Polyneuropathy in a Critically Ill Patient with Severe Malaria and Multiorganic Dysfunction
Keywords:
Polyneuropathies, Malaria, Patients.Abstract
Introduction: a critically ill patient´s polyneuropathy is a acute sensory-motor axonal neuropathy that occurs in 60-80% of severely ill patients, often it could be subclinical or unimportant, but it should be suspected in all patients after 2-to-3-week stay in intensive care who starts 2-5 days after admission to the intensive care unit of the Girassol Clinic (People´s Republic of Angola) or from the beginning of the systemic inflammatory response. The course of the disease is monophasic and self-limiting. It may present itself with variable intensity tetraparesis, hypotonia, muscular hypotrophy, with or without sensory disorders (distal hypoesthesia, paresthesia), with rare involvement of cranial nerves.Case presentation: a 28-year-old patient was admitted to the Intensive Care Unit of Girassol Clinic (People´s Republic of Angola) with a diagnosis of severe malaria with multiorganic dysfunction, while prolonged mechanical ventilation is presented. After seven days of evolution, tetraparesis appeared, which is an acute respiratory failure. Its timely detection and empirical treatment, combined with immunoglobulins and plasmapheresis, permitted a total recovery.
Conclusions: a critically ill patient´s polyneuropathy as in the presented case of a patient with critical malaria, should be detected in all patients with sensory-motor alterations, above all in the recovery stage. It is important the differentiating diagnosis regarding Guillain Barre. The treatment is based on sepsis proper management with multiorganic dysfunction syndrome, hyperglycemia control, and favoring factors as the most effective measure to avoid it.
Downloads
References
1. Lacomis D, Petrella JT, Guliani M. Causes of neuromuscular weakness in the intensive care unit: a study of ninety-two patients. Muscle Nerve 1998;21:610-7.
2. Li et al. Reversible tetraplegia after percutaneous nephrostolithotomy and septic shock: a case of critical illness polyneuropathy and myopathy with acute onset and complete recovery. BMC Nephrology 2013,14:36 http://www.biomedcentral.com/1471-2369/14/36
3. Bolton CF, Gilber JJ, Hahn AF , Sibbald WJ. Polyneuropathy in critically ill patients. J Neurol Neurosur Ps 1984;47:1223-31. http://jnnp.bmj.com/content/49/5/563.shor.
4. R.E. Dalton1, R.S. Tripathi, E.E. Abel2, D.S. Kothari, M.S. Firstenberg, S.P. Stawicki3, T.J. Papadimos. Polyneuropathy and myopathy in the elderly. HSR Proceedings in Intensive Care and Cardiovascular Anesthesia 2012, Vol. 4. http://www.hsrproceedings.org/allegati/numeri/hsrp-04-015.pdf.
5. Lorena Cerda A. Evolución neurológica y funcional en pacientes con polineuropatia de paciente crítico. Revisión de literatura y reporte de casos. Rev Hosp Clín Univ Chile 2011; 22: 230-7
6. Hermans G, de Jonghe B, Bruyninckx F, et al. Interventions for preventing critical illness polyneuropathy and critical illness myopathy. Cochrane Database Syst Rev. 2009: CD00683. http://www.update-software.com/BCP/WileyPDF/EN/CD006832.pdf
7. Friedrich O: Critical illness myopathy: sepsis-mediated failure of the peripheral nervous system. Eur J Anaesthesiol Suppl 2008, 42:73–82. http://www.nature.com/nrneurol/journal/v5/n7/abs/nrneurol.2009.75.htm.
8. Latronico N, Bolton CF: Critical illness polyneuropathy and myopathy: a major cause of muscle weakness and paralysis. Lancet Neurol 2011, 10:931–941
9. Matthew H: Inpatient Management of Guillain-Barré Syndrome. Neurohospitalist. 2011 April; 1(2):78–84 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3726082/pdf/10.1177_1941875210396379.pdf
10.Novak P, Vidmar G, Kuret Z, Bizovičar N: Rehabilitation of critical illness polyneuropathy and myopathy patients: an observational study. Int J Rehabil Res 2011, 34:336–342. http://www.ncbi.nlm.nih.gov/pubmed/22067549.
11. Koch S, Spuler S, Deja M, Bierbrauer J, Dimroth A, Behse F, Spies CD, Wernecke KD, Weber-Carstens S: Critical illness myopathy is frequent: accompanying neuropathy protracts ICU discharge. J Neurol Neurosurg Psychiatry 2011, 82:287–293 http://jnnp.bmj.com/content/82/3/287.short.
12. Magalhães et al. Finding malaria hot-spots in northern Angola: the role of individual, household and environmental factors within a meso-endemic area Malaria Journal 2012, 11:385 http://www.malariajournal.com/content/11/1/385.
13. Fortes et al. Evaluation of prevalence’s of pfdhfr and pfdhps mutations in Angola. Malaria Journal 2011, 10:22 http://www.malariajournal.com/content/10/1/22.
Published
How to Cite
Issue
Section
License
Authors who have publications with this journal agree to the following terms: Authors will retain their copyrights and grant the journal the right of first publication of their work, which will be publication of their work, which will be simultaneously subject to the Creative Commons Attribution License (CC-BY-NC 4.0) that allows third parties to share the work as long as its author and first publication in this journal are indicated.
Authors may adopt other non-exclusive license agreements for distribution of the published version of the work (e.g.: deposit it in an institutional telematic archive or publish it in a volume). Likewise, and according to the recommendations of the Medical Sciences Editorial (ECIMED), authors must declare in each article their contribution according to the CRediT taxonomy (contributor roles). This taxonomy includes 14 roles, which can be used to represent the tasks typically performed by contributors in scientific academic production. It should be consulted in monograph) whenever initial publication in this journal is indicated. Authors are allowed and encouraged to disseminate their work through the Internet (e.g., in institutional telematic archives or on their web page) before and during the submission process, which may produce interesting exchanges and increase citations of the published work. (See The effect of open access). https://casrai.org/credit/