ITAP TT1 MC - Glaucoma – Sept 17 1 ITAP MANAGED CARE WORKING GROUP TASK TEAM 1: CHRONIC DISEASE CONDITIONS (CDL’s) – GLAUCOMA – Explanatory note to the Managed Care minimum reporting data specification (excel spreadsheet) The aim of the project is to measure the value added by managed care organisations, by means of capturing, measuring and reporting on clinical process indicators to demonstrate the clinical outcome/s achieved. Hence this is by no means a representation of the full protocol, policy or guideline on Glaucoma management. Additionally, these process indicators and or outcomes achieved will be reported on within the Annual statutory returns.
32
Embed
ITAP MANAGED CARE WORKING GROUP TASK TEAM 1: … Documents... · 2018-04-05 · ITAP TT1 MC - Glaucoma – Sept 17 1 ITAP MANAGED CARE WORKING GROUP TASK TEAM 1: CHRONIC DISEASE CONDITIONS
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
Transcript
ITAP TT1 MC - Glaucoma – Sept 17
1
ITAP MANAGED CARE WORKING GROUP
TASK TEAM 1: CHRONIC DISEASE CONDITIONS (CDL’s)
– GLAUCOMA –
Explanatory note to the Managed Care minimum reporting data specification (excelspreadsheet)
The aim of the project is to measure the value added by managed care organisations, by means of capturing, measuring and reporting onclinical process indicators to demonstrate the clinical outcome/s achieved. Hence this is by no means a representation of the full protocol,policy or guideline on Glaucoma management.
Additionally, these process indicators and or outcomes achieved will be reported on within the Annual statutory returns.
ITAP TT1 MC - Glaucoma – Sept 17
2
Meetings and discussions were held with industry representatives and subject matter experts prior to finalising the minimum dataspecification.
1) Goal
The value of managing a disease is to establish measurable goals that result in quality of care.(Diagnosis, treatment and care of all beneficiaries should be in line with evidence base medicine, cost effectiveness and affordability).
· Maintain the individuals visual function and related quality of life at a sustainable cost.· Lower IOP and slow rate of visual field deterioration. Target IOP is specific to each individual.· Prevent complications and optimally manage the progression of disease.
2) Identification of beneficiaries that have Glaucoma / or registered on a managed care program
Please ensure the relevant consent has been obtained and confidentially maintained when obtaining personal health information.
Identification of beneficiaries registered on the program may include· Registered on chronic and or disease management programs· ICD-10 Codes or other relevant clinical coding· Anatomical Therapeutic Chemical Classification System (ATC Class)· National stock numbers (State stock code)
3) Minimum data specification: Process indicators, clinical outcomes and data
The level of Active Management of Glaucoma will depend on the nature of the contract, the level of services covered and the feestructure for those services, e.g. screening, medication, procedures etc.
The minimum required fields for the effective collection of appropriate data to demonstrate the value of the managed careinterventions for the below mentioned categories are detailed by way of process indicators (see attached spreadsheet).
· Diagnosis
The diagnosis of Glaucoma is made by the specified registered practitioner.o Congenital Glaucomao Closed Angle Glaucomao Open Angle Glaucoma
The service providers must be registered with their relevant statutory bodies and as indicated by discipline coded list providedby BHF.
4) Treatment – Glaucoma
Congenital Glaucoma Closed Angle Glaucoma Open Angle Glaucoma
Surgery / Medication Medication, Laser and / or Drainage /Cataract Surgery
Medication (first line / Second line)
Drainage surgery
ITAP TT1 MC - Glaucoma – Sept 17
4
Medication:
- S01E - Antiglaucoma preparations and miotics
* Please note these recommendations do not replace the published algorithms, PMB entitlements etc. It is a means of measuring thevalue and quality of care provided.
* The above is merely the initial phase of the ITAP Task Team 1- CDL project and as such is not exhaustive.
Full details can be seen on the accompanying excel spreadsheets.
5) Clinical Outcomes measures
· Number of all cause admissions· Number of admissions for Glaucoma· Number of Beneficiaries treated on medication alone· Number of Beneficiaries that had surgery· Number of beneficiaries that had repeated surgery / theatre· Cost of medication pre-surgery versus post-surgery
* Information in regards to ICD-10 coding may be found on the following sitehttp://www.health.gov.za/index.php/shortcodes/2015-03-29-10-42-47/2015-06-10-09-23-36/2015-06-10-09-26-11
6) Reporting (MCO and Scheme)*Definitions will be the same utilised within the Annual statutory returns – see Circular 10 of 2015. For full detailshttp://www.medicalschemes.com/files/Circulars/Circular10Of2015.pdf
All reports to be submitted to the Scheme for inclusion in the Annual Statutory Returns. Please complete the section relevant to theservice rendered by your organisation.
