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1.
J Low Genit Tract Dis ; 28(2): 169-174, 2024 Apr 01.
Article in English | MEDLINE | ID: mdl-38346422

ABSTRACT

OBJECTIVE: Topical corticosteroid (TC) phobia (TCP) is common in subjects affected with chronic inflammatory skin diseases who need prolonged corticosteroid treatments. The aim of this study was to assess TCP in women affected with vulvar lichen sclerosus (VLS). MATERIALS AND METHODS: This observational, cross-sectional study included adult patients with VLS who either started or were undergoing a TC treatment at our vulva unit between May 2022 and May 2023. All patients completed the self-administered TOPICOP questionnaire, which is validated for measuring concerns, worries, and beliefs about TC use. The scores obtained were analyzed in relation to demographic, history, and clinical data. RESULTS: The majority of the 165 (92.1%, 66.5 ± 11.9 years) included patients who had previously undergone TC treatments, mostly for VLS; 81.8% of them had received information about TCs, mainly from dermatologists (86.7%). The median global TOPICOP score was 16.7% (interquartile range. 8.3-30.6), corresponding to a raw median value of 6.0 (interquartile range, 3.0-11.0). The median subscores for the 2 TOPICOP domains, namely, mistaken beliefs and worries about TCs, were equal to each other. At multivariate analysis, none of the collected variables showed a significant association with the degree of TCP. CONCLUSIONS: In our VLS patients, TCP resulted rather low, probably because of the small skin area being treated and the high percentage of women who had already used TCs and who had received information about them from a dermatologist. This latter point suggests that adequate counseling could be a strong basis for greater awareness and serenity in the long-term use of TCs.


Subject(s)
Dermatologic Agents , Phobic Disorders , Skin Diseases , Vulvar Lichen Sclerosus , Adult , Humans , Female , Vulvar Lichen Sclerosus/complications , Vulvar Lichen Sclerosus/drug therapy , Cross-Sectional Studies , Glucocorticoids/therapeutic use , Adrenal Cortex Hormones/therapeutic use , Phobic Disorders/chemically induced , Phobic Disorders/complications , Phobic Disorders/drug therapy
3.
Psychiatry Res ; 228(3): 571-5, 2015 Aug 30.
Article in English | MEDLINE | ID: mdl-26141602

ABSTRACT

The inhalation of 35% carbon dioxide (CO2) induces panic and anxiety in people with panic disorder (PD) and in people with various other psychiatric disorders. The anxiogenic effect of CO2 in people with eating disorders has received sparse attention despite the fact that PD and bulimia nervosa (BN) have several common psychological and neurobiological features. This study compared CO2-reactivity across three groups of participants: females with BN, females with PD, and female controls without known risk factors for enhanced CO2-reactivity (e.g., social anxiety disorder, first degree relatives with PD). Reactivity was measured by self-reported ratings of panic symptomatology and subjective anxiety, analyzed as both continuous variables (change from room-air to CO2) and dichotomous variables (positive versus negative responses to CO2). Analyses of each outcome measure demonstrated that CO2-reactivity was similar across the BN and PD groups, and reactivity within each of these two groups was significantly stronger than that in the control group. This is the first study to demonstrate CO2-hyperreactivity in individuals with BN, supporting the hypothesis that reactivity to this biological paradigm is not specific to PD. Further research would benefit from examining transdiagnostic mechanisms in CO2-hyperreactivity, such as anxiety sensitivity, which may account for this study's results.


