Safety and efficacy of inhaled nitric oxide in the management of hypoxemic respiratory failure in adults with acute respiratory distress syndrome

Duchscherer G, Guo B
Record ID 32007000487
English
Authors' objectives: This report will examine the published scientific evidence regarding the safety and efficacy of inhaled nitric oxide (iNO) in the management of hypoxemic respiratory failure in adult ARDS patients. The goal of this project is to produce new insights on the use of this experimental therapy. Therefore, the information provided may provide the support for a more selective allocation of this therapy in the Calgary Health Region and in other healthcare jurisdictions.
Authors' results and conclusions: No published HTAs or clinical practice guidelines for the use of iNO in this population were identified. The results from one systematic review, five RCTs, and one follow-up study indicate that there is now more evidence to suggest that using iNO in ARDS does not translate into improvements in mortality as compared to conventional management with or without placebo.
Authors' recommendations: People with ARDS from a non-pulmonary infection source (such as sepsis) and those with multiorgan failure or an irreversible underlying condition have poor outcomes in general. iNO in this population does not appear to alter outcomes, and therefore its use should be reconsidered. A transient improvement in oxygenation can be expected in approximately 60% of people who receive iNO early in the progression of ARDS (within 72 hours). This improvement, when present, is typically evident within 10 minutes from initiation of the therapy, and may be present for up to 48 hours. Beyond this time, continued use should be re-evaluated on the basis of the patient's current condition, including an assessment for potential complications. iNO should be used in concentrations of less than 40 parts per million (ppm), with the best available evidence indicating a range of 5 to 10 ppm as being most effective (when there is a response in oxygenation present). Daily dose assessment or challenges should be conducted throughout the duration of use in order to re-establish optimal dosing. Discontinuation of iNO in a stepwise approach should be conducted if there is no ongoing positive response in oxygenation or in intensity of ventilation. The use of iNO is not without potential and serious complications. Although the incidence of serious complications was not clinically significant in the studies presented, one must not forget that even a slight complication in a critically ill ARDS patient can have serious results. While there have been suggestions that iNO may be considered as a last resort in the most severely refractory hypoxemic patients to obviate the need for more expensive therapeutic options such as extracorporeal membrane oxygenation; the degree of benefit in this population however has yet to be studied and therefore has not been established.
Authors' methods: Review
Details
Project Status: Completed
Year Published: 2007
English language abstract: An English language summary is available
Publication Type: Not Assigned
Country: Canada
MeSH Terms
  • Adult
  • Bronchodilator Agents
  • Humans
  • Nitric Oxide
  • Respiratory Distress Syndrome
  • Respiratory Insufficiency
Contact
Organisation Name: Institute of Health Economics
Contact Address: 1200, 10405 – Jasper Avenue, Edmonton, AB T5J 3N4, Canada. Tel: +1 780 448 4881 Fax: +1 780 448 0018
Contact Name: info@ihe.ca
Contact Email: info@ihe.ca
Copyright: Institute of Health Economics (IHE)
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.