6.1 By Managed Care Organisation: Management out of hospital
- Time period: Benefit year (Reporting period – Start and end)- Per benefit option- Per Scheme- Member- Beneficiary- Service Date (Benefit Year)- Gender – Male / Female- Age (Age of the beneficiary is to be calculated as the Year of Reporting - Year of Birth)
a) Program Demographics
Year: Bi-Annual
Actual number of beneficiariesregistered for Glaucoma on thePharmacy Benefit and or Activedisease management program
(Longer than 6 months onprogram)
Number of new registrations inthe period
Number of beneficiaries who leftprogram *
Male Female Male Female Male FemaleUnder 11 to 44 to 910 to 1415 to 1920 to 2425 to 2930 to 34
ITAP TT1 MC - Glaucoma – Sept 17
6
35 to 3940 to 4445 to 4950 to 5455 to 5960 to 6465 to 6970 to 7475 to 7980 to 8485 andaboveTotal
*Left the program – This may include various reason codes i.e. left the scheme, death, suspensions etc.
b) Clinical Management
Year:Annual
Total Number of beneficiariestreated with medication only
Total Number of Beneficiaries thathad surgery (Laser / DrainageSurgery)
Total Number of Beneficiariesidentified with 2 or more co-morbidities
AgeGroups Female Male Female Male Male Female
Under 11 to 44 to 910 to 14
ITAP TT1 MC - Glaucoma – Sept 17
7
15 to 1920 to 2425 to 2930 to 3435 to 3940 to 4445 to 4950 to 5455 to 5960 to 6465 to 6970 to 7475 to 7980 to 8485 andaboveTotal
Co-morbiditieso Hypertensiono Diabeteso Eye Injuryo Cortisone use
6.2 Management in Hospital
- Time period: 1 January to 31 December (Service dates / financial year), define per quarter- Per benefit option- Per Scheme- Hospital Admissions:
ITAP TT1 MC - Glaucoma – Sept 17
8
o All cause admissionso Glaucoma admissions
- Hospital Categoryo Day Admissiono Long Stayo Readmission
- Gender- Age
Admission definitions
§ Glaucoma related admission - please refer to attached list of ICD10 Codes.§ Mortality / Exit codes – Where a hospital notifies the schemes / MCO / Administrator that a member is
deceased. See attached§ Emergency room – Definition as per Circular 10 of 2015§ Hospital admission
· A day case is when admission day is same as discharge date
· A long stay is when discharge date is after the admission day.
· A re-admission is when a patient from hospital is readmitted within 90 days of previous discharge date.
ITAP TT1 MC - Glaucoma – Sept 17
9
a) Hospital Category: Day Case
Scheme Total numberof
admissions(All Cause)
Total numberof admissions
(Glaucoma)Related
Admission per category Mortality(Exit
Codes =Expire)
Claimedamount
Riskpaid
amountSurgical Medical Paediatric EmergencyRoom (Only)
Male Female Male Female Male Female Male Female
b) Hospital Category: Long Stay
Scheme Total numberof
admissions(All Cause)
Total numberof related
admissions(Glaucoma)
Admission per category Mortality(Exit
Codes =Expire)
Claimedamount
Riskpaid
amountSurgical Medical Paediatric EmergencyRoom (Only)
Male Female Male Female Male Female Male Female
c) Hospital Category: Re-admission
Scheme Total numberof
admissions(All Cause)
Total numberof related
admissions(Glaucoma)
Admission per category Mortality(Exit
Codes =Expire)
Claimedamount
Riskpaid
amountSurgical Medical Paediatric EmergencyRoom (Only)
Male Female Male Female Male Female Male Female
7) References· Task Team 1 of the Managed Care ITAP working group;· Standard treatment guidelines and Essential medicine list· Circular 10 of 2015· South African Glaucoma Society
Entry andVerification
ProcessIndicators
Disease ManagementProgram Algorithm Outcomes Data Spec
ICD10 Description ATC Class ATC Class Investigation Tariff Code Tariff Description Program Algorithm Outcome Data specsH40 Glaucoma S01E Antiglaucoma preparations and miotics Initial Diagnosis Date of Diagnosis CDL Algorithm No of hosp admissions (All Cause) MembershipH40.0 Glaucoma suspect 3009
Basic capital equipment used in own rooms by ophthalmologists. Only to becharged at first and follow-up consultations. Not to be charged for post-operativefollow-up consultations Date of Registration No of hosp admissions (Glaucoma) Scheme name
H40.1 Primary open-angle glaucoma 3014 Tonometry per test with maximum of 2 tests for provocative tonometry (one or botheyes) Number of beneficiaries treated with medication only Option name
H40.2 Primary angle-closure glaucoma 3003 Fundus contact lens or 90 D lens examination (not to be charged with item 3004 oritem 3012) Numer of beneficiaries that underwent surgery Member No
H40.3 Glaucoma secondary to eyetrauma
3002Gonioscopy Dependent code
H40.4 Glaucoma secondary to eyeinflammation
3026 Digital Tomography of optic nerve with Scanning Laser Ophthalmoscope (SLO).Limited to two exams per annum Number of beneficiaries who post surgery Date of birth
