Watershed stroke

Brain ischemia
T1 MRI of an ischemic stroke in the brain without (left) and with (right) contrast.
Classification and external resources

A watershed stroke or watershed infarct is defined as ischemia that is localized to the vulnerable border zones between the tissues supplied via the Anterior, Posterior and Middle Cerebral arteries.[1](Note that the actual blood stream blockage/restriction site can be located far away from the infarcts. See "Pathogenesis" followed.) Watershed locations are those border-zone regions in the brain supplied by the major cerebral arteries where blood supply is decreased. Watershed strokes are a concern because they comprise approximately 10% of all ischemic stroke cases.[2] The watershed zones themselves are particularly susceptible to infarction from global ischemia as the distal nature of the vasculature predisposes these areas to be most sensitive to profound hypoperfusion.[1]

Watershed strokes are localized to two primary regions of the brain, and are termed cortical watersheds (CWS) and internal watersheds (IWS).[3] Patients with many different cardiovascular diseases have a higher likelihood of experiencing a blood clot or loss of blood flow in border-zone regions of the brain. The resulting symptoms differ based on the affected area of the brain. A CT scan and MRI are used for diagnosis, and afterward several treatment options are available, including the removal of atherosclerotic plaque and a physical widening of the clogged blood vessel. Long-term care is focused around three areas: rehabilitative therapy, surgical interventions, and prevention of future watershed strokes. Going forward, research to combat watershed strokes is focusing on various topics, such as stem cell research.

Terminology and location

Ventricles and Arteries

Schematic representation showing relations of the ventricles to the surface of the brain.

Schematic representation of the Circle of Willis, arteries of the brain and brain stem.

Anatomical terms of neuroanatomy

Watershed strokes are named because they affect the distal watershed areas of the brain. The original terminology came from the German literature, which used the analogy of an irrigation system. The German scholars compared the blood flow in distal arterial territories of the brain to the last field on a farm, which was the area with the least supply of water and therefore most vulnerable to any reduction in flow.[4] In a medical context, the term "watershed" refers to those areas of the brain that receive dual blood supply from the branching ends of two large arteries.[4]

These events are localized to two primary regions of the brain:

  1. Cortical watershed strokes (CWS), or outer brain infarcts, are located between the cortical territories of the anterior cerebral artery (ACA), middle cerebral artery (MCA), and posterior cerebral artery (PCA).[3]
  2. Internal watershed strokes (IWS), or subcortical brain infarcts, are located in the white matter along and slightly above the lateral ventricle, between the deep and the superficial arterial systems of the MCA, or between the superficial systems of the MCA and ACA.[3]

Nonetheless, within the literature itself, there exists confusion over the terminology used to describe cortical (outer brain) infarcts and subcortical (inner brain) infarcts. Besides watershed, border-zone is another common term used to refer to areas of the brain between the ends of two adjacent arteries. Other less used terms include: borderland, end zone, boundary zone, and terminal zone. These varying terms have arisen from the considerable anatomic variability both in the cerebral vascular structure and the territories of the brain that they supply.[4]

Causes and risk factors

Watershed strokes are caused by ischemia or a lack of blood flow to the brain.[2] There are several causes of ischemia, including embolism and atherosclerosis. There are several conditions that can predispose someone to watershed stroke by increasing the likelihood that insufficient blood supply will be able to reach the brain. People with many different cardiovascular diseases have a higher likelihood of experiencing a clot or a plaque that impedes flow through a blood vessel.[3] Cardiovascular diseases that increase the risk of ischemia include:

Signs and symptoms

Stroke signs and symptoms in general

Watershed stroke symptoms are due to the reduced blood flow to all parts of the body, specifically the brain, thus leading to brain damage. Initial symptoms, as promoted by the American Stroke Association, are FAST (stroke), representing F = Facial weakness (droop), A = Arm weakness (drift), S = Speech difficulty (slur), and T = Time to act (priority of intervention).[8]

All strokes are considered a medical emergency. Any one of these symptoms, whether seen alone or in combination, should be assumed to be stroke until proven otherwise. Emergency medical help should be sought IMMEDIATELY if any or all of these symptoms are seen or experienced. Early diagnosis and timely medical intervention can drastically reduce the severity of a stroke, limit damage to the brain, improve the chances of a full recovery and reduce recovery times massively.

