SoP LibraryIschaemic heart disease

Statement of Principles

Ischaemic heart disease — DVA SoP factors

Every factor in the Repatriation Medical Authority Statements of Principles for Ischaemic heart disease. DVA can only accept a claim for Ischaemic heart disease if at least one of these factors is met and connected to your service. Reasonable Hypothesis (RH) applies to operational service; Balance of Probabilities (BoP) applies to peacetime service.

Source: Repatriation Medical Authority Statements of Principles as held by the Veterans Health Centre. SoPs are amended and replaced regularly; always confirm the current instrument at rma.gov.au before relying on it.

Ischaemic heart disease

RH No. 27 of 2025 · BoP No. 28 of 2025106 factors

Meaning of ischaemic heart disease: For the purposes of this Statement of Principles, ischaemic heart disease: (a) means a cardiac disease in which inadequate coronary blood supply to part of the heart leads to infarction or periodic ischaemia; (b) includes: (i) myocardial infarction (ST elevation myocardial infarction (STEMI), and non-ST elevation myocardial infarction NSTEMI)); (ii) angina pectoris (including unstable angina and Prinzmetal angina); (iii) ischaemic cardiomyopathy; and (iv) acute coronary syndrome (including STEMI, NSTEMI, and unstable angina); and (c) excludes: (i) coronary artery disease without ischaemia; (ii) myocardial infarction due to generalised hypoxia, vascular shock, or cardiac arrest;

Reasonable Hypothesis (RH) — Statement of Principles No. 27 of 2025

At least one of the following factors must as a minimum exist before it can be said that a reasonable hypothesis has been raised connecting ischaemic heart disease or death from ischaemic heart disease with the circumstances of a person's relevant service:

  1. (1)
    having hypertension before clinical onset or clinical worsening;
  2. (2)
    having diabetes mellitus before clinical onset or clinical worsening;
  3. (3)
    being obese or overweight for at least the 5 years before clinical onset or clinical worsening;

    Note: being obese or overweight is defined in the Schedule 1 - Dictionary.

  4. (4)
    having persistently abnormal blood lipid levels before clinical onset or clinical worsening, as indicated by any of the following: (a) a serum high density lipoprotein cholesterol level less than 1.0 mmol/L; (b) a serum low density lipoprotein cholesterol level greater than 4.0 mmol/L; (c) a total serum cholesterol level greater than 5.5 mmol/L; (d) the regular administration of drug therapy to normalise previously elevated blood lipid levels;
  5. (5)
    where smoking has not ceased before clinical onset or clinical worsening: (a) smoking an average of at least 1 cigarette per day, or the equivalent thereof in other tobacco products, for at least the 1 year before clinical onset or clinical worsening; or (b) smoking at least one half of one pack-year before clinical onset or clinical worsening;

    Note: one pack-year is defined in the Schedule 1 - Dictionary.

  6. (6)
    where smoking has ceased before clinical onset or clinical worsening: (a) having smoked at least one half of one pack-year but less than 5 pack-years, before clinical onset or clinical worsening, and the clinical onset or clinical worsening has occurred within 5 years of smoking cessation; or (b) having smoked at least 5 pack-years but less than 20 pack-years, before clinical onset or clinical worsening, and the clinical onset or clinical worsening occurred within 20 years of smoking cessation; or (c) having smoked at least 20 pack-years before clinical onset or clinical worsening;

    Note: one pack-year is defined in the Schedule 1 - Dictionary.

  7. (7)
    where exposure to second-hand tobacco smoke has not ceased, being exposed to second-hand tobacco smoke exhaled by others in an enclosed space for at least 1,000 hours before clinical onset or clinical worsening;
  8. (8)
    where exposure to second-hand tobacco smoke has ceased: (a) being exposed to second-hand tobacco smoke exhaled by others in an enclosed space for at least 1,000 hours but less than 5,000 hours before clinical onset or clinical worsening, and the clinical onset or clinical worsening has occurred within 5 years of the last exposure to second-hand tobacco smoke; or (b) being exposed to second-hand tobacco smoke exhaled by others in an enclosed space for at least 5,000 hours before clinical onset or clinical worsening;
  9. (9)
    where the use of smokeless tobacco has not ceased, using smokeless tobacco on more days than not for at least 1 year before clinical onset or clinical worsening;

    Note: smokeless tobacco is defined in the Schedule 1 - Dictionary.

