Diagnosis ICD-10 F 01 Vascular dementia (disease treatment)

ACVA ICD 10 code is a classification on the basis of which the most accurate diagnosis is made, indicating the specific area of ​​cerebrovascular accident. This scale is accepted all over the world and helps the patient to seek help with a ready-made diagnosis in a clinic in any other country. In this case, the doctor at the foreign medical center will fully understand the previously made diagnosis and quickly select the necessary therapy.

In this scale, there are 10 types of diseases with codes from I 60 to I 69. Let's consider each type separately.

I60 Subarachnoid hemorrhage

Includes: rupture of cerebral aneurysm

Excludes: consequences of subarachnoid hemorrhage (I69.0)

I60.0 Subarachnoid hemorrhage from the carotid sinus and bifurcation

I60.1 Subarachnoid hemorrhage from the middle cerebral artery

I60.2 Subarachnoid hemorrhage from the anterior communicating artery

I60.3 Subarachnoid hemorrhage from the posterior communicating artery

I60.4 Subarachnoid hemorrhage from the basilar artery

I60.5 Subarachnoid hemorrhage from the vertebral artery

I60.6 Subarachnoid hemorrhage from other intracranial arteries

I60.7 Subarachnoid hemorrhage from intracranial artery, unspecified

I60.8 Other subarachnoid hemorrhage

I60.9 Subarachnoid hemorrhage, unspecified

Strokes

The definition of “stroke” means a violation of the integrity of the arterial wall with blood entering nearby tissues. This disease has serious consequences - disruption of the neural network in the cortex due to hematoma, which leads to loss of physical and cognitive abilities.

In the ICD 10 scale, strokes occupy 3 gradations.

  • I 60 is a subarachnoid hemorrhage when a vessel ruptures between the arachnoid and pia mater. This code has 5 subtypes of the disease, which are determined by the location of the damaged artery. Additional encoding is indicated using a dot.
  • I 61 – parenchymal (intracerebral) hemorrhage. A rupture of a blood vessel in the inner region of the brain, where the gray and white matter is located. This code also contains 5 additional subtypes that define a specific break area.
  • I 62 – the location of the hemorrhage is unknown. The doctor identified the fact of a stroke, but the specific area of ​​damage was not found. This code has 3 additional subtypes.

The consequences of the hemorrhagic type of stroke are included in the headings of the ICD 10 scale. These deviations develop against the background of a stroke and can cause lifelong disability for the patient. Such pathologies need to be treated urgently in order to exclude a very likely fatal outcome (about 30% of patients die within five years due to subsequent complications).

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I63 Cerebral infarction

Includes: occlusion and stenosis of the cerebral and precerebral arteries causing cerebral infarction

Excludes: complications after cerebral infarction (I69.3)

I63.0 Cerebral infarction caused by thrombosis of precerebral arteries

I63.1 Cerebral infarction caused by embolism of precerebral arteries

I63.2 Cerebral infarction caused by unspecified occlusion or stenosis of precerebral arteries

I63.3 Cerebral infarction caused by thrombosis of cerebral arteries

I63.4 Cerebral infarction caused by cerebral artery embolism

I63.5 Cerebral infarction caused by unspecified occlusion or stenosis of cerebral arteries

I63.6 Cerebral infarction caused by cerebral vein thrombosis, non-pyogenic

I63.8 Other cerebral infarction

I63.9 Cerebral infarction, unspecified

Remaining classification

Above is a key classification of problems with blood flow in the brain, which reflects the most commonly diagnosed conditions. Let's consider what other cases, diseases and complications of stroke there are, which are covered by separate codes on the ICD 10 scale:

  • I 64 – placed if the clinical picture is unclear and the patient has symptoms of both an ischemic attack and hemorrhage.
  • I 67 – the disease is associated with impaired blood circulation in the brain, but is neither a heart attack nor a stroke.
  • I 68 – disturbance of blood flow in the brain as a consequence of another disease.
  • I 69 – complications after cerebrovascular accident.