After the initial stroke, other symptoms depend on the area of the brain affected. If one of the three central nervous system pathways is affected, symptoms can include numbness, reduced sensation, and hyperreflexia.

Most often, the side of the brain damaged results in body defects on the opposite side. Since the cranial nerves originate from the brainstem, damage to this area can lead to defects in the function of these nerves. Symptoms can include altered breathing, problems with balance, drooping of eyelids, and decreased sensation in the face.[9]

Damage to the cerebral cortex may lead to aphasia or confusion and damage to the cerebellum may lead to lack of motor movement.[9]

Watershed stroke signs and symptoms

Stroke presentations which are particularly suggestive of a watershed stroke include bilateral visual loss, stupor, and weakness of the proximal limbs, sparing the face, hands and feet.

Diagnosis

Diagnosis of a cerebral vascular accident begins with a general neurological examination, used to identify specific areas of resulting injury. A CT scan of the brain is then used to identify any cerebral hemorrhaging. An MRI with special sequences called diffusion-weighted MR imaging (DWI), is very sensitive for locating areas of an ischemic based stroke, such as a watershed stroke.

Further diagnosis and evaluation of a stroke includes evaluation of the blood vessels in the neck using either Doppler ultrasound, MR-angiography or CT-angiography, or formal angiography. An echocardiogram may be performed looking for a cardiac source of emboli. Blood tests for risk factors also may be ordered, including cholesterol levels, triglyceride levels, homocysteine levels, and blood coagulation tests.

Classification systems

  1. Thrombosis or embolism due to atherosclerosis of a large artery
  2. Embolism of cardiac origin
  3. Occlusion of a small blood vessel[12]

Pathogenesis

Although many imaging techniques are used to document watershed strokes, their pathogenesis remains controversial. It may involve various mechanisms such as systemic hypotension, microemboli, severe arterial stenosis, ICA occlusion or a combination of these.[3]

Hypotension

A sharp drop in blood pressure is the most frequent cause of watershed infarcts. The most frequent location for a watershed stroke is the region between the anterior cerebral artery and middle cerebral artery. These events caused by hypotension do not usually cause the blood vessel to rupture.[2]

Microemboli

Microemboli have not been experimentally proven to cause watershed strokes. It is unclear whether they are a cause or an effect of a watershed stroke.[13] With watershed strokes, platelet aggregates block the small meningeal arteries in watershed regions creating a microembolism. Microemboli usually form as thrombi, and can block arteries outright. On the other hand, they often detach, move into blood circulation, and eventually block smaller downstream branches of arteries causing a thromboembolism. Generally, emboli travel as far outward as their size permits along the vascular branches of the brain. Using this hypothesis, microemboli are viewed as the cause of the infarct rather than secondary events. Nevertheless, secondary thrombi do form after infarcts, and therefore it has been difficult to distinguish between emboli and thrombi in watershed locations.[2] The best supporting evidence is correlative; patients display subcortical abnormalities on CT scans and present more microembolic signals during a carotid endarterectomy.[13]

Microemboli can be common in some high-risk patients, such as those with carotid stenosis. However, in healthier patients strokes do not usually result from microemboli.[13]

ICA occlusions

Internal carotid artery

Arteries of the neck. The internal carotid arteries arise from the common carotid arteries - labeled Common caroti on the figure.

