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Effect of a Parenteral Emulsion With Omega3 on PPHN

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Prijava Registriraj se
Veza se sprema u međuspremnik
StatusAktivan, ne regrutira
Sponzori
Coordinación de Investigación en Salud, Mexico

Ključne riječi

Sažetak

The purpose of this study is to evaluate the effect of a parenteral emulsion containing n-3 long-chain polyunsaturated fatty acids (LC-PUFA) in fish oil on clinical outcomes, markers of inflammation and oxidative stress, and pain in neonates with persistent pulmonary hypertension of the newborn (PPHN) compared with those who receive an emulsion containing soy oil and medium-chain triglycerides (MCT) without n-3 LC-PUFA.

Opis

Background. Persistent pulmonary hypertension of the newborn (PPHN), is a syndrome characterized by difficulty to provide normal pulmonary vasodilatation at birth or after birth, which may be related with right ventricular dysfunction, congenital diaphragmatic hernia, sepsis, and meconium aspiration. This condition is understudied. PPHN causes pulmonary vascular resistance (PVR) that decreases left pulmonary artery flow (LPA), meaning that blood cannot be oxygenated in the lungs, leading to low oxygen delivery to all organs. Expensive medication along with ventilator support may help, but the latter and PPHN increase the production of the inflammatory mediators such as pro-inflammatory cytokines and markers of oxidative stress, which cause cell toxicity. When patients have PPHN secondary to a diaphragmatic hernia, they undergo corrective surgery, which further increases the production of inflammatory markers and worsens oxidative stress. As a result, the pain of the surgery also worsens the hypoxemia and respiratory insufficiency in the newborn. PPHN is associated with bronchopulmonary dysplasia (BPD), a chronic lung disease. To date, there is no effective treatment for neonates with PPHN, and around one-third of patients may not respond to current management, leading to death up to 33% of the infants in developed countries. In Mexico, the mortality rate from PPHN reaches 80%, which is an unacceptable outcome at a high cost. Therefore, the prevention or reduction of the severity of PPHN is actively sought.

Previous reports have shown that the n-3 long-chain polyunsaturated fatty acids (LC-PUFA), such as docosahexaenoic acid (DHA) improves the nutritional status and clinical outcomes in septic newborn reduce systemic inflammation and organ dysfunction in newborns who underwent cardiovascular surgery with a shorter stay in the neonatal intensive care unit. In addition, those babies received lower amounts of analgesics. Other authors have shown that n-3 LC-PUFA reduces oxidative stress. In experimental models of PPHN, the EPA and DHA from Omegaven (fish oil) increased pulmonary artery flow and decrease the pulmonary vascular resistance. In the current project, it is hypothesized that n-3 LC-PUFA improves clinical outcomes such as decreasing pulmonary vascular resistance and markers of inflammation and oxidative stress but increases LPA flow in neonates with PPHN. This hypothesis has not been evaluated in PPHN.

Objective. The purpose of this study is to evaluate the effect of a parenteral emulsion containing n-3 LC-PUFA in fish oil on clinical outcomes, markers of inflammation and oxidative stress, and pain in neonates with PPHN compared with those who receive an emulsion containing soy and medium-chain triglycerides (MCT) without n-3 LC-PUFA.

Methodology. A double-blind clinical trial will be carried out in Mexican newborns diagnosed with PPHN. Control group will receive intravenous nutrition support including a lipid emulsion based on soy oil plus MCT (control group) and the intervention group will receive a lipid emulsion based on soy oil, MCT, olive oil and fish oil (n-3 LC-PUFA group); both groups will receive a dose of lipid between 3-4 g/kg/d, through total parenteral nutrition (TPN) for at least 14 days and a maximum of 21 days.

The effect of n-3 LC-PUFA will be evaluated on:

1. Clinical outcomes, nutritional status, perception od pain

2. Markers of inflammation

3. Oxidative stress markers

To compare the groups, the Exact Fisher´s, Student's t or U-Mann-Whitney tests will be applied as appropriate. To adjust the effect of n-3 LC-PUFA for confounders such as fatty acid background and medication, Repeated Measures ANOVA and binary logistic regression will be performed.

