-
Je něco špatně v tomto záznamu ?
Changes in Fetal Hemoglobin Associated with Erythrocyte Transfusions Are Clinically Relevant in SpO2 Targeting: A Retrospective Cohort Observational Study
TE. Bachman, TA. Nguyen, L. Tejkl, R. Plavka
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, pozorovací studie
PubMed
40159229
DOI
10.1159/000545306
Knihovny.cz E-zdroje
- MeSH
- analýza krevních plynů MeSH
- fetální hemoglobin * metabolismus analýza MeSH
- gestační stáří MeSH
- kyslík * krev MeSH
- lidé MeSH
- novorozenec nedonošený * krev MeSH
- novorozenec MeSH
- retrospektivní studie MeSH
- saturace kyslíkem * MeSH
- transfuze erytrocytů * škodlivé účinky MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- novorozenec MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
INTRODUCTION: There is a broad awareness of shifts in the oxygen hemoglobin dissociation (ODC) relationship associated with fetal hemoglobin (HbF) changes. However, quantification of the shift has been limited. Aim was to quantify the shift of partial oxygen tension (PO2) associated with HbF and with changes after transfusion of adult erythrocytes (TAE) in preterm infants. METHODS: This is a single-center, retrospective observational analysis of blood gas samples. The shifts of ODC and PO2 related to HbF were evaluated in two models. Either HbF or TAE status (0, 1, ≥2) were used as the independent variable. Multivariate analysis was used to correct for confounding effects (gestational age, postnatal age, source of blood gas sample as well as pH, SO2, and PCO2). RESULTS: There were 3,452 blood gas observations analyzed from 2,464 infants whose median gestational age was 334 weeksdays (IQR 296-363). With SpO2 between 90 and 95%, the ODC was shifted to the left (13 mm Hg, 1.3 kPa). After adjusting for confounding variables, the number of TAEs (0, 1, ≥2), was highly significantly related to a shift (p < 0.001), consistent with the percent HbF level (p < 0.001). Based on the multivariate model (i.e., holding confounding parameters constant), with a SpO2 of 92% the PaO2 could be expected to shift markedly higher with 2 or more TAEs in an extremely preterm infant (7.3 mm Hg, 0.97 kPa). CONCLUSION: While preliminary, these data suggest that in vulnerable preterm infants a change to a slightly lower SpO2 target range following TAE could maintain equivalent PaO2 exposure.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25022662
- 003
- CZ-PrNML
- 005
- 20251023080517.0
- 007
- ta
- 008
- 251014s2025 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1159/000545306 $2 doi
- 035 __
- $a (PubMed)40159229
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Bachman, Thomas E $u Department of Biomedical Technology, Faculty of Biomedical Engineering, Czech Technical University in Prague, Kladno, Czechia
- 245 10
- $a Changes in Fetal Hemoglobin Associated with Erythrocyte Transfusions Are Clinically Relevant in SpO2 Targeting: A Retrospective Cohort Observational Study / $c TE. Bachman, TA. Nguyen, L. Tejkl, R. Plavka
- 520 9_
- $a INTRODUCTION: There is a broad awareness of shifts in the oxygen hemoglobin dissociation (ODC) relationship associated with fetal hemoglobin (HbF) changes. However, quantification of the shift has been limited. Aim was to quantify the shift of partial oxygen tension (PO2) associated with HbF and with changes after transfusion of adult erythrocytes (TAE) in preterm infants. METHODS: This is a single-center, retrospective observational analysis of blood gas samples. The shifts of ODC and PO2 related to HbF were evaluated in two models. Either HbF or TAE status (0, 1, ≥2) were used as the independent variable. Multivariate analysis was used to correct for confounding effects (gestational age, postnatal age, source of blood gas sample as well as pH, SO2, and PCO2). RESULTS: There were 3,452 blood gas observations analyzed from 2,464 infants whose median gestational age was 334 weeksdays (IQR 296-363). With SpO2 between 90 and 95%, the ODC was shifted to the left (13 mm Hg, 1.3 kPa). After adjusting for confounding variables, the number of TAEs (0, 1, ≥2), was highly significantly related to a shift (p < 0.001), consistent with the percent HbF level (p < 0.001). Based on the multivariate model (i.e., holding confounding parameters constant), with a SpO2 of 92% the PaO2 could be expected to shift markedly higher with 2 or more TAEs in an extremely preterm infant (7.3 mm Hg, 0.97 kPa). CONCLUSION: While preliminary, these data suggest that in vulnerable preterm infants a change to a slightly lower SpO2 target range following TAE could maintain equivalent PaO2 exposure.
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a retrospektivní studie $7 D012189
- 650 12
- $a fetální hemoglobin $x metabolismus $x analýza $7 D005319
- 650 _2
- $a novorozenec $7 D007231
- 650 12
- $a kyslík $x krev $7 D010100
- 650 12
- $a novorozenec nedonošený $x krev $7 D007234
- 650 12
- $a transfuze erytrocytů $x škodlivé účinky $7 D017707
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a gestační stáří $7 D005865
- 650 _2
- $a analýza krevních plynů $7 D001784
- 650 12
- $a saturace kyslíkem $7 D000089382
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a pozorovací studie $7 D064888
- 700 1_
- $a Nguyen, Truong An $u Department of Gynaecology, Obstetrics and Neonatology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia
- 700 1_
- $a Tejkl, Leos $u Department of Biomedical Technology, Faculty of Biomedical Engineering, Czech Technical University in Prague, Kladno, Czechia
- 700 1_
- $a Plavka, Richard $u Department of Gynaecology, Obstetrics and Neonatology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia
- 773 0_
- $w MED00184905 $t Neonatology $x 1661-7819 $g Roč. 122, č. 4 (2025), s. 407-413
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/40159229 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20251014 $b ABA008
- 991 __
- $a 20251023080522 $b ABA008
- 999 __
- $a ok $b bmc $g 2417431 $s 1260825
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 122 $c 4 $d 407-413 $e 20250329 $i 1661-7819 $m Neonatology $n Neonatology $x MED00184905
- LZP __
- $a Pubmed-20251014