Anatomical terminology

Thrombi at the split of the internal carotid artery in the neck may cause watershed infarcts between the territories of the anterior cerebral artery and the middle cerebral artery. The resulting watershed infarcts in carotid artery blockages have mostly been considered to be due to a reduced blood flow, similar to that of hypotension.[2] Imaging studies in severe internal carotid artery (ICA) disease report an incidence of watershed stroke ranging from 19% to 64%.[3] Almost 40% of these watershed infarcts are attributed to narrowing of the carotid artery, which produces the reduced blood flow.[3]

However, a different possible explanation has emerged. Alternatively, the vascular occlusion could be the result of microemboli from the carotid thrombi before the lumen becomes completely blocked.[2] In this scenario, the clotting becomes too severe and the clot breaks free. The resulting traveling clot is known as an embolus (plural emboli). The wall of internal carotid artery just distal to the bifurcation (split) is a common site of atherosclerosis because of the unique hemodynamic effects caused by the blood flow divider. As a result, thrombi formation is more prevalent there.[13] In general, researches have observed that this microembolization is a frequent phenomenon during the build-up of cerebral thrombi.[2] The resulting emboli are pieces of calcified plaque. If these microemboli are 0.1 mm in diameter, they might pass into the small branches of the vascular system. There they may be destroyed by protective cellular defenses, or they may cause a stroke.[13] Altogether, these considerations suggest that the watershed infarcts in carotid thrombosis are caused by microembolization from mural thrombi, thrombi adherent to the vessel wall, rather than by blood flow disturbances.[2]

Treatment

Carotid endarterectomy

Often considered one of the safest ways to treat symptomatic carotid stenosis, carotid endarterectomy is a procedure by which a surgeon gently removes atherosclerotic plaque. Blood flow hopefully then returns to normal, increasing oxygen concentration to normal amounts in watershed areas of the brain.

There is the potential for complications, including disturbing portions of the plaque leading to a stroke or heart attack during or after surgery. Small risks of bleeding and infection exist as well.[14]

Percutaneous treatments of carotid stenosis

In this type of procedure, a narrowed blood vessel is expanded via angioplasty or stenting. A thin angiography catheter is inserted in a large groin blood vessel and advanced to the stenosis. Percutaneous treatment is less invasive than endarterectomy, usually requiring only local anesthesia. Endarterectomy is still considered safer though, as percutaneous treatments can lead to accidental dislodging of plaque or even arterial rupturing.[14]

Carotid angioplasty

During carotid angioplasty, an angiography cather with a small deflated balloon attached on the tip is advanced to a carotid stenosis. The ballon is then inflated slowly, forcing the narrowed portion of the vessel to expand.

Carotid stenting

Carotid stenting follows a similar procedure. Rather than using a balloon, a stent (metal mesh-like tube) is placed over the atherosclerotic plaque in the hopes of stabilizing it and allowing for increased blood flow to watershed portions of the brain.

Long-term care and rehabilitation

Watershed strokes are seldom fatal, but they can lead to neuromuscular degeneration, as well as dementia.[3] This degeneration at the watershed regions of the brain can lead to difficulties with movement and motor coordination, as well as speech. Long-term care is focused around three areas: rehabilitative therapy, surgical interventions, and prevention of future watershed strokes.

Rehabilitative therapies

Long-term rehabilitative therapy for watershed stroke patients involves physical, occupational, and speech and language therapies. Physical therapy can be used to enhance motor function in the legs and arms that has been impacted by stroke.[15] Occupational therapies can be provided to help to alleviate cognitive impairments that result from watershed stroke,[16] as well as to improve fine motor function that was damaged as a result of the stroke.[17] Stroke can also cause impairments in speech production secondary to neurocognitive and neuromuscular impairments, and therefore speech and language therapies are often a component of long-term care for stroke patients. Intensive speech and language therapy has been shown to improve speech deficits associated with aphasia resulting from stroke.[18]

Surgical interventions

Endovascular interventions, including surgical revascularization, can increase blood flow in the area of the stroke, thereby decreasing the likelihood that insufficient blood flow to the watershed regions of the brain will result in subsequent strokes.[14] Neuroscientists are currently researching stem cell transplantation therapies to improve recovery of cebreral tissue in affected areas of the brain post-stroke. Should this intervention be proven effective, it will greatly increase the number of neurons in the brain that can recover from a stroke.[19]