I66 Occlusion and stenosis of cerebral arteries not leading to cerebral infarction

Included:

obstruction (complete) (partial), narrowing, thrombosis, embolism: middle, anterior and posterior cerebral arteries and cerebellar arteries, not causing cerebral infarction

Excludes: conditions causing cerebral infarction (I63.-)

I66.0 Occlusion and stenosis of the middle cerebral artery

I66.1 Occlusion and stenosis of the anterior cerebral artery

I66.2 Occlusion and stenosis of the posterior cerebral artery

I66.3 Occlusion and stenosis of the cerebellar arteries

I66.4 Occlusion and stenosis of multiple and bilateral cerebral arteries

I66.8 Blockage and stenosis of another cerebral artery

I66.9 Occlusion and stenosis of cerebral artery, unspecified

I69 Consequences of cerebrovascular diseases

Note: The term “consequences” includes conditions specified as such, as residual effects, or as conditions that persist for a year or more from the onset of the causative condition.

I69.0 Consequences of subarachnoid hemorrhage

I69.1 Consequences of intracranial hemorrhage

I69.2 Sequelae of other non-traumatic intracranial hemorrhage

I69.3 Consequences of cerebral infarction

I69.4 Consequences of stroke, not specified as cerebral hemorrhage or infarction

I69.8 Sequelae of other and unspecified cerebrovascular diseases

Cerebrovascular diseases (I60-I69)

Incl.: with mention of hypertension (conditions in I10 and I15.-) Use additional code, if desired, to identify presence of hypertension. Excl.: transient cerebral ischemic attacks and related syndromes (G45.-) traumatic intracranial haemorrhage (S06.-) vascular dementia (F01.-)

I60 Subarachnoid hemorrhage

Excl.: sequelae of subarachnoid haemorrhage (I69.0)

I60.0 Subarachnoid haemorrhage from carotid siphon and bifurcation
I60.1 Subarachnoid haemorrhage from middle cerebral artery
I60.2 Subarachnoid haemorrhage from anterior communicating artery
I60.3 Subarachnoid haemorrhage from posterior communicating artery
I60.4 Subarachnoid haemorrhage from basilar artery
I60.5 Subarachnoid haemorrhage from vertebral artery
I60.6 Subarachnoid haemorrhage from other intracranial arteries

Multiple involvement of intracranial arteries

I60.7 Subarachnoid haemorrhage from intracranial artery, unspecified

Ruptured (congenital) berry aneurysm NOS

  • Subarachnoid haemorrhage from: cerebral
  • communicating
  • artery NOS
I60.8 Other subarachnoid haemorrhage

Meningeal haemorrhage Rupture of cerebral arteriovenous malformation

I60.9 Subarachnoid haemorrhage, unspecified

I61 Intracerebral haemorrhage

Excl.: sequelae of intracerebral haemorrhage (I69.1)

I61.0 Intracerebral haemorrhage in hemisphere, subcortical

Deep intracerebral haemorrhage

I61.1 Intracerebral haemorrhage in hemisphere, cortical

Cerebral lobe haemorrhage Superficial intracerebral haemorrhage

I61.2 Intracerebral haemorrhage in hemisphere, unspecified
I61.3 Intracerebral haemorrhage in brain stem
I61.4 Intracerebral haemorrhage in cerebellum
I61.5 Intracerebral haemorrhage, intraventricular
I61.6 Intracerebral haemorrhage, multiple localized
I61.8 Other intracerebral haemorrhage
I61.9 Intracerebral haemorrhage, unspecified

I62 Other nontraumatic intracranial haemorrhage

Excl.: sequelae of intracranial haemorrhage (I69.2)

I62.0 Subdural haemorrhage (acute)(nontraumatic)
I62.1 Nontraumatic extradural haemorrhage

Nontraumatic epidural hemorrhage

I62.9 Intracranial haemorrhage (nontraumatic), unspecified

I63 Cerebral infarction

Incl.: occlusion and stenosis of cerebral and precerebral arteries, resulting in cerebral infarction Excl.: sequelae of cerebral infarction (I69.3)

I63.0 Cerebral infarction due to thrombosis of precerebral arteries
I63.1 Cerebral infarction due to embolism of precerebral arteries
I63.2 Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries
I63.3 Cerebral infarction due to thrombosis of cerebral arteries
I63.4 Cerebral infarction due to embolism of cerebral arteries
I63.5 Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries
I63.6 Cerebral infarction due to cerebral venous thrombosis, nonpyogenic
I63.8 Other cerebral infarction
I63.9 Cerebral infarction, unspecified