H40.5 Glaucoma secondary to other eyedisorders
3027Fundus photography 0-5 days post-operative procedure - Theatre revisist Gender
H40.6 Glaucoma secondary to drugs 3028 Optical Coherent Tomography (OCT) of Optic nerve or macula: Per eye - annual Repeat surgery - 60 to 360 days post initial surgeryH40.8 Other glaucoma 3017 Retinal threshold test inclusive of computer disc storage for Delta of Statpak
programs - annual ClaimsH40.9 Glaucoma, unspecified 3020 Special eye investigations: Pachymetry: Only when own instrument is used, per
eye. Only in addition to corneal surgery (once per life) Number of drops before vs after surgery (180days) Date of serviceH42.8 Glaucoma in other diseases
classified elsewhere Cost of drops before surgery versus cost of drops after surgery Doctor typeQ15.0 Congenital glaucoma Practice number
3026 Digital Tomography of optic nerve with Scanning Laser Ophthalmoscope (SLO).Limited to two exams per annum (Old technology) ICD -10 Code
Other 3027 Fundus photography (Annually) DSP: Y or NH42 Glaucoma in diseases classified
elsewhere3028
Optical Coherent Tomography (OCT) of Optic nerve or macula: Per eye Tariff Code / UPFSH42.0 Glaucoma in endocrine,
3020Special eye investigations: Pachymetry: Only when own instrument isused, per eye. Only in addition to corneal surgery (Once in life time) ATC Class
3009 Basic capital equipment used in own rooms by ophthalmologists. Only to becharged at first and follow-up consultations. Not to be charged for post-operativefollow-up consultations. (x3 per year) CPT Code
3014 Fundus contact lens or 90 D lens examination (not to be charged with item 3004 oritem 3012) (x3 per year) Claimed Amount
3003 Fundus contact lens or 90 D lens examination (not to be charged with item 3004 oritem 3012) (x3 per year) Benefit Amount
3002 Gonioscopy. (x3 per year) Member Amount3017 Retinal threshold test inclusive of computer disc storage for Delta of Statpak
programs. (x2 per year) Length of StayLevel of Care
Surgery Exit Reason code
3021
Special eye investigations: Retinal function assessment including refractionafter ocular surgery (within four months), maximum two examinations.(x2 per year)
3080Examination of eyes under general anaesthetic where no surgery is done.(x4 per year) Clinical results
FEV13061 Drainage operation
3062Implantation of aqueous shunt device/seton in glaucoma (additional toitem 3061)
3063 Cyclocryotherapy or cyclodiathermy Program3064 Laser trabeculoplasty Date of Diagnosis3065 Removal of blood from anterior chamber Date of Registration3067 Goniotomy3149 Iridectomy or iridotomy by open operation as isolated procedure
3153Iridectomy or iridotomy by laser or photocoagulation as isolatedprocedure (maximum one procedure)
3157 Division of anterior synechiae as isolated procedure3158 Repair iris as in dialysis: Anterior chamber reconstruction3199 Repair of conjunctiva by grafting3196 Diamond knife: Use of own diamond knife during intraocular surgery
3201Laser apparatus (ophthalmic): Hire fee for one or both eyes done in onesitting (Not to be used with IOL Master)
Management
GlaucomaSurgery
CPT Code Description65855 Trabeculoplasty by laser surgery, 1 or more sessions (defined treatment series)66150 Fistulisation of sclera for glaucoma; trephination with iridectomy66155 Fistulisation of sclera for glaucoma; thermocauterisation with iridectomy66160 Fistulisation of sclera for glaucoma; sclerectomy with punch or scissors, with iridectomy66165 Fistulisation of sclera for glaucoma; iridencleisis or iridotasis66170 Fistulisation of sclera for glaucoma; trabeculectomy ab externo in absence of previous surgery66172 Fistulisation of sclera for glaucoma; trabeculectomy ab externo with scarring from previous ocular surgery or trauma
(includes injection of antifibrotic agents)
ITAP TT1 MC - Haemophilia _Sept 2017
1
ITAP MANAGED CARE WORKING GROUP
TASK TEAM 1: CHRONIC DISEASE CONDITIONS (CDL’s)
– HAEMOPHILIA –
Explanatory note to the Managed Care minimum reporting data specification (excelspreadsheet)
The aim of the project is to measure the value added by managed care organisations, by means of capturing, measuring and reporting onclinical process indicators to demonstrate the clinical outcome/s achieved. Hence this is by no means a representation of the full protocol,policy or guideline on Haemophilia management.
Additionally, these process indicators and or outcomes achieved will be reported on within the Annual statutory returns.
ITAP TT1 MC - Haemophilia _Sept 2017
2
Meetings and discussions were held with industry representatives and subject matter experts prior to finalising the minimum dataspecification.