Prevention of future strokes

There are several interventions that are often used to help prevent the recurrence of a watershed stroke; namely, nutritional interventions, as well as antiplatelet, anticoagulant, and statin drug use. Nutritional interventions, including increased consumption of certain amino acids, antioxidants, B-group vitamins, and zinc, have been shown to increase the recovery of neurocognitive function after a stroke.[20] Antiplatelet drugs, such as aspirin, as well as anticoagulants, are used to help prevent blood clots and therefore embolisms, which can cause watershed strokes. Statin drugs are also used to control hyperlipidemia, another risk factor for watershed stroke.

Current and future research

Stem cell transplantation

Ischemic stroke is still a major health concern and studies are being conducted to determine the pathway in which brain damage occurs to identify targets for intervention. Stem cell transplantation may help in intervention to improve cell recovery and regeneration.[19]

Strokes after cardiac surgery

Although the mechanism is not entirely understood, the likelihood of a watershed stroke increases after cardiac surgery. An experiment conducted in a five-year span studied the diagnosis, etiology, and outcome of these postoperative strokes. It was observed that intraoperative decrease in blood pressure may lead to these strokes and patients who have undergone aortic procedures are more likely to have bilateral watershed infarcts. Furthermore, bilateral watershed strokes are associated with poor short-term outcomes and are most reliably observed by diffusion-weighted imaging MRI. Thus future clinical research and practice should focus on the identification of bilateral stroke characteristics. This identification can help discover affected areas and increase correct diagnosis.[21]

Deep watershed infarcts

Hemodynamic impairment is thought to be the cause of deep watershed infarcts, characterized by a rosary-like pattern. However new studies have shown that microembolism might also contribute to the development of deep watershed infarcts. The dual contribution of hemodynamic impairment and microembolism would result in different treatment for patients with these specific infarcts.[22]

Basilar artery (BA) stenting

While intracranial artery stenting is used for same side stoke prevention, basilar artery stenting may help to improve parallel, accessory blood flow. The stent may also lead to termination of recurrent middle cerebral artery (MCA) strokes.[23]

Penumbra imaging

The area around the damaged ischemia is known as the penumbra. This viable area has the ability to regenerate with the help of pharmacological treatment however most patients with penumbra are left untreated. New research is being conducted in metabolic suppression, direct energy delivery, and selective drug delivery to help salvage this area of the brain after a stroke.[24]

CLEVSRKNC peptide

This new drug has been shown to home to ischemic stroke tissue as well as apoptotic neuronal cells of the penumbra region. This discovery may help in creating selective drug delivery for stroke patients.[25]

Liposomal drug delivery

Nanoliposomes are currently being researched for specific drug delivery due to their ph-sensitive and high blood–brain barrier diffusion characteristics. Many advantages of these drugs include:

  1. Drugs can be maintained in the active state while encapsulated.
  2. Being encapsulated provides direct access to target tissue
  3. Prevention of non-specific binding
  4. Allows for a high concentration of drug

Due to the fact that acidic environment and low blood flow are prominent characteristic of the penumbra area, liposomal drugs seem to be well suited.[24]