I64 Stroke, not specified as haemorrhage or infarction

Incl.: Cerebrovascular accident NOS Excl.: sequelae of stroke (I69.4)

I65 Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction

Inc.:

  • embolism
  • narrowing
  • obstruction (complete)(partial)
  • thrombosis
  • of basilar, carotid or vertebral arteries, not resulting in cerebral infarction

Excl.: when causing cerebral infarction (I63.-)

I65.0 Occlusion and stenosis of vertebral artery
I65.1 Occlusion and stenosis of basilar artery
I65.2 Occlusion and stenosis of carotid artery
I65.3 Occlusion and stenosis of multiple and bilateral precerebral arteries
I65.8 Occlusion and stenosis of other precerebral artery
I65.9 Occlusion and stenosis of unspecified precerebral artery

Precerebral artery NOS

I66 Occlusion and stenosis of cerebral arteries, not resulting in cerebral infarction

Inc.:

  • embolism
  • narrowing
  • obstruction (complete)(partial)
  • thrombosis
  • of middle, anterior and posterior cerebral arteries, and cerebellar arteries, not resulting in cerebral infarction

Excl.: when causing cerebral infarction (I63.-)

I66.0 Occlusion and stenosis of middle cerebral artery
I66.1 Occlusion and stenosis of anterior cerebral artery
I66.2 Occlusion and stenosis of posterior cerebral artery
I66.3 Occlusion and stenosis of cerebellar arteries
I66.4 Occlusion and stenosis of multiple and bilateral cerebral arteries
I66.8 Occlusion and stenosis of other cerebral artery

Occlusion and stenosis of perforating arteries

I66.9 Occlusion and stenosis of unspecified cerebral artery

I67 Other cerebrovascular diseases

Excl.: sequelae of the listed conditions (I69.8)

I67.0 Dissection of cerebral arteries, nonruptured

Excl.: ruptured cerebral arteries (I60.7)

I67.1 Cerebral aneurysm, nonruptured

Cerebral:

  • aneurysm NOS
  • arteriovenous fistula, acquired

Excl.: congenital cerebral aneurysm, nonruptured (Q28.-) ruptured cerebral aneurysm (I60.-)

I67.2 Cerebral atherosclerosis

Atheroma of cerebral arteries

I67.3 Progressive vascular leukoencephalopathy

Binswanger disease Excl.: subcortical vascular dementia (F01.2)

I67.4 Hypertensive encephalopathy
I67.5 Moyamoya disease
I67.6 Nonpyogenic thrombosis of intracranial venous system

Nonpyogenic thrombosis of:

  • cerebral vein
  • intracranial venous sinus

Excl.: when causing infarction (I63.6)

I67.7 Cerebral arteritis, not elsewhere classified
I67.8 Other specified cerebrovascular diseases

Acute cerebrovascular insufficiency NOS Cerebral ischaemia (chronic)

I67.9 Cerebrovascular disease, unspecified

I68* Cerebrovascular disorders in diseases classified elsewhere

I68.0* Cerebral amyloid angiopathy (E85.-†)
I68.1* Cerebral arteritis in infectious and parasitic diseases classified elsewhere

Cerebral arteritis:

  • listerial (A32.8†)
  • syphilitic (A52.0†)
  • tuberculous (A18.8†)
I68.2* Cerebral arteritis in other diseases classified elsewhere

Cerebral arteritis in systemic lupus erythematosus (M32.1†)

I68.8* Other cerebrovascular disorders in diseases classified elsewhere

Uraemic apoplexia in chronic kidney disease (N18.5†)

I69 Sequelae of cerebrovascular disease

Note: Category I69 is to be used to indicate conditions in I60-I67.1 and I67.4-I67.9 as the cause of sequelae, themselves classified elsewhere. The “sequelae” include conditions specified as such or as late effects, or those present one year or more after onset of the causal condition. Not to be used for chronic cerebrovascular disease. Code these to I60-I67.

I69.0 Sequelae of subarachnoid haemorrhage
I69.1 Sequelae of intracerebral hemorrhage
I69.2 Sequelae of other nontraumatic intracranial haemorrhage
I69.3 Sequelae of cerebral infarction
I69.4 Sequelae of stroke, not specified as haemorrhage or infarction

PSYCHIATRIC

ICD-10 Preface.

