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1. |
A NEW YEAR |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 1-2
JOHN SOMBERG,
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ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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2. |
Superior Oblique Tendon Resection or Inferior Oblique Muscle Recession in Vertical Deviations |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 3-8
James Luton,
Stanley Muenzler,
Robin Smart,
Clinton Corder,
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摘要:
This study reports the results on patients undergoing superior oblique (SO) tendon resections with or without inferior oblique (IO) muscle recession to correct vertical deviations. The design of this study was nonrandomized, baseline-controlled, and postsurgical versus presurgical and was performed in a solo practice affiliated with a university ophthalmology department. One hundred ninety-five patients underwent surgery. Patients were evaluated presurgically and postoperatively in the major fields of muscle action. Resections were based on measurements at 14 inches in the field of major function of the SO. The surgical approach was a radial, rather than circumferential, incision extending from the limbus to the tarsus parallel to the lateral border of the superior rectus, followed by resection of the SO tendon. Surgery resulted in improved fusion in 78% of the cases. Average deviation in the left superior oblique field in SO tendon resection only (n = 14) was reduced from 11.0 to 1.7 prism diopters, and fusion improved 85% after treatment. In 181 cases of SO tendon resection or IO recession, the left superior oblique field was reduced from 15.8 to 3.6 diopters. SO tendon resection was successfully utilized to treat underacting SO muscle and vertical deviations. A radial incision facilitated the surgical procedure, and its use is recommended to those performing the surgery.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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3. |
Lack of Pharmacokinetic Drug Interactions Between Tiagabine and Carbamazepine or Phenytoin |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 9-16
Linda Gustavson,
Allen Cato,
Samuel Boellner,
Guoliang Cao,
Jiang Qian,
Helen Guenther,
Kenneth Sommerville,
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摘要:
Two single-center, open-label studies examined the potential effects of tiagabine on the pharmacokinetics and safety of carbamazepine and phenytoin at steady state. Twelve adult patients with seizures controlled by an individualized fixed dosage of antiepilepsy medication (carbamazepine or phenytoin) participated in each study. On day 1, the pharmacokinetics of the baseline antiepilepsy drug were determined. On days 2 through 18, tiagabine was titrated from 8 to 48 mg/d (or the maximum tolerated dose up to 48 mg/d), and the usual fixed dosage of carbamazepine or phenytoin was continued. The pharmacokinetic assessment was repeated on day 18. There were no statistically significant differences in carbamazepine, carbamazepine epoxide, and phenytoin pharmacokinetic parameters when either drug was administered alone or in combination with tiagabine. In each study, 11 of 12 patients (92%) experienced treatment-emergent adverse events after tiagabine was added. The most frequent adverse events were dizziness, headache, difficulty concentrating, drowsiness, and tremor. Most symptoms were mild or moderate in severity and resolved without further treatment, although tiagabine dosage reductions were required by 4 patients in the carbamazepine study and by 3 patients in the phenytoin study. There were no clinically important effects on physical examination or neurologic test results, laboratory values, or vital signs. The results suggest that addition of tiagabine to a fixed regimen of either carbamazepine or phenytoin is generally well tolerated and that carbamazepine and phenytoin steady-state pharmacokinetics are unaffected by the addition of tiagabine.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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4. |
Effects of Delapril in Combination With Indapamide on Blood Pressure and Left Ventricular Mass in Elderly Hypertensive Patients |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 17-24
Domenico Acanfora,
David Lowenthal,
Giuseppe Furgi,
Luigi Trojano,
Costantino Picone,
Antonio Nicolino,
Gian Iannuzzi,
Antimo Papa,
Franco Rengol,
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摘要:
