Queen's Cancer Center Kuakini

CLIA Laboratory Citation Details

2
Total Citations
3
Total Deficiencyies
3
Unique D-Tags
CMS Certification Number 12D0699363
Address 321 N Kuakini St #402, Honolulu, HI, 96817
City Honolulu
State HI
Zip Code96817
Phone(808) 691-8777

Citation History (2 surveys)

Survey - September 3, 2024

Survey Type: Standard

Survey Event ID: U2Q911

Deficiency Tags: D5221 D6019

Summary:

Summary Statement of Deficiencies D5221 EVALUATION OF PROFICIENCY TESTING PERFORMANCE CFR(s): 493.1236(d) All proficiency testing evaluation and verification activities must be documented. This STANDARD is not met as evidenced by: Based on a review of American Association of Bioanalysts (AAB) proficiency testing records and an interview with the testing personnel on 09/03/2024 at 3:00 PM, it was revealed that the laboratory failed to ensure its hematology proficiency testing evaluation and verification activities were documented. The findings include: 1. 2023 Nonchemistry M1 event: The laboratory reported an Erythrocytes-3 part diff result of 4.07 on Specimen 1. The intended response range was 4.12 to 4.64. 2. 2023 Nonchemistry (Blood cell identification) M2 event: The laboratory reported Bacteria for Specimen 10. The intended response was Yeast. 3. 2023 Nonchemistry (Educational Challenge) M2 Event: The laboratory reported Lymphocyte; atypical, Downey, variant for Specimen 6. The intended response was Blast undifferentiated. The testing personnel stated the laboratory selected the wrong result code as it does not report abnormal hematology slide results. 4. 2024 Nonchemistry (Blood cell identification) M1 event: The laboratory reported Metamyelocyte for Specimen 3. The intended response was Myelocyte. The testing personnel stated the laboratory selected the wrong result code was it does not report abnormal hematology slide results. 5. 2024 Nonchemistry (Blood cell identification) M2 event: The laboratory reported Monocyte, any stage for Specimen 10. The intended response was Lymphocyte, reactive. 6. The testing personnel stated the laboratory's AAB Medical Laboratory Evaluation (MLE) Proficiency Testing Service Proficiency Test

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Survey - March 11, 2021

Survey Type: Standard

Survey Event ID: 0NM511

Deficiency Tags: D6107

Summary:

Summary Statement of Deficiencies D6107 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1445(e)(15) The laboratory director must specify, in writing, the responsibilities and duties of each consultant and each supervisor, as well as each person engaged in the performance of the preanalytic, analytic, and postanalytic phases of testing, that identifies which examinations and procedures each individual is authorized to perform, whether supervision is required for specimen processing, test performance or result reporting and whether supervisory or director review is required prior to reporting patient test results. This STANDARD is not met as evidenced by: Based on a review of laboratory procedures and an interview with the General Supervisor and testing personnel on 03/11/2021 at 3:00 p.m., it was determined that the Laboratory Director failed to specify in writing, the responsibilities and duties of each consultant and supervisor, as well as each person engaged in the pre-analytic, analytic, and post analytic phases of hematology testing, that identifies which examinations and procedures each individual is authorized to perform, whether supervision is required for specimen processing test performance or result reporting and whether supervisory or director review is required prior to reporting patient test results. The findings include: 1. The testing personnel stated her responsibilities and duties were described in the Laboratory Manager Job Description to include Administrative Duties, Efficient Workflow Environment, Quality Control, Maintenance and Education. The Laboratory Manager Job Description stated that the testing personnel was responsible to "establish quality standards, supervise QC, inspect staff's work and adjusts laboratory policies and procedures as needed when standards are not met". For high complexity testing, the Laboratory Director may delegate the establishment and maintenance of quality assessment and quality control programs to the Technical Supervisor. The Laboratory Director was designated as the Technical Supervisor on the Laboratory Personnel Report Form CMS 209. 2. The Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 2 -- responsibilities and duties delegated by the Laboratory Director to the General Supervisor were not available for review. -- 2 of 2 --

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