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2.
Sci Rep ; 10(1): 11856, 2020 07 16.
Article En | MEDLINE | ID: mdl-32678248

Dengue induces a spectrum of severity in humans from the milder dengue fever to severe disease, or dengue hemorrhagic fever (DHF). Chymase is a candidate biomarker that may aid dengue prognosis. This prospective study aimed to identify whether warning signs of severe dengue, including hypovolemia and fluid accumulation, were associated with elevated chymase. Serum chymase levels were quantified prospectively and longitudinally in hospitalized pediatric dengue patients in Sri Lanka. Warning signs were determined based on daily clinical assessments, laboratory tests and ultrasound findings. Chymase was significantly elevated during the acute phase of disease in DHF or Severe dengue, defined by either the 1997 or 2009 WHO diagnosis guidelines, and persisted longer in the most severe patients. Chymase levels were higher in patients with narrow pulse pressure and clinical warning signs such as severe leakage, fluid accumulation, pleural effusion, gall-bladder wall thickening and rapid haematocrit rise concurrent with thrombocytopenia. No association between chymase and liver enlargement was observed. This study confirms that serum chymase levels are associated with DHF/Severe dengue disease in hospitalized pediatric patients. Chymase levels correlate with warning signs of vascular dysfunction highlighting the possible functional role of chymase in vascular leakage during dengue.


Chymases/blood , Dengue Virus/pathogenicity , Hypovolemia/diagnosis , Pleural Effusion/diagnosis , RNA, Viral/blood , Severe Dengue/diagnosis , Thrombocytopenia/diagnosis , Biomarkers/blood , Child , Child, Preschool , Dengue Virus/genetics , Dengue Virus/isolation & purification , Female , Hospitalization , Humans , Hypovolemia/blood , Hypovolemia/pathology , Hypovolemia/virology , Longitudinal Studies , Male , Pleural Effusion/blood , Pleural Effusion/pathology , Pleural Effusion/virology , Prognosis , Prospective Studies , Severe Dengue/blood , Severe Dengue/pathology , Severe Dengue/virology , Severity of Illness Index , Sri Lanka , Thrombocytopenia/blood , Thrombocytopenia/pathology , Thrombocytopenia/virology , Viral Load
3.
Cardiorenal Med ; 10(4): 209-216, 2020.
Article En | MEDLINE | ID: mdl-32460302

As the coronavirus disease 2019 (COVID-19) continues to spread across the globe, the knowledge of its epidemiology, clinical features, and management is rapidly evolving. Nevertheless, the data on optimal fluid management strategies for those who develop critical illness remain sparse. Adding to the challenge, the fluid volume status of these patients has been found to be dynamic. Some present with several days of malaise, gastrointestinal symptoms, and consequent hypovolemia requiring aggressive fluid resuscitation, while a subset develop acute respiratory distress syndrome with renal dysfunction and lingering congestion necessitating restrictive fluid management. Accurate objective assessment of volume status allows physicians to tailor the fluid management goals throughout this wide spectrum of critical illness. Conventional point-of-care ultrasonography (POCUS) enables the reliable assessment of fluid status and reducing the staff exposure. However, due to specific characteristics of COVID-19 (e.g., rapidly expanding lung lesions), a single imaging method such as lung POCUS will have significant limitations. Herein, we suggest a Tri-POCUS approach that represents concurrent bedside assessment of the lungs, heart, and the venous system. This combinational approach is likely to overcome the limitations of the individual methods and provide a more precise evaluation of the volume status in critically ill patients with COVID-19.


Betacoronavirus , Coronavirus Infections/complications , Hypovolemia/diagnostic imaging , Hypovolemia/virology , Pneumonia, Viral/complications , Point-of-Care Systems , Ultrasonography , Acute Kidney Injury/diagnostic imaging , Acute Kidney Injury/etiology , COVID-19 , Coronavirus Infections/diagnostic imaging , Critical Illness , Humans , Hypovolemia/complications , Male , Middle Aged , Pandemics , Pneumonia, Viral/diagnostic imaging , SARS-CoV-2
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