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1.
Intern Med J ; 46(6): 669-76, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27059169

ABSTRACT

BACKGROUND: The Barwon area in Australia has one of the highest incidence rates of inflammatory bowel disease (IBD) and therefore is an ideal location to study the impact of environmental exposures on the disease's development. AIM: To study these exposures prior to the development of IBD in a population-based cohort. METHOD: One hundred and thirty-two incident cases (81 Crohn disease (CD) and 51 ulcerative colitis (UC)) from an IBD registry and 104 controls replied to the International Organization of Inflammatory Bowel Diseases environmental questionnaire. This included 87 questions about pre-illness exposures that included childhood illnesses, vaccinations, breastfeeding, house amenities, pets and swimming, diet and smoking. RESULTS: The factors associated with CD included smoking (odds ratio (OR): 1.42, confidence interval (CI): 1-2.02, P = 0.029); childhood events, including tonsillectomy (OR: 1.74, CI: 1.15-2.6, P = 0.003) and chicken pox infection (OR: 3.89, CI: 1.61-9.4, P = 0.005) and pre-diagnosis intake of frequent fast food (OR: 2.26, CI: 1.76-4.33, P = 0.003). In UC, the risk factors included smoking (OR: 1.39, CI: 1.1-1.92, P = 0.026) and pre-diagnosis intake of frequent fast food (OR: 2.91, CI: 1.54-5.58, P < 0.001), and high caffeine intake was protective (OR: 0.51, 95% CI: 0.3-0.87, P = 0.002). Other protective exposures for UC included high fruit intake (OR: 0.59, CI: 0.4-0.88, P = 0.003) and having pets as a child (OR: 0.36, CI: 0.2-0.79, P = 0.001). CONCLUSION: This first Australian population-based study of environmental risk factors confirms that smoking, childhood immunological events and dietary factors play a role in IBD development; while high caffeine intake and pet ownership offer a protective effect.


Subject(s)
Diet , Inflammatory Bowel Diseases/epidemiology , Life Style , Adolescent , Adult , Aged , Australia/epidemiology , Case-Control Studies , Chickenpox/epidemiology , Child , Fast Foods/adverse effects , Female , Humans , Logistic Models , Male , Middle Aged , Odds Ratio , Registries , Risk Factors , Smoking/epidemiology , Surveys and Questionnaires , Tonsillectomy/statistics & numerical data , Young Adult
2.
Aliment Pharmacol Ther ; 37(4): 438-44, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23278192

ABSTRACT

BACKGROUND: Inflammatory bowel disease can impact on a patient's ability to maintain normal physical and mental function, and fulfil their social, family and work roles. Aspects of disability in IBD have received little attention. AIM: To develop, validate and apply a questionnaire directed towards evaluating these disease aspects. METHODS: A literature review on disability in IBD was undertaken, and opinion about aspects of disability to measure was sought from six IBD-specialised gastroenterologists. A questionnaire was developed, and IBD patients completed the new disability questionnaire, the SF-36 and the short-IBD (SIBDQ - 10 point). A subgroup of patients completed the questionnaire again 4 weeks later. Healthy volunteers were studied as a control group. RESULTS: A total of 116 IBD out-patients were approached, of whom 81 (52 Crohn's disease and 28 ulcerative colitis) participated. Nineteen patients were re-evaluated at 4 weeks. Twenty-five controls were studied. All subscales demonstrated good Cronbach's alpha reliability and reproducibility. There was a significant inverse correlation between the disability score and the SIBDQ and between the disability score and the SF36 and a positive correlation with the Crohn's Disease Activity Index (CDAI) (all P < 0.001). Disability differed between ulcerative colitis and controls, but not between active and inactive disease. CONCLUSIONS: The new disability questionnaire is sensitive for detecting disability, is reliable and reproducible, and correlates with disease activity in Crohn's disease, but not ulcerative colitis. Further prospective testing is now needed in the longer term, larger patient populations and in different countries and ethnicities.


Subject(s)
Colitis, Ulcerative/diagnosis , Crohn Disease/diagnosis , Disability Evaluation , Activities of Daily Living , Adolescent , Adult , Aged , Case-Control Studies , Disabled Persons , Female , Humans , Male , Middle Aged , Quality of Life , Reproducibility of Results , Severity of Illness Index , Surveys and Questionnaires , Young Adult
6.
Anaesthesia ; 36(1): 10-5, 1981 Jan.
Article in English | MEDLINE | ID: mdl-6110384

ABSTRACT

Sixty patients scheduled for day case surgery were allocated into two groups in a double-blind study. One group received temazepam 20 mg or 30 mg orally 1 hour before surgery whilst the second group received a placebo of identical appearance. The use of temazepam was followed by a greater frequency of sedation and anxiolysis and with fewer problems at induction. The time to awaken, the level of postoperative sedation and the ability to walk unaided were similar in both groups. Postoperative sequelae were less frequent in the temazepam group. Temazepam is advocated as a suitable drug for premedication in day case surgery.


Subject(s)
Ambulatory Surgical Procedures , Anti-Anxiety Agents , Preanesthetic Medication , Temazepam , Adolescent , Adult , Aged , Anti-Anxiety Agents/pharmacology , Anxiety/prevention & control , Clinical Trials as Topic , Double-Blind Method , Female , Hemodynamics/drug effects , Humans , Hypnotics and Sedatives , Male , Middle Aged , Placebos , Temazepam/adverse effects , Temazepam/pharmacology
7.
Anaesthesia ; 35(1): 60-4, 1980 Jan.
Article in English | MEDLINE | ID: mdl-6104935

ABSTRACT

Fifty healthy female patients scheduled for surgery were randonly allocated into two groups in a double-blind study. One group received lorazepam 2.5 mg orally at 2200 h on the evening before surgery as night sedation, and again at 0800 h on the morning before surgery as premedication. The second group received diazepam 10 mg orally at the samte times. The quality of sleep the night before surgery was superior in the lorazepam group (p less than 0.02). The frequency of effective sedation produced pre-operatively was similar in both groups. Although the incidence of amnesia for visual stimuli following lorazapam was higher (p less than 0.05) than with diazepam, there was no difference in the recall of auditory and painful stimuli. The overall incidence of side effects was similar for each drug and at the dosage used no difference was found in the time to awaken from anaesthesia.


Subject(s)
Anti-Anxiety Agents , Diazepam , Lorazepam , Preanesthetic Medication , Sleep/drug effects , Adult , Aged , Anesthesia, General , Anti-Anxiety Agents/therapeutic use , Clinical Trials as Topic , Diazepam/therapeutic use , Double-Blind Method , Female , Humans , Lorazepam/therapeutic use , Mental Recall/drug effects , Middle Aged , Postoperative Period , Random Allocation
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