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Neurocritical Care

, Volume 29, Issue 3, pp 525–525 | Cite as

Neurological Disease Triggering Takotsubo Syndrome

  • Josef Finsterer
  • Anna Bersano
Letter to the Editor
  • 289 Downloads

With interest we read the article by Morris et al. [1] about a retrospective study of patients with acute neurological disease, who also experienced Takotsubo syndrome (TTS). We have the following comments and concerns.

TTS has not only been reported in association with epilepsy, subarachnoid bleeding, ischemic, stroke, intracerebral bleeding, migraine, Guillain–Barre syndrome, and traumatic brain injury as mentioned in the article by Morris et al., but also in association with amyotrophic lateral sclerosis, mitochondrial disorder, thrombolysis of ischemic stroke, non-convulsive status epilepticus, zoster virus encephalitis, HLTV1-associated myelopathy, myasthenia gravis, Miller–Fisher syndrome, posterior reversible encephalopathy syndrome, syndrome of inadequate ADH secretion, transient global amnesia, multiple sclerosis, baclofen withdrawal, post-anoxic encephalopathy, Alzheimer’s disease, myotonic dystrophy type 1, acute disseminated encephalomyelitis, eclampsia, delirium, panhypopituitarism, and botulism.

A main disadvantage of the study is that only ICD9 was applied. According to ICD10, the identifier for TTS is I51.81 [2]. Was this code also considered during the recruitment of patients with acute neurological disease and TTS? Due to ignoring of the ICD10 system, a number of patients might have been missed during the search for appropriate patients.

Interestingly, the authors included hypertensive encephalopathy to the list of acute neurological disorders [1]. However, we do not regard hypertensive encephalopathy as “acute.” It is a chronic disease developing due to chronic arterial hypertension. The authors may mean an acute hypertensive crisis, for example, due to pheochromocytoma previously reported in association with TTS [3], but this is not an acute neurological disease.

A further shortcoming of the study is that only diagnoses at dismissal from the hospital were considered. Mentioning TTS with an acute neurological disease on the report does not mean that these diagnoses are causally linked, and does not clarify whether there was a timely relation. A patient may have been admitted for ischemic stroke but may have developed TTS 4 weeks later due to a completely different trigger. Furthermore, TTS may have been the initial event leading to admission and the neurological disease may have developed long after recovery from TTS, thus excluding a causal relation. However, both diagnoses may commonly appear on the report about the hospitalization.

In summary, this interesting study could be more meaningful if additional neurological disorders would have been considered as triggers of TTS, if the ICD10 codes for TTS would have been additionally used, and if the time relation between the neurological event and TTS would have been clarified.

References

  1. 1.
    Morris NA, Chatterjee A, Adejumo OL, Chen M, Merkler AE, Murthy SB, Kamel H. The risk of Takotsubo cardiomyopathy in acute neurological disease. Neurocrit Care. 2018.  https://doi.org/10.1007/s12028-018-0591-z.CrossRefPubMedPubMedCentralGoogle Scholar
  2. 2.
    International Statistical Classification of Diseases and Related Health Problems 10th Revision Volume 2 Instruction manual, 2010 Edition, http://www.who.int/classifications/icd/ICD10Volume2_en_2010.pdf.
  3. 3.
    Demea AD, Dunca DG, Radu RA, Agoşton-Coldea L. Takotsubo syndrome induced by malignant pheochromocytoma in a patient with type 2 papillary renal cell carcinoma—a case report. Clujul Med. 2018;91:242–4.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2018

Authors and Affiliations

  1. 1.Krankenanstalt RudolfstiftungViennaAustria
  2. 2.Division Cerebrovascular Disease Unit, IRCCS Foundation “C. Besta”Neurological InstituteMilanItaly

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