1) Goal
The value of managing a disease is to establish measurable goals that result in quality of care.(Diagnosis, treatment and care of all beneficiaries should be in line with evidence base medicine, cost effectiveness and affordability).
· Prevent complications and optimally manage the progression of disease.
2) Identification of beneficiaries that have Haemophilia/ or registered on a managed care program
Please ensure the relevant consent has been obtained and confidentially maintained when obtaining personal health information.
Identification of beneficiaries registered on the program may include· Registered on chronic and or disease management programs· ICD-10 Codes or other relevant clinical coding· Anatomical Therapeutic Chemical Classification System (ATC Class)· National stock numbers (State stock code)
3) Minimum data specification: Process indicators, clinical outcomes and data
The level of Active Management of Haemophilia will depend on the nature of the contract, the level of services covered and the feestructure for those services, e.g. screening, medication, procedures etc.
The minimum required fields for the effective collection of appropriate data to demonstrate the value of the managed careinterventions for the below mentioned categories are detailed by way of process indicators (see attached spreadsheet).
The diagnosis of Haemophilia is made by the specified registered practitioner.Distinguish between hereditary and acquired haemophilia
· InvestigationsPathology (Blood)
o Factor VIII related antigeno Coagulation factors: Quantitativeo Full blood counto Platelet counto Fibrinogen titreo Partial thromboplastin timeo Prothrombin indexo Therapeutic drug level: Dosageo Bleeding timeo Blood volume, dye methodo Coagulation factor inhibitor assay
ScreeningDue to continuation treatment and receiving plasma product, beneficiaries to be screened for
o HIVo Hepatitis
Pregnancy – beneficiaries that are at risk to be screened and offered genetic counselling.
· Discipline Type
The service providers must be registered with their relevant statutory bodies and as indicated by discipline coded list providedby BHF.
4) Treatment – Haemophilia
ITAP TT1 MC - Haemophilia _Sept 2017
4
ATC Description
B02AA02 Tranexamic acidB02BD02 Coagulation factor VIIIB02BD03 Factor VIII inhibitor bypassing activityB02BD08 Eptacog Alfa (Activated)B02BD04 Coagulation factor IX
B02BD06Von Willebrand factor and coagulation factor VIII incombination
H01BA Vasopressin and analoguesH01BA02 Desmopressin
* Please note these recommendations do not replace the published algorithms, PMB entitlements etc. It is a means of measuring thevalue and quality of care provided.
* The above is merely the initial phase of the ITAP Task Team 1- CDL project and as such is not exhaustive.
Full details can be seen on the accompanying excel spreadsheets.
5) Clinical Outcomes measures
· Number of all cause admissions· Number of admissions for haemophilia
§ Major Bleeds§ Minor Bleeds
· Number of beneficiaries with target joints
ITAP TT1 MC - Haemophilia _Sept 2017
5
· All-cause mortality
* Information in regards to ICD-10 coding may be found on the following sitehttp://www.health.gov.za/index.php/shortcodes/2015-03-29-10-42-47/2015-06-10-09-23-36/2015-06-10-09-26-11
6) Reporting (MCO and Scheme)*Definitions will be the same utilised within the Annual statutory returns – see Circular 10 of 2015. For full detailshttp://www.medicalschemes.com/files/Circulars/Circular10Of2015.pdf
All reports to be submitted to the Scheme for inclusion in the Annual Statutory Returns. Please complete the section relevant to theservice rendered by your organisation.
6.1 By Managed Care Organisation: Management out of hospital
- Time period: Benefit year (Reporting period – Start and end)- Per benefit option- Per Scheme- Member- Beneficiary- Service Date (Benefit Year)- Gender – Male / Female- Age (Age of the beneficiary is to be calculated as the Year of Reporting - Year of Birth)
a) Program Demographics
Year: Bi-Annual
Actual number of beneficiariesregistered for Haemophilia on thePharmacy Benefit and or Activedisease management program
Under 11 to 44 to 910 to 1415 to 1920 to 2425 to 2930 to 3435 to 3940 to 4445 to 4950 to 5455 to 5960 to 6465 to 6970 to 7475 to 7980 to 8485 andaboveTotal
*Left the program – This may include various reason codes i.e. left the scheme, death, suspensions etc.
b) Clinical Management
ITAP TT1 MC - Haemophilia _Sept 2017
7
Year:Annual
Number of beneficiaries withMinor /Major Bleedsadmissions
Number of beneficiaries withtarget joints
Number of beneficiariestreated with Radio-Isotopes Total Number of Beneficiaries
identified with 2 or more co-morbidities
AgeGroups Female Male Female Male
Female MaleMale Female
Under 11 to 44 to 910 to 1415 to 1920 to 2425 to 2930 to 3435 to 3940 to 4445 to 4950 to 5455 to 5960 to 6465 to 6970 to 7475 to 7980 to 8485 andaboveTotal
6.2 Management in Hospital
- Time period: 1 January to 31 December (Service dates / financial year), define per quarter
ITAP TT1 MC - Haemophilia _Sept 2017
8
- Per benefit option- Per Scheme- Hospital Admissions:
o All cause admissionso Haemophilia admissions
- Hospital Categoryo Day Admissiono Long Stayo Re-admission
- Gender- Age
Admission definitions
§ Haemophilia related admission - please refer to attached list of ICD10 Codes.§ Mortality / Exit codes – Where a hospital notifies the schemes / MCO / Administrator that a member is
deceased. See attached§ Emergency room – Definition as per Circular 10 of 2015§ Hospital admission
· A day case is when admission day is same as discharge date
· A long stay is when discharge date is after the admission day.