References

  1. 1 2 Porth, C.M. (2009). Pathophysiology: Concepts of Altered Health States (Eighth Edition). Philadelphia: Wolters Kluwer Health | Lippincott Williams & Wilkins. p. 1301. ISBN 978-16054-7390-1.
  2. 1 2 3 4 5 6 7 8 9 Torvik, A. (1984). "The pathogenesis of watershed infarcts in the brain". Stroke. 15 (2): 221–3. PMID 6701929. doi:10.1161/01.STR.15.2.221.
  3. 1 2 3 4 5 6 7 8 9 Momjian-Mayor, I; Baron, J.C. (2005). "The Pathophysiology of Watershed Infarction in Internal Carotid Artery Disease: Review of Cerebral Perfusion Studies". Stroke. 36 (3): 567–77. PMID 15692123. doi:10.1161/01.STR.0000155727.82242.e1.
  4. 1 2 3 Bladin, C. F.; Chambers, B. R.; Donnan, G. A. (1993). "Confusing stroke terminology: Watershed or borderzone infarction?". Stroke. 24 (3): 477–8. PMID 8446987. doi:10.1161/01.STR.24.3.477.
  5. ↑ Miklossy, J. (2003). "Cerebral hypoperfusion induces cortical watershed microinfarcts which may further aggravate cognitive decline in Alzheimer's disease". Neurological Research. 25 (6): 605–10. PMID 14503014. doi:10.1179/016164103101202048.
  6. 1 2 3 Donnan, G.A.; Fisher, M; MacLeod, M.; Davis, S. M. (2008). "Stroke". The Lancet. 371 (9624): 1612–23. PMID 18468545. doi:10.1016/S0140-6736(08)60694-7.
  7. ↑ Verduzco, L. A.; Nathan, D. G. (2009). "Sickle cell disease and stroke". Blood. 114 (25): 5117–25. PMID 19797523. doi:10.1182/blood-2009-05-220921.
  8. ↑ Harbison, J.; Massey, A.; Barnett, L.; Hodge, D.; Ford, G. A. (1999). "Rapid ambulance protocol for acute stroke". The Lancet. 353 (9168): 1935. PMID 10371574. doi:10.1016/S0140-6736(99)00966-6.
  9. 1 2 Martini, F, Nath, J, Bartholomew, E 2012. "Fundamentals of Anatomy & Physiology.", p. 742-43. Pearson Education Inc, San Francisco. ISBN 9780321709332.
  10. ↑ Bamford, J.; Sandercock, P.; Dennis, M.; Warlow, C.; Burn, J. (1991). "Classification and natural history of clinically identifiable subtypes of cerebral infarction". The Lancet. 337 (8756): 1521–6. PMID 1675378. doi:10.1016/0140-6736(91)93206-O. Later publications distinguish between "syndrome" and "infarct", based on evidence from imaging. "Syndrome" may be replaced by "hemorrhage" if imaging demonstrates a bleed. See Internet Stroke Center. "Oxford Stroke Scale". Retrieved 2008-11-14.
  11. ↑ Bamford, J.M. (2000). "The Role of the Clinical Examination in the Subclassification of Stroke". Cerebrovascular Diseases. 10: 2–4. PMID 11070389. doi:10.1159/000047582.
  12. ↑ Adams, H. P.; Bendixen, B. H.; Kappelle, L. J.; Biller, J.; Love, B. B.; Gordon, D. L.; Marsh, E. E. (1993). "Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment". Stroke. 24 (1): 35–41. PMID 7678184. doi:10.1161/01.STR.24.1.35.
  13. 1 2 3 4 5 Grotta, JC; Alexandrov, AV (2001). "Preventing stroke: Is preventing microemboli enough?". Circulation. 103 (19): 2321–2. PMID 11352876. doi:10.1161/01.CIR.103.19.2321.
  14. 1 2 3 Mathews, Marlon S.; Sharma, J.; Snyder, K. V.; Natarajan, S. K.; Siddiqui, A. H.; Hopkins, L. N.; Levy, E. I. (2009). "Safety, Effectiveness, and Practicality of Endovascular Therapy Within the First 3 Hours of Acute Ischemic Stroke Onset". Neurosurgery. 65 (5): 860–5; discussion 865. PMID 19834397. doi:10.1227/01.NEU.0000358953.19069.E5.