Subject(s)
Bulimia Nervosa/chemically induced , Bulimia Nervosa/diagnosis , Carbon Dioxide/administration & dosage , Panic Disorder/chemically induced , Panic Disorder/diagnosis , Administration, Inhalation , Adolescent , Adult , Bulimia Nervosa/blood , Carbon Dioxide/blood , Female , Humans , Panic Disorder/blood , Phobic Disorders/blood , Phobic Disorders/chemically induced , Phobic Disorders/diagnosis , Risk Factors , Young Adult
4.
Twin Res Hum Genet ; 15(4): 473-82, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22854069

ABSTRACT

BACKGROUND: Previous studies examined caffeine use and caffeine dependence and risk for the symptoms, or diagnosis, of psychiatric disorders. The current study aimed to determine if generalized anxiety disorder (GAD), panic disorder, phobias, major depressive disorder (MDD), anorexia nervosa (AN), or bulimia nervosa (BN) shared common genetic or environmental factors with caffeine use, caffeine tolerance, or caffeine withdrawal. METHOD: Using 2,270 women from the Virginia Adult Twin Study of Psychiatric and Substance Use Disorders, bivariate Cholesky decomposition models were used to determine if any of the psychiatric disorders shared genetic or environmental factors with caffeine use phenotypes. RESULTS: GAD, phobias, and MDD shared genetic factors with caffeine use, with genetic correlations estimated to be 0.48, 0.25, and 0.38, respectively. Removal of the shared genetic and environmental parameter for phobias and caffeine use resulted in a significantly worse fitting model. MDD shared unique environmental factors (environmental correlation=0.23) with caffeine tolerance; the genetic correlation between AN and caffeine tolerance and BN and caffeine tolerance were 0.64 and 0.49, respectively. Removal of the genetic and environmental correlation parameters resulted in significantly worse fitting models for GAD, phobias, MDD, AN, and BN, which suggested that there was significant shared liability between each of these phenotypes and caffeine tolerance. GAD had modest genetic correlations with caffeine tolerance, 0.24, and caffeine withdrawal, 0.35. CONCLUSIONS: There was suggestive evidence of shared genetic and environmental liability between psychiatric disorders and caffeine phenotypes. This might inform us about the etiology of the comorbidity between these phenotypes.


Subject(s)
Anorexia Nervosa/chemically induced , Anxiety Disorders/chemically induced , Bulimia/chemically induced , Caffeine/adverse effects , Depressive Disorder, Major/chemically induced , Diseases in Twins/chemically induced , Panic Disorder/chemically induced , Phobic Disorders/chemically induced , Substance Withdrawal Syndrome/genetics , Substance-Related Disorders/genetics , Adult , Anorexia Nervosa/genetics , Anorexia Nervosa/psychology , Anxiety Disorders/genetics , Anxiety Disorders/psychology , Bulimia/genetics , Bulimia/psychology , Depressive Disorder, Major/genetics , Depressive Disorder, Major/psychology , Diseases in Twins/genetics , Diseases in Twins/psychology , Female , Gene-Environment Interaction , Humans , Panic Disorder/genetics , Panic Disorder/psychology , Phenotype , Phobic Disorders/genetics , Phobic Disorders/psychology , Registries , Risk Factors , Substance Withdrawal Syndrome/psychology , Substance-Related Disorders/psychology , Virginia
5.
Environ Health Perspect ; 120(6): 817-23, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22538241

ABSTRACT

BACKGROUND: Different lines of evidence suggest that low-level lead exposure could be a modifiable risk factor for adverse psychological symptoms, but little work has explored this relation. OBJECTIVE: We assessed whether bone lead--a biomarker of cumulative lead exposure--is associated with depression and anxiety symptoms among middle-age and elderly women. METHODS: Participants were 617 Nurses' Health Study participants with K-shell X-ray fluorescence bone lead measures and who had completed at last one Mental Health Index 5-item scale (MHI-5) and the phobic anxiety scale of the Crown-Crisp Index (CCI) assessment at mean ± SD age of 59 ± 9 years (range, 41-83 years). With exposure expressed as tertiles of bone lead, we analyzed MHI-5 scores as a continuous variable using linear regression and estimated the odds ratio (OR) of a CCI score ≥ 4 using generalized estimating equations. RESULTS: There were no significant associations between lead and either outcome in the full sample, but associations were found among premenopausal women and women who consistently took hormone replacement therapy (HRT) between menopause and bone lead measurement (n = 142). Compared with women in the lowest tertile of tibia lead, those in the highest scored 7.78 points worse [95% confidence interval (CI): -11.73, -3.83] on the MHI-5 (p-trend = 0.0001). The corresponding OR for CCI ≥ 4 was 2.79 (95% CI: 1.02, 7.59; p-trend = 0.05). No consistent associations were found with patella lead. CONCLUSIONS: These results provide support for an association of low-level cumulative lead exposure with increased depressive and phobic anxiety symptoms among older women who are premenopausal or who consistently take postmenopausal HRT.