· A re-admission is when a patient from hospital is readmitted within 90 days of previous discharge date.
ITAP TT1 MC - Haemophilia _Sept 2017
9
a) Hospital Category: Day Case
Scheme Total number ofadmissions (All
Cause)
Total number ofadmissions
(HaemophiliaRelated)
Admission per category Mortality(Exit Codes
= Expire)
Claimedamount
Riskpaid
amountSurgical Medical Paediatric EmergencyRoom (Only)
Male Female Male Female Male Female Male Female
b) Hospital Category: Long Stay
Scheme Total numberof
admissions(All Cause)
Total numberof related
admissions(Haemophilia)
Admission per category Mortality(Exit
Codes =Expire)
Claimedamount
Riskpaid
amountSurgical ICU / SICU /HC
Medical Paediatric EmergencyRoom (Only)
Male Female Male Female Male Female Male Female Male Female
c) Hospital Category: Re-admission
Scheme Total numberof admissions
(All Cause)
Total number ofrelated admissions
(Haemophilia)
Admission per category Mortality(Exit Codes
= Expire)
Claimedamount
Riskpaid
amountSurgical Medical Paediatric EmergencyRoom (Only)
Male Female Male Female Male Female Male Female
7) References· Task Team 1 of the Managed Care ITAP working group;· Standard treatment guidelines and Essential medicine list· Circular 10 of 2015· Haemophiliac Society
Disease ManagementProgram Algorithm Outcomes Data Spec
ICD10 Description - Haemophilia ATC Class ATC Class Investigation Tariff Code Tariff Description Program Algorithm Outcome Data specsD66 Hereditary factor VIII deficiency Haemophilia (Hereditary) Date of Diagnosis CDL Alogrithm No of hosp admissions (All Cause) MembershipD67 Hereditary factor IX deficiency B02AA02 Tranexamic acid FBC 3755 Full blood count (including items 3739, 3762, 3783, 3785, 3791) Date of Registration No of hosp admissions (Hemophilia) Scheme name
B02BD02 Coagulation factor VIII Platelets 3797 Platelet count Casualty visits Option name
Haemophilia (Acquired) B02BD03 Factor VIII inhibitor bypassing activityPlatelet functionstudies 3795 Platelet aggregation per aggregant (require a min of 6) Mortality (all cause) Member No
D68.4 Acquired coagulation factor deficiency B02BD08 Eptacog Alfa (Activated factor VIIa) Fibrogen 3825 Fibrinogen titre Number of Surgeries (Frequency) Dependent code
B02BD04 Coagulation factor IXVon Willebrandfactor
3758Factor VIII related antigen (determine severity) (initial workup) Number of Radio Isotopes (frequency) Date of birth
B02BD06Von Willebrand factor and coagulation factor VIII incombination
Factor XIIIQuantitive
3757Coagulation factors: Quantitative
Number of beneficiaries with 'complications' (See secondary codestab) per system Gender
H01BA02 DesmopressinFactor XIIIQualitative 3744 Fibrin stabilizing factor (urea test) Number of beneficairies with target jointsPTT 3837 Partial thromboplastin time (Mixing studies x3) Claims
Thrombin time 3841 Thrombin time (screen)
Radio IsotopesSee attachedATC codes Number of beneficiaries treated with radio-Isotopes Date of service
Ristocetin co-factor 3857 Ristocetin Cofactor Doctor typeINR 3805 Prothrombin index Practice numberDrug Levels 3806 Therapeutic drug level: Dosage ICD -10 CodeD-Dimer(qualitative) 3854 XDP (Dimer test or equivalent latex slide test) DSP: Y or ND- Dimer(Quantatitive) 3856 D-Dimer (quantitative) Tariff Code / UPFSFDP 3853 Fibrin degeneration products (latex slide) Nappi codes
HIV antibodies 3932 Antibodies to human immunodeficiency virus (HIV): ELISA Program3999 Albumin Date of Diagnosis4001 Alkaline phosphatase Date of Registration4131 Alanine aminotransferase (ALT)4009 Bilirubin: Total4010 Bilirubin: Conjugated4117 Protein: Total4130 Aspartate aminotransferase (AST)4134 Gamma glutamyl transferase (GGT)4531 Hepatitis: Per antigen or antibody3942 Hepatitis Rapid Viral Ab
Genetic testing (Factor 8 and 9) - Once off (Maternity to be screened)Genetic councellor
501Rehabilitation where the pathology requires the undivided attention of thephysiotherapist. Rule 008 does not apply. Duration: 30min.
