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1.
J Thorac Cardiovasc Surg ; 114(4): 666-71, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9338654

ABSTRACT

OBJECTIVE: Recent studies suggest that urodilatin from the kidneys rather than atrial natriuretic factor from the heart is the more important member of the family of natriuretic peptides involved in the normal regulation of renal sodium and water excretion. We thus examined the relationship between natriuresis, urodilatin, and atrial natriuretic factor in patients after cardiopulmonary bypass, a procedure known to increase levels of atrial natriuretic factor significantly. METHODS: Excretion rates of sodium and water were correlated with the excretion of urodilatin and with circulating levels of atrial natriuretic factor, antidiuretic hormone, aldosterone, and plasma renin activity during a period of 16 hours in 12 patients having had coronary artery bypass operations and with approximately a 400% elevation in levels of atrial natriuretic factor. RESULTS: Natriuresis did not correlate with atrial natriuretic factor, antidiuretic hormone, aldosterone, or plasma renin activity. Excretion rates of urodilatin, however, correlated significantly with excretion rates of sodium (r = 0.74, p = 0.03), urine flow (r = 0.83, p = 0.01), and with levels of serum sodium (r = 0.82, p = 0.01). CONCLUSION: These results suggest an important role for urodilatin, greater than that of atrial natriuretic factor, in the regulation of renal excretion of sodium and water after cardiopulmonary bypass surgery.


Subject(s)
Atrial Natriuretic Factor/physiology , Cardiopulmonary Bypass , Coronary Artery Bypass , Natriuresis/physiology , Peptide Fragments/physiology , Adult , Aged , Aldosterone/blood , Atrial Natriuretic Factor/blood , Atrial Natriuretic Factor/urine , Case-Control Studies , Diuretics/blood , Female , Humans , Kidney/physiology , Male , Middle Aged , Peptide Fragments/urine , Postoperative Period , Renin/blood , Time Factors , Vasopressins/blood
2.
Eur Heart J ; 16(6): 852-8, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7588931

ABSTRACT

Since recent results have suggested that the relative neuroendocrine response to physical activity is exaggerated following cardiac transplantation, we studied the haemodynamic-neuroendocrine responses to mental stress, and to physical exercise, in heart transplant recipients free of antihypertensive medication. Ten patients were studied 1.7 years (mean) after transplantation and compared with 10 age-matched controls. Plasma levels of catecholamines, renin activity, aldosterone, atrial natriuretic factor, calcitonin gene-related peptide (CGRP), and endothelin were measured, together with blood pressure and heart rate, during mental stress and graded, submaximal ergometry. Mental stress increased blood pressure in both groups (P < 0.02), but heart rate in controls only (P < 0.05). Noradrenaline did not change. Adrenaline rose in controls only (P < 0.05). Plasma renin activity increased in both groups (P < 0.02), while aldosterone increased in controls only P < 0.02). Atrial natriuretic factor, and endothelin were higher in patients (P < 0.01). Mental stress, however, did not induce any changes. No significant differences were found in relative changes (delta %), except for plasma renin activity which was greater in controls (P < 0.05). During ergometry, only delta % noradrenaline was greater in patients (P < 0.05). delta % for all other parameters were either of the same order as in controls, or blunted. Thus, apart from noradrenaline, cardiac transplant recipients, not receiving antihypertensive medication, do not show an exaggeration in the relative neuroendocrine response to mental or physical stress.


Subject(s)
Heart Transplantation , Neurotransmitter Agents/blood , Physical Exertion , Stress, Psychological/blood , Adolescent , Adult , Female , Hemodynamics , Humans , Male , Middle Aged , Neurosecretory Systems/physiopathology
3.
Monatsschr Kinderheilkd ; 141(8): 655-8, 1993 Aug.
Article in German | MEDLINE | ID: mdl-8377770

ABSTRACT

A 7 year old girl in whom an interstitial deletion of the short arm of a chromosome no. 4 had been discovered [46, XX, del(4)(p15.2p16)] is moderately retarded and exhibits some mild craniofacial dysmorphies. Cardiological examination revealed a PDA and an ASD. From seven similar cases published up to now a typical phenotype cannot be concluded. Dermatoglyphics show a remarkable frequency of digital arches but the diagnostic significance is questioned by this observation.


Subject(s)
Chromosome Deletion , Chromosomes, Human, Pair 4 , Intellectual Disability/genetics , Child , Chromosome Aberrations , Chromosome Disorders , Dermatoglyphics , Ductus Arteriosus, Patent/genetics , Female , Heart Septal Defects, Atrial/genetics , Humans , Neurologic Examination , Phenotype , Syndrome
5.
Klin Padiatr ; 205(3): 176-9, 1993.
Article in German | MEDLINE | ID: mdl-8394475

ABSTRACT

We report the case of a premature female newborn of the 35th gestational week with a congenital mesoblastic nephroma. The tumor was prenatally diagnosed in the 32nd week of gestation. By close sonographic controls, rapid enlargement was verified towards the end of the 35th week of gestation. This was probably caused by hemorrhage into the tumor. Anemia and postnatal disseminated intravascular coagulation followed. Cesarean section was done, because the anemia was suspected by Doppler sonographic evaluation. Disseminated intravascular coagulation could not be sufficiently controlled by conservative means but only by surgical removal of the tumor. The tumor turned out to be a congenital mesoblastic nephroma by histologic evaluation. Despite postoperative anuria and catecholamine dependency, our patient eventually showed a very favourable outcome. Diagnosis, clinical behavior and therapy of this tumor with a generally good prognosis are described and discussed.