Subject(s)
Depression/epidemiology , Environmental Exposure/statistics & numerical data , Lead/toxicity , Phobic Disorders/epidemiology , Age Factors , Bone and Bones/chemistry , Depression/chemically induced , Estrogen Replacement Therapy/statistics & numerical data , Female , Humans , Linear Models , Menopause/psychology , Odds Ratio , Phobic Disorders/chemically induced , Risk Factors , Spectrometry, X-Ray Emission , United States/epidemiology
6.
Nicotine Tob Res ; 14(2): 176-83, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22025539

ABSTRACT

INTRODUCTION: Previous studies have shown links between anxiety and depression and chronic obstructive pulmonary disease (COPD), but little is known about possible mechanisms of this association. The current study examined whether the observed relationship between anxiety and depression and COPD is explained by confounding due to cigarette smoking and lifetime nicotine dependence. METHODS: Data were drawn from the National Comorbidity Survey Replication, a community-based representative sample of adults in the United States. RESULTS: Analyses suggest that the association between anxiety disorders and COPD appears to be largely explained by confounding by former cigarette smoking and lifetime nicotine dependence. The association between mood disorders and COPD appears to be largely explained by confounding by lifetime nicotine dependence. CONCLUSIONS: These findings provide initial evidence suggesting that the association between anxiety, depression, and COPD may be at least partly attributable to confounding by cigarette smoking and nicotine dependence. Efforts toward prevention of chronic lung disease may be more effective if treatment and prevention efforts aimed at smoking cessation address mental health problems.


Subject(s)
Anxiety/epidemiology , Depression/epidemiology , Pulmonary Disease, Chronic Obstructive/epidemiology , Smoking/adverse effects , Tobacco Use Disorder/epidemiology , Adolescent , Adult , Aged , Anxiety/chemically induced , Comorbidity , Depression/chemically induced , Diagnostic and Statistical Manual of Mental Disorders , Female , Humans , Logistic Models , Male , Mental Disorders/chemically induced , Mental Disorders/epidemiology , Middle Aged , Odds Ratio , Phobic Disorders/chemically induced , Phobic Disorders/epidemiology , Pulmonary Disease, Chronic Obstructive/chemically induced , Smoking/epidemiology , Smoking/psychology , Time Factors , Tobacco Use Disorder/psychology , Young Adult
7.
Travel Med Infect Dis ; 9(2): 82, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21310662

ABSTRACT

A woman is described who developed fear of flying because she took mefloquine as malaria prophylaxis prior to the flight. Mefloquine, because of its potential neurotoxicity, should not be used for persons with fear of flying.


Subject(s)
Aircraft , Antimalarials/adverse effects , Mefloquine/adverse effects , Phobic Disorders/chemically induced , Antimalarials/administration & dosage , Dizziness/chemically induced , Doxycycline/administration & dosage , Female , HIV Infections/complications , HIV Infections/drug therapy , Humans , Malaria/prevention & control , Mefloquine/administration & dosage , Middle Aged , Nausea/chemically induced
8.
Psychiatry Res ; 169(2): 149-53, 2009 Sep 30.
Article in English | MEDLINE | ID: mdl-19698996