We present a single-blinded, placebo-controlled trial of the effects on blood pressure and left ventricular mass and of the safety of a combined antihypertensive treatment with delapril, a new nonsulfhydryl angiotensin-converting enzyme inhibitor, and indapamide, a sulfonamide diuretic. We studied 28 elderly patients aged 65–85 years (mean age, 69 ± 1) with sitting systolic/diastolic blood pressure of 160–200/95–115 mm Hg (at the end of the placebo period). After a 2-week placebo run-in, patients took 30 mg delapril in combination with 1.25 mg indapamide once daily for 24 weeks. Twenty-four-hour ambulatory blood pressure was monitored and M- and B-mode echo-cardiography were performed before and after 24 weeks of treatment. Blood pressure decreased from 156 ± 1.5/101 ± 1 mm Hg before treatment to 133 ± 1/73 ± 1 mm Hg after treatment. The total blood pressure burden also decreased; the percentage of measurements with a systolic blood pressure ≥ 140 mm Hg and a diastolic blood pressure ≥ 90 mm Hg decreased from 48.7% ± 5%/31.5% ± 4.3% to 23.5% ± 4%/20.5% ± 2.9% (p < 0.0005 and p > 0.05). The area under the curve of the 24-hour blood pressure decreased from 250 ± 41/103 ± 21 mm Hg to 97 ± 21/37 ± 8.5 mm Hg (p < 0.001 and p < 0.005). The left ventricular mass index (LVMI) in the 15 patients with pretreatment left ventricular hypertrophy was reduced after therapy from 167.5 ± 8.5 g/m2to 152.2 ± 7.6 g/m2(p < 0.05). A positive correlation was observed between percent changes of the area under the curve of the 24-hour diastolic blood pressure and percent changes of LVMI (r = 0.6; p < 0.05) in the 15 patients with left ventricular hypertrophy. Only 2 patients reported side effects: 1 developed skin rash and 1 developed headache. The safety of the treatment was confirmed by laboratory tests. In elderly hypertensive patients, the combination of delapril and indapamide at low doses reduced blood pressure and had favorable effects on LVMI with few side effects.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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5. |
Clinical and Neurohormonal Effects of Nicardipine Hydrochloride in Patients With Severe Chronic Heart Failure Receiving Angiotensin‐Converting Enzyme Inhibitor Therapy |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 25-32
Daniel Benatar,
Veronica Hall,
Srinivas Reddy,
Mihai Gheorghiade,
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摘要:
It has been proposed that worsening of heart failure with dihydropyridines, such as nicardipine, is related to the activation of the neuroendocrine system. To test this, we evaluated 20 patients with severe heart failure (mean age, 55 ± 13 years; New York Heart Association functional class III; left ventricular ejection fraction, 18% ± 8% on maintenance therapy with captopril, digoxin, and diuretics) who were randomized to nicardipine (60 or 90 mg/d) or placebo during a 4-month double-blind protocol. The following measurements were obtained at baseline, monthly, and at 4 months or last follow-up visit: rest and exercise radionuclide ventriculography, maximal treadmill time, 6-minute walking test distance, serum norepinephrine and aldosterone concentrations, and plasma renin activity. During the follow-up period, worsening of heart failure occurred in 6 patients in the nicardipine group and in 2 patients in the placebo group (p = 0.06). The maximal treadmill time for a 6-minute walking distance and exercise radionuclide ejection fraction at the last follow-up visit did not change in patients who did not deteriorate with heart failure in the placebo or nicardipine groups as compared with baseline values. In this study group of patients with severe heart failure receiving therapy with digoxin, captopril, and diuretics, nicardipine was associated with worsening heart failure without an apparent activation of the neurohormones. However, because of the small number of patients and a significant number of patients who deteriorated during the follow-up period, no definitive conclusions can be made.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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6. |
Hepatic Encephalopathy and Role of Antibenzodiazepines |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 33-36
J. Hammond,
F. Ahmad,
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摘要:
The majority of pharmacological agents are designed to accomplish a specific effect based on the established mechanisms of a disease. However, there are a few examples in which investigation of a pharmacological action has led to a previously unknown mechanism, i.e. the drug effect was observed initially before its mechanism became known. For example, the opiates had been in use for their analgesic effect for centuries before the question of endogenous substances that might explain the presence of opiate binding sites in the central nervous system (CNS) was raised, leading to the discovery of the opioids. A somewhat analogous development has occurred in another investigative arena, the observation that the administration of the benzodiazepine antagonist, flumazenil, has reversed the encephalopathy of hepatic failure. This has refocused research to discover whether one or more endogenous substances that bind to the benzodiazepine receptor in the CNS are responsible for the inhibition of CNS function of advanced liver failure. The investigative impetus was initiated by observations that patients with liver failure were highly vulnerable to benzodiazepines; therapeutic dosages precipitated coma or near-coma, and this effect was prolonged. The question was raised whether any given patient presenting with a coma-like state associated with advanced liver dysfunction might have received a benzodiazepine in the recent past, under circumstances over-looked or not recorded, that might be a contributing factor to the patient's condition. This led to testing the effects of the antagonist, with transitory success in arousing patients or improving their level of stupor. Further inquiry revealed that this improvement in mental function occurred in the absence of prior exposure to benzodiazepines. There followed a search for endogenous substances capable of binding to the benzodiazepine receptor, with CNS inhibitory effects. These investigations have resulted in the identification of several substances that may play a role in encephalopathy and can be displaced from the CNS receptor by properly designed antagonists—an ongoing investigative effort.