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Difficult-to-wean: High index of suspicion
Patient: Female, 57 Final Diagnosis: Syryngomyelia • cervical Symptoms: Acute respiratory insufficiency Medication: — Clinical Procedure: — Specialty: Pulmonology OBJECTIVE: Rare disease BACKGROUND: Failed planned extubation occurs in a minority of patients with acute respiratory failure requiring i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004791/ https://www.ncbi.nlm.nih.gov/pubmed/24790685 http://dx.doi.org/10.12659/AJCR.890284 |
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author | Gelaye, Alehegn Patel, Brijesh Farra, Wassim Kole, Bruce |
author_facet | Gelaye, Alehegn Patel, Brijesh Farra, Wassim Kole, Bruce |
author_sort | Gelaye, Alehegn |
collection | PubMed |
description | Patient: Female, 57 Final Diagnosis: Syryngomyelia • cervical Symptoms: Acute respiratory insufficiency Medication: — Clinical Procedure: — Specialty: Pulmonology OBJECTIVE: Rare disease BACKGROUND: Failed planned extubation occurs in a minority of patients with acute respiratory failure requiring invasive mechanical ventilation. In patients presenting with acute respiratory failure with no identifiable cardiopulmonary causes, uncommon conditions, such as cervical spondylotic myelopathy, should be considered. In very rare instances, when cervical spondylotic myelopathy and syringomyelia present concomitantly, they can be devastating. CASE REPORT: A 57-year-old woman visited the emergency room (ER) after feeling unwell for several days. She was brought to the ER with acute respiratory distress and obtunded state with GCS of 6/15. She was hypotensive and agonally breathing. Her initial neurologic evaluation was unrevealing. Based on these findings, she was intubated. Over the next several days, she was difficult to wean from the ventilator and had persistent respiratory acidosis. After a short-lived extubation, the patient was again re-intubated. This time the neurologic evaluation showed decreased movements of all muscle groups against gravity and forces, with generalized weakness. An MRI of the brain and cervical spine demonstrated moderate degenerative disc disease and syringomyelia extending from C2 to C7 level. The patient underwent de-compression laminectomy. After failing several weaning trials, she underwent bronchoscopically-assisted tracheotomy. CONCLUSIONS: Acute cardiopulmonary and intensive care unit-acquired neuromuscular conditions have been attributed as a major cause of difficult weaning and extubation. Failure to identify and correct other rare combinations (such as cervical degenerative disc disease and syringomyelia) may cause acute respiratory failure and subsequent failure to wean and extubation, resulting in high rates of mortality and morbidity. |
format | Online Article Text |
id | pubmed-4004791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40047912014-04-30 Difficult-to-wean: High index of suspicion Gelaye, Alehegn Patel, Brijesh Farra, Wassim Kole, Bruce Am J Case Rep Articles Patient: Female, 57 Final Diagnosis: Syryngomyelia • cervical Symptoms: Acute respiratory insufficiency Medication: — Clinical Procedure: — Specialty: Pulmonology OBJECTIVE: Rare disease BACKGROUND: Failed planned extubation occurs in a minority of patients with acute respiratory failure requiring invasive mechanical ventilation. In patients presenting with acute respiratory failure with no identifiable cardiopulmonary causes, uncommon conditions, such as cervical spondylotic myelopathy, should be considered. In very rare instances, when cervical spondylotic myelopathy and syringomyelia present concomitantly, they can be devastating. CASE REPORT: A 57-year-old woman visited the emergency room (ER) after feeling unwell for several days. She was brought to the ER with acute respiratory distress and obtunded state with GCS of 6/15. She was hypotensive and agonally breathing. Her initial neurologic evaluation was unrevealing. Based on these findings, she was intubated. Over the next several days, she was difficult to wean from the ventilator and had persistent respiratory acidosis. After a short-lived extubation, the patient was again re-intubated. This time the neurologic evaluation showed decreased movements of all muscle groups against gravity and forces, with generalized weakness. An MRI of the brain and cervical spine demonstrated moderate degenerative disc disease and syringomyelia extending from C2 to C7 level. The patient underwent de-compression laminectomy. After failing several weaning trials, she underwent bronchoscopically-assisted tracheotomy. CONCLUSIONS: Acute cardiopulmonary and intensive care unit-acquired neuromuscular conditions have been attributed as a major cause of difficult weaning and extubation. Failure to identify and correct other rare combinations (such as cervical degenerative disc disease and syringomyelia) may cause acute respiratory failure and subsequent failure to wean and extubation, resulting in high rates of mortality and morbidity. International Scientific Literature, Inc. 2014-04-22 /pmc/articles/PMC4004791/ /pubmed/24790685 http://dx.doi.org/10.12659/AJCR.890284 Text en © Am J Case Rep, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Articles Gelaye, Alehegn Patel, Brijesh Farra, Wassim Kole, Bruce Difficult-to-wean: High index of suspicion |
title | Difficult-to-wean: High index of suspicion |
title_full | Difficult-to-wean: High index of suspicion |
title_fullStr | Difficult-to-wean: High index of suspicion |
title_full_unstemmed | Difficult-to-wean: High index of suspicion |
title_short | Difficult-to-wean: High index of suspicion |
title_sort | difficult-to-wean: high index of suspicion |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004791/ https://www.ncbi.nlm.nih.gov/pubmed/24790685 http://dx.doi.org/10.12659/AJCR.890284 |
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