Datumi

Posljednja provjera: 06/30/2020
Prvo podneseno: 07/07/2019
Predviđena prijava poslana: 07/21/2019
Prvo objavljeno: 07/23/2019
Posljednje ažuriranje poslano: 07/15/2020
Posljednje ažuriranje objavljeno: 07/19/2020
Stvarni datum početka studija: 08/11/2019
Procijenjeni datum primarnog završetka: 06/30/2022
Procijenjeni datum završetka studije: 06/30/2022

Stanje ili bolest

Pulmonary Hypertension of Newborn
Diaphragm Defect

Intervencija / liječenje

Dietary Supplement: Parenteral emulsion

Faza

-

Grupe ruku

RukaIntervencija / liječenje
Experimental: Omega 3
The experimental group will receive a parenteral emulsion containing soy oil, MCT, olive oil and n-3 LCPUFA in fish oil
Sham Comparator: Control group
The Control group will receive a parenteral emulsion containing soy oil and MCT

Kriterij prihvatljivosti

Spolovi koji ispunjavaju uvjete za studijAll
Prihvaća zdrave volontereDa
Kriteriji

Inclusion Criteria:

- The requirement of TPN for at least 14 days

- Clinical, gasometric, and echocardiographic diagnosis of pulmonary arterial hypertension associated with diaphragm defect.

- Gestational age >34 weeks.

- Written informed consent signed by both parents after an explanation of the objectives, procedures and possible risks and benefits of the research, along with the signature of two witnesses

Exclusion Criteria:

- Diagnosis of complex congenital cardiopathy with PPHN

- Cyanotic congenital cardiology defect

- Insufficiency of the tricuspid valve

- Immunosuppressive disease. HIV has been associated with PPHN and human herpesvirus with vascular remodeling, perivascular macrophages, and lung fibrosis

- Clinical entities that preclude the total parenteral nutrition for one day or longer.

- Presence of profuse and persistent hemorrhage at any level

Elimination criteria

- Parents who withdraw their consent.

- Starting a drug at doses for nonclotting treatment such as heparin, enoxaparin.

- Development of profuse and persistent hemorrhage at any level after receiving vitamin K treatment.

Ishod

Primarne mjere ishoda

1. Change on Systolic pressure of pulmonary artery [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

measured by echocardiography in millimeters of mercury (mm/Hg)

2. Change on Mean pressure of the pulmonary artery [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

measured by echocardiography in mm//Hg

3. Change on Pulmonary output [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

measured by echocardiography in units

4. Change on Cardiac output [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

measured by echocardiography in mL/min

5. Change on Preductal partial pressure of oxygen (PaO2) [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

Measure the amount of oxygen in blood measured by gasometry in arterial blood in mmHg

6. Change on Preductal and postductal oxygen saturation (SatO2) [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

It is a measure of oxygenation in hemoglobin. It is preductal if the measurement id on hand, and postductal if it is on foot, determined by an pulse oximeter in percentage

7. Change on Inspired fraction of oxygen (FiO2) [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

Oxygen concentration supplied by ventilation support in percentage

8. Change on Nutritional status [Before surgery (baseline), day 7, day 14 and day 21 post-surgery.]

Measurement of body weight in grams, length and head circumference in centimeters to obtain an eutrophic or undernutrition outcome using the Fenton's standard reference of growth and/or World Health Organization as appropriate for preterm or term infants, respectively.

9. Change of pain perception [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]

Pain will be measured with COMFORT scale computed by the sum of 8 sections with scores from 1 to 5. The sum will be scored as mild (<10 points), moderate (10-20 points) and severe (>20 points)

Sekundarne mjere ishoda

1. Concentration of plasma cytokines as inflammatory markers [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day, and day 14 post-surgery.]

Determination of pro and anti-inflammatory cytokines interleukin (IL)-1beta, tumoral necrosis factor-alpha, IL-6, IL-8, IL-10, IL-12 (p70) (pg/milliliter) in plasma by luminex-based immunoassay.

2. Concentration of inflammatory derived-lipid mediators [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day, and day 14 post-surgery.]

Determination lipid mediators such as eicosanoids and resolvin(s) in ng/ml by liquid chromatography coupled to mass spectrometry.

3. Concentration of total free thiols [At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.]

This will be measured in urine by ELISA in pg/milliliter

4. Concentration of nitrotyrosine [At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.]

This will be measured in urine by ELISA in micromol per liter (uM)

5. Concentration of reduced/oxidized glutathione ratio (GSH/GSSG) [At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.]

This will be measured in urine by ELISA in uM/milliliter

6. Concentration of 8-hydroxy-2-deoxyguanosine (8OHgD) [At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.]

This will be measured in urine by ELISA in pg/milliliter

7. Concentration of Ratio of F2-isoprostanes (F2-isop) and F2-isofurans (F2-isof) [At study entry, before surgery (2 baselines), and once a day until day 7 after surgery, then at 14 and 21 days-post-surgery.]

This ratio will be measured in urine in nmol/liter by Liquid chromatography coupled to mass spectrometry.

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