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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7. |
DopaminePharmacologic and Therapeutic Aspects |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 37-44
Manuel Velasco,
Augusta Luchsinger,
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摘要:
Dopamine is a biogenic amine synthesized in the hypothalamus, in the arcuate nucleus, the caudad, and various areas of the central and peripheral nervous system. It has been widely established that dopamine and its agonists play an important role in cardiovascular, renal, hormonal, and central nervous system regulation through stimulation of alpha and beta adrenergic and dopaminergic receptors. There are several agonists of dopamine-2 (DA2) dopaminergic receptors, such as bromocriptine, pergolide, lisuride, quinpirole, and carmoxirole, which inhibit norepinephrine release and produce a decrease in arterial blood pressure; in some cases, bromocriptine and pergolide also reduce heart rate. From a therapeutic point of view, the above-mentioned agonists are used for treating Parkinson's disease, acting over DA2dopaminergic receptors of the nigrostriatal system. Bromocriptine and the other dopaminergic agonists mentioned act over DA2receptors of the tuberoinfundibular system, inhibiting prolactin release and decreasing hyperprolactinemia and tumor size. Among DA, receptor agonists, we can mention fenoldopam, piribedil, ibopamine, SKF 3893, and apomorphine (nonspecific). Activation of these receptors decreases peripheral resistance, inducing lowering of arterial blood pressure and increases in heart rate, sympathetic tone, and activity of the renin aldosterone system. Among DA2receptor antagonists, we can mention metoclopramide, domperidone, sulpiride, and haloperidol. From a therapeutic point of view, metoclopramide and domperidone are used in gastric motility disorders, and haloperidol is used in psychotic alterations. Antagonists of DA1receptors are SCH23390 and clozapine. Clozapine is used for treating schizophrenia.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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8. |
Management of Opportunistic Infections in Acquired Immunodeficiency Syndrome. I. Treatment |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 45-50
Seymour Schlager,
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摘要:
A case report of a patient infected with human immunodeficiency virus (HIV) is described. The patient presents with a multitude of medical complaints that are of acute or subacute onset. The medical examination of these complaints is described and includes algorithms for the diagnosis and treatment of the most common HIV-related opportunistic infections, includingPneumocystis cariniipneumonia, toxoplasmosis,Mycobacterium aviumcomplex, cytomegalovirus infection, and cryptococcal meningitis.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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9. |
Clinical Therapeutic ConferenceRecurrent Venous Thrombotic and Thromboembolic Disease |
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American Journal of Therapeutics,
Volume 5,
Issue 1,
1998,
Page 51-51
Michael Freedman,
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摘要:
Recurrent venous thrombotic and thromboembolic disease, once thought to be an uncommon entity, is increasingly being recognized. Etiologies of recurrent deep venous thrombosis usually include elements of Virchow's triad. Venous stasis (e.g., immobilization, congestive heart failure, acute myocardial infarction, obesity), hypercoagulability (e.g., malignancy, inflammatory bowel disease, hyperhomocysteinemia, protein C resistance, antithrombin III, protein C or S deficiency) and endothelial trauma (e.g., surgical trauma, venous trauma, in-dwelling venous instrumentation) are risk factors. Diagnosis is dependent on objective testing, including venography duplex Doppler (color) ultrasonography and impedance plethysmography. Treatment is usually started with heparin or low-molecular-weight heparin and advanced to warfarin (adjusted to international normalized ratio). Prophylaxis may continue using low-molecular-weight heparin, warfarin, venacaval interruption (Greenfield filter), or concomitant use of the platelet-active agent indobufen and graduated compression stockings.
ISSN:1075-2765
出版商:OVID
年代:1998
数据来源: OVID
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