Effect of a Parenteral Emulsion With Omega3 on PPHN
Kata kunci
Abstrak
Deskripsi
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.
tanggal
Terakhir Diverifikasi: | 06/30/2020 |
Pertama Dikirim: | 07/07/2019 |
Perkiraan Pendaftaran Telah Dikirim: | 07/21/2019 |
Pertama Diposting: | 07/23/2019 |
Pembaruan Terakhir Dikirim: | 07/15/2020 |
Pembaruan Terakhir Diposting: | 07/19/2020 |
Tanggal Mulai Studi Sebenarnya: | 08/11/2019 |
Perkiraan Tanggal Penyelesaian Utama: | 06/30/2022 |
Perkiraan Tanggal Penyelesaian Studi: | 06/30/2022 |
Kondisi atau penyakit
Intervensi / pengobatan
Dietary Supplement: Parenteral emulsion
Tahap
Kelompok Lengan
Lengan | Intervensi / pengobatan |
---|---|
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 |
Kriteria kelayakan
Jenis Kelamin yang Layak untuk Belajar | All |
Menerima Relawan Sehat | Iya |
Kriteria | 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. |
Hasil
Ukuran Hasil Utama
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.]
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.]
3. Change on Pulmonary output [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]
4. Change on Cardiac output [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]
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.]
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.]
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.]
8. Change on Nutritional status [Before surgery (baseline), day 7, day 14 and day 21 post-surgery.]
9. Change of pain perception [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day 14 and day 21 post-surgery.]
Ukuran Hasil Sekunder
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.]
2. Concentration of inflammatory derived-lipid mediators [Before surgery (baseline), 24 hour, 48 hour, 72 hour, day 7, day, and day 14 post-surgery.]
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.]
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.]
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.]
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.]
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.]