502
Hydrotherapy where the pathology requires the undivided attention of thephysiotherapist. Rule 008 does not apply. Duration: 30min.
Home RX Nursing - 88 practice
030
Where a consultation was not performed and the nurse attended to or visited thepatient with the sole purpose of administering intramuscular or intravenousmedication. The route of administration of medication to be stated, as well as thename of the medication. Oral, rectal, vaginal medication excluded as well as theapplication of topical medicine.
Note:* first 20 exposures to be performed in a facility with emergency facilities
Target jointA target joint is a joint in which 3 or more spontaneous bleeds have occurred withina consecutive 6-month period.
DentalScreening (Bi-
Nurse (88)
Entry and Verification Process Indicators
Screening (Plasma products given hence screening) - Annually
Hepatitis
Liver FunctionTest (annual)
Physiotherapy -Rehabilitation
Diagnostic
Management
Tariff CodeTariff Description
3641 Tracer test3642 Repeat of further tracer tests for same investigation: Half of above fee
3643If both tracer and therapeutic procedures are done, half fee of tracer test to be chargedplus therapeutic fee
3645 Other organ scanning with use of relevant radio isotopes
Discipline Sub-discipline Discipline-description Sub-Discipline description002 000 Nutritionist003 000 Accredited Blood and Blood Product Couriers004 000 Chiropractors008 000 Homoeopaths009 001 Ambulance Service Basic Life Support Service009 002 Ambulance Service Intermediate Life Support Service009 003 Ambulance Service Advance Life Support Service009 004 Ambulance Service Provincial Ambulance Service010 000 Anaesthetists012 000 Dermatology014 000 General Medical Practice015 000 Specialist Family Medicine016 000 Independent Practice Specialist Obstetrics and Gynaecology016 001 Independent Practice Sub Specialist Obstetrics and Gynaecology Critical Care016 002 Independent Practice Sub Specialist Obstetrics and Gynaecology Gynaecological Oncology016 003 Independent Practice Sub Specialist Obstetrics and Gynaecology Medical Genetics016 004 Independent Practice Sub Specialist Obstetrics and Gynaecology Maternal and Foetal Medicine016 005 Independent Practice Sub Specialist Obstetrics and Gynaecology Reproductive Medicine016 006 Independent Practice Sub Specialist Obstetrics and Gynaecology Infectious Diseases017 000 Pulmonology018 000 Independent Practice Specialist Medicine018 001 Independent Practice Subspecialist Medicine Clinical Haematology018 002 Independent Practice Subspecialist Medicine Nephrology018 003 Independent Practice Subspecialist Medicine Cardiology018 004 Independent Practice Subspecialist Medicine Endocrinology018 005 Independent Practice Subspecialist Medicine Pulmonology018 006 Independent Practice Subspecialist Medicine Critical Care018 007 Independent Practice Subspecialist Medicine Geriatric Medicine018 008 Independent Practice Subspecialist Medicine Medical Genetics018 009 Independent Practice Subspecialist Medicine Infectious Diseases018 010 Independent Practice Subspecialist Medicine Gastroenterology018 011 Independent Practice Subspecialist Medicine Medical Oncology018 012 Independent Practice Subspecialist Medicine Rheumatology019 000 Gastroenterology020 000 Neurology021 000 Cardiology021 001 Cardiology Independent Practice Sub Specialist Medicine021 002 Cardiology Independent Practice Sub Specialist Paediatrics021 003 Cardiology Independent Practice Sub Specialist Special Merit022 000 Psychiatry023 000 Medical Oncology024 000 Independent Practice Specialist Neurosurgery024 001 Independent Practice Sub Specialist Neurosurgery Critical Care025 000 Nuclear Medicine026 000 Ophthalmology027 000 Clinical Haemotology027 001 Clinical Haematology Independent Practice Sub Specialist Pathology (Haematological)027 002 Clinical Haematology Paediatrics027 003 Clinical Haematology Medicine028 000 Orthopaedics029 000 Occupational Medicine Independent Practice Specialist
