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  • 1
    ISSN: 1432-1440
    Keywords: Psoriasis ; Lipid infusion ; n-3 fatty acids ; Neutrophil leukotriene generation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Twenty patients hospitalized for acute psoriasis guttata with a minimum 10% of body surface area involvement (range 10–90%) completed a 10-day trial in which they were randomly allocated to receive daily infusions with either an n-3 fatty acid based lipid emulsion [100 ml/day with 2.1 g eicosapentaenoic (EPA) and 21 g docosahexaenoic acid (DHA)] or a conventional n-6 lipid emulsion (EPA+DHA〈0.1 g/100 ml). The severity of disease was evaluated by scoring daily erythema, infiltration, and desquamation and by a subjective scoring of clinical manifestations offered by the patients. Leukotriene (LT) and platelet-activating factor (PAF) generation were investigated in ionophore-stimulated neutrophils obtained on days 0, 1, 3, 5, 10, and 40. Moderate improvement in clinical manifestations was noted in the n-6 group (changes in score systems between 16–25% from baseline within 10 days). In contrast, the severity of disease markedly decreased in all patients of the n-3 group, with improvements in all score systems ranging between 45% and 76% within 10 days (P〈0.05 for each variable). The difference in response to the two regimens was evident within 4–7 days after onset of lipid infusion. A more than ten fold increase in neutrophil EPA-derived 5-1ipoxygenase product formation (LTB5, its omega-oxidation products, non-enzymatic degradation products of LTA5 and 5-hydroxyeicosapentaenoic acid) was noted in the n-3 group but not in the n-6 group. Neutrophil PAF generation increased in the n-6 group but decreased in the n-3 group. In conclusion, modulation of eicosanoid metabolism by intravenous n-3 fatty acid supplementation appears to exert a rapid beneficial effect on inflammatory skin lesions in acute guttate psoriasis.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1238
    Keywords: Key words Primary pulmonary hypertension ; Pulmonary selective vasodilatation ; Right heart decompensation ; Low output failure ; Inhaled iloprost ; Prostacyclin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective: The treatment of decompensated right ventricular failure with vasodilators is difficult due to reduced systemic pressure and/or ventilation/perfusion (V/Q) mismatch with hypoxemia. In a recent study we demonstrated that inhaled vasodilatory prostanoids may offer a new strategy to achieve pulmonary selective vasodilatation and improvement of right ventricular function. We applied this new approach to a patient with circulatory shock due to primary pulmonary hypertension (PPH), complicated by a pulmonary infiltrate, who did not tolerate intravenous prostacyclin. Design: Case report. Setting: Intensive Care Unit (ICU), Medizinische Klinik Gießen, Germany. Patient: A 45-year-old woman with PPH presenting with decompensated right heart failure (ascites, pleural effusion), circulatory shock and commencing renal and hepatic failure, despite maximum therapy including the use of catecholamines. Intervention: Intermittent inhalation of aerosolized iloprost, the stable analogue of prostacyclin, and comparison to inhaled nitric oxide (NO). Subsequent long-term therapy with aerosolized iloprost, 150 μg/day. Measurements and results: In response to inhaled iloprost, pulmonary arterial pressure (PAP) decreased from 65 to 61 mmHg, cardiac index (CI) increased from 1.25 to 1.85 l/min per m2, and pulmonary vascular resistance (PVR) decreased from 2416 to 1549 dyn/s per cm5 while inhaled NO decreased the PVR from 2280 to 1920 dyn/s per cm5 without a decrease in PAP. Both of these interventions increased the arterial pO2 but did not change the systemic arterial pressure. In contrast, intravenous prostacyclin was not tolerated, due to systemic side effects. During repeated inhalations with iloprost, the baseline hemodynamics and gas exchange improved dramatically and renal and liver functions normalized. During 1 year of continued therapy, the clinical status improved very much, concomitant with improved hemodynamics, and the patient has been taken off the transplantation list. Conclusions: Inhalation of aerosolized iloprost may offer a new life-saving strategy in near desperate cases of pulmonary hypertension in which intravenous prostacyclin cannot be applied due to severe side effects.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Der Internist 38 (1997), S. 453-460 
    ISSN: 1432-1289
