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1.
G Ital Cardiol (Rome) ; 20(11): 651-657, 2019 Nov.
Article in Italian | MEDLINE | ID: mdl-31697272

ABSTRACT

BACKGROUND: The purpose of this study was to use hypnosis in patients with congenital heart disease undergoing transesophageal echocardiography (TEE). METHODS: From January 2016 to July 2017, 50 adult patients undergoing TEE were randomly assigned to two groups: TEE in hypnosis (n = 23), TEE in sedation (n = 27). Vital parameters (heart rate [HR], blood pressure [BP], oxygen saturation [SO2] before, during and after the procedure) and drug administration were recorded. The State-Trait Anxiety Inventory was performed before and after TEE, the memory and experience of TEE through a structured interview were assessed. RESULTS: All patients in the hypnosis group performed TEE without any sedation. As for anxiety before TEE, no significant differences were observed between groups; after TEE all patients were less anxious than at the beginning (p<0.001) with a greater decrease in patients of the hypnosis group (p<0.001). Before TEE, there were no significant differences also in HR, BP and SO2. During TEE in both groups a similar increase in HR and BP was found (p<0.001), whereas SO2 values remained stable. In the responses to the structured interview, 94% of patients in the sedation group remembered everything vs 36% of the hypnosis group (p<0.05). No differences were found in the other answers between the two groups. CONCLUSIONS: Hypnosis in TEE is useful to improve the emotional experience of patients with congenital heart disease.


Subject(s)
Echocardiography, Transesophageal/methods , Heart Defects, Congenital/diagnostic imaging , Hypnosis/methods , Hypnotics and Sedatives/administration & dosage , Adult , Aged , Anxiety/prevention & control , Blood Pressure/physiology , Echocardiography, Transesophageal/psychology , Female , Heart Defects, Congenital/psychology , Heart Rate/physiology , Humans , Male , Middle Aged , Young Adult
2.
Eur J Pediatr ; 170(12): 1569-75, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21814782

ABSTRACT

Reflex vagal hypertonia (RVH) has been identified as a possible cause of sudden unexpected death in infants during the first year of life. Homatropine methylbromide (HM) is an anticholinergic drug known to inhibit muscarinic acetylcholine receptors, thus affecting the parasympathetic nervous system. The aim of the present study was to investigate the effects of HM on 24-h Holter electrocardiographic signs of RVH (pre-HM treatment vs post-HM treatment; post-HM treatment vs a control group of healthy infants). A total of 50 patients (mean age, 6.1 ± 2.7 months; 28 males, 22 females; 12 born pre-term) affected by RVH were enrolled in the study. Pre-HM treatment vs post-HM treatment: statistically significant differences were detected for higher heart rate, lower heart rate, mean heart rate, longer sinusal pause, presence of advanced atrio-ventricular blocks, and systolic blood pressure (p < 0.001, p < 0.00001, p < 0.02, p < 0.00001, p < 0.05, and p < 0.04, respectively). A statistically significant correlation was revealed between HM-administered dose and both average heart rate and systolic blood pressure (r = 0.93, p < 0.0001; r = 0.94, p < 0.0001, respectively). No significant differences were detected between post-HM treatment electrocardiographic data and those of the control group. By antagonizing action of the vagus nerve of the parasympathetic system on the heart, thus increasing cardiac frequency, HM treatment appears to feature a good safety profile and be highly effective in preventing transient infantile hypervagotonia, the potential cause of several cases of sudden unexpected death during the first year of life.


Subject(s)
Autonomic Nervous System Diseases/complications , Sudden Infant Death/prevention & control , Tropanes/administration & dosage , Vagus Nerve/physiopathology , Administration, Oral , Autonomic Nervous System Diseases/drug therapy , Autonomic Nervous System Diseases/physiopathology , Dose-Response Relationship, Drug , Drug Administration Schedule , Electrocardiography, Ambulatory , Female , Follow-Up Studies , Heart Rate , Humans , Infant , Male , Retrospective Studies , Sudden Infant Death/etiology , Treatment Outcome , Vagus Nerve/drug effects
3.
J Matern Fetal Neonatal Med ; 23 Suppl 3: 30-3, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20873974

ABSTRACT

Supraventricular tachycardia (SVT), being atrioventricular re-entry the underlying mechanism, is the most frequent tachyarrhythmia requiring a medical treatment in infants with no cardiac disease. The acute treatment of a single episode of SVT has generally an excellent prognosis. An antiarrhythmic prophylaxis of SVT recurrences is usually recommended during the first year of life. Although many efficient drugs are available for the SVT treatment, a careful risk-benefit analysis of each single case should suggest the correct drug choice.


Subject(s)
Anti-Arrhythmia Agents/therapeutic use , Choice Behavior , Infant, Newborn, Diseases/drug therapy , Tachycardia, Supraventricular/drug therapy , Chemoprevention/methods , Choice Behavior/physiology , Decision Making/physiology , Humans , Infant, Newborn , Infant, Newborn, Diseases/prevention & control , Secondary Prevention , Tachycardia, Supraventricular/prevention & control
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