030 000 Otorhinolaryngology031 000 Rheumatology032 000 Paediatrics Independent Practice Specialist032 001 Paediatrics Independent Practice Sub Specialist Neurology032 002 Paediatrics Independent Practice Sub Specialist Developmental Paediatrics032 003 Paediatrics Independent Practice Sub Specialist Medical Oncology032 004 Paediatrics Independent Practice Sub Specialist Infectious Diseases032 005 Paediatrics Independent Practice Sub Specialist Medical Genetics032 006 Paediatrics Independent Practice Sub Specialist Endocrinology032 007 Paediatrics Independent Practice Sub Specialist Gastroenterology032 008 Paediatrics Independent Practice Sub Specialist Neonatology032 009 Paediatrics Independent Practice Sub Specialist Pulmonology032 010 Paediatrics Independent Practice Sub Specialist Rheumatology032 011 Paediatrics Independent Practice Sub Specialist Nephrology032 012 Paediatrics Independent Practice Sub Specialist Critical Care032 013 Paediatrics Independent Practice Sub Specialist Cardiology032 014 Paediatrics Independent Practice Sub Specialist Clinical Haematology034 000 Physical Medicine035 000 Emergency Medicine Independent Practice Specialist036 000 Plastic and Reconstructive Surgery037 000 Medical technology037 001 Medical technology Blood Transfusion Technology037 002 Medical technology Cardiology037 003 Medical technology Chemical Pathology037 004 Medical technology Clinical Pathology037 005 Medical technology Cytotechnology037 006 Medical technology Forensic Pathology037 007 Medical technology Haematology037 008 Medical technology Histopathological Technique037 009 Medical technology Lung Function037 010 Medical technology Microbiology037 011 Medical technology Parasitology037 012 Medical technology Pharmacology037 013 Medical technology Virology037 014 Medical technology Immunology037 015 Medical technology Radio-Isotope Technology038 000 Diagnostic Radiology039 000 Radiography039 001 Radiography Diagnosis039 002 Radiography Therapy039 003 Radiography Nuclear Medicine039 004 Radiography Ultrasound040 000 Independent Practice Specialist Radiation Oncology042 000 Surgery Independent Practice Specialist042 001 Surgery Independent Practice Sub Specialist Vascular Surgery042 002 Surgery Independent Practice Sub Specialist Critical Care042 003 Surgery Independent Practice Sub Specialist Gastroenterology042 005 Surgery Independent Practice Sub Specialist Trauma Surgery044 000 Cardio Thoracic Surgery046 000 Urology047 000 Drug & Alcohol Rehab (Department of Health)047 001 Drug & Alcohol Rehab (Welfare)
048 000 Travel Clinic049 001 Sub-Acute Facilities General Care049 002 Sub-Acute Facilities Psychiatry049 003 Sub-Acute Facilities Physical Rehab049 004 Sub-Acute Facilities All Services049 005 Sub-Acute Facilities Post Natal Unit049 006 Sub-Acute Facilities Psychiatric/Post Natal049 007 Sub-Acute Facilities Rehab/Post Natal049 008 Sub-Acute Facilities Specialised Psychiatric Unit Only050 000 Group practices050 009 Group Practice Primary Care050 010 Delayed Children Development Clinic WELFARE & DOH051 000 Group practices/Hospitals052 000 Pathology Independent Practice Specialist052 001 Pathology Independent Practice Sub-Specialist Anatomy052 002 Pathology Independent Practice Sub-Specialist Chemical052 003 Pathology Independent Practice Sub-Specialist Clinical052 004 Pathology Independent Practice Sub-Specialist Forensic052 006 Pathology Independent Practice Sub-Specialist Medical Genetics052 007 Pathology Independent Practice Sub-Specialist Microbiology052 008 Pathology Independent Practice Sub-Specialist Infectious Diseases052 009 Pathology Independent Practice Sub-Specialist Virology054 000 General Dental Practice055 000 Mental Health Institutions056 000 Provincial Hospitals056 001 Provincial Hospitals District Hospital056 002 Provincial Hospitals Regional Hospital056 003 Provincial Hospitals Tertiary/Academic Hospital056 004 Provincial Hospitals DOH Oral healthcare Centre056 009 Provincial Hospitals Primary Care056 010 Provincial Hospitals DOH Orthotics & Prosthetics Centre056 011 Provincial Hospitals Central Hospital056 012 Provincial Hospitals Specialised Hospital056 013 Provincial Hospitals Small District Hospital056 014 Provincial Hospitals Medium District Hospital056 015 Provincial Hospitals Large District Hospital057 000 Private Hospitals ('A' - Status)057 001 Private Hospitals ('A' - Status) +ICU +Theatre Less than 100 beds057 002 Private Hospitals ('A' - Status) #NAME?057 003 Private Hospitals ('A' - Status) #NAME?057 004 Private Hospitals ('A' - Status) #NAME?057 005 Private Hospitals ('A' - Status) #NAME?057 006 Private Hospitals ('A' - Status) #NAME?057 008 Private Hospital Lesotho #NAME?057 100 Private Hospitals ('A' - Status) Mine Hospilals057 200 Private Hospitals ('A' - Status) State subsidised058 000 Private Hospitals ('B' - Status)059 000 Private Rehab Hospital (Acute)060 000 Pharmacies060 001 Pharmacies Consultant Pharmacy061 000 Pharmacotherapist062 000 Maxillo-facial and Oral Surgery