    Keywords: Schlüsselwörter Stickstoffmonoxid ; ARDS ; Stickstoffmonoxid ; pulmonale Hypertonie ; NO ; ARDS ; NO ; pulmonale Hypertonie ; Pulmonale Hypertonie ; Stickstoffmonoxid ; ARDS ; Stickstoffmonoxid ; Prostaglandin ; ARDS ; Prostaglandin ; pulmonale Hypertonie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung Gerade die hohe Letalität des Adult Respiratory Distress Syndrome (ARDS) und der schweren pulmonalen Hypertonie läßt sich nach neuen Behandlungsmethoden suchen, mittels derer möglichst selektiv eine pulmonale Vasodilatation und ein besserer Gasaustausch erzielt werden könnten. Daß Stickstoffmonoxid (NO), am besten inhalativ appliziert, hier eine therapeutische Option sein könnte, liegt nahe. Die vorliegende Arbeit gibt einen Überblick über die NO-Wirkungen und die leider erheblichen Nebenwirkungen im pulmonalen Bereich. Es wird aber auch auf andere Möglichkeiten hingewiesen, besonders auf Prostaglandine, die ebenfalls im c-GMP- und c-AMP-Signaltransduktionsweg bei der Modulierung des Tonus der glatten Gefäßmuskulatur wirksam eingesetzt werden können.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1750
    Keywords: Adult respiratory distress syndrome ; Antiinflammatory therapy ; Vasodilator inhalation ; Surfactant application ; Artificial ventilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The complex pathophysiology of adult respiratory distress syndrome (ARDS) makes preventive and therapeutic concepts difficult. Ample experimental evidence indicates that ARDS can be prevented by blocking systemic inflammatory agents. Clinically, only heparin, for inhibition of coagulation phenomena, is presently used among this array of approaches. Corticosteroids have not proven to be beneficial in ARDS. Alternative antiinflammatory agents are being proposed and are under current clinical investigation (e.g. indomethacin, acetylcysteine, αl-proteinase inhibitor, antitumor necrosis factor, interleukin 1 receptor antagonist, platelet-activating factor antagonists). Symptomatic therapeutic strategies in early ARDS include selective pulmonary vasodilation (preferably by inhaled vasorelaxant agents) and optimal fluid balance. Transbronchial surfactant application, presently tested in pilot studies, may be available for ARDS patients in the near future and may have acute beneficial effects on gas exchange, pulmonary mechanics, and lung hemodynamics; its impact on survival cannot be predicted at the present time. Strong efforts should be taken to reduce secondary nosocomial pneumonia in ARDS patients and thus avoid the vicious circle of pneumonia, sepsis from lung infection, and perpetuation of multiple organ dysfunction syndrome. Optimal respirator therapy should be directed to ameliorate gas-exchange conditions acutely but at the same time should aim at minimizing potentially aggravating side effects of artificial ventilation (barotrauma, O2 toxicity). Several new techniques of mechanical ventilation and the concept of permissive hypercapnia address these aspects. Approaches with extracorporeal CO2 removal and oxygenation are being used in specialized centers.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-1420
    Keywords: Key words Acute/adult respiratory distress syndrome ; prostacyclin ; primary pulmonary hypertension ; nitric oxide ; Schlüsselwörter Acute/adult respiratory distress syndrome ; Prostazyklin ; Primäre pulmonale Hypertonie ; Stickstoffmonoxid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Trotz ihrer ausgeprägten vasodilatativen Potenz in der pulmonalen Strombahn sind die Indikationen zur intravenösen Applikation der vasodilatativen Prostanoide PGE1 und PGI2 durch fehlende pulmonale und intrapulmonale Selektivität begrenzt. Ein therapeutischer Ansatz stellt die ambulante intravenöse Dauertherapie bei Patienten mit primärer pulmonaler Hypertonie (PPH) vor (Herz-)Lungentransplantation dar. Bei Patienten mit adult respiratory distress syndrome (ARDS) führen PGE1 und PGI2 zu einer Abnahme des gesamtperipheren Widerstandes (fehlende pulmonale Selektivität), und die generelle pulmonale Vasodilatation induziert oder verstärkt Ventilations-Perfusions-Verteilungsstörungen mit begleitender Verschlechterung des Gasaustausches (fehlende intrapulmonale Selektivität). Die transbronchiale PGI2-Applikation (Aerosol) dagegen erzielt eine pulmonale und intrapulmonale Selektivität, die ein fast identisches Wirkungsprofil erreicht, wie der selektive pulmonale Vasodilatator Stickstoffmonoxid (NO). Darüber hinaus liegen erste Langzeiterfahrungen mit der repetitiven Aerosol-Applikation des länger wirkenden Iloprost bei Patienten mit schwerster pulmonaler Hypertonie vor.