ABSTRACT

Studies have demonstrated the vulnerability of anxiety disorder patients to challenge tests. Our aim was to observe if panic disorder (PD) patients and generalized social anxiety disorder (GSAD) and performance social anxiety disorder (PSAD) patients respond in a similar way to the induction of anxiety symptoms and panic attacks by an oral caffeine challenge test. We compared 28 PD patients, 25 GSAD patients, 19 PSAD, and 26 control subjects after a 480-mg caffeine test. The patients had not received psychotropic drugs for at least a 4-week period. In a randomized double-blind experiment performed in two occasions 7 days apart, 480 mg of caffeine and a caffeine-free solution were administered and anxiety scales were administered before and after each test. A panic attack was induced in 17 (60.7%) PD patients, 4 (16.0%) GSAD patients, and 10 (52.6%) PSAD patients, during the caffeine test. None of the control subjects had a panic attack after the caffeine intake. Neither patients nor any control subject had a panic attack after drinking the caffeine-free solution. Our data suggest that there is an association between PD and PSAD hyperreactivity to an oral caffeine challenge test. The PD and PSAD patients had a higher number of induced panic attacks, some specific anxiety symptoms, and a more severe anxiety response than GSAD patients and normal volunteers.


Subject(s)
Caffeine , Central Nervous System Stimulants , Panic Disorder/chemically induced , Panic Disorder/diagnosis , Phobic Disorders/chemically induced , Phobic Disorders/diagnosis , Adolescent , Adult , Analysis of Variance , Caffeine/adverse effects , Central Nervous System Stimulants/adverse effects , Double-Blind Method , Humans , Middle Aged , Psychiatric Status Rating Scales , Social Behavior , Surveys and Questionnaires , Young Adult
9.
Psychother Psychosom Med Psychol ; 59(3-4): 117-23, 2009.
Article in German | MEDLINE | ID: mdl-19350471

ABSTRACT

This paper presents the Social Phobia Psychotherapy Research Network (SOPHO-NET). SOPHO-NET is among the five research networks on psychotherapy funded by "Bundesministerium für Bildung und Forschung". The research program encompasses a coordinated group of studies of social phobia. In the central project (Study A), a multi-center randomized controlled trial, refined models of manualized cognitive-behavioral therapy (CBT) and manualized short-term psychodynamic psychotherapy (STPP) are compared in the treatment of social phobia. A sample of n=512 outpatients will be randomized to either CBT, STPP or wait list. For quality assurance and treatment integrity, a specific project has been established (Project Q). Study A is complemented by four interrelated projects focusing on attachment style (Study B1), cost-effectiveness (Study B2), polymorphisms in the serotonin transporter gene (Study C1) and on structural and functional deviations of hippocampus and amygdala (Study C2). Thus, the SOPHO-NET program allows for a highly interdisciplinary research of psychotherapy in social phobia.


Subject(s)
Phobic Disorders/genetics , Phobic Disorders/psychology , Phobic Disorders/therapy , Psychotherapy , Cognitive Behavioral Therapy , Humans , Multicenter Studies as Topic , Phobic Disorders/chemically induced , Phobic Disorders/economics , Polymorphism, Genetic , Psychotherapy, Brief , Quality Assurance, Health Care , Randomized Controlled Trials as Topic , Research
11.
Neurosci Biobehav Rev ; 32(7): 1267-76, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18619675

ABSTRACT

Specific phobias, including animal phobias, are the most common anxiety disorders, and have a strong innate and genetic component. Research on the neurobiology and environmental constraints of innate fear of predators in rodents may be useful in elucidating mechanisms of animal phobias in humans. The present article reviews research on innate fear in rats to trimethylthiazoline (TMT), an odor originally isolated from fox feces. TMT induces unconditioned freezing and other defensive responses that are regulated by the dose of TMT and the shape of the testing environment. Contextual conditioning induced by TMT occurs, but is constrained by the environment. Lesion studies indicate the amygdala circuitry subserving fear conditioning is not necessary for unconditioned fear to TMT. Additionally, a medial hypothalamic defensive circuit also appears not necessary for unconditioned freezing to TMT, whereas circuits that include the medial nucleus of the amygdala and the bed nucleus of the stria terminalis are essential. The importance of these findings of innate predator odor fear in rodents to animal phobias in humans is discussed.