  10. (10)
    where the use of smokeless tobacco has ceased: (a) using smokeless tobacco on more days than not for at least 1 year but less than 5 years before clinical onset or clinical worsening, and the clinical onset or clinical worsening has occurred within 5 years of ceasing to use smokeless tobacco; or (b) using smokeless tobacco on more days than not for at least 5 years before clinical onset or clinical worsening;

    Note: smokeless tobacco is defined in the Schedule 1 - Dictionary.

  11. (11)
    an inability to undertake any physical activity greater than 3 METs for at least the 5 years before clinical onset or clinical worsening;

    Note: MET (metabolic equivalent) is a unit of measure of the level of physical capability of the cardiorespiratory system. For example, 1 MET = cardiorespiratory effort associated with a person sitting, 3-4 METs = cardiorespiratory effort associated with a person walking at average walking pace (5 km/h) or light gardening.

  12. (12)
    being sedentary for a cumulative total of at least 10 hours per day on more days than not for at least the 5 years before clinical onset or clinical worsening;

    Note: being sedentary is defined in the Schedule 1 - Dictionary.

  13. (13)
    an inability to consume an average of at least 100 grams per day of vegetables or fruits, for at least the 5 years before clinical onset or clinical worsening;
  14. (14)
    having chronic kidney disease before clinical onset or clinical worsening as indicated by one of the following: (a) a glomerular filtration rate of less than 60 mL/min/1.73 m2 for at least 3 months; (b) albuminuria with an albumin to creatinine ratio of at least 3 milligrams/millimole for at least 3 months; (c) kidney damage, as evidenced by renal biopsy, imaging studies, urinary sediment abnormalities or other markers of abnormal renal function; (d) having had a kidney transplant;
  15. (15)
    having hypothyroidism for at least 2 years within the 10 years before clinical onset or clinical worsening;

    Note: Hashimoto thyroiditis can cause hypothyroidism.

  16. (16)
    having Hashimoto thyroiditis for at least 2 years within the 10 years before clinical onset or clinical worsening;
  17. (17)
    having received a cumulative equivalent dose of at least 0.5 sievert of ionising radiation to the heart at least 1 year before clinical onset or clinical worsening;

    Note: cumulative equivalent dose is defined in the Schedule 1 - Dictionary.

  18. (18)
    having radiotherapy for cancer, where the heart was in the field of radiation, before clinical onset or clinical worsening;
  19. (19)
    inhaling, ingesting or having cutaneous contact with 1,2 propylene glycol dinitrate (Otto fuel II): (a) for a cumulative period of at least 1,000 hours within a consecutive period of 10 years, before clinical onset or clinical worsening; and (b) where the first exposure occurred at least 5 years before clinical onset or clinical worsening; and if that exposure has ceased before clinical onset or clinical worsening, then that onset or worsening occurred within 25 years of cessation;
  20. (20)
    undergoing a procedure involving catheterisation of the affected coronary artery within the 30 days before clinical onset or clinical worsening of myocardial infarction or unstable angina;
  21. (21)
    having infective endocarditis at the time of the clinical onset of myocardial infarction;
  22. (22)
    having syphilis involving the coronary arteries at the time of clinical onset or clinical worsening;
  23. (23)
    having one of the following vasculitides at the time of clinical onset or clinical worsening: (a) antineutrophilic cytoplasmic antibody (ANCA) associated vasculitis; (b) Behcet disease; (c) eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome); (d) giant cell (temporal) arteritis; (e) granulomatosis with polyangiitis (Wegener granulomatosis); (f) IgA vasculitis (Henoch-Schönlein purpura); (g) microscopic polyangiitis; (h) mucocutaneous lymph node syndrome (Kawasaki disease); (i) non-specific autoimmune vasculitis; (j) polyarteritis nodosa; (k) Takayasu arteritis;
  24. (24)
    having thromboangiitis obliterans (Buerger disease) before the clinical onset of myocardial infarction;
  25. (25)
    having one of the following systemic inflammatory rheumatological diseases at the time of clinical onset or clinical worsening: (a) ankylosing spondylitis; (b) dermatomyositis; (c) inflammatory bowel disease; (d) polymyositis; (e) psoriasis; (f) psoriatic arthritis; (g) rheumatoid arthritis; (h) Sjögren syndrome; (i) systemic lupus erythematosus; (j) systemic sclerosis;
  26. (26)
    having a hypercoagulable state that results in thrombosis of a coronary artery at the time of clinical onset or clinical worsening;