    Notes: Summary The vasodilatory prostanoids PGE1 and PGI2 possess strong vasodilatory potency in the pulmonary circulation. Their application is, however, limited by the lack of pulmonary and intrapulmonary selectivity. By use of chronic ambulatory PGI2-infusion, patients with primary pulmonary hypertension (PPH) may be bridged for (heart-) lung transplantation. In patients with adult respiratory distress syndrome (ARDS), PGE1 and PGI2 lower the pulmonary vascular resistance, but may also decrease the systemic pressure (limited pulmonary selectivity) and increase ventilation-perfusion-mismatch, accompanied by an impairment of gas exchange (limited intrapulmonary selectivity). Application of PGI2 via the transbronchial route (aerosol) may achieve pulmonary and intrapulmonary selectivity with an efficacy profile comparable to that of the selective pulmonary vasodilator nitric oxide (NO). Repetitive aerosol application of the stable PGI2 analogue iloprost is under consideration for long-term treatment of patients with severe pulmonary hypertension such as primary pulmonary hypertension.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Intensivmedizin und Notfallmedizin 36 (1999), S. 104-125 
    ISSN: 1435-1420
    Keywords: Key words Acute/adult respiratory distress syndrome ; nitric oxide ; prostacyclin ; surfactant ; mechanical ventilation ; liquid ventilation ; membrane oxygenation? ; Schlüsselwörter Acute/adult respiratory distress syndrome ; Stickstoffmonoxid ; Prostazyklin ; Surfactant ; mechanische Beatmung ; Liquidventilation ; extrakorporale Membranoxygenierung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Diese Übersicht faßt die aktuell diskutierten Therapiestrategien beim ARDS vor dem Hintergrund ihrer klinischen Etablierbarkeit zusammen. Die vorgestellten Behandlungskonzepte reichen von antiinflammatorischen Therapieansätzen über Stickstoffmonoxid und Surfactant bis zu neuen Beatmungsstrategien.
    Notes: Summary This review summarizes actually discussed therapeutic strategies in ARDS and their possible role for clinical use. The presented therapeutic modalities include antiinflammatory treatment, nitric oxide and surfactant and new ventilation regimes.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1435-1285
    Keywords: Key words Acute/adult respiratory distress syndrome –¶pulmonary hypertension –¶inhalative therapy –¶sepsis-nitric oxide – prostacyclin– ARDS and pulmonary hypertension – new aspects of the inhalative therapy ; Schlüsselwörter Acute/adult respiratory distress syndrome –¶Pulmonale Hypertonie –¶inhalative Therapie –¶Sepsis-Stickstoffmonoxid –¶Prostazyklin –¶ARDS und pulmonale Hypertonie – Neue Aspekte der inhalativen Therapie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die chronische pulmonale Hypertonie und das septische Lungenversagen (ARDS) sind Krankheiten mit völlig unterschiedlichen Auslösern, die zu einer Störung der transpulmonalen Blutströmung führen. Die Beeinträchtigung der Hämodynamik im kleinen Kreislauf beruht auf einer pathologischen Gefäßverengung, die sowohl eine Überlastung des rechten Ventrikels als auch eine gravierende Störung des Gasaustausches durch Perfusionsfehlverteilungen verursachen kann. Die unterschiedlichen auf die Vaskularisation einwirkenden Schädigungsmechanismen können dabei sowohl eine irreversible als auch eine reversible Verengung der Lungengefäße bewirken. Prinzipiell bestehen drei Möglichkeiten durch pharmakologische Intervention die Widerstandserhöhung zu beeinflussen: • Aufhebung eines dauerhaft erhöhten Vasotonus durch Relaxation der glatten Gefäßmuskulatur (Angriffspunkt der Vasodilatatoren). • Beeinflussung einer thrombusbedingten Obliteration der Lungenstrombahn (Embolie, in situ Thrombose) durch Antikoagulanzien oder Fibrinolitika (nur im Akutstadium). • Beeinflussung des strukturellen Gefäßumbaus (vaskuläres Remodelling) durch Einsatz von antiinflammatorischen und antiproliferativen Agenzien bei der chronischen pulmonalen Hypertonie. Die systemische (intravenöse, oder orale) Gabe von vasodilatativen Agenzien ist sowohl bei der Sepsis als auch bei der chronischen pulmonalen Hypertonie mit erheblichen Nachteilen behaftet: • Antagonisierung der hypoxischen pulmonalen Vaskonstriktion und damit Zunahme der Ventilations-Perfusions-Verteilungsstörung (Abfall der arteriellen Oxygenierung). • Unerwünschte systemische Effekte der Vasodilatatoren (Verstärkung der meist vorbestehenden systemischen Hypotension). Der wesentliche Vorteil des inhalativen Applikationsmodus ist die pulmonale Anreicherung der Agenzien (pulmonale Selektivität) mit bevorzugter Deposition gerade in den gut belüfteten Alveolarbezirken (intrapulmonale Selektivität). Die erwünschte Abnahme des pulmonal-vaskulären Widerstandes ist so gleichzeitig mit einer Optimierung der intrapulmonalen Perfusionsverteilung und einer Verbesserung des Gasaustausches verbunden. Erste positive Erfahrungen mit dieser Vorgehensweise wurden bei beatmeten Patienten mit septischem Lungenversagen unter Einsatz von inhaliertem NO und aerosoliertem Prostazyklin gewonnen. Der Einsatz des stabilen Prostazyklinanalogons Iloprost (Ilomedin) ermöglichte aufgrund der längeren Halbwertszeit der Substanz einen intermittierenden Inhalationsmodus und so eine ambulante Selbstbehandlung von Patienten mit chronischer pulmonaler Hypertonie.
