
It is the policy of DSI Laboratories to provide services in
compliance with all state and federal governance for all operations.
We strive to be consistent with the highest standards of business
and professional ethics. Examples of such policy topics include
but are not limited to, patient confidentiality, diagnosis
coding, anti-kickback statutes, professional courtesy and
medical necessity practices. DSI is committed to compliance
with all applicable regulatory agencies including but not
limited to CLIA, State of Florida Agency for Health Care Administration,
the Centers for Medicare and Medicaid (CMS) and the College
of American Pathologists. It is our expectation that organizations
and individuals utilizing our services have instituted similar
policies to ensure compliance with regulatory requirements.
DSI encourages all personnel and clients to contact the Compliance
Officer if they have any concerns regarding compliance issues
and that all such inquiries or comments will be kept in the
strictest confidence possible consistent with the need to
investigate all situations.
DSI Laboratories is committed to comply with the Health
Insurance Portability and Accountability Act (HIPAA) Privacy,
Security and Electronic Transmission Standards. DSI has
implemented policies, processes and procedures designed
to secure the protected health information (PHI) provided
to us by our patients and their providers. Audits are conducted
for compliance and effectiveness.
The State of Florida Agency for Health Care Administration
limits the information that can be shared directly with
patients under Florida Administrative Code 59A-7.000. Laboratory
results must be reported directly to the authorized person
who has ordered the test. Because the laws of Florida are
more strict than those of HIPAA, we are not permitted to
release results to patients unless we are instructed to
do so by the ordering authority. Other information such
as billing data can be released to the patient or designated
entity with an appropriate release form. Please contact
the Compliance Officer for specific instructions.

DSI Laboratories has a rigorous Quality Assurance program
located here in our regional facilities that monitors and
audits all instrumentation used in processing the specimens
we receive from our clients. All instruments are tested and
calibrated on a regular basis to ensure quality results. Spot
checks are performed and specimens are re-tested at random
intervals to monitor performance.
All DSI Laboratories participate in the College of American
Pathologists Proficiency Testing Programs in which unknown
samples are analyzed and the results compared to other laboratories
in the United States. In addition, each assay contains a
minimum of one normal and abnormal control period. All results
are correlated and processed daily. If an analyte shows
a variation greater than expected for the procedure, the
testing system is reviewed and corrective action is taken.
A preventative maintenance program is in place to be efficiency
of each instrument within the Laboratory.
Inspection programs by the College of American Pathologists
consist of a CAP-appointed panel of practicing Pathologists
and other laboratory professionals from the state of Florida.
Our laboratories have consistently scored well in both proficiency
and inspection programs and are fully accredited. All DSI
laboratories are also inspected and accredited by the State
of Florida.
DSI Laboratories Compliance Department randomly audits
requisitions or orders from all clients. Each requisition
or order is monitored for 26 different items to ensure accurate
reporting and testing of specimens and the best quality
care possible. Some of the items audited are ensuring all
necessary information, such as diagnosis or patient information,
is on the requisitions or orders and correctly entered into
our systems. Other audit items ensure the correct tests
are ordered and results are sent to all necessary providers.
Our Compliance area also provides education for all Registration
Associates, and works with the Marketing area to provide
necessary information for our Clients. The Compliance and
Billing areas have worked extensively with our local Medicare
Part B provider to ensure we have up to date Medicare Advance
Beneficiary Notice information, which is shared with our
Clients.
The Compliance area also audits the billing process. In
this area, claims are randomly checked to ensure all information
gathered at Registration is carried accurately through to
the billing process. The billing process is further audited
to ensure compliance with Medicare and Medicaid regulations.
Billing processes are carefully monitored to ensure any
overpayments are returned promptly to the correct payor
either through refund checks or notification to carriers
so they can deduct overpayments from future remittances.
All orders must be submitted in writing by a licensed practitioner
authorized to order laboratory tests. DSI provides test
requisitions which may be preprinted with the clients
name and address and tailored to their practice. Instructions
for completion of test requisitions are listed in the General
Collection Guidelines section of this manual. There are
standard panels and profiles that DSI performs based on
AMA approved CPT codes. All reflex testing and additional
panels and profiles are outlined in the Test Directory section
of this manual which is also available online.
Reflex Profiles are tests that provide our clients with a screening test which will automatically generate an order for a confirmatory or additional test(s) according to our established protocol. This ordering convenience eliminates any delays in obtaining additional testing. This list provides the commonly ordered reflex panels offered by our laboratory. In many cases, the profile is the default order. Please refer to the requisition or ordering manual at www.dsilabs.com which identifies and explains all reflex profiles. If you wish to order a test without reflex, please specify these instructions on your order. Reflex testing may incur additional charges for the additional testing.