    Note: Some examples of hypercoagulable state include acquired antithrombin III deficiency, disseminated intravascular coagulation, secondary thrombocytosis and acute myeloid leukaemia.

  27. (27)
    having one of following clinically significant disorders of mental health for at least the 5 years before clinical onset or clinical worsening; (a) adjustment disorder; (b) agoraphobia; (c) anxiety disorder; (d) depressive disorder; (e) panic disorder; (f) posttraumatic stress disorder; (g) schizophrenia; or (h) social anxiety disorder;

    Note: clinically significant disorder of mental health is defined in the Schedule 1 - Dictionary.

  28. (28)
    taking combined estrogen-progestogen contraception within the 4 weeks before clinical onset or clinical worsening of myocardial infarction or unstable angina;
  29. (29)
    taking any of the following medications, within the 24 hours before clinical onset or clinical worsening: (a) alemtuzumab; (b) aromatase inhibitors; (c) bevacizumab; (d) capecitabine; (e) dextroamphetamine; (f) docetaxel; (g) ephedrine; (h) ergotamine; (i) fluorouracil; (j) methylphenidate; (k) paclitaxel; (l) phentermine; (m) pseudoephedrine; (n) the kinase inhibitors, axitinib, cabozantinib, dasatinib, erlotinib, lenvatinib, midostaurin, nilotinib, nintedanib, pazopanib, ponatinib, regorafenib, sorafenib; or (o) triptans, including sumatriptan;
  30. (30)
    being treated with antipsychotic agents or macrolide antibiotics within the 24 hours before the clinical onset or clinical worsening of myocardial infarction;
  31. (31)
    taking a non-topical, non-steroidal, anti-inflammatory drug, excluding aspirin and paracetamol, for a continuous period of at least 3 days before clinical onset or clinical worsening, where the last dose of the drug was taken within the 7 days before clinical onset or clinical worsening;

    Note: non-steroidal, anti-inflammatory drug is defined in the Schedule 1 - Dictionary.

  32. (32)
    having bilateral orchidectomy (orchiectomy) before clinical onset or clinical worsening;
  33. (33)
    taking one of the following anti-androgen medications for at least the 7 days before clinical onset or clinical worsening: (a) abiraterone; (b) androgen receptor blockers, including apalutamide, bicalutamide, darolutamide, enzalutamide, and cyproterone acetate; or (c) gonadotrophin releasing hormone agonists, including goserelin and leuprorelin;
  34. (34)
    inhaling, ingesting or having cutaneous contact with the phenoxy acid herbicides 2,4-dichlorophenoxyacetic acid (2,4-D) or 2,4,5- trichlorophenoxyacetic acid (2,4,5-T): (a) for a cumulative period of at least 1,000 hours within a consecutive period of 10 years, before clinical onset or clinical worsening; and (b) where the first exposure occurred at least 5 years before clinical onset or clinical worsening; and if that exposure has ceased before clinical onset or clinical worsening, then that onset or worsening occurred within 25 years of cessation;
  35. (35)
    inhaling, ingesting or having cutaneous contact with a chemical agent contaminated by 2,3,7,8-tetrachlorodibenzo-para-dioxin (TCDD): (a) for a cumulative period of at least 1,000 hours within a consecutive period of 10 years, before clinical onset or clinical worsening; and (b) where the first exposure occurred at least 5 years before clinical onset or clinical worsening; and if that exposure has ceased before clinical onset or clinical worsening, then that onset or worsening occurred within 25 years of cessation;

    Note: inhaling, ingesting or having cutaneous contact with a chemical agent contaminated by 2,3,7,8-tetrachlorodibenzo-para-dioxin (TCDD) is defined in the Schedule 1 - Dictionary.