Subject(s)
Amygdala/drug effects , Behavior, Animal/drug effects , Fear/drug effects , Neural Pathways/drug effects , Phobic Disorders/chemically induced , Thiazoles/pharmacology , Amygdala/physiology , Animals , Anxiety/chemically induced , Disease Models, Animal , Environment , Humans , Hypothalamus/drug effects , Odorants , Rats
14.
Psychiatry Res ; 134(1): 37-42, 2005 Mar 30.
Article in English | MEDLINE | ID: mdl-15808288

ABSTRACT

The current investigation uses a large non-clinical sample of undergraduate college students (N=189) to investigate schizotypal traits among cannabis and non-cannabis users, as well as the temporal order of the onset of these traits and cannabis use. Findings suggest that regular cannabis users are significantly more prone to cognitive and perceptual distortions as well as disorganization, but not interpersonal deficits, than non-regular users and those who have never used. Additionally, the onset of schizotypal symptoms generally precedes the onset of cannabis use. The findings do not support a causal link between cannabis use and schizotypal traits.


Subject(s)
Marijuana Abuse/psychology , Schizotypal Personality Disorder/psychology , Adolescent , Adult , Cannabinoids/adverse effects , Cognition Disorders/chemically induced , Cognition Disorders/diagnosis , Cognition Disorders/psychology , Female , Humans , Interpersonal Relations , Male , Marijuana Abuse/diagnosis , Perceptual Distortion , Personality Inventory/statistics & numerical data , Phobic Disorders/chemically induced , Phobic Disorders/diagnosis , Phobic Disorders/psychology , Psychometrics/statistics & numerical data , Reference Values , Schizotypal Personality Disorder/diagnosis , Social Behavior , Students/psychology , Surveys and Questionnaires
15.
J Dev Behav Pediatr ; 26(2): 123-7, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15827464

ABSTRACT

Difficulty swallowing solids and/or liquids accompanied by intense anxiety that results in restricted eating patterns or complete avoidance of eating may not have an easily identified underlying medical cause. This type of "eating disorder," which has also been described as "choking phobia," may occur in the absence of body image distortion, fear of becoming fat, or the desire to be thinner. The primary complaint in these children may be physical discomfort accompanied by high anxiety. Negative consequences can be severe and include social withdrawal, family distress, and deleterious effects on the child's physical health. Prompt recognition in the pediatric setting is, therefore, critical to avoid escalation of symptoms and treatment delays. Three pediatric cases of severe choking phobia refractory to prior intervention are presented in which rapid and sustained improvement followed low-dose therapy with a selective serotonin reuptake inhibitor (SSRI). Possible predictors of response to low-dose SSRI treatment in children with choking phobia and future avenues for investigation are explored.


Subject(s)
Feeding and Eating Disorders/chemically induced , Phobic Disorders/chemically induced , Selective Serotonin Reuptake Inhibitors/adverse effects , Child , Dose-Response Relationship, Drug , Female , Humans , Male , Selective Serotonin Reuptake Inhibitors/administration & dosage , Selective Serotonin Reuptake Inhibitors/therapeutic use
16.
J Neurobiol ; 62(3): 386-96, 2005 Feb 15.
Article in English | MEDLINE | ID: mdl-15547935

ABSTRACT

Insects, like vertebrates, exhibit spatially complex locomotor activity patterns when foraging or navigating. Open field studies recently showed that Drosophila avoids central zones and stays at the periphery, an effect that can be interpreted as centrophobism and/or thigmotaxis. In this study, we further characterized this phenomenon and studied the responsible underlying neural mechanisms. The implication of the Drosophila mushroom bodies (MBs) in olfactory learning and memory processes is well documented. In an open field situation in which fly locomotor activity is recorded by video tracking, we show that center avoidance is greatly diminished in flies with hydroxyurea-ablated MBs, suggesting a new role for these structures. Furthermore, the temperature-sensitive allele of the dynamin gene shibire was expressed in various enhancer-trap P[GAL4] lines, disrupting synaptic transmission in different MB lobes. Specifically blocking the gamma lobes alters centrophobism/thigmotaxis while blocking the alpha/beta lobes does not, suggesting a functional specialization of MB lobes. Drosophila may serve as a new model system for elucidating the genetic and neural bases of such complex phenomena as centrophobism/thigmotaxis.


