Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Failure of noninvasive prediction of pulmonary hypertension in patients with idiopathic pulmonary fibrosis

F. Salajka, V. Bartos, J. Novosad, J. St'ásek, J. Bis, M. Brtko, P. Polanský, V. Koblízek, V. Sedlák,

. 2011 ; 75 (3) : 172-7.

Jazyk angličtina Země Itálie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc12023987

BACKGROUND: Pulmonary hypertension (PH) in patients with advanced idiopathic pulmonary fibrosis (IPF) is a complication connected with unfavorable prognosis. Great efforts have been made in attempting to establish a reliable non-invasive method which would enable detection of this complication. In this context a formula using pulmonary function parameters was published with outstanding results. METHODS: We tested the formula in 27 IPF patients who underwent a lung function examination, cardiac ultrasonography and catheterisation on the same day. RESULTS: Pulmonary hypertension was detected by catheterisation in 17 patients (63%). In our group, contrary to the published data, the aforementioned formula was neither useful for detecting patients with a high probability of PH nor as a means of calculating the mean pulmonary artery pressure in individual patients (p = 0.502 and p = 0.833, respectively). Ultrasound examination reached borderline correlation with the values measured by catheterisation when we compare patients with relevant results (r = 0.531, p = 0.051). However, the examination gave no usable results in 13 patients (48%). CONCLUSION: Our data suggests that no reliable, noninvasive method is currently available for detecting and confirming PH in IPF patients. We did not confirm the usefulness of the published formula. Further carefully organised studies will be necessary to verify or refute it.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc12023987
003      
CZ-PrNML
005      
20200710094211.0
007      
ta
008      
120815s2011 it f 000 0#eng||
009      
AR
024    7_
$a 10.4081/monaldi.2011.218 $2 doi
035    __
$a (PubMed)22428220
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a it
100    1_
$a Salajka, František, $d 1953- $7 mzk2003183706 $u Department of Pneumology, University Hospital and Charles University Faculty of Medicine, Hradec Kralove, Czech Republic. salajka@fnhk.cz
245    10
$a Failure of noninvasive prediction of pulmonary hypertension in patients with idiopathic pulmonary fibrosis / $c F. Salajka, V. Bartos, J. Novosad, J. St'ásek, J. Bis, M. Brtko, P. Polanský, V. Koblízek, V. Sedlák,
520    9_
$a BACKGROUND: Pulmonary hypertension (PH) in patients with advanced idiopathic pulmonary fibrosis (IPF) is a complication connected with unfavorable prognosis. Great efforts have been made in attempting to establish a reliable non-invasive method which would enable detection of this complication. In this context a formula using pulmonary function parameters was published with outstanding results. METHODS: We tested the formula in 27 IPF patients who underwent a lung function examination, cardiac ultrasonography and catheterisation on the same day. RESULTS: Pulmonary hypertension was detected by catheterisation in 17 patients (63%). In our group, contrary to the published data, the aforementioned formula was neither useful for detecting patients with a high probability of PH nor as a means of calculating the mean pulmonary artery pressure in individual patients (p = 0.502 and p = 0.833, respectively). Ultrasound examination reached borderline correlation with the values measured by catheterisation when we compare patients with relevant results (r = 0.531, p = 0.051). However, the examination gave no usable results in 13 patients (48%). CONCLUSION: Our data suggests that no reliable, noninvasive method is currently available for detecting and confirming PH in IPF patients. We did not confirm the usefulness of the published formula. Further carefully organised studies will be necessary to verify or refute it.
650    _2
$a senioři $7 D000368
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a srdeční katetrizace $7 D006328
650    _2
$a lidé $7 D006801
650    _2
$a plicní hypertenze $x diagnóza $x etiologie $x patofyziologie $x ultrasonografie $7 D006976
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    _2
$a prognóza $7 D011379
650    _2
$a prospektivní studie $7 D011446
650    _2
$a plicní fibróza $x komplikace $x patofyziologie $7 D011658
650    _2
$a reprodukovatelnost výsledků $7 D015203
650    _2
$a respirační funkční testy $7 D012129
650    _2
$a senzitivita a specificita $7 D012680
655    _2
$a časopisecké články $7 D016428
700    1_
$a Bartoš, Vladimír, $d 1976- $7 hka2011667947
700    1_
$a Novosad, J
700    1_
$a Šťásek, Josef, $d 1955- $7 xx0063485
700    1_
$a Bis, J
700    1_
$a Brtko, M
700    1_
$a Polanský, P
700    1_
$a Koblízek, V
700    1_
$a Sedlák, V
773    0_
$w MED00003404 $t Monaldi archives for chest disease Archivio Monaldi per le malattie del torace Fondazione clinica del lavoro, IRCCS [and] Istituto di clinica tisiologica e malattie apparato respiratorio, Università di Napoli, Secondo ateneo $x 1122-0643 $g Roč. 75, č. 3 (2011), s. 172-7
856    41
$u https://pubmed.ncbi.nlm.nih.gov/22428220 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y m $z 0
990    __
$a 20120815 $b ABA008
991    __
$a 20200710094210 $b ABA008
999    __
$a ok $b bmc $g 946135 $s 781315
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2011 $b 75 $c 3 $d 172-7 $i 1122-0643 $m Monaldi archives for chest disease $n Monaldi Arch Chest Dis $x MED00003404
LZP    __
$a Pubmed-20120815/12/02

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...