  36. (36)
    inhaling chronically polluted air for at least 1,000 hours, within the 5 years before clinical onset or clinical worsening;

    Note: chronically polluted air is defined in the Schedule 1 - Dictionary.

  37. (37)
    consuming an average daily intake of at least 12 grams (200 millimoles) per day of salt (sodium chloride) for at least the 5 years before clinical onset or clinical worsening;
  38. (38)
    having periodic, heavy alcohol consumption for the 1 year before clinical onset or clinical worsening;

    Note: periodic, heavy alcohol consumption is defined in the Schedule 1 - Dictionary.

  39. (39)
    having sleep apnoea for at least the 1 year before clinical onset or clinical worsening;
  40. (40)
    an inability to sleep for an average of at least 5 hours daily for at least the 1 year before clinical onset or clinical worsening;
  41. (41)
    undertaking night shift work on at least 120 nights per year, for at least the 10 years before clinical onset or clinical worsening;

    Note: night shift work is defined in the Schedule 1 - Dictionary.

  42. (42)
    having infection with human immunodeficiency virus for at least the 5 years before clinical onset or clinical worsening;
  43. (43)
    having periodontitis for at least the 5 years before clinical onset or clinical worsening;
  44. (44)
    having gout or hyperuricaemia for at least the 5 years before clinical onset or clinical worsening;

    Note: hyperuricaemia is defined in the Schedule 1 - Dictionary.

  45. (45)
    undertaking physical activity of 5 METS or more within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: MET (metabolic equivalent) is a unit of measure of the level of physical capability of the cardiorespiratory system. For example, 1 MET = cardiorespiratory effort associated with a person sitting, 3-4 METs = cardiorespiratory effort associated with a person walking at average walking pace (5 km/h) or light gardening.

  46. (46)
    experiencing a category 1A stressor within the 48 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: category 1A stressor is defined in the Schedule 1 - Dictionary.

  47. (47)
    experiencing a category 1B stressor within the 48 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: category 1B stressor is defined in the Schedule 1 - Dictionary.

  48. (48)
    experiencing an acute severe stressful event that causes a sudden, intense emotional or psychological response within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  49. (49)
    experiencing the death of a family member or close friend within the 4 weeks before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  50. (50)
    using one of the following illicit drugs within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease: (a) amphetamines or amphetamine derivatives, including methamphetamine, 3, 4-methylenedioxymethamphetamine (Ecstasy or MDMA); (b) cocaine; (c) D-lysergic acid diethylamide; (d) marijuana; (e) Khat and synthetic cathinones, including alpha- pyrrolidinopentiophenone, 4- methylmethcathinone (4-MMC), and 3-methylmethcathinone (3-MMC);
  51. (51)
    having an episode of acute cholinergic poisoning from exposure to an organophosphorus ester within the 1 week before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: acute cholinergic poisoning and organophosphorus ester are defined in the Schedule 1 - Dictionary.

  52. (52)
    being exposed to: (a) an ambient temperature of 38 degrees Celsius or above; or (b) an ambient temperature of zero degrees Celsius or below; for a period of at least 6 hours within the 1 week before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  53. (53)
    inhaling polluted air, for at least 2 hours within the 1 week before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: polluted air is defined in the Schedule 1 - Dictionary.

  54. (54)
    being envenomated by a snake, scorpion, wasp, bee, hornet, spider, centipede, fish or jellyfish within the 24 hours before the clinical onset of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  55. (55)
    having an acute hypersensitivity reaction (including anaphylaxis) involving the coronary arteries within the 24 hours before the clinical onset of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  56. (56)
    having infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) within the 3 months before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) and sudden death from ischaemic heart disease;

    Note: SARS-CoV-2 is the virus which causes coronavirus disease 2019 (COVID-19).