    Notes: Summary Chronic pulmonary hypertension and septic lung failure display different clinical features resulting in severe disturbances in the pulmonary circulation. In these diseases, the pulmonary bloodflow is impaired by a pathologic constriction of blood vessels that may lead to right ventricular overloading as well as serious worsening of gas exchange mainly caused by ventilation/perfusion mismatch. Various mechanisms deteriorating the vascular function may induce both an irreversible and a reversible contraction of pulmonary vessels, respectively. Two pharmacological approaches exist to reduce the vascular resistance: • Reduction of the increased vascular tone by relaxation of vascular smooth muscle cells (effect of vasodilators). • Inhibition of thrombus-mediated obliteration of the lung perfusion by use of anti-coagulatory and fibrinolytic drugs. • Prevention of the structural reorganization of pulmonary vessels (vascular remodeling) by use of vasodilators with anti-inflammatory and anti-proliferative potency such as prostanoids. The systemic (intravenous or oral) application of vasodilative agents in sepsis and chronic pulmonary hypertension has, however, important side effects: • Antagonism of the hypoxic pulmonary vasoconstriction aggravates the ventilation/perfusion mismatch (decrease in arterial oxygenation). • Side effects of these vasodilators (systemic hypotension). The inhalative route of application is superior because of the pulmonary enrichment of the applied agent (pulmonary selectivity). Furthermore, a preferential deposition in the well-ventilated areas of the lung is achieved (intrapulmonary selectivity). Thus, the decrease in pulmonary-vascular resistance is paralleled by both optimized ventilation-perfusion matching and subsequently improved gas exchange. First clinical studies with inhaled nitric oxide and aerosolized prostacyclin have been performed in intubated and mechanically ventilated patients with septic lung failure. At present, the use of the long-acting prostacyclin analogue ilomedin for ambulant treatment of patients with chronic pulmonary hypertension is under investigation.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Intensivmedizin und Notfallmedizin 34 (1997), S. 499-500 
    ISSN: 1435-1420
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Intensivmedizin und Notfallmedizin 37 (2000), S. 671-673 
    ISSN: 1435-1420
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Intensivmedizin und Notfallmedizin 37 (2000), S. 251-256 
    ISSN: 1435-1420
    Keywords: Key words¶Acute respiratory failure –¶acute respiratory distress syndrome (ARDS) –¶hypoxemic respiratory failure –¶lung edema –¶non-invasive ventilation (NIV) – pneumonia ; Schlüsselwörter¶Akutes Lungenversagen (ARDS) – Akute respiratorische Insuffizienz – Hypoxämisches respiratorisches¶Versagen – Lungenödem –¶Non-invasive Beatmung (NIV) – Pneumonie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die non-invasive Beatmung (NIV) ist als Alternative zur konventionellen mechanischen Beatmung bei akuter Exazerbation einer chronisch obstruktiven Lungenerkrankung (COPD) anerkannt. Im Gegenteil dazu ist der Stellenwert und die Effizienz der NIV bei Patienten mit akutem Lungenversagen bei anderer Genese als einer COPD noch unklar. Ziel dieser Übersicht ist es den Stellenwert der NIV für das akute hypoxämische Lungenversagen zu bestimmen.
    Notes: Summary Non-invasive ventilation (NIV) has been proposed as an efficient alternative to conventional mechanical ventilation during acute exacerbation of chronic obstructive pulmonary disease (COPD). In contrast, the value and benefit of NIV used in patients suffering from acute respiratory failure unrelated to COPD remain unclear. The objective of this overview is to determine the role of NIV in acute hypoxemic respiratory failure.
    Type of Medium: Electronic Resource
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