Subject(s)
Behavior, Animal/physiology , Motor Activity/physiology , Mushroom Bodies/physiology , Analysis of Variance , Animals , Animals, Genetically Modified , Disease Models, Animal , Drosophila , Female , Hydroxyurea/toxicity , Male , Mushroom Bodies/drug effects , Mushroom Bodies/injuries , Nucleic Acid Synthesis Inhibitors/toxicity , Phobic Disorders/chemically induced , Phobic Disorders/physiopathology , Sex Factors , Thermosensing/genetics , Video Recording/methods
17.
Psychol Rep ; 95(1): 192-6, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15460375

ABSTRACT

This case study concerns a 26-yr.-old male who had consumed large amounts of Ecstasy seven years previously. He stated that his increasingly intensive use of ecstasy over a 4-yr. period had led to the emergence of multiple psychiatric and psychological problems. Given these problems, he stopped using Ecstasy, but the problems had not resolved despite seven years of abstinence. The neurocognitive profile was very similar to that shown by current heavy Ecstasy users, with deficits in immediate and delayed verbal recall, moderately impaired memory function, but normal expressive language ability and perceptual functioning. Extremely high pathology was evident, including depression and phobic anxiety. Severe problems with sleep and sex were also reported. Further studies involving larger groups of abstinent former users are needed; adverse sequelae associated with intensive Ecstasy use may sometimes be enduring.


Subject(s)
Adrenergic Uptake Inhibitors/toxicity , Depressive Disorder/chemically induced , Memory Disorders/chemically induced , N-Methyl-3,4-methylenedioxyamphetamine/toxicity , Neuropsychological Tests , Phobic Disorders/chemically induced , Psychoses, Substance-Induced/diagnosis , Substance Withdrawal Syndrome/diagnosis , Substance-Related Disorders/rehabilitation , Adult , Depressive Disorder/diagnosis , Erectile Dysfunction/chemically induced , Erectile Dysfunction/psychology , Follow-Up Studies , Humans , Male , Memory Disorders/diagnosis , Memory Disorders/psychology , Panic Disorder/chemically induced , Panic Disorder/diagnosis , Panic Disorder/psychology , Phobic Disorders/diagnosis , Phobic Disorders/psychology , Psychoses, Substance-Induced/psychology , Sleep Wake Disorders/chemically induced , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/psychology , Substance Withdrawal Syndrome/psychology , Substance-Related Disorders/psychology
18.
J Consult Clin Psychol ; 71(2): 243-50, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12699019

ABSTRACT

Treatment of phobias is sometimes followed by a return of fear. Animal and human research has shown that changes in external and internal contexts between the time of treatment and follow-up tests often enhance return of fear. The present study examined whether shifts in caffeine (C) state would enhance return of fear. Participants who were highly afraid of spiders (n = 43) were treated in 1-session exposure-based therapy and tested for follow-up 1 week later. Participants were randomly assigned to 1 of 4 groups and received either placebo (P) or C at treatment and follow-up sessions: CC, PP, CP, and PC. Results demonstrated state-dependent learning. Participants experiencing incongruent drug states during treatment and follow-up (CP and PC) exhibited greater return of fear than those experiencing congruent drug states (CC and PP).