  57. (57)
    having influenza or a lower respiratory tract infection within the 30 days before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  58. (58)
    being pregnant within the 6 weeks before the clinical onset or the clinical worsening of acute myocardial infarction or sudden death from ischaemic heart disease;
  59. (59)
    having a hypertensive emergency or crisis within the 48 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: hypertensive emergency or crisis is defined in the Schedule 1 - Dictionary.

  60. (60)
    having atrial fibrillation or atrial flutter within the 30 days before the clinical onset of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  61. (61)
    having bilateral oophorectomy before the age of 45 years, before clinical onset or clinical worsening;
  62. (62)
    inability to obtain appropriate clinical management for ischaemic heart disease before clinical worsening;

Balance of Probabilities (BoP) — Statement of Principles No. 28 of 2025

44 factors

At least one of the following factors must exist before it can be said that, on the balance of probabilities, ischaemic heart disease or death from ischaemic heart disease is connected with the circumstances of a person's relevant service:

  1. (1)
    having hypertension before clinical onset or clinical worsening;
  2. (2)
    having diabetes mellitus before clinical onset or clinical worsening;
  3. (3)
    being obese for at least the 5 years before clinical onset or clinical worsening;

    Note: being obese is defined in the Schedule 1 - Dictionary.

  4. (4)
    having persistently abnormal blood lipid levels before clinical onset or clinical worsening, as indicated by any of the following: (a) a serum high density lipoprotein cholesterol level less than 1.0 mmol/L; (b) a serum low density lipoprotein cholesterol level greater than 4.0 mmol/L; (c) a total serum cholesterol level greater than 5.5 mmol/L; (d) the regular administration of drug therapy to normalise previously elevated blood lipid levels;
  5. (5)
    where smoking has not ceased before clinical onset or clinical worsening: (a) smoking an average of at least 1 cigarette per day, or the equivalent thereof in other tobacco products, for at least the 1 year before clinical onset or clinical worsening; or (b) smoking at least one half of one pack-year before clinical onset or clinical worsening;

    Note: one pack-year is defined in the Schedule 1 - Dictionary.

  6. (6)
    where smoking has ceased before clinical onset or clinical worsening: (a) having smoked at least one half of one pack-year but less than 5 pack-years, before clinical onset or clinical worsening, and the clinical onset or clinical worsening has occurred within 5 years of smoking cessation; or (b) having smoked at least 5 pack-years but less than 20 pack-years, before clinical onset or clinical worsening, and the clinical onset or clinical worsening occurred within 20 years of smoking cessation; or (c) having smoked at least 20 pack-years before clinical onset or clinical worsening;

    Note: one pack-year is defined in the Schedule 1 - Dictionary.

  7. (7)
    where exposure to second-hand tobacco smoke has not ceased, being exposed to second-hand tobacco smoke exhaled by others in an enclosed space for at least 1,000 hours before clinical onset or clinical worsening;
  8. (8)
    where exposure to second-hand tobacco smoke has ceased: (a) being exposed to second-hand tobacco smoke exhaled by others in an enclosed space for at least 1,000 hours but less than 5,000 hours before clinical onset or clinical worsening, and the clinical onset or clinical worsening has occurred within 5 years of the last exposure to second-hand tobacco smoke; or (b) being exposed to second-hand tobacco smoke exhaled by others in an enclosed space for at least 5,000 hours before clinical onset or clinical worsening;
  9. (9)
    an inability to undertake any physical activity greater than 3 METs for at least the 5 years before clinical onset or clinical worsening;

    Note: MET (metabolic equivalent) is a unit of measure of the level of physical capability of the cardiorespiratory system. For example, 1 MET = cardiorespiratory effort associated with a person sitting, 3-4 METs = cardiorespiratory effort associated with a person walking at average walking pace (5 km/h) or light gardening.

