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  • 11
    ISSN: 1432-1440
    Keywords: Captopril ; Kidney function ; Essential hypertension ; Renovascular hypertension ; Renal parenchymatous hypertension
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To study long-term effects of captopril on renal function in patients with various forms of severe hypertension, serum creatinine values were monitored in 76 patients under captopril therapy over a period of up to 3 years. Three different groups were formed: (1) patients with essential hypertension (n=37); (2) patients with renovascular hypertension (n=20); (3) patients with renal parenchymatous hypertension (n=19). In each of the three groups reduction in blood pressure was accompanied by increases in serum creatinine. However, both changes were more pronounced in patients with renovascular hypertension. In this group only the rise in creatinine was statistically significant and showed a slight progression with duration of captopril treatment. Group specific analysis revealed that the increase was smaller in patients with unilateral (n=16) renovascular disease than in those with bilateral (n=4) involvement, but in the former it was still significantly higher than in patients with essential or renal parenchymatous hypertension. Separation of patients according to the underlying disease of renovascular hypertension showed that renal function deteriorated less in patients with arteriosclerotic origin (n=10) than in those with fibromuscular dysplasia (n=8). Statistical evaluation of subjects with renovascular and essential hypertension still revealed significant differences in creatinine when the patients with initial plasma renin activity (PRA) below and above 6 ng/ml·3 h were compared separately. A significant correlation (r=0.73;P〈0.05) between blood pressure reduction and creatinine changes was obtained only for patients with renovascular hypertension. Finally, in all three groups of patients creatinine changes were statistically independent from daily dosages of captopril. From these data we conclude that sustained impairment of kidney function by captopril is mainly restricted to patients with renovascular hypertension and possibly results from the combined effects of low renal perfusion pressure and interference with intrarenal regulation of glomerular filtration rate by a postulated angiotensin-II-mediated mechanism.
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 62 (1984), S. 925-930 
    ISSN: 1432-1440
    Keywords: Transdermal therapeutic systems (TTS) ; Clonidine ; Essential hypertension ; Skin allergy ; Clonidine allergy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Skin patches of a clonidine transdermal therapeutic system (clonidine-TTS) with a constant release rate of either 0.1 or 0.2 mg clonidine/24 h continuously over 7 days were used in 32 essential hypertensives. These self-adhesive drug delivery systems (3.5 cm2), which were affixed to the upper outer arm, were changed by the patients at weekly intervals. During a mean observation period of 7 months (range 1–19 months) transdermal clonidine reduced the blood pressure from 162±15/107±5 mmHg to normal values (diastolic ≦95 mmHg) in 63% of our patients. However, chronic use of clonidine-TTS was accompanied by a high frequency of contact dermatitis (type IV allergy) in nearly half of our patients (n=15, 47%). In 11 of these 15 patients transdermal clonidine administration had to be stopped because of intolerable local skin reactions (pruritus, erythema, vesiculation, and/or infiltration). Subsequent patch testing with all components of clonidine-TTS was performed in eight cases. Whereas in seven cases an allergic contact dermatitis to clonidine was found, only one patient showed an allergy to another component of clonidine-TTS (polyisobutylene). We conclude that this strikingly high incidence of local allergic skin reactions limits the use of clonidine-TTS in essential hypertension.
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 60 (1982), S. 161-170 
    ISSN: 1432-1440
    Keywords: Patient compliance ; Methods of measurement ; Determinants of compliance ; Compliance improving strategies ; Patientencompliance ; Bestimmungsmethoden ; compliancevermindernde Faktoren ; compliancefördernde Maßnahmen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Verschiedene Untersuchungen über die Compliance oder Therapiedisziplin von Patienten haben gezeigt, daß zwischen 20 bis 50% der Patienten vor allem in der Langzeittherapie die ärztlichen Verordnungen nicht oder nur ungenügend befolgen. Die Non-Compliance ist damit seit der Einführung wirksamer Medikamente insbesondere in der Behandlung der essentiellen Hypertonie, bei Fettstoffwechselstörungen, sowie bei Patienten unter tuberkulostatischer Therapie oder prophylaktischer Chemotherapie zu einem der wichtigsten therapielimitierenden Faktoren geworden. Die Einnahmedisziplin verschlechtert sich im Laufe der Behandlung zusehends. In den ersten vier Monaten ist mit einem Abfall der Compliancerate um 30% zu rechnen, nach 5 Jahren