Subject(s)
Caffeine/adverse effects , Fear , Phobic Disorders/chemically induced , Spiders , Adolescent , Adult , Animals , Female , Humans , Male , Random Allocation , Surveys and Questionnaires
19.
Neurology ; 60(7): 1130-5, 2003 Apr 08.
Article in English | MEDLINE | ID: mdl-12682319

ABSTRACT

OBJECTIVE: To evaluate the efficacy and safety of risperidone in children and adults with Tourette syndrome. METHODS: This was an 8-week, randomized, double-blind, placebo-controlled trial. The primary outcome measure was the Total Tic score of the Yale Global Tic Severity Scale (YGTSS). RESULTS: Thirty-four medication-free subjects (26 children and 8 adults) ranging in age from 6 to 62 years (mean = 19.7 +/- 17.0 years) participated. YGTSS Total Tic scores were similar at baseline (26.0 +/- 5.1 for risperidone vs 27.4 +/- 8.5 for placebo). After 8 weeks of treatment (mean daily dose of 2.5 +/- 0.85), the 16 subjects on risperidone showed a 32% reduction in tic severity from baseline, compared to a 7% reduction for placebo patients (n = 18) (F[2,64] = 6.07; p = 0.004). The 12 children randomized to risperidone showed a 36% reduction in tic symptoms compared to an 11% decrease in the 14 children on placebo (F[2,48] = 6.38; p = 0.004). Two children on risperidone showed acute social phobia, which resolved with dose reduction in one subject but resulted in medication discontinuation in the other. A mean increase in body weight of 2.8 kg was observed in the risperidone group compared to no change in placebo (F[2,64] = 10.68; p = 0.0001). No extrapyramidal symptoms and no clinically significant alterations in cardiac conduction times or laboratory measures were observed. CONCLUSION: Risperidone appears to be safe and effective for short-term treatment of tics in children or adults with Tourette syndrome. Longer-term studies are needed to evaluate the durability of efficacy and safety over time.


Subject(s)
Risperidone/therapeutic use , Tics/drug therapy , Tourette Syndrome/drug therapy , Adolescent , Adult , Antipsychotic Agents/adverse effects , Antipsychotic Agents/therapeutic use , Body Weight/drug effects , Child , Diagnostic Techniques, Neurological , Dopamine Antagonists/adverse effects , Dopamine Antagonists/therapeutic use , Dose-Response Relationship, Drug , Double-Blind Method , Erectile Dysfunction/chemically induced , Female , Heart Conduction System/drug effects , Humans , Male , Middle Aged , Phobic Disorders/chemically induced , Risperidone/adverse effects , Severity of Illness Index , Tics/etiology , Tourette Syndrome/complications , Treatment Outcome
20.
Contemp Top Lab Anim Sci ; 42(2): 20-5, 2003 Mar.
Article in English | MEDLINE | ID: mdl-19757620

ABSTRACT

Acetaminophen administration is gaining popularity as a postsurgical analgesic in many rodent labs despite reports that animals may consume suboptimal doses as a result of taste neophobia. The present study evaluated the presence, duration, and extent of acetaminophen neophobia in adult male and female rats (Long Evans) with the intent of developing a protocol for administration of this analgesic in the rodent surgery lab. After a 7-day baseline period in which average water consumption, food consumption, and body weight were established for 32 rats (20 females and 12 males), cherry-flavored acetaminophen was administered (6 mg/ml) in the animals' water bottles for an additional 7 days. Fluid consumption, food consumption, and weight were monitored during this period of drug exposure. Male rats displayed a transient period (1 day) of reduced fluid consumption followed by elevated fluid consumption on subsequent days. Female animals displayed normal to elevated fluid consumption on all days of drug exposure. Both male and female animals, however, decreased their food intake after drug exposure and subsequently lost weight. Recommendations for the oral administration of acetaminophen as a postsurgical analgesic are discussed.


Subject(s)
Acetaminophen/administration & dosage , Analgesia/veterinary , Analgesics, Non-Narcotic/administration & dosage , Behavior, Animal/drug effects , Drinking Behavior/drug effects , Flavoring Agents/administration & dosage , Phobic Disorders/prevention & control , Administration, Oral , Animals , Body Weight/drug effects , Drinking/drug effects , Eating/drug effects , Female , Male , Pain, Postoperative/prevention & control , Pain, Postoperative/veterinary , Phobic Disorders/chemically induced , Rats , Rats, Long-Evans
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