  10. (10)
    having chronic kidney disease before clinical onset or clinical worsening as indicated by one of the following: (a) a glomerular filtration rate of less than 45 mL/min/1.73 m2 for at least 3 months; (b) albuminuria with an albumin to creatinine ratio of at least 3 milligrams/millimole for at least 3 months; (c) kidney damage, as evidenced by renal biopsy, imaging studies, urinary sediment abnormalities or other markers of abnormal renal function; (d) having had a kidney transplant;
  11. (11)
    having Hashimoto thyroiditis for at least 2 years within the 10 years before clinical onset or clinical worsening;
  12. (12)
    having radiotherapy for cancer, where the heart was in the field of radiation, before clinical onset or clinical worsening;
  13. (13)
    undergoing a procedure involving catheterisation of the affected coronary artery within the 30 days before clinical onset or clinical worsening of myocardial infarction or unstable angina;
  14. (14)
    having infective endocarditis at the time of the clinical onset of myocardial infarction;
  15. (15)
    having syphilis involving the coronary arteries at the time of clinical onset or clinical worsening;
  16. (16)
    having one of the following vasculitides at the time of clinical onset or clinical worsening: (a) antineutrophilic cytoplasmic antibody (ANCA) associated vasculitis; (b) Behcet disease; (c) eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome); (d) giant cell (temporal) arteritis; (e) granulomatosis with polyangiitis (Wegener granulomatosis); (f) IgA vasculitis (Henoch-Schönlein purpura); (g) microscopic polyangiitis; (h) mucocutaneous lymph node syndrome (Kawasaki disease); (i) non-specific autoimmune vasculitis; (j) polyarteritis nodosa; (k) Takayasu arteritis;
  17. (17)
    having one of the following systemic inflammatory rheumatological diseases at the time of clinical onset or clinical worsening: (a) dermatomyositis; (b) polymyositis; (c) psoriasis; (d) psoriatic arthritis; (e) rheumatoid arthritis; (f) Sjögren syndrome; (g) systemic lupus erythematosus; (h) systemic sclerosis;
  18. (18)
    having a hypercoagulable state that results in thrombosis of a coronary artery at the time of clinical onset or clinical worsening;

    Note: Some examples of hypercoagulable state include acquired antithrombin III deficiency, disseminated intravascular coagulation, secondary thrombocytosis and acute myeloid leukaemia.

  19. (19)
    having one of following clinically significant disorders of mental health for at least the 5 years before clinical onset or clinical worsening; (a) adjustment disorder; (b) agoraphobia; (c) anxiety disorder; (d) depressive disorder; (e) panic disorder; (f) posttraumatic stress disorder; (g) schizophrenia; or (h) social anxiety disorder;

    Note: clinically significant disorder of mental health is defined in the Schedule 1 - Dictionary.

  20. (20)
    taking combined estrogen-progestogen contraception within the 4 weeks before clinical onset or clinical worsening of myocardial infarction or unstable angina;
  21. (21)
    taking any of the following medications, within the 24 hours before clinical onset or clinical worsening: (a) alemtuzumab; (b) aromatase inhibitors; (c) bevacizumab; (d) capecitabine; (e) docetaxel; (f) ephedrine; (g) ergotamine; (h) fluorouracil; (i) paclitaxel; (j) phentermine; (k) pseudoephedrine; (l) the kinase inhibitors, axitinib, cabozantinib, dasatinib, erlotinib, lenvatinib, midostaurin, nilotinib, nintedanib, pazopanib, ponatinib, regorafenib, sorafenib; or (m) triptans, including sumatriptan;
  22. (22)
    being treated with antipsychotic within the 24 hours before the clinical onset or clinical worsening of myocardial infarction;
  23. (23)
    taking a non-topical, non-steroidal, anti-inflammatory drug, excluding aspirin and paracetamol, for a continuous period of at least 7 days before clinical onset or clinical worsening, where the last dose of the drug was taken within the 7 days before clinical onset or clinical worsening;

    Note: non-steroidal, anti-inflammatory drug is defined in the Schedule 1 - Dictionary.

