• Je něco špatně v tomto záznamu ?

Early diagnosis of solitary functioning kidney: comparing the prognosis of kidney agenesis and multicystic dysplastic kidney

H. Flogelova, K. Bouchalova, O. Smakal, J. Halek, K. Langova, K. Cizkova

. 2024 ; 39 (9) : 2645-2654. [pub] 20240415

Jazyk angličtina Země Německo

Typ dokumentu časopisecké články, srovnávací studie

Perzistentní odkaz   https://www.medvik.cz/link/bmc24019195
E-zdroje Online Plný text

NLK ProQuest Central od 1996-08-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 1996-08-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest) od 1996-08-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1996-08-01 do Před 1 rokem
Family Health Database (ProQuest) od 1996-08-01 do Před 1 rokem

BACKGROUND: Individuals with congenital solitary functioning kidney (SFK) are at an increased risk of kidney damage. According to some studies, the risk is higher in unilateral kidney agenesis (UKA) than in unilateral multicystic dysplastic kidney (UMCDK). We hypothesized that with early detection of children with UKA and UMCDK, there would be no difference in the presence of hypertension, proteinuria, and reduced glomerular filtration rate (GFR) between UKA and UMCDK. METHODS: Based on a long-term follow-up protocol, we evaluated a cohort of 160 children followed from birth for SFK (84 with UKA and 76 with UMCDK) detected by prenatal or routine neonatal ultrasound screening. Hypertension, proteinuria, and reduced GFR were monitored as markers of kidney damage. We compared the characteristics and outcomes of the subgroups of children with UKA and UMCDK. RESULTS: GFR was reduced in 42 (26.2%) children, of whom 41 showed only mild reduction. Hypertension and proteinuria were found in 22 (13.8%) and 14 (8.8%) children, respectively. Combined kidney damage was present in 57 (35.6%) children. The UMCDK and UKA subgroups differed in GFR at final examination, with UMCDK patients being significantly more likely to have normal GFR compared to UKA patients (82% vs. 67%; p = 0.039). CONCLUSIONS: One third of the children showed signs of SFK damage, albeit mild. Patients with UKA had reduced GFR significantly more often than those with UMCDK, but did not differ in the rates of hyperfiltration injury or congenital anomalies of the kidneys and urinary tract (CAKUT) in SFK.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc24019195
003      
CZ-PrNML
005      
20241024111652.0
007      
ta
008      
241015s2024 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00467-024-06360-2 $2 doi
035    __
$a (PubMed)38622348
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Flogelova, Hana $u Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 779 00, Olomouc, Czech Republic. Hana.Flogelova@seznam.cz $1 https://orcid.org/0000000329955735 $7 xx0096386
245    10
$a Early diagnosis of solitary functioning kidney: comparing the prognosis of kidney agenesis and multicystic dysplastic kidney / $c H. Flogelova, K. Bouchalova, O. Smakal, J. Halek, K. Langova, K. Cizkova
520    9_
$a BACKGROUND: Individuals with congenital solitary functioning kidney (SFK) are at an increased risk of kidney damage. According to some studies, the risk is higher in unilateral kidney agenesis (UKA) than in unilateral multicystic dysplastic kidney (UMCDK). We hypothesized that with early detection of children with UKA and UMCDK, there would be no difference in the presence of hypertension, proteinuria, and reduced glomerular filtration rate (GFR) between UKA and UMCDK. METHODS: Based on a long-term follow-up protocol, we evaluated a cohort of 160 children followed from birth for SFK (84 with UKA and 76 with UMCDK) detected by prenatal or routine neonatal ultrasound screening. Hypertension, proteinuria, and reduced GFR were monitored as markers of kidney damage. We compared the characteristics and outcomes of the subgroups of children with UKA and UMCDK. RESULTS: GFR was reduced in 42 (26.2%) children, of whom 41 showed only mild reduction. Hypertension and proteinuria were found in 22 (13.8%) and 14 (8.8%) children, respectively. Combined kidney damage was present in 57 (35.6%) children. The UMCDK and UKA subgroups differed in GFR at final examination, with UMCDK patients being significantly more likely to have normal GFR compared to UKA patients (82% vs. 67%; p = 0.039). CONCLUSIONS: One third of the children showed signs of SFK damage, albeit mild. Patients with UKA had reduced GFR significantly more often than those with UMCDK, but did not differ in the rates of hyperfiltration injury or congenital anomalies of the kidneys and urinary tract (CAKUT) in SFK.
650    _2
$a lidé $7 D006801
650    _2
$a ženské pohlaví $7 D005260
650    12
$a multicystické dysplastické ledviny $x diagnóza $x komplikace $x patofyziologie $7 D021782
650    _2
$a mužské pohlaví $7 D008297
650    12
$a solitární ledvina $x komplikace $x diagnóza $x patofyziologie $7 D000075529
650    12
$a ledviny $x abnormality $x patofyziologie $x diagnostické zobrazování $7 D007668
650    12
$a hodnoty glomerulární filtrace $7 D005919
650    12
$a časná diagnóza $7 D042241
650    _2
$a novorozenec $7 D007231
650    _2
$a prognóza $7 D011379
650    12
$a proteinurie $x etiologie $x diagnóza $7 D011507
650    _2
$a kojenec $7 D007223
650    _2
$a předškolní dítě $7 D002675
650    _2
$a dítě $7 D002648
650    _2
$a hypertenze $x diagnóza $x etiologie $x epidemiologie $x patofyziologie $7 D006973
650    _2
$a následné studie $7 D005500
650    _2
$a vrozené vady $x diagnóza $x diagnostické zobrazování $7 D000013
650    _2
$a novorozenecký screening $x metody $7 D015997
650    _2
$a nemoci ledvin $x vrozené $7 D007674
655    _2
$a časopisecké články $7 D016428
655    _2
$a srovnávací studie $7 D003160
700    1_
$a Bouchalova, Katerina $u Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 779 00, Olomouc, Czech Republic
700    1_
$a Smakal, Oldrich $u Department of Urology, University Hospital Olomouc, Olomouc, Czech Republic
700    1_
$a Halek, Jan $u Department of Neonatology, University Hospital Olomouc, Olomouc, Czech Republic
700    1_
$a Langova, Katerina $u Department of Medical Biophysics, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic
700    1_
$a Cizkova, Katerina $u Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic
773    0_
$w MED00003733 $t Pediatric nephrology (Berlin, Germany) $x 1432-198X $g Roč. 39, č. 9 (2024), s. 2645-2654
856    41
$u https://pubmed.ncbi.nlm.nih.gov/38622348 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20241015 $b ABA008
991    __
$a 20241024111645 $b ABA008
999    __
$a ok $b bmc $g 2201812 $s 1231168
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2024 $b 39 $c 9 $d 2645-2654 $e 20240415 $i 1432-198X $m Pediatric nephrology (Berlin, Germany) $n Pediatr Nephrol $x MED00003733
LZP    __
$a Pubmed-20241015

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...