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| 3502521 |
Urinalysis
- Urinalysis with Reflex Microscopic
(microscopic performed only if chemstrip is positive)
- Chemstrip Urinalysis
- Microscopic Urinalysis
|
81001*
81003
81015 |
| 3502531 |
Urinalysis
- Urinalysis with Reflex Microscopic
& Culture
(microscopic performed only if chemstrip is positive;
culture performed if chemstrip or microscopic
is positive)
- Chemstrip Urinalysis
- Microscopic Urinalysis
- Urine Culture (Organism Identification
/ Organism Susceptibility (billed separately at
additional charge)
|
81001*
81003
81015
87086 |
| 1008200 |
Hepatitis B
Panel
- Hepatitis B Virus Surface Antigen,
Hepatitis B Core Antibody, Total, and Hepatitis
B Surface Antibody with Reflex to Hepatitis B
Core Antibody, IgM
- Hepatitis B Surface Antigen (HbsAg)
- Hepatitis B Surface Antibody (anti-HBs)
- Hepatitis B Core Antibody,
Total (Combined IgG & IgM) [anti-HBc (Total)]*
- Hepatitis B Core Antibody, IgM
(Acute) [anti-HBc (IgM)]
*If anti-HBc Total is 'positive', anti-HBc (IgM)
reflex testing is performed to determine whether
the patient has "acute" infection with
Hepatitis B Virus
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87340
86706
86704
86705 |
| 5000460 |
Hepatitis B
Surface Antigen
- Hepatitis B Surface Antigen with
Reflex to Hepatitis B Surface Antigen Neutralization
Confirmatory Test
- (Neutralization procedure performed
if HBsAg is positive)
- Hepatitis B Surface Antigen (HbsAg)(cannot
be ordered separately)
- Hepatitis B Surface Antigen Neutralization
Confirmatory Test(cannot be ordered separately)
|
87340
86382 |
| 2000880 |
Sickle Screen
- Sickle Screen with Reflex Hemoglobin
Electrophoresis
- (Hemoglobin Electrophoresis performed
if Sickle Screen is positive)
- Sickle Screen
- Hemoglobin Electrophoresis
|
85660
83020 |
| 5000158 |
Lyme Disease
Serology
- Lyme (IgM/IgG) Antibody with Reflex
to Lyme Western Blot
(Lyme (IgM/IgG) antibody screen performed with
reflex to confirmatory Western Blot testing if
screen is positive)
- Lyme IgM/IgG Antibody Screen
by EIA
- Lyme Western Blot
|
86618
86617 (x2) |
| 5020019 |
HIV Serology
- HIV-1&2
Antibody Screen with Reflex to HIV- Western Blot)
(HIV Western Blot confirmation performed if HIV
screen is reactive)
- HIV-1&2
Antibody Screen (EIA)
- HIV-1 Western
Blot
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86703
86689 |
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| 5002013 |
Neutrophil Cytoplasmic Antibody
- Neutrophil Cytoplasmic Antibody (ANCA) with Reflex to Myeloperoxidase Antibody, IgG (MPO) , Serine Protease 3 Antibody, IgG (PR3) , Glomerular Basement Membrane IgG
(If ANCA by IFA is positive or atypical, MPO and PR3 will be performed)
- Neutrophil Cytoplasmic Antibody (ANCA)
- Myeloperoxidase Antibody, IgG (MPO)
- Serine Protease 3 Antibody, IgG (PR3)
- GBM IgG
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86255 83516 83516 |
| 5000760 |
Syphilis Serology
- RPR with Reflex to FTA (RPR with reflex to FTA-abs confirmation if RPR is reactive)
- RPR (cannot be ordered separately)
- FTA-abs
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86592 86781 |
| 1001586 |
Protein Electrophoresis
- Protein Electrophoresis (Serum & Urine) with Reflex Testing
(If initial serum or urine protein Electrophoresis is abnormal, one or more follow-up tests will be performed)
- Protein Electrophoresis, Serum (PE S)
- Protein Electrophoresis, Urine (PE U R)
- Immunofixation, Serum (IFE S)
- Immunofixation, Urine (IFE U)
- C-Reactive Protein (CRP)
- Quantitative Immunoglobulins (QIM: IgG, IgA, IgM)
- Beta 2 Microglobulin (B2M)
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84155, 84165 84156, 84166 86334
86325 86140 82784x3 82232
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| 5002120 |
ANA Screen, Reflex to Titer by IFA
- ANA Screen
(If initial screen is positive, titer will be performed by IFA methodology.) |
86038,86039 |
| 5002140 |
Autoimmune Reflex Panel (If ANA negative, no further testing)
- ANA Screen automatic reflex testing for ANA pattern and titer by IFA
- DNA Scleroderma Antibody (ENA-Scl-70)
- Sjogren Antibody (SSA) Jo-1 Antibody (ENA-Jo-1)
- Sjogren Antibody (SSB) Histone Antibody
- Smith Antibody Centromere Antibody
- Ribonucleic Protein antibody (ENA-RNP)
- Rheumatoid Arthritis Factor
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86038,86039 86225,
86235 x 8 86431
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| 3000601 |
Platelet Function Screen
- Platelet Function Screen, (if results greater than 183 sec confirmatory test ordered)
- Platelet Function Confirmation (cannot be ordered separately)
|
85572 x 2 |
| 6000563 |
Respiratory Syncytial Virus DFA Smear Reflex to
Viral Respiratory Culture
- RSV DFA Smear (if negative, reflex to Culture)
- Viral Culture Complete Respiratory
|
87280
87252,87254 |
| 8100215 |
Liquid Based SurePath/ThinPrep Pap Test
Reflex to HPV
- Thin Layer(SurePath/ThinPrep) Liquid Based Pap Test
- HPV Screen
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88142 87621
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| 0030181 |
Lupus Anticoagulant Panel with Reflex
APTT (If the Partial Thromboplastin Time and Dilute Russell Viper Venom Time are normal, no further testing will be performed. If abnormal, these tests are ordered and performed:)
- Protime
- APTT 1:1 Mix (Cannot be ordered separately)
- Platelet Neutralization (Cannot be ordered separately)
- Dilute Russell Viper Venom Time (Cannot be ordered separately)
- Smith Antibody Centromere Antibody
- Dilute Russell Viper Venom Time Confirmation (Cannot be ordered separately)
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85610 85730 85613 If positive add 85735
85613 x 2 85597 |
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