Response to Vasopressin Analogues in Diabetes Insipidus

1976 ◽  
Vol 295 (7) ◽  
pp. 393-394 ◽  
2015 ◽  
Vol 172 (3) ◽  
pp. 243-250 ◽  
Author(s):  
L A Behan ◽  
M Sherlock ◽  
P Moyles ◽  
O Renshaw ◽  
C J T Thompson ◽  
...  

Context and objectivePatients with cranial diabetes insipidus (CDI) are at risk of developing both hypernatraemia and hyponatraemia, due to the condition itself or secondary to treatment with vasopressin-analogues or during administration of i.v. fluids. We aimed to assess the frequency and impact of dysnatraemias in the inpatient (INPT) and outpatient (OPT) setting in desmopressin-treated CDI, comparing those with normal thirst with those with abnormal thirst.DesignThe study included 192 patients with cranial diabetes, who were identified from the Beaumont Pituitary Database, a tertiary referral centre. Retrospective case note audit was performed and the clinical and biochemical information of 147 patients with CDI were available for analysis.ResultsA total of 4142 plasma sodium measurements for 137 patients with normal thirst, and 385 plasma sodium measurements for ten patients with abnormal thirst were analysed. In those with normal thirst, the most common OPT abnormality was mild hyponatraemia (pNa+ 131–134 mmol/l) in 27%, while 14.6% had more significant hyponatraemia (pNa+ ≤130 mmol/l). Of those patients with normal thirst, 5.8% were admitted due to complications directly related to hyponatraemia. Compared with patients with normal thirst, those with abnormal thirst were more likely to develop significant OPT hypernatraemia (20% vs 1.4%, P=0.02) and significant INPT hyponatraemia (50% vs 11.1%, P 0.02).ConclusionOPT management of CDI is complicated by a significant incidence of hyponatraemia. In contrast, OPT hypernatraemia is almost exclusively a complication seen in adipsic CDI, who also had more frequent INPT hyponatraemia. CDI associated with thirst disorder requires increased physician attention and patient awareness of potential complications.


Author(s):  
C. N. Sun ◽  
H. J. White ◽  
E. J. Towbin

Diabetes insipidus and compulsive water drinking are representative of two categories of antidiuretic hormone (ADH) lack. We studied a strain of rats with congenital diabetes insipidus homozygote (DI) and normal rats on an isocaloric fortified dilute milk diet. In both cases, the collecting tubules could not concentrate urine. Special staining techniques, Alcian Blue-PAS for light microscopy and lanthanum nitrate for electron microscopy were used to demonstrate the changes in interstitial mucopolysaccharides (MPS). The lanthanum staining was done according to the method of Khan and Overton.Electron microscopy shows cytoplasmic lesions, vacules, swelling and degenerating mitochondria and intercellular spaces (IS) in the collecting tubule cells in DI and rats on milk diet.


2018 ◽  
Vol 24 ◽  
pp. 178-179
Author(s):  
Sabrina Huq ◽  
Mahalakshmi Honasoge ◽  
Ebru Sulanc
Keyword(s):  

2004 ◽  
Vol 10 ◽  
pp. 22
Author(s):  
Carolyn Narvacan-Montano ◽  
Thelma D. Crisostomo
Keyword(s):  

2006 ◽  
Vol 12 ◽  
pp. 60
Author(s):  
Jann M. Johnston ◽  
Camille Marie Buonocore ◽  
Adrianna Katarzyna Wegrecki ◽  
Imran Mohammed

2009 ◽  
Vol 66 (11) ◽  
pp. 765-768
Author(s):  
Curzio Solcà ◽  
Anja Kruse
Keyword(s):  

Die Krankengeschichte eines Patienten mit angeborenem renalen Diabetes insipidus wird dargestellt. Die Pathogenese und therapeutischen Modalitäten werden diskutiert.


1969 ◽  
Vol 68 (1, Pt.1) ◽  
pp. 38-44 ◽  
Author(s):  
Genaro M. Palmieri ◽  
Samuel Taleisnik

Sign in / Sign up

Export Citation Format

Share Document