  15. ↑ Winter, Jackie; Hunter, S.; Sim, J.; Crome, P. (2011). Winter, Jackie, ed. "Hands-on therapy interventions for upper limb motor dysfunction following stroke". Cochrane Database of Systematic Reviews (6): CD006609. PMID 21678359. doi:10.1002/14651858.CD006609.pub2.
  16. ↑ Hoffmann, Tammy; Bennett, S.; Koh, C. L.; McKenna, K. T. (2010). Hoffmann, Tammy, ed. "Occupational therapy for cognitive impairment in stroke patients". Cochrane Database of Systematic Reviews (9): CD006430. PMID 20824849. doi:10.1002/14651858.CD006430.pub2.
  17. ↑ Legg, L.; Drummond, A.; Leonardi-Bee, J.; Gladman, J R F; Corr, S.; Donkervoort, M.; Edmans, J.; Gilbertson, L.; et al. (2007). "Occupational therapy for patients with problems in personal activities of daily living after stroke: Systematic review of randomised trials". BMJ. 335 (7626): 922. PMC 2048861 Freely accessible. PMID 17901469. doi:10.1136/bmj.39343.466863.55.
  18. ↑ Brady, Marian C; Kelly, H.; Godwin, J.; Enderby, P.; Campbell, P. (2016). Brady, Marian C, ed. "Speech and language therapy for language problems after a stroke". Cochrane Database Syst Rev (6): 1–4. PMID 27245310. doi:10.1002/14651858.CD000425.pub4.
  19. 1 2 Jablonska, A.; Lukomska, B. (2011). "Stroke induced brain changes: Implications for stem cell transplantation". Acta Neurobiologiae Experimentalis. 71 (1): 74–85. PMID 21499328.
  20. ↑ Aquilani, R.; Sessarego, P.; Iadarola, P.; Barbieri, A.; Boschi, F. (2011). "Nutrition for Brain Recovery After Ischemic Stroke: An Added Value to Rehabilitation". Nutrition in Clinical Practice. 26 (3): 339–45. PMID 21586419. doi:10.1177/0884533611405793.
  21. ↑ Gottesman, R. F.; Sherman, P. M.; Grega, M. A.; Yousem, D. M.; Borowicz Jr, L. M.; Selnes, O. A.; Baumgartner, W. A.; McKhann, G. M. (2006). "Watershed Strokes After Cardiac Surgery: Diagnosis, Etiology, and Outcome". Stroke. 37 (9): 2306–11. PMID 16857947. doi:10.1161/01.STR.0000236024.68020.3a.
  22. ↑ Moustafa, R. R.; Momjian-Mayor, I.; Jones, P. S.; Morbelli, S.; Day, D.; Aigbirhio, F.; Fryer, T.; Warburton, E.; Baron, J. (2011). "Microembolism Versus Hemodynamic Impairment in Rosary-Like Deep Watershed Infarcts: A Combined Positron Emission Tomography and Transcranial Doppler Study". Stroke. 42 (11): 3138–43. PMID 21852602. doi:10.1161/STROKEAHA.111.616334.
  23. ↑ Titsworth, W; Civelek, A; Abou-Chebl, A (2010). "Use of far field basilar artery stenting for recurrent middle cerebral artery ischemia". Journal of NeuroInterventional Surgery. 3 (1): 57–61. PMID 21990791. doi:10.1136/jnis.2009.001958.
  24. 1 2 Liu, S; Levine, S; Winn, H (2010). "Targeting ischemic penumbra: Part I - from pathophysiology to therapeutic strategy". Journal of experimental stroke & translational medicine. 3 (1): 47–55. PMC 2896002 Freely accessible. PMID 20607107. doi:10.6030/1939-067x-3.1.47.
  25. ↑ Hong, H; Choi, J; Kim, Y; Lee, H; Kwak, W; Yoo, J; Lee, J; Kwon, T; et al. (2008). "Detection of apoptosis in a rat model of focal cerebral ischemia using a homing peptide selected from in vivo phage display". Journal of Controlled Release. 131 (3): 167–72. PMID 18692101. doi:10.1016/j.jconrel.2008.07.020.
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