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1.
Colorectal Dis ; 15(3): 374-9, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22849324

ABSTRACT

AIM: The advent of rescue medical therapy (cyclosporin or infliximab) and laparoscopic surgery has shifted the paradigm in managing steroid refractory acute severe ulcerative colitis (ASUC). We investigated prospectively the impact of rescue therapy on timing and postoperative complications of urgent colectomy and subsequent restorative surgery for steroid refractory ASUC. METHOD: All consecutive presentations of steroid refractory ASUC at the Royal Brisbane Hospital (1996-2009) were entered in the study. Data collated included demographics, clinical and laboratory parameters on admission, medical therapy and operative and postoperative details. Steroid refractory ASUC patients undergoing immediate colectomy were compared with those failing rescue therapy and requiring same admission colectomy. RESULTS: Of 108 steroid refractory ASUC presentations, 19 (18%) received intravenous steroids only and proceeded directly to colectomy. Rescue medical therapy was instituted in 89 (82%) patients with 30 (34%) failing to respond and proceeding to colectomy. There was no significant difference in the median time from admission to colectomy for rescue therapy compared with steroid-only cases (12 vs 10 days, P = 0.70) or 30-day complication rates (27%vs 47%, P = 0.22). The interval from colectomy to a subsequent restorative procedure was significantly longer for patients who failed rescue therapy (12 vs 5 months, P = 0.02). Furthermore 30-day complications following pouch surgery were significantly higher in patients who failed rescue therapy (32%vs 0%, P = 0.01). CONCLUSION: Rescue therapy in steroid refractory ASUC is not related to delay in urgent colectomy or increased post-colectomy complications.


Subject(s)
Colectomy/methods , Colitis, Ulcerative/surgery , Steroids/therapeutic use , Acute Disease , Adolescent , Adult , Aged , Aged, 80 and over , Colitis, Ulcerative/drug therapy , Female , Humans , Male , Middle Aged , Treatment Outcome , Young Adult
6.
J Prosthet Dent ; 63(6): 707-12, 1990 Jun.
Article in English | MEDLINE | ID: mdl-2163447

ABSTRACT

The epidemic of acquired immunodeficiency syndrome has initiated a number of regulations, at both the federal and state level, that impact directly on the practice of dentistry. During the past 5 to 6 years, guidelines have been published that specifically and generally state those procedures which should be implemented in the dental practice with regard to infectious disease control. However, confusion remains regarding these procedural guidelines and the differences that exist between municipal, state, and federal regulations. The ensuing discussion (1) reviews the historical background of the guidelines, (2) reflects on the current Occupational Safety and Health Administration guidelines as they relate to the dental practice, (3) summarizes the role of the regulatory agencies, (4) discusses federal and state statutes that have impact on the dental practitioner, and (5) describes the possible legal implications that these regulations may have on the dental practice.


Subject(s)
Centers for Disease Control and Prevention, U.S. , Communicable Disease Control/legislation & jurisprudence , Legislation, Dental , United States Occupational Safety and Health Administration , Acquired Immunodeficiency Syndrome/prevention & control , Forecasting , Hepatitis B/prevention & control , Humans , Legislation, Dental/trends , Practice Management, Dental/legislation & jurisprudence , State Government , United States
7.
Chronicle ; 53(3): 38-9, 44-5, 1990 May.
Article in English | MEDLINE | ID: mdl-2279452
8.
Chronicle ; 51(7): 100-1, 104-5, 1988 Dec.
Article in English | MEDLINE | ID: mdl-3271201
9.
Br J Clin Pharmacol ; 9(4): 341-9, 1980 Apr.
Article in English | MEDLINE | ID: mdl-7378250

ABSTRACT

1 A system is described for screening new chemical entities in normal human subjects, which is designed to search for novel drug actions at an early stage of drug development. 2 In single (subject) blind experiments, doses are increased incrementally from one subject to next, with immediate feed-back of results from each dose. 3 As many physiological variables as possible are recorded, for which a purpose-designed apparatus system was constructed, and connected to a computer. 4 To overcome problems of inter-subject variability, the need for sensitivity, and to identify drug-related effects from the mass of data generated, a novel data management system was developed, and physiological profiles of volunteer subjects were built up to provide control data. 5 Results from a validation experiment in which isoprenaline was infused intravenously at different rates are presented and discussed.


Subject(s)
Drug Evaluation/methods , Dose-Response Relationship, Drug , Electrocardiography , Hemodynamics/drug effects , Humans , Informed Consent , Pharmaceutical Preparations/administration & dosage , Pharmaceutical Preparations/metabolism , Respiration/drug effects , Saliva/metabolism
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