In the early 1960s, the World Health Organization began active work on a program aimed at improving the diagnosis and classification of mental disorders.
At that time, WHO held a series of meetings at which representatives of various disciplines and schools of psychiatry from around the world summarized the then existing knowledge in this area. WHO stimulated and conducted research into classification criteria and diagnostic reproducibility. In addition, procedures for joint diagnostic assessments of clinical material based on the study of videotaped interviews with patients and other methods were developed and disseminated. As a result of numerous proposals to improve the classification of mental disorders, the 8th revision of the International Classification of Disease (ICD-8) was carried out during the widest consultations. A special glossary has been developed to define each category of mental disorder in ICD-8. Work on the above program also led to the creation of a team of individuals and a network of national centers dealing with the problems of improving psychiatric classification. The 1970s saw increased interest in improving psychiatric taxonomy throughout the world. This was facilitated by the expansion of international contacts, the organization of several international collaborative studies and the emergence of the possibility of new forms of therapy. The development of specific classification criteria has been encouraged in a number of countries to improve diagnostic reproducibility. In particular, the American Psychiatric Association developed and disseminated the 3rd revision of the Diagnostic and Statistical Manual, which included the use of operational criteria in its classification system.

In 1978, WHO entered into a long-term project with the US Administration on Alcohol and Drug Abuse to further improve the classification and diagnosis of mental disorders and alcohol and drug use problems. In a series of workshops that brought together scientists from different psychiatric traditions, knowledge in their respective fields was reviewed and recommendations for further research were developed. These recommendations were summarized at a major international conference in Copenhagen, Denmark in 1982.

Several major studies have been undertaken to implement the recommendations of the Copenhagen Conference. One of them, which involved centers in 17 countries, aimed to develop the Composite International Diagnostic Interview, an instrument that would be suitable for conducting epidemiological studies of mental disorders in general populations in different countries. Another major project focused on developing an assessment tool suitable for use by clinicians. Another study was devoted to the development of an instrument to assess personality disorders in different countries.

In addition, several more dictionaries with clear definitions of terms have been prepared and are being prepared. Work on these projects was fruitfully associated with the development of definitions of mental and behavioral disorders in the International Statistical Classification of Diseases and Related Health Problems (ICD-10). The translation of diagnostic criteria into diagnostic algorithms included in assessment tools has proven useful in identifying inconsistencies, points of contention, and repetition that can be eliminated. On the other hand, work on ICD-10 has helped in the development of assessment tools. The final result was the creation of a clear system of ICD-10 criteria and assessment tools that can provide the data needed to classify disorders according to the criteria included in Chapter V(F) of ICD-10.

The Copenhagen Conference also recommended that the positions of the various schools of psychiatry be presented in publications on the sources of the ICD-10 classification. As a result, several major publications appeared.

The first book among the publications compiled on the basis of Chapter V (F) of ICD-10 was the glossary “Clinical Descriptions and Diagnostic Guidelines”. It represents the culmination of the efforts of many people who have worked on it over a number of years. In the course of this work, several large projects were prepared, each of which came out after numerous consultations with groups of experts, national and international psychiatric associations and individual consultants. The 1987 project led to trials at 40 national centers, an unprecedented study of its kind aimed at improving psychiatric diagnosis. The results of these trials were used to prepare the final clinical guidelines.

The text presented in this book has also been widely reviewed. Researchers and clinicians from 32 countries participated. Subsequent publications will include a version for general practitioners, a multi-axis version of the classification, a series of publications detailing more specific problems (for example, on the assessment and classification of mental retardation), as well as reference materials allowing comparison of relevant terms in ICD-10, ICD-10 9 and ICD-8.

With the accumulation of experience and the expansion of our knowledge, it should be possible to further improve the classification of mental disorders. This task will be assigned primarily to those WHO centers that participated in the preparation of this classification.

There are numerous publications from national centers based on and related to ICD-10 research. A complete list of these and reprints of the articles can be obtained on request from the Department of Mental Health, WHO, 1211 Geneva 27, Switzerland.

Classification is a way of seeing the world at a certain time stage. Without a doubt, scientific progress and experience with the present research criteria will require their revision and updating. I hope that such a revision will be the result of the same cordial and productive international scientific cooperation as in the preparation of this classification.

Norman Sartorius

Director of the WHO Division of Mental Health

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