How Do We Monitor Oxygenation during the Management of PPHN? Alveolar, Arterial, Mixed Venous Oxygen Tension or Peripheral Saturation?
Autor: | Munmun Rawat, Praveen Chandrasekharan, Satyan Lakshminrusimha |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Pediatric Research Initiative oxygen tension Review Mixed Venous Oxygen Tension 03 medical and health sciences 0302 clinical medicine Clinical Research 030225 pediatrics medicine.artery Internal medicine Hypoxic pulmonary vasoconstriction medicine 030212 general & internal medicine Lung Pediatric medicine.diagnostic_test business.industry lcsh:RJ1-570 lcsh:Pediatrics Oxygenation respiratory system Oxygen tension Pulse oximetry medicine.anatomical_structure Pediatrics Perinatology and Child Health Circulatory system Pulmonary artery Cardiology Vascular resistance PPHN oxygenation business |
Zdroj: | Children Children (Basel, Switzerland), vol 7, iss 10 Children, Vol 7, Iss 180, p 180 (2020) |
ISSN: | 2227-9067 |
Popis: | Oxygen is a pulmonary vasodilator and plays an important role in mediating circulatory transition from fetal to postnatal period. Oxygen tension (PO2) in the alveolus (PAO2) and pulmonary artery (PaO2) are the main factors that influence hypoxic pulmonary vasoconstriction (HPV). Inability to achieve adequate pulmonary vasodilation at birth leads to persistent pulmonary hypertension of the newborn (PPHN). Supplemental oxygen therapy is the mainstay of PPHN management. However, optimal monitoring and targeting of oxygenation to achieve low pulmonary vascular resistance (PVR) and optimizing oxygen delivery to vital organs remains unknown. Noninvasive pulse oximetry measures peripheral saturations (SpO2) and a target range of 91–95% are recommended during acute PPHN management. However, for a given SpO2, there is wide variability in arterial PaO2, especially with variations in hemoglobin type (HbF or HbA due to transfusions), pH and body temperature. This review evaluates the role of alveolar, preductal, postductal, mixed venous PO2, and SpO2 in the management of PPHN. Translational and clinical studies suggest maintaining a PaO2 of 50–80 mmHg decreases PVR and augments pulmonary vasodilator management. Nevertheless, there are no randomized clinical trials evaluating outcomes in PPHN targeting SpO2 or PO2. Also, most critically ill patients have umbilical arterial catheters and postductal PaO2 may not be an accurate assessment of oxygen delivery to vital organs or factors influencing HPV. The mixed venous oxygen tension from umbilical venous catheter blood gas may assess pulmonary arterial PO2 and potentially predict HPV. It is crucial to conduct randomized controlled studies with different PO2/SpO2 target ranges for the management of PPHN and compare outcomes. |
Databáze: | OpenAIRE |
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