- MeSH
- lidé MeSH
- poranění páteře * diagnostické zobrazování klasifikace terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- přehledy MeSH
xiv, 471 stran : ilustrace (některé barevné), portréty ; 28 cm
Vysokoškolská učebnice, která se zaměřuje na základy ortopedie a traumatologie.
- MeSH
- ortopedie MeSH
- traumatologie MeSH
- Konspekt
- Ortopedie. Chirurgie. Oftalmologie
- Učební osnovy. Vyučovací předměty. Učebnice
- NLK Obory
- ortopedie
- traumatologie
- NLK Publikační typ
- učebnice vysokých škol
- kolektivní monografie
It is commonly assumed that changes in plasma strong ion difference (SID) result in equal changes in whole blood base excess (BE). However, at varying pH, albumin ionic-binding and transerythrocyte shifts alter the SID of plasma without affecting that of whole blood (SIDwb), i.e., the BE. We hypothesize that, during acidosis, 1) an expected plasma SID (SIDexp) reflecting electrolytes redistribution can be predicted from albumin and hemoglobin's charges, and 2) only deviations in SID from SIDexp reflect changes in SIDwb, and therefore, BE. We equilibrated whole blood of 18 healthy subjects (albumin = 4.8 ± 0.2 g/dL, hemoglobin = 14.2 ± 0.9 g/dL), 18 septic patients with hypoalbuminemia and anemia (albumin = 3.1 ± 0.5 g/dL, hemoglobin = 10.4 ± 0.8 g/dL), and 10 healthy subjects after in vitro-induced isolated anemia (albumin = 5.0 ± 0.2 g/dL, hemoglobin = 7.0 ± 0.9 g/dL) with varying CO2 concentrations (2-20%). Plasma SID increased by 12.7 ± 2.1, 9.3 ± 1.7, and 7.8 ± 1.6 mEq/L, respectively (P < 0.01) and its agreement (bias[limits of agreement]) with SIDexp was strong: 0.5[-1.9; 2.8], 0.9[-0.9; 2.6], and 0.3[-1.4; 2.1] mEq/L, respectively. Separately, we added 7.5 or 15 mEq/L of lactic or hydrochloric acid to whole blood of 10 healthy subjects obtaining BE of -6.6 ± 1.7, -13.4 ± 2.2, -6.8 ± 1.8, and -13.6 ± 2.1 mEq/L, respectively. The agreement between ΔBE and ΔSID was weak (2.6[-1.1; 6.3] mEq/L), worsening with varying CO2 (2-20%): 6.3[-2.7; 15.2] mEq/L. Conversely, ΔSIDwb (the deviation of SID from SIDexp) agreed strongly with ΔBE at both constant and varying CO2: -0.1[-2.0; 1.7], and -0.5[-2.4; 1.5] mEq/L, respectively. We conclude that BE reflects only changes in plasma SID that are not expected from electrolytes redistribution, the latter being predictable from albumin and hemoglobin's charges.NEW & NOTEWORTHY This paper challenges the assumed equivalence between changes in plasma strong ion difference (SID) and whole blood base excess (BE) during in vitro acidosis. We highlight that redistribution of strong ions, in the form of albumin ionic-binding and transerythrocyte shifts, alters SID without affecting BE. We demonstrate that these expected SID alterations are predictable from albumin and hemoglobin's charges, or from the noncarbonic whole blood buffer value, allowing a better interpretation of SID and BE during in vitro acidosis.
BACKGROUND: Several studies explored the interdependence between Paco2 and bicarbonate during respiratory acid-base derangements. The authors aimed to reframe the bicarbonate adaptation to respiratory disorders according to the physical-chemical approach, hypothesizing that (1) bicarbonate concentration during respiratory derangements is associated with strong ion difference; and (2) during acute respiratory disorders, strong ion difference changes are not associated with standard base excess. METHODS: This is an individual participant data meta-analysis from multiple canine and human experiments published up to April 29, 2021. Studies testing the effect of acute or chronic respiratory derangements and reporting the variations of Paco2, bicarbonate, and electrolytes were analyzed. Strong ion difference and standard base excess were calculated. RESULTS: Eleven studies were included. Paco2 ranged between 21 and 142 mmHg, while bicarbonate and strong ion difference ranged between 12.3 and 43.8 mM, and 32.6 and 60.0 mEq/l, respectively. Bicarbonate changes were linearly associated with the strong ion difference variation in acute and chronic respiratory derangement (β-coefficient, 1.2; 95% CI, 1.2 to 1.3; P < 0.001). In the acute setting, sodium variations justified approximately 80% of strong ion difference change, while a similar percentage of chloride variation was responsible for chronic adaptations. In the acute setting, strong ion difference variation was not associated with standard base excess changes (β-coefficient, -0.02; 95% CI, -0.11 to 0.07; P = 0.719), while a positive linear association was present in chronic studies (β-coefficient, 1.04; 95% CI, 0.84 to 1.24; P < 0.001). CONCLUSIONS: The bicarbonate adaptation that follows primary respiratory alterations is associated with variations of strong ion difference. In the acute