Literature DB >> 27711045

Non-invasive inhaled nitric oxide in the treatment of hypoxemic respiratory failure in term and preterm infants.

R Sahni1, X Ameer1, K Ohira-Kist1, J-T Wung1.   

Abstract

OBJECTIVES: Inhaled nitric oxide (iNO) is effective in conjunction with tracheal intubation (TI) and mechanical ventilation (MV) for treating arterial pulmonary hypertension and hypoxemic respiratory failure (HRF) in near-term and term newborns. Non-invasive respiratory support with nasal continuous positive airway pressure (CPAP) is increasingly used to avoid morbidity associated with TI and MV, yet the effectiveness of iNO delivery via nasal CPAP remains unknown. To evaluate the effectiveness of iNO delivered via the bubble nasal CPAP system in term and preterm newborns with HRF. STUDY
DESIGN: Electronic medical records from all infants admitted to the neonatal intensive care unit (NICU) during 2005 to 2014 (n=10, 895) were screened for treatment with iNO therapy for HRF. Detailed data on population characteristics and cardiorespiratory, iNO and respiratory support indices were abstracted for all infants, who were administered iNO non-invasively using bubble nasal CPAP. Change in relevant indices at baseline (before initiating non-invasive iNO) and at 3, 6, 12 and 24 h after non-invasive iNO therapy were analyzed using repeated measures analysis of variance.
RESULTS: Of 795 infants treated with iNO (7.3% of total NICU admissions) over a 10-year period, 107 infants (13.4% of iNO treated) with birth weight 2448±1112 g and gestational age 35.3±5.8 weeks received iNO non-invasively. 25 infants received iNO exclusively non-invasively, whereas in remaining 82 infants non-invasive route followed invasive delivery via TI and MV. Indications for using non-invasive iNO included idiopathic pulmonary hypertension (39%), congenital heart disease (37%), bronchopulmonary dysplasia (10%), meconium aspiration syndrome (9%) and congenital diaphragmatic hernia (5%). Over the 24 h following initiation of non-invasive iNO, fractional oxygen requirements decreased (0.38 to 0.32; P<0.0005) and SpO2 increased (90.7 to 91.6%; P<0.01) with no significant changes in heart rate, respiratory rate, blood pressure, pH and PaCO2. On average non-invasive iNO was initiated on day of life 9 with a maximal dose was 20 p.p.m. The average duration of iNO therapy and the duration over which it was weaned off were 134 and 51 h, respectively. Analysis of environmental gases during non-invasive iNO therapy revealed median ambient nitrogen dioxide and nitric oxide levels of 0.30 and 0.01 p.p.m., respectively.
CONCLUSIONS: Initiation of iNO in infants on bubble nasal CPAP or continuation of iNO in infants transitioning from MV to bubble nasal CPAP is associated with improved oxygenation during HRF in term and preterm infants. Non-invasive iNO may have a synergistic effect with airway recruitment strategies such as nasal CPAP.

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Year:  2016        PMID: 27711045     DOI: 10.1038/jp.2016.164

Source DB:  PubMed          Journal:  J Perinatol        ISSN: 0743-8346            Impact factor:   2.521


  28 in total

1.  American Academy of Pediatrics. Committee on Fetus and Newborn. Use of inhaled nitric oxide.

Authors: 
Journal:  Pediatrics       Date:  2000-08       Impact factor: 7.124

2.  Nitric oxide reduces the sequestration of polymorphonuclear leukocytes in lung by changing deformability and CD18 expression.

Authors:  Y Sato; K R Walley; M E Klut; D English; Y D'yachkova; J C Hogg; S F van Eeden
Journal:  Am J Respir Crit Care Med       Date:  1999-05       Impact factor: 21.405

3.  Occupational exposure during nitric oxide inhalational therapy in a pediatric intensive care setting.

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Journal:  Intensive Care Med       Date:  1996-09       Impact factor: 17.440

4.  Inhaled nitric oxide in preterm infants undergoing mechanical ventilation.

Authors:  Roberta A Ballard; William E Truog; Avital Cnaan; Richard J Martin; Philip L Ballard; Jeffrey D Merrill; Michele C Walsh; David J Durand; Dennis E Mayock; Eric C Eichenwald; Donald R Null; Mark L Hudak; Asha R Puri; Sergio G Golombek; Sherry E Courtney; Dan L Stewart; Stephen E Welty; Roderic H Phibbs; Anna Maria Hibbs; Xianqun Luan; Sandra R Wadlinger; Jeanette M Asselin; Christine E Coburn
Journal:  N Engl J Med       Date:  2006-07-27       Impact factor: 91.245

5.  Inhaled nitric oxide in full-term and nearly full-term infants with hypoxic respiratory failure.

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Journal:  N Engl J Med       Date:  1997-02-27       Impact factor: 91.245

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Journal:  Chest       Date:  1996-06       Impact factor: 9.410

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Authors:  C Jones
Journal:  Intensive Crit Care Nurs       Date:  1998-12       Impact factor: 3.072

8.  Low-dose nitric oxide therapy for persistent pulmonary hypertension of the newborn. Clinical Inhaled Nitric Oxide Research Group.

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Journal:  N Engl J Med       Date:  2000-02-17       Impact factor: 91.245

9.  Delivery characteristics of a combined nitric oxide nasal continuous positive airway pressure system.

Authors:  R Lindwall; C G Frostell; P A Lönnqvist
Journal:  Paediatr Anaesth       Date:  2002-07       Impact factor: 2.556

10.  Venous admixture (Qva/Q) and true shunt (Qs/Qt) in ARF patients: effects of PEEP at constant FIO2.

Authors:  A Pesenti; A Riboni; R Marcolin; L Gattinoni
Journal:  Intensive Care Med       Date:  1983       Impact factor: 17.440

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  1 in total

Review 1.  Critical role of nitric oxide in impeding COVID-19 transmission and prevention: a promising possibility.

Authors:  Rajalakshmi Rajendran; Anjana Chathambath; Abdullah G Al-Sehemi; Mehboobali Pannipara; Mazhuvancherry Kesavan Unnikrishnan; Lotfi Aleya; Roshni Pushpa Raghavan; Bijo Mathew
Journal:  Environ Sci Pollut Res Int       Date:  2022-03-08       Impact factor: 5.190

  1 in total

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