ist nur noch ein Fünftel bis ein Viertel der Patienten therapietreu. Die Zuverlässigkeit der Patienten läßt sich mit indirekten Bestimmungsmethoden wie Patientenbefragung, Pillenzählen oder aufgrund der Therapiewirkungen abschätzen. Eine genaue Ermittlung der Compliancerate erfordert die Bestimmung der Medikamente oder Markersubstanzen im Serum oder Urin. Die Ergebnisse von Untersuchungen über compliancebestimmende Faktoren sind zum Teil widersprüchlich. Als gesichert kann hingegen gelten, daß psychische Erkrankungen insbesondere Schizophrenie, ein komplexes Therapieschema mit hoher täglicher Tablettenzahl, Therapien, welche eine Änderung von Lebensgewohnheiten erfordern, eine langdauernde Behandlung und ungenügende, schlecht organisierte Nachkontrollen mit langen Wartezeiten für den Patienten eine schlechte Therapiedisziplin zeigen. Im weiteren beeinflussen das Krankheitsbewußtsein sowie die Einstellung der Familie das Einnahmeverhalten der Patienten. Compliancefördernde Maßnahmen richten sich nach den Faktoren, welche die Therapietreue der Patienten negativ beeinflussen. Entsprechend sollte durch eine Verwendung von „Slow-Release“-Präparaten die tägliche Tablettenzahl möglichst klein gehalten werden. Bei mehreren Tabletteneinnahmen pro Tag ist ein schriftlicher Verordnungszettel („aide-memoire“) von Nutzen. Durch regelmäßige engmaschige Nachkontrollen mit festen Terminen und kurzen Wartezeiten sollte in der Langzeittherapie die „drop-out“-Rate reduziert werden. Eine zusätzliche Betreuung durch paramedizinisches Personal zeigt ebenso wie der Einsatz von Therapiegruppen vor allem in der Betreuung von übergewichtigen Patienten und Hypertonikern einen günstigen Effekt auf die Compliance. Die Beteiligung des Patienten an der Behandlung und Überwachung seiner Erkrankung z.B. durch Blutdruckselbstmessung bei den wenig symptomatischen Hypertonikern führt zu einer deutlichen Verbesserung der Einnahmedisziplin. Bei Therapien, welche eine Änderung von Lebensgewohnheiten erfordern (Diät, Alkoholabstinenz, Nikotinabstinenz u.a.), sollte die Familie (Ehefrau) in den Therapieplan miteinbezogen werden. Die Patientencompliance verdient aufgrund ihrer praktischen Bedeutung (Nichterreichen des Therapieziels, Beeinflussung von Ergebnissen der Arzneimittelforschung, unnötige Kosten) eine vermehrte Beachtung im Rahmen der Patientenbetreuung. Compliancevermindernde Faktoren sollten möglichst eliminiert und Maßnahmen zur Verbesserung der Therapiedisziplin ergriffen werden.
    Notes: Summary Several studies concerning compliance or drug adherence of patients have shown, that between 20–50% of the patients in particular during long term therapy do not or only insufficiently follow doctor's advice. Thus, since the introduction of potent drugs, non-compliance has become one of the most important therapy limiting factors in particular in the management of essential hypertension, disorders of lipid metabolism, tuberculosis and chemo-prophylaxis. Compliance decreases during treatment. During the first four months a decline of compliance rate of 30% must be expected, after five years only 20–25% of the patients are still compliant. Patients' cooperation may be estimated by indirect methods such as patient interview, pill-counting or therapeutic outcome. An exact determination of compliance requires measurements of blood levels or urinary excretion of the medicaments or marker. The results of studies about the determinants of compliance are conflicting. However, it seems to be proved, that a psychiatric diagnosis in particular schizophrenia, a complex therapeutic regimen with a high number of daily tablets, therapies which include a behavioral change, longterm therapy and a inefficient follow-up system with long waiting time for the patient are associated with non-compliance. In addition, patients perception of the disease and family support are influencing drug adherence. Compliance improving strategies were derived from the determinants which diminish patients' drug adherence. By using slow release medicaments the number of daily tablets should be minimalized. If several tablets must be taken daily an “aide-memoire” may be useful. The drop-out rate should be reduced by regular scheduled follow-up visits with short waiting time. In addition, follow-up care by a nurse or a diet adviser as well as therapy groups show a compliance improving effect in particular in patients with overweight or hypertension. The participation of the patient in therapy and follow-up for instance by blood pressure selfmeasurement in the mostly symptomless hypertensives increases markedly drug adherence. In therapies which necessitate behavioral changes (diet, alcohol abstinence, stop of smoking) the family should be integrated in the therapeutical procedure. Because of its practical importance (unsatisfactory therapeutical outcome, influence on results of pharmacological studies, costs) compliance should be taken into account in patient's care. Compliance decreasing factors should be eliminated and strategies for improving drug adherence should be performed.
