0% pH Blood Gas (#0315) 0% PO2 Blood gas (#0325) 0% PCO2 Blood Gas (#0335) 2. Review of the laboratory

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Survey - April 20, 2022

Survey Type: Special, Standard

Survey Event ID: DJ8111

Deficiency Tags: D0000 D5211 D5555 D5791 D0000 D5211 D5555 D5791

Summary:

Summary Statement of Deficiencies D0000 An announced, on site, routine recertification survey was conducted at Summers County ARH Hospital Laboratory on April 19th and April 20th of 2022, by the West Virginia Office of Laboratory Services. The laboratory was assessed for compliance with the Federal Clinical Laboratory Improvement Amendment (CLIA) regulations under 42 CFR 493. Specific deficiencies are explained below. D5211 EVALUATION OF PROFICIENCY TESTING PERFORMANCE CFR(s): 493.1236(a) The laboratory must review and evaluate the results obtained on proficiency testing performed as specified in subpart H of this part. This STANDARD is not met as evidenced by: Based on record review and interview the laboratory failed to document the evaluation of results for 5 of 5 College of American Pathologists (CAP) proficiency testing (PT) events in Immunohematology for 2021. Findings: 1. Review of 2021 CAP Immunohematology PT records identified 5 of 5 event results had no documentation of review by the technical supervisor. 2. Review of the 2nd event 2021 identified a score of 80% for the analyte 0855 Antibody Detection. No

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Survey - September 16, 2020

Survey Type: Standard

Survey Event ID: UVIT11

Deficiency Tags: D2000 D3015 D3015

Summary:

Summary Statement of Deficiencies D2000 ENROLLMENT AND TESTING OF SAMPLES CFR(s): 493.801 Each laboratory must enroll in a proficiency testing (PT) program that meets the criteria in subpart I of this part and is approved by HHS. The laboratory must enroll in an approved program or programs for each of the specialties and subspecialties for which it seeks certification. The laboratory must test the samples in the same manner as patients' specimens. For laboratories subject to 42 CFR part 493 published on March 14, 1990 (55 FR 9538) prior to September 1, 1992, the rules of this subpart are effective on September 1, 1992. For all other laboratories, the rules of this subpart are effective January 1, 1994. This CONDITION is not met as evidenced by: Based on a review of the laboratory American Proficiency Institute (API) proficiency testing (PT) records and an interview with the laboratory manager, the laboratory failed to enroll in an approved program for Microbiology and Routine Chemistry for the 1st and 2nd testing events of 2020 and no other testing was performed to establish and maintain the accuracy of the testing procedures, in accordance with 493.1236 (c) (1). Findings: 1. A review of 2019 and 2020 API PT records identified no enrollment for Microbiology- Bacteriology PT of the Film Array BioFire GI panel, Respiratory panel, and Meningitis panel for testing events 1 and 2 of 2020. 2. A review of 2019 and 2020 API PT records identified no enrollment for Chemistry- Core Chemistry and Hematology PT of Respiratory Therapy testing pCO2, pH, pO2, Carboxyhemoglobin, Hemoglobin (Blood Oximetry), Methemoglobin, and Oxyhemoglobin for testing events 1 and 2 of 2020. 3. A review of the PT records for the API Microbiology and Core Chemistry 2020 testing events (1 and 2), identified an investigation and

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