Subject(s)
Disseminated Intravascular Coagulation/congenital , Hemorrhage/congenital , Kidney Neoplasms/congenital , Ultrasonography, Prenatal , Wilms Tumor/congenital , Blood Coagulation Tests , Disseminated Intravascular Coagulation/diagnostic imaging , Disseminated Intravascular Coagulation/pathology , Disseminated Intravascular Coagulation/surgery , Female , Hemorrhage/diagnostic imaging , Hemorrhage/pathology , Hemorrhage/surgery , Humans , Infant, Newborn , Kidney/pathology , Kidney Neoplasms/diagnostic imaging , Kidney Neoplasms/pathology , Kidney Neoplasms/surgery , Nephrectomy , Pregnancy , Wilms Tumor/diagnostic imaging , Wilms Tumor/pathology , Wilms Tumor/surgery
6.
Pediatr Radiol ; 22(7): 527-8, 1992.
Article in English | MEDLINE | ID: mdl-1491913

ABSTRACT

Moyamoya disease is a rare vascular anomaly of the cerebral arteries. The etiology of the disease has not yet been clearly identified. We report the noninvasive diagnosis of Moyamoya disease in a patients with a very early onset of symptoms in infancy. The diagnosis was made by colour coded Doppler sonography and confirmed by angiography at the age of 6 months, following two episodes of cerebral infarction. A bilateral encephalodurosynangiosis was performed at the age of 7 months with subsequent slight improvement of the neurological deficits. Colour Doppler sonography revealed early vascularisation from the fascia temporalis graft into the arachnoid space. At the age of 10 months the patient developed arterial hypertension caused by left renal artery stenosis. Our case suggests, that in infancy Moyamoya disease can be suspected noninvasively by colour Doppler sonography of the cerebral arteries. Patients should be carefully screened for possible extracranial arterial stenoses which may develop in the course of time. Encephalodurosynangiosis seems to be a good therapeutic option for patients with severe neurological symptoms.


Subject(s)
Cerebral Arteries/diagnostic imaging , Moyamoya Disease/diagnostic imaging , Renal Artery Obstruction/diagnostic imaging , Female , Follow-Up Studies , Humans , Infant , Moyamoya Disease/complications , Moyamoya Disease/surgery , Renal Artery Obstruction/etiology , Renal Artery Obstruction/therapy , Ultrasonography
7.
Monatsschr Kinderheilkd ; 138(9): 596-604, 1990 Sep.
Article in German | MEDLINE | ID: mdl-2172804

ABSTRACT

Between 1979 and 1989 21 renal tumors (8 girls and 13 boys) were diagnosed and treated in the Pediatric Hospital of the University of Erlangen. Additionally, there was evidence of nephroblastomatosis in 5 children with Beckwith-Wiedemann Syndrome and hemihypertrophy. One of these infants developed a Wilms' tumor at the age of 3 1/2 years. The most frequent tumor was the Wilms' tumor, which was diagnosed in 14 children. Wilms' tumor are sonographically well delineated, round or oval tumors which often enclose small cysts (72%) but rarely calcifications (5%) and show inhomogenous liver like echogenicity. Metastasis in liver, spleen or abdomen occurred in 2 infants. The most frequent renal tumor in neonates was the mesoblastic nephroma (3 infants). All mesoblastic nephromas were well delineated round tumors with inhomogenous echo-texture and equal or increased echogenicity in comparison to the liver. They often enclosed small cysts but no metastasis or calcifications. Angiomyolipomas of the kidneys could be diagnosed in two children with tuberous sclerosis. These tumors were echogenic nodules spread all over the kidney. We found multilocular nephroblastomas with multiple irregularly delineated cysts in one child. In an other child multiple renal lymphomas simulating solid tumors with liver-like echogenicity could be found.


Subject(s)
Hemangioma/diagnosis , Kidney Neoplasms/diagnostic imaging , Lipoma/diagnosis , Lymphoma/diagnosis , Wilms Tumor/diagnostic imaging , Adolescent , Child , Child, Preschool , Diagnosis, Differential , Female , Humans , Infant , Infant, Newborn , Kidney/pathology , Male , Ultrasonography
8.
Circulation ; 70(6): 923-8, 1984 Dec.
Article in English | MEDLINE | ID: mdl-6499148

ABSTRACT

We analyzed data from 68 consecutive patients with congestive cardiomyopathy to evaluate the prognostic significance of quantitative morphologic findings in left ventricular myocardium as compared with the prognostic significance of left ventricular hemodynamics. Left ventricular endomyocardial biopsy specimens were obtained from all patients during diagnostic heart catheterization. Myocardial fiber diameter, volume fraction of interstitial fibrosis, and intracellular volume fraction of myofibrils were determined by light-microscopic morphometry. All patients had normal coronary arteriograms, but reduced left ventricular ejection fractions. There were 23 deaths during a mean follow-up period of 1124 days. Multivariate regression analysis (Cox model) revealed that left ventricular ejection fraction (p less than .00001) and left ventricular systolic pressure (p less than .01), but not morphometric findings in biopsy specimens, were independent predictors of cardiac death. Thus, morphologic findings in the left ventricular myocardium do not contribute significantly to the prognostic evaluation in patients with congestive cardiomyopathy studied by hemodynamic and angiographic methods.


Subject(s)
Cardiomyopathy, Dilated/pathology , Heart Failure/pathology , Hemodynamics , Adult , Cardiomyopathy, Dilated/mortality , Cardiomyopathy, Dilated/physiopathology , Diastole , Female , Germany, West , Humans , Male , Middle Aged , Myocardium/pathology , Prognosis , Stroke Volume , Systole
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