Coral Springs Holistic Pediatrics Llc

CLIA Laboratory Citation Details

3
Total Citations
8
Total Deficiencyies
7
Unique D-Tags
CMS Certification Number 10D1054722
Address 9750 Nw 33rd St Ste 216, Coral Springs, FL, 33065
City Coral Springs
State FL
Zip Code33065
Phone(954) 752-8446

Citation History (3 surveys)

Survey - May 12, 2022

Survey Type: Special

Survey Event ID: DSGJ11

Deficiency Tags: D2016 D6000 D0000 D2130 D6016

Summary:

Summary Statement of Deficiencies D0000 A desk review survey of the laboratory's proficiency test results was performed on May 12, 2022 for Coral Springs Holistic Pediatrics. Coral Springs Holistic Pediatrics is not in compliance with the Code of Federal Regulations (CFR), Part 493, Laboratory Requirements. 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 review of the laboratory's proficiency testing records for 2021 and 2022, the laboratory did not have successful performance in proficiency testing in the specialty of hematology. Refer to D2130. Findings include: Review of the American Proficiency Institute (API) proficiency testing records and the review of the Centers 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 -- for Medicare & Medicaid Services (CMS) 153 and 155 reports, on May 12, 2022 on or about 10:00 AM, showed that the laboratory had unsatisfactory testing scores for the analytes, white blood cell count (WBC), red blood cell count (RBC), hemoglobin (HGB), hematocrit (HCT), platelets (PLT), and white blood cell differential (WBC Diff) for two out of three testing events in 2021 and 2022. 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 the review of the Centers for Medicare & Medicaid Services (CMS) 153 and 155 reports and the laboratory's proficiency testing records, the laboratory did not have successful performance in proficiency testing in the specialty of hematology for the listed analytes. Findings include: On May 12, 2022 on or about 10:00 AM the American Proficiency Institute (API) proficiency testing records and the CMS 153 and 155 reports were reviewed. The review showed that the laboratory failed to achieve satisfactory performance for the analytes, WBC, RBC, HGB, HCT, PLT, WBC Differential, as shown below. Event #2, 2021 WBC-0% RBC-0% HGB-0% HCT-0% PLT-0% WBC Differential-0% Event #1, 2022 WBC-0% RBC-0% HGB- 0% HCT-0% PLT-0% WBC Differential-0% 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 the review of the laboratory's proficiency testing records, the laboratory director failed to ensure that the laboratory maintained a satisfactory score in proficiency testing for analytes found in the specialty of hematology. Findings include: On May 12, 2022, on or about 10:00 AM, the American Proficiency Institute (API) proficiency records and the Centers for Medicare & Medicaid Service (CMS) 153 and 155 reports were reviewed. The review showed that the laboratory had unsatisfactory testing scores for two out of three testing events for the analytes, WBC, RBC, HGB, HCT, PLT, WBC differential, in the specialty of hematology. The laboratory director is responsible for ensuring that the laboratory maintains successful participation in proficiency testing. Refer to D2130. D6016 LABORATORY DIRECTOR RESPONSIBILITIES 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 -- 2 of 3 -- required under Subpart H of this part; This STANDARD is not met as evidenced by: Based on the review of the laboratory's proficiency testing scores, the laboratory director failed to ensure that the laboratory performed proficiency testing in such a manner as to achieve and maintain successful participation in proficiency testing for analytes found in the specialty of hematology. Findings Include: The review of the American Proficiency Institute (API) proficiency testing records and the Centers for Medicare & Medicaid Services (CMS) 153 and 155 reports on May 12, 2022, on or about 10:00 AM showed that the laboratory received unsatisfactory proficiency testing scores for two out of three testing events for the analytes shown below. Event #2, 2021 WBC-0% RBC-0% HGB-0% HCT-0% PLT-0% WBC Differential-0% Event #1, 2022 WBC-0% RBC-0% HGB-0% HCT-0% PLT-0% WBC Differential- 0% -- 3 of 3 --

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Survey - January 7, 2021

Survey Type: Standard

Survey Event ID: IBTD11

Deficiency Tags: D0000 D2128

Summary:

Summary Statement of Deficiencies D0000 A recertification survey conducted on 1/6/2021 to1/7/2021, found the Coral Springs Holistic Pediatrics clinical laboratory was not in compliance with 42 CFR Part 493, Requirements for Laboratories. D2128 HEMATOLOGY CFR(s): 493.851(e) (1) For any unsatisfactory analyte or test performance or testing event for reasons other than a failure to participate, the laboratory must undertake appropriate training and employ the technical assistance necessary to correct problems associated with a proficiency testing failure. (2) For any unacceptable analyte or testing event score, remedial action must be taken and documented, and the documentation must be maintained by the laboratory for two years from the date of participation in the proficiency testing event. This STANDARD is not met as evidenced by: Based on record review and interview, the laboratory failed to receive a passing analyte score of 80 % for white blood cell differential , granulocytes, monocytes/mids and lymphocytes in hematology for the second proficiency testing (PT)event of American Proficiency Institute (API) in 2020. Findings Included: Review of the API proficiency testing revealed the laboratory received unsatisfactory analyte scores in the second event of PT for hematology in 2020 for the following : 1. White blood cell differential received a score of 33%. 2. Granulocytes received a score of 0%. 3. Monocytes/Mids received a score of 40%. 4. Lymphocytes received a score of 60%. On 1-6-2021 at 3:34pm , The office manager confirmed the laboratory did not receive a passing analyte score of 80 % for white blood cell differential , granulocytes, monocytes/mids and lymphocytes in hematology for the second PT event of API in 2020. 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 - October 18, 2018

Survey Type: Standard

Survey Event ID: FHD111

Deficiency Tags: D5413

Summary:

Summary Statement of Deficiencies D5413 TEST SYSTEMS, EQUIPMENT, INSTRUMENTS, REAGENT CFR(s): 493.1252(b) The laboratory must define criteria for those conditions that are essential for proper storage of reagents and specimens, accurate and reliable test system operation, and test result reporting. The criteria must be consistent with the manufacturer's instructions, if provided. These conditions must be monitored and documented and, if applicable, include the following: (1) Water quality. (2) Temperature. (3) Humidity. (4) Protection of equipment and instruments from fluctuations and interruptions in electrical current that adversely affect patient test results and test reports. This STANDARD is not met as evidenced by: Based on Hematology analyzer Drew 3 user manual review and interview with testing personnel (TP) # A, the laboratory failed to document room temperature and humidity requirement to assure optimal operation of the analyzer during 2016, 2017, 2018. Findings include: Review of the Drew 3 manual indicates that the operation temperature range is 18 to 32 C and humidity below 80 %. There was no log available for documenting the temperature and humidity of the laboratory room. During an interview on 10/18/2018 at 11:30 a.m., the TP # A confirmed that there was no documentation of room and humidity control check. 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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