East Side Oncology Associates Pllc

CLIA Laboratory Citation Details

2
Total Citations
12
Total Deficiencyies
6
Unique D-Tags
CMS Certification Number 33D2143178
Address 35 West 45th Street, 6th Floor, New York, NY, 10036
City New York
State NY
Zip Code10036
Phone212 400-8384
Lab DirectorROBERT GELFAND

Citation History (2 surveys)

Survey - October 3, 2023

Survey Type: Standard

Survey Event ID: X9IZ11

Deficiency Tags: D2009 D2009

Summary:

Summary Statement of Deficiencies D2009 TESTING OF PROFICIENCY TESTING SAMPLES CFR(s): 493.801(b)(1) The individual testing or examining the samples and the laboratory director must attest to the routine integration of the samples into the patient workload using the laboratory's routine methods. This STANDARD is not met as evidenced by: Based on review of the proficiency testing (PT) results and interview with the testing personnel (TP), the laboratory director (LD) failed to sign the proficiency testing attestation form. Findings: 1. It was noted that TP signed and dated the American Proficiency Institute attestation forms from 2021 through 2023; however, there was no documentation of LD review and signature. 2. Electronic PT result submissions did not include a signed copy of the online attestation form. 3. Confirmed findings by interview with the TP on October 3, 2023, at 12:30 P.M. Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 1 --

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Survey - April 20, 2020

Survey Type: Special

Survey Event ID: RWF511

Deficiency Tags: D2016 D2130 D2131 D6000 D6016 D2016 D2130 D2131 D6000 D6016

Summary:

Summary Statement of Deficiencies D2016 SUCCESSFUL PARTICIPATION CFR(s): 493.803(a)(b)(c) (a) Each laboratory performing nonwaived testing must successfully participate in a proficiency testing program approved by CMS, if applicable, as described in subpart I of this part for each specialty, subspecialty, and analyte or test in which the laboratory is certified under CLIA. (b) Except as specified in paragraph (c) of this section, if a laboratory fails to participate successfully in proficiency testing for a given specialty, subspecialty, analyte or test, as defined in this section, or fails to take remedial action when an individual fails gynecologic cytology, CMS imposes sanctions, as specified in subpart R of this part. (c) If a laboratory fails to perform successfully in a CMS- approved proficiency testing program, for the initial unsuccessful performance, CMS may direct the laboratory to undertake training of its personnel or to obtain technical assistance, or both, rather than imposing alternative or principle sanctions except when one or more of the following conditions exists: (1) There is immediate jeopardy to patient health and safety. (2) The laboratory fails to provide CMS or a CMS agent with satisfactory evidence that it has taken steps to correct the problem identified by the unsuccessful proficiency testing performance. (3) The laboratory has a poor compliance history. This CONDITION is not met as evidenced by: Based on a proficiency testing (PT) desk review of the Center for Medicare and Medicaid Services (CMS) PT reports and PT records from the American Proficiency Institute (API) PT program, the laboratory failed to participate and perform successfully in a PT program, approved by CMS, for the specialty Hematology and the test analytes Cell Identification (Cell I.D.)/White Blood Cell Differential (WBC Diff.) Red Blood Cell Count (RBC), Hematocrit (Hct), Hemoglobin (Hgb), White Blood Cell Count (WBC) and Platelet. The following scores were assigned Specialty Hematology 2019 second event = 36% 2019 third event = 100% 2020 first event = 0% [non-participation] WBC/RBC/Hct/Hgb/Cell I.D. 2019 second event = 40% 2019 Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 3 -- third event = 100% 2020 first event = 0% [non-participation] Platelet 2019 second event = 20% 2019 third event = 100% 2020 first event = 0% [non-participation] This is considered unsuccessful PT performance. Refer to D2130 and D2131. D2130 HEMATOLOGY CFR(s): 493.851(f) Failure to achieve satisfactory performance for the same analyte in two consecutive events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on a PT desk review of the CMS PT reports and PT records from the API PT program, the laboratory failed to participate and perform successfully in a PT program, approved by CMS, for the test analytes Cell I.D., RBC, WBC, Hct, Hgb and Platelets. The following scores were assigned Cell I.D./RBC/WBC/Hct/Hgb 2019 second event = 40% 2019 third event = 100% 2020 first event = 0% [non- participation] Platelets 2019 second event = 20% 2019 third event = 100% 2020 first event = 0% [non-participation] This is considered unsuccessful PT performance. D2131 HEMATOLOGY CFR(s): 493.851(g) Failure to achieve an overall testing event score of satisfactory performance for two consecutive testing events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on a proficiency testing (PT) desk review of the Center for Medicare and Medicaid Services (CMS) PT reports and PT records from the American Proficiency Institute (API) PT program, the laboratory failed to participate and perform successfully in a PT program, approved by CMS, for the specialty Hematology. The following scores were assigned 2019 second event = 36% 2019 third event = 100% 2020 first event = 0% [non-participation] This is considered unsuccessful PT performance. D6000 MODERATE COMPLEXITY LABORATORY DIRECTOR CFR(s): 493.1403 The laboratory must have a director who meets the qualification requirements of 493. 1405 of this subpart and provides overall management and direction in accordance with 493.1407 of this subpart. This CONDITION is not met as evidenced by: Based on PT desk review of the PT CMS data reports and API PT program records, the laboratory director failed to fulfill the laboratory director's responsibilities and ensure that the laboratory achieved a satisfactory performance and successfully participate in a PT program, for the specialty Hematology and test analytes WBC, RBC, Cell I.D., Hct, Hgb and Platelets. Refer to D6016. D6016 LABORATORY DIRECTOR RESPONSIBILITIES -- 2 of 3 -- CFR(s): 493.1407(e)(4)(i) The laboratory director is responsible for the overall operation and administration of the laboratory, including the employment of personnel who are competent to perform test procedures, and record and report test results promptly, accurate, and proficiently and for assuring compliance with the applicable regulations. (e) The laboratory director must-- (e)(4)(i) Ensure that the proficiency testing samples are tested as required under Subpart H of this part; This STANDARD is not met as evidenced by: Based on PT desk review of the PT CMS data reports and API PT program records, the laboratory director failed to fulfill the laboratory director's responsibilities and ensure that the laboratory achieved a satisfactory performance and successfully participate in a PT program, for the specialty Hematology and the test analytes WBC, RBC, Cell I.D., Hct, Hgb and Platelets. The following scores were assigned: Specialty Hematology 2019 second event = 36% 2019 third event = 100% 2020 first event = 0% [non-participation] WBC/RBC/Hct/Hgb/Cell I.D. 2019 second event = 40% 2019 third event = 100% 2020 first event = 0% [non-participation] Platelet 2019 second event = 20% 2019 third event = 100% 2020 first event = 0% [non-participation] This is considered unsuccessful PT performance. . -- 3 of 3 --

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