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1.
Am J Perinatol ; 38(S 01): e92-e101, 2021 08.
Article in English | MEDLINE | ID: mdl-32120418

ABSTRACT

OBJECTIVE: This study aimed to establish neonatal serum triglyceride (TG) level reference ranges during lipid infusion and correlate peak TG with neonatal outcomes. STUDY DESIGN: This is a retrospective review of 356 neonates with 696 TG measures obtained in four neonatal intensive care units between 2015 and 2017. TG was evaluated collectively to establish a reference range and a threshold limit. To analyze the effects of a higher TG threshold, neonates were categorized by their peak TG: <180 (TG<180), 180 to 400 (TG180-400), and > 400 mg/dL (TG>400). Univariable and multivariable regression models were constructed to compare peak TG to patient characteristic and clinical outcomes. RESULTS: The frequency of TG > 400 mg/dL was 5% and found only in neonates weighing < 1.5 kg. Neonates in the TG180-400 (n = 91) group were significantly lower in birth weight and gestational age, had lower 5-minute APGAR scores, and had increased ventilatory requirement when compared with neonates in the TG<180 (n = 240) group (all p < 0.001). The TG180-400 group had increased risk of severe intraventricular hemorrhage (p = 0.02) and bronchopulmonary dysplasia (p = 0.03). Elevated TG was associated with mortality (odds ratio [OR]: 14.4, p < 0.001) in univariable analysis, but the relationship weakened (OR: 4.4, p = 0.05) after adjusting for comorbidities in multivariable logistic regression. CONCLUSION: It is unclear if the adverse outcomes seen in neonates with higher peak TG were due to elevated TG alone, or whether illness severity predicted the increased TG. More prospective studies are needed to further delineate the relationships.


Subject(s)
Fat Emulsions, Intravenous , Hypertriglyceridemia/mortality , Infant, Newborn/blood , Parenteral Nutrition , Triglycerides/blood , Birth Weight , Bronchopulmonary Dysplasia/blood , Bronchopulmonary Dysplasia/etiology , Cerebral Intraventricular Hemorrhage/blood , Cerebral Intraventricular Hemorrhage/etiology , Fat Emulsions, Intravenous/administration & dosage , Fat Emulsions, Intravenous/adverse effects , Female , Gestational Age , Humans , Hypertriglyceridemia/complications , Infant, Small for Gestational Age , Intensive Care Units, Neonatal , Logistic Models , Male , Odds Ratio , Reference Values , Retrospective Studies , Risk Factors , Triglycerides/adverse effects
2.
Ann Pharmacother ; 54(11): 1109-1143, 2020 11.
Article in English | MEDLINE | ID: mdl-32483988

ABSTRACT

OBJECTIVE: To compile and synthesize the available literature describing medical cannabis use across various disease states. DATA SOURCES: PubMed, EBSCO, and Google Scholar searches were conducted using MeSH and/or keywords. STUDY SELECTION AND DATA EXTRACTION: Studies were included if they described the use of cannabis-based products and medications in the treatment of a predefined list of disease states in humans and were published in English. The extraction period had no historical limit and spanned through April 2019. DATA SYNTHESIS: Evidence was compiled and summarized for the following medical conditions: Alzheimer disease, amyotrophic lateral sclerosis, autism, cancer and cancer-associated adverse effects, seizure disorders, human immunodeficiency virus, inflammatory bowel disease, multiple sclerosis (MS), nausea, pain, posttraumatic stress disorder, and hospice care. RELEVANCE TO PATIENT CARE AND CLINICAL PRACTICE: Based on identified data, the most robust evidence suggests that medical cannabis may be effective in the treatment of chemotherapy-induced nausea and vomiting, seizure disorders, MS-related spasticity, and pain (excluding diabetic neuropathy). Overall, the evidence is inconsistent and generally limited by poor quality. The large variation in cannabis-based products evaluated in studies limits the ability to make direct comparisons. Regardless of the product, a gradual dose titration was utilized in most studies. Cannabis-based therapies were typically well tolerated, with the most common adverse effects being dizziness, somnolence, dry mouth, nausea, and euphoria. CONCLUSIONS: As more states authorize medical cannabis use, there is an increasing need for high-quality clinical evidence describing its efficacy and safety. This review is intended to serve as a reference for clinicians, so that the risks and realistic benefits of medical cannabis are better understood.


Subject(s)
Drug Utilization Review/trends , Medical Marijuana/therapeutic use , Clinical Trials as Topic , Humans , Medical Marijuana/administration & dosage , Medical Marijuana/adverse effects , Multiple Sclerosis/drug therapy , Nausea/drug therapy , Pain/drug therapy , Practice Guidelines as Topic , Vomiting/drug therapy
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