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 62 (1984), S. 470-476 
    ISSN: 1432-1440
    Keywords: Adrenal carcinomas ; Aldosterone secretion ; Hypokalemic alkalosis ; Operation ; Chemotherapy with o,p′-DDD
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the present study two patients with aldosterone-producing adrenal carcinomas are reported. The clinical features were characterized by hypertension and severe hypokalemia with muscular weakness, flaccid paralysis of arms and legs, diarrhea and polyuria. In both cases excessively high plasma aldosterone levels and suppressed plasma renin activity were found. In contrast to most other cases with aldosterone-secreting tumours plasma cortisol, urinary free cortisol excretion, 17-hydroxy- and 17-ketosteroids were in the normal range. There was no clinical evidence of oversecretion of sex hormones. After adrenalectomy blood pressure and serum potassium normalized and the clinical symptoms disappeared. Plasma aldosterone and urinary aldosterone secretion returned to normal, while plasma renin activity remained low. Three and a half and 6 months later primary aldosteronism and the associated clinical symptoms reappeared due to hormonally active metastases. After introducing the antitumour drug o,p′-DDD in patient 1 aldosterone secretion normalized and the clinical status of the patient markedly improved. However, 10 months after diagnosis the patient died due to a haemorrhage from a liver metastasis. In patient 2 tumour-invaded regional lymph nodes were surgically removed with only minor changes in the hormone pattern.
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 63 (1985), S. 361-363 
    ISSN: 1432-1440
    Keywords: Primary aldosteronism ; Captopril ; Spironolactone ; Renin-angiotensin ; Converting-enzyme ; Secondary hypertension
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In three patients with primary aldosteronism, the acute effect of a single dose of captopril on the elevated mean arterial blood pressure (MAP) was studied before and after 4 weeks of treatment with spironolactone. Before spironolactone therapy, captopril did not cause any drop in MAP. Four weeks later, after an oral daily dose of 400 mg spironolactone, MAP was still elevated in all three patients, though electrolyte abnormalities were fully corrected. Since plasma renin activity (PRA) was increased to values above the normal range, the acute effect of captopril on MAP was tested again. A single dose of 25 mg captopril then caused a fall in MAP to normal. These data reveal the conversion from a renin-independent to a renindependent kind of hypertension after spironolactone therapy in three patients with primary aldosteronism syndrome. This might be of pathogenetic and therapeutic interest.
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  • 16
    ISSN: 0168-9002
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
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  • 17
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Instruments and Methods in Physics Research Section A: 250 (1986), S. 228-232 
    ISSN: 0168-9002
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 24 (1968), S. 340-341 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Arginine has been converted into a suitable pyrimidine derivative to permit its qualitative analysis in the presence of other amino acids by means of mass spectrometric and gas-chromatographic techniques.
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 28 (1985), S. 89-91 
    ISSN: 1432-1041
    Keywords: atenolol ; pindolol ; sleep disturbance ; β-blockers ; dreaming ; fatigue ; hypertension ; lipophilicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary This randomized crossover out-patient study was designed to compare the antihypertensive effects of atenolol and pindolol. After a wash-out period of two weeks in pretreated cases, 107 patients with essential hypertension were given either atenolol 100 mg once-daily or pindolol 20 mg slow release (SR) once-daily. Both atenolol and pindolol lowered blood pressure over the 24 week period. The diastolic blood pressure reduction was significantly greater (p〈0.01) with atenolol than with pindolol. Before β-blocker therapy, many patients had already experienced side-effects such as fatigue, sleep disturbances and dreams. This probably relates to the high sensitivity of the analogue scale used to assess side-effects, and to the high incidence of such symptoms in untreated patients. As the study progressed there was a reduction in the frequency of fatigue (p〈0.03) and dreams (p〈0.05) in both groups, whereas sleep disturbances significantly increased under pindolol (p〈0.05) but decreased under atenolol (p〈0.05). The only important side-effect difference between the two β-blockers was the higher incidence of sleep disturbances with pindolol which may be due to the higher lipophilicity of this β-blocker.
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 61 (1983), S. 803-805 
    ISSN: 1432-1440
    Keywords: Obesity ; Hypertension ; Intracellular sodium ; Intracellular calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Intracellular activities of sodium and calcium were determined in red cells of patients with obesity. Compared to normal people mean intracellular sodium and calcium were higher in obese patients. However, increased intracellular sodium and calcium could only be observed in those patients with obesity suffering from hypertension or showing a familial disposition to hypertension. In contrast there was no difference in intracellular sodium and calcium between obese normotensives lacking a familial disposition to hypertension and normal people. Thus, our results suggest, that the observed variations in intracellular sodium and calcium in obesity are due to an enhanced blood pressure or a familial disposition to hypertension and not specific for obesity.
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