  24. (24)
    having bilateral orchidectomy (orchiectomy) before clinical onset or clinical worsening;
  25. (25)
    taking one of the following anti-androgen medications for at least the 7 days before clinical onset or clinical worsening: (a) abiraterone; (b) androgen receptor blockers, including apalutamide, bicalutamide, darolutamide, enzalutamide, and cyproterone acetate; or (c) gonadotrophin releasing hormone agonists, including goserelin and leuprorelin;
  26. (26)
    an inability to sleep for an average of at least 5 hours daily for at least the 1 year before clinical onset or clinical worsening;
  27. (27)
    having infection with human immunodeficiency virus for at least the 5 years before the clinical onset or clinical worsening of myocardial infarction;
  28. (28)
    having gout at the time of clinical onset or clinical worsening of myocardial infarction;
  29. (29)
    undertaking physical activity of 6 METS or more within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: MET (metabolic equivalent) is a unit of measure of the level of physical capability of the cardiorespiratory system. For example, 1 MET = cardiorespiratory effort associated with a person sitting, 3-4 METs = cardiorespiratory effort associated with a person walking at average walking pace (5 km/h) or light gardening.

  30. (30)
    experiencing a category 1A stressor within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: category 1A stressor is defined in the Schedule 1 - Dictionary.

  31. (31)
    experiencing a category 1B stressor within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: category 1B stressor is defined in the Schedule 1 - Dictionary.

  32. (32)
    experiencing an acute severe stressful event that causes a sudden, intense emotional or psychological response within the 12 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  33. (33)
    experiencing the death of a family member or close friend within the 1 week before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  34. (34)
    using one of the following illicit drugs within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease: (a) amphetamines or amphetamine derivatives, including methamphetamine, 3, 4-methylenedioxymethamphetamine (Ecstasy or MDMA); (b) cocaine; (c) marijuana; (d) Khat and synthetic cathinones, including alpha- pyrrolidinopentiophenone, 4- methylmethcathinone (4-MMC), and 3-methylmethcathinone (3-MMC);
  35. (35)
    having an episode of acute cholinergic poisoning from exposure to an organophosphorus ester within the 1 week before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: acute cholinergic poisoning and organophosphorus ester are defined in the Schedule 1 - Dictionary.

  36. (36)
    being exposed to: (a) an ambient temperature of 38 degrees Celsius or above; or (b) an ambient temperature of zero degrees Celsius or below; for a period of at least 6 hours within the 1 week before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  37. (37)
    being envenomated by a snake, scorpion, wasp, bee, hornet, spider, centipede, fish or jellyfish within the 24 hours before the clinical onset of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  38. (38)
    having an acute hypersensitivity reaction (including anaphylaxis) involving the coronary arteries within the 12 hours before the clinical onset of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  39. (39)
    having infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) within the 3 months before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) and sudden death from ischaemic heart disease;

    Note: SARS-CoV-2 is the virus which causes coronavirus disease 2019 (COVID-19).

  40. (40)
    having influenza or a lower respiratory tract infection within the 30 days before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  41. (41)
    being pregnant within the 6 weeks before the clinical onset or the clinical worsening of acute myocardial infarction or sudden death from ischaemic heart disease;
  42. (42)
    having a hypertensive emergency or crisis within the 24 hours before the clinical onset or the clinical worsening of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;

    Note: hypertensive emergency or crisis is defined in the Schedule 1 - Dictionary.

  43. (43)
    having atrial fibrillation or atrial flutter within the 30 days before the clinical onset of acute coronary syndrome (including myocardial infarction) or sudden death from ischaemic heart disease;
  44. (44)
    inability to obtain appropriate clinical management for ischaemic heart disease before clinical worsening;

A VHC Diagnostic Assessment addresses each of these factors one by one against your service record and clinical history. See how a VHC DVA claim works, see all fees ($600 + GST per stage) or book an appointment.

About Dr Thomas Perkins

One doctor. Every report.

Founding doctor of the Veterans Health Centre in Ipswich, Queensland, and one of Australia's most experienced practitioners in veterans' medicolegal medicine.

Dr Perkins has spent more than thirteen years working exclusively with current and former ADF members — treating their conditions, writing their reports and navigating the DVA system alongside them. With over 100,000 claims submitted and 2,000 Permanent Impairment Assessments completed, he has seen precisely what separates an accepted claim from a rejected one at every level, from initial liability to the Veterans' Review Board.

Every chart review, diagnostic assessment, impairment rating and appeal that leaves this clinic is personally overseen by Dr Perkins. No template, no locum, no hand-off.

0429 146 039 reception@vhc.org.au

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