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About:
Management of Severe Malaria and Severe Dengue in Resource-Limited Settings
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Management of Severe Malaria and Severe Dengue in Resource-Limited Settings
Creator
Wills, Bridget
Nguyen, Mai
Dondorp, Arjen
Schultz, M
Schultz, Marcus
Hoang, Thi
Dondorp, A
Dünser, M
Dünser, Martin
Mer, Mervyn
Nakibuuka, Jane
Hoang, M
Mer, M
Mohanty, S
Mohanty, Sanjib
Thwaites, C
Wills, ·
source
PMC
abstract
This chapter summarizes recommendations on important aspects of the management of patients with severe malaria and severe dengue. Severe falciparum malaria requires rapid parasitological diagnosis by microscopy or rapid diagnostic test (RCT) and prompt initiation of parenteral artesunate. Fluid bolus therapy should be avoided in patients without hypotensive shock, and we suggest initial (24 h) crystalloid fluid therapy of 2–4 mL/kg/h, which may subsequently be reduced to 1 mL/kg/h in patients receiving additional fluids, e.g., through enteral tube feeding. In the minority of those patients presenting with hypotensive shock, we suggest fluid bolus therapy (30 mL/kg) with an isotonic crystalloid and early initiation of vasopressor support. Enteral feeding in non-intubated adult patients with cerebral malaria can start after 60 h, to avoid aspiration pneumonia. There are insufficient data to suggest this in pediatric cerebral malaria. The diagnosis of severe dengue is commonly with a combined dengue antigen (NS1) and antibody RDT. No antiviral treatment is currently available. Dengue shock results from capillary leakage, although hemorrhage or depression of myocardial contractility can contribute. The World Health Organization guidelines recommend restoration of the circulation guided by pulse pressure, capillary refill time, hematocrit, and urine output. Large (>15 mL/kg) rapid (<30 min) fluid boluses should be avoided, but prompt fluid administration with crystalloids is essential and should be restricted as soon as the critical phase is over to avoid pulmonary edema. Corticosteroids are not recommended, neither is platelet transfusion for thrombocytopenia in the absence of active bleeding or other risk factors.
has issue date
2019-02-09
(
xsd:dateTime
)
bibo:doi
10.1007/978-3-030-03143-5_9
bibo:pmid
32091688
has license
cc-by
sha1sum (hex)
7358517c091cf2b4d0e035e7d12d4fef2d1deb4b
schema:url
https://doi.org/10.1007/978-3-030-03143-5_9
resource representing a document's title
Management of Severe Malaria and Severe Dengue in Resource-Limited Settings
has PubMed Central identifier
PMC7123178
has PubMed identifier
32091688
schema:publication
Sepsis Management in Resource-limited Settings
resource representing a document's body
covid:7358517c091cf2b4d0e035e7d12d4fef2d1deb4b#body_text
is
schema:about
of
named entity 'Management'
named entity 'starch'
named entity 'dengue shock syndrome'
named entity 'dengue'
named entity 'falciparum malaria'
named entity 'dengue shock syndrome'
named entity 'infection'
named entity 'saline'
named entity 'pulse pressure'
named entity 'South America'
named entity 'fluid management'
named entity 'crystalloid fluid'
named entity 'albumin'
named entity 'hematocrit'
named entity 'ClinicalTrials.gov'
named entity 'observational study'
named entity 'case fatality rate'
named entity 'SSC'
named entity 'Hemorrhage'
named entity 'thrombocytopenia'
named entity 'cerebral malaria'
named entity 'falciparum malaria'
named entity 'febrile'
named entity 'thrombocytopathy'
named entity 'dengue'
named entity 'platelet transfusion'
named entity 'dengue'
named entity 'cerebral malaria'
named entity 'Acute respiratory distress syndrome'
named entity 'albumin'
named entity 'arterial hypertension'
named entity 'immunological'
named entity 'Surviving Sepsis Campaign'
named entity 'Corticosteroids'
named entity 'cytotoxic'
named entity 'lung'
named entity 'lung'
named entity 'pregnant women'
named entity 'WHO'
named entity 'hypotension'
named entity 'severe malaria'
named entity 'cerebral malaria'
named entity 'Dengue shock syndrome'
named entity 'fluid therapy'
named entity 'Aedes'
named entity 'Prophylactic'
named entity 'colloid'
named entity 'dengue'
named entity 'hypotensive'
named entity 'intravenous glucose'
named entity 'pathophysiologic'
named entity 'enteral'
named entity 'falciparum malaria'
named entity 'cellular immune responses'
named entity 'pediatric'
named entity 'urine output'
named entity 'colloids'
named entity '2.2'
named entity 'Corticosteroids'
named entity 'SSC'
named entity 'hypovolemia'
named entity 'dengue'
named entity 'dengue virus'
named entity 'SSC'
named entity 'severe malaria'
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