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1.
Mil Med ; 166(12): 1038-45, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11778399

ABSTRACT

The preparation of military primary care physicians for practice in operational environments has taken on greater importance during the past decade. The Department of Defense military-unique curriculum identifies the elements that should be incorporated into residency training programs to accomplish comprehensive training in operational matters. We describe efforts to integrate the military-unique curriculum into internal medicine residency, including obstacles encountered, so that other programs may learn from our experience.


Subject(s)
Curriculum , Internal Medicine/education , Military Medicine/education , Humans , United States
2.
Clin Pharm ; 3(6): 638-43, 1984.
Article in English | MEDLINE | ID: mdl-6509877

ABSTRACT

The bioavailability of pseudoephedrine and triprolidine from combination and single-ingredient products was evaluated in a randomized, four-way crossover study. Healthy men volunteers received single doses of a tablet containing triprolidine hydrochloride and pseudoephedrine hydrochloride, a syrup containing the same two drugs, and single-ingredient tablets of each drug. Blood samples were collected before each dose and at 13 sampling times over 24 hours for determination of drug concentrations by radioimmunoassay. Observed peak concentration (Cmax), corresponding observed peak time (tmax), area under the plasma drug concentration-time curve from dosing to time infinity (AUC), and the ratio between plasma clearance and extent of bioavailability (CL/F) were determined. Nonlinear regression analysis was used to obtain estimates of lag time for absorption, first-order rate constant for absorption, first-order rate constant for elimination, and ratio between volume of distribution and extent of bioavailability. Data were analyzed for 19 of 20 men entering the study; data were complete for 16 of these. Pseudoephedrine concentrations were significantly different for the combination tablet and the syrup at four sampling times; no significant differences were found between pseudoephedrine concentrations for the combination tablet and single-ingredient tablet. Cmax, tmax, AUC, and CL/F for pseudoephedrine were not significantly different for the three formulations. Triprolidine concentrations at 8 hours were significantly higher for the combination tablet than for the single-ingredient tablet, and tmax for triprolidine was significantly higher for the combination tablet than for the syrup. For both pseudoephedrine and triprolidine, the combination tablet was bioequivalent to the syrup and to the single-drug tablets.


Subject(s)
Ephedrine/metabolism , Pyridines/metabolism , Triprolidine/metabolism , Adolescent , Adult , Biological Availability , Drug Combinations , Ephedrine/administration & dosage , Humans , Hydrogen-Ion Concentration , Kinetics , Male , Radioimmunoassay , Solubility , Triprolidine/administration & dosage
3.
Br J Clin Pharmacol ; 18(1): 86-9, 1984 Jul.
Article in English | MEDLINE | ID: mdl-6204666

ABSTRACT

The abilities of triprolidine 2.5 mg and pseudoephedrine 60 mg, alone and in combination, to protect against an increase in nasal airway resistance (NAR) after histamine challenge were determined in eighteen individuals with grass pollen allergy. The study was conducted outside the pollen season using a double-blind, placebo controlled crossover design. The prior administration of pseudoephedrine 60 mg and triprolidine 2.5 mg alone or in combination was superior to placebo in reducing the increase in NAR after challenge with 1.0% histamine. However, such NAR measurements did not differentiate between pseudoephedrine 60 mg and triprolidine 2.5 mg administered alone or in combination. Challenge with 0.1% histamine failed to discriminate between any of the test medications.


Subject(s)
Airway Resistance/drug effects , Ephedrine/therapeutic use , Histamine , Nasal Decongestants/therapeutic use , Pyridines/therapeutic use , Rhinitis, Allergic, Seasonal/drug therapy , Triprolidine/therapeutic use , Adult , Clinical Trials as Topic , Double-Blind Method , Drug Therapy, Combination , Ephedrine/administration & dosage , Humans , Nasal Decongestants/administration & dosage , Nasal Provocation Tests , Triprolidine/administration & dosage
4.
Ann Allergy ; 48(2): 87-92, 1982 Feb.
Article in English | MEDLINE | ID: mdl-6175254

ABSTRACT

A single capsule of sustained release pseudoephedrine (SUDAFED S.A., Burroughs Wellcome Co.) was shown by objective and subjective measurements to be superior to placebo in relieving nasal congestion associated with allergic rhinitis. The drug had no discernible effect on (1) the degree of wetness perceived in the mouth or nose, (2) a complex of symptoms which included sneezing, coughing, sniffing, swallowing, itching of eyes and nose or (3) number of nose blows. The study was marked by an absence of serious adverse reactions.


Subject(s)
Ephedrine/therapeutic use , Rhinitis, Allergic, Seasonal/drug therapy , Adult , Airway Resistance/drug effects , Delayed-Action Preparations , Ephedrine/adverse effects , Female , Headache/chemically induced , Humans , Male , Middle Aged , Mouth Mucosa/metabolism , Nasal Decongestants/therapeutic use , Nasal Mucosa/metabolism , Sleep Stages/drug effects , Smoking
5.
J Int Med Res ; 10(5): 341-7, 1982.
Article in English | MEDLINE | ID: mdl-6128282

ABSTRACT

Pseudoephedrine and triprolidine, administered every 6 hours as a combination, made separate and distinct contributions to the treatment of allergic rhinitis. Furthermore, the combination was perceived by the patients as being clinically superior to either of its components or placebo.


Subject(s)
Ephedrine/therapeutic use , Histamine H1 Antagonists/therapeutic use , Pyridines/therapeutic use , Rhinitis, Allergic, Seasonal/drug therapy , Triprolidine/therapeutic use , Clinical Trials as Topic , Double-Blind Method , Drug Combinations/therapeutic use , Humans , Placebos , Pseudoephedrine
6.
Ann Allergy ; 47(2): 87-91, 1981 Aug.
Article in English | MEDLINE | ID: mdl-7258744

ABSTRACT

A double-blind, parallel, placebo-controlled study was performed to assess the efficacy of a combination drug product containing the antihistamine, triprolidine, and the sympathomimetic, pseudoephedrine, in the treatment of allergic rhinitis. Allergic rhinitis was defined on the basis of coexistent nasal congestion and an aggregate symptom complex score which exceeded a pre-established value. Pseudoephedrine and triprolidine were shown to make distinct and separate contributions to the treatment of allergic rhinitis defined in this manner.


Subject(s)
Ephedrine/therapeutic use , Pyridines/therapeutic use , Rhinitis, Allergic, Seasonal/drug therapy , Triprolidine/therapeutic use , Airway Resistance/drug effects , Double-Blind Method , Drug Evaluation , Drug Therapy, Combination , Female , Humans , Male , Placebos
7.
Arch Surg ; 114(5): 616-22, 1979 May.
Article in English | MEDLINE | ID: mdl-36057

ABSTRACT

The relationship between liver blood flow and hepatic metabolism remains unclear. An animal model as well as a methodology that permits simultaneous assessment of both of these functions are proposed. Several fractions of inspired oxygen were used to produce arterial oxygen levels commonly seen in clinical practice; these ranged from hyperoxemia to established hypoxemia. Over this range there were no considerable changes in transhepatic blood flow, but there were considerable changes in hepatic metabolism as shown by measurements of the hepatic parenchymal pH, transhepatic oxygen consumption, and lactic acid use. Of these, the parenchymal pH seems to be the most sensitive indicator of metabolic events.


Subject(s)
Liver Circulation , Liver/metabolism , Animals , Dogs , Hemoglobins , Hydrogen-Ion Concentration , Lactates/blood , Models, Biological , Oxygen/blood , Oxygen Consumption
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