090 004 Clinical services Eye Prosthetic Supplier090 005 Clinical services Breast Prosthetic Supplier090 006 Clinical services Cardiac Prosthetic Supplier090 007 Clinical services Stomal/appliances Supplier090 008 Clinical services Medical General Supplier090 009 Clinical services FAMSA (family and marriage counselling)090 011 Clinical services Oncology units (not owned by hospital)090 013 Clinical services Diabetes Appliances090 014 Clinical Services Compression Bandaging & Bone Healing System090 015 Clinical Services Parenteral Nutrition (TPN) - homecare091 000 Biokinetics092 000 Periodontics093 000 Dental Technician094 000 Prosthodontic095 000 Dental therapy096 000 Community dentistry097 000 Independent Practice Specialist Public Health Medicine098 000 Oral pathology101 000 Naturopathy102 000 Osteopathy103 000 Phytotherapy104 000 Ayurveda Ayurveda Practitioner104 001 Ayurveda Primary Healthcare Advisor104 002 Ayurveda Yoga Therapist105 000 Acupuncturist106 000 Therapeutic Aromatherapist107 000 Therapeutic Massage Therapist108 000 Therapeutic Reflexologist109 000 Unani-Tibb110 000 Clinical Pharmacokineticist111 000 Radiopharmacist112 000 Independent Practice Specialist Clinical Pharmacology113 000 Oral Hygiene114 000 Paediatric Surgery Independent Practice Specialist115 000 Medical Genetics
Haemophilia Related ComplicationsRespiratoryHaemorrhage from respiratory passages R04.0 EpistaxisHaemorrhage from respiratory passages R04.1 Haemorrhage from throatHaemorrhage from respiratory passages R04.2 HaemoptysisHaemorrhage from respiratory passages R04.8 Haemorrhage from other sites in respiratory passagesHaemorrhage from respiratory passages R04.9 Haemorrhage from respiratory passages, unspecified
JointM25.0 HaemarthrosisM25.00 Haemarthrosis, multiple sitesM25.01 Haemarthrosis, shoulder regionM25.02 Haemarthrosis, upper armM25.03 Haemarthrosis, forearmM25.04 Haemarthrosis, handM25.05 Haemarthrosis, pelvic region and thighM25.06 Haemarthrosis, lower legM25.07 Haemarthrosis, ankle and footM25.08 Haemarthrosis, other siteM25.09 Haemarthrosis, site unspecified
DentalGingivitis and periodontal diseases K05 Gingivitis and periodontal diseasesGingivitis and periodontal diseases K05.0 Acute gingivitisGingivitis and periodontal diseases K05.1 Chronic gingivitisGingivitis and periodontal diseases K05 Gingivitis and periodontal diseasesGingivitis and periodontal diseases K05.0 Acute gingivitisGingivitis and periodontal diseases K05.1 Chronic gingivitisDental caries K02 Dental cariesDental caries K02.0 Caries limited to enamelDental caries K02.1 Caries of dentineDental caries K02.2 Caries of cementumDental caries K02.3 Arrested dental cariesDental caries K02.4 OdontoclasiaDental caries K02.5 Caries with pulp exposureDental caries K02.8 Other dental cariesDental caries K02.9 Dental caries, unspecified
GITVascular disorders of intestine K55.2 Angiodysplasia of colonPeptic ulcer, site unspecified K27.0 Peptic ulcer, site unspecified, acute with haemorrhagePeptic ulcer, site unspecified K27.2 Peptic ulcer, site unspecified, acute with both haemorrhage and perforationPeptic ulcer, site unspecified K27.4 Peptic ulcer, site unspecified, chronic or unspecified with haemorrhagePeptic ulcer, site unspecified K27.6 Peptic ulcer, site unspecified, chronic or unspecified with both haemorrhage and perforationOther diseases of digestive system K92.1 MelaenaOther diseases of digestive system K92.0 Haematemesis
GenitourinaryRecurrent and persistent haematuria N02 Recurrent and persistent haematuriaRecurrent and persistent haematuria N02.0 Recurrent and persistent haematuria, minor glomerular abnormalityRecurrent and persistent haematuria N02.1 Recurrent and persistent haematuria, focal and segmental glomerular lesionsRecurrent and persistent haematuria N02.2 Recurrent and persistent haematuria, diffuse membranous glomerulonephritisRecurrent and persistent haematuria N02.3 Recurrent and persistent haematuria, diffuse mesangial proliferative glomerulonephritisRecurrent and persistent haematuria N02.4 Recurrent and persistent haematuria, diffuse endocapillary proliferative glomerulonephritisRecurrent and persistent haematuria N02.5 Recurrent and persistent haematuria, diffuse mesangiocapillary glomerulonephritisRecurrent and persistent haematuria N02.6 Recurrent and persistent haematuria, dense deposit diseaseRecurrent and persistent haematuria N02.7 Recurrent and persistent haematuria, diffuse crescentic glomerulonephritisRecurrent and persistent haematuria N02.8 Recurrent and persistent haematuria, otherRecurrent and persistent haematuria N02.9 Recurrent and persistent haematuria, unspecified
PregnancyAntenatal screening Z36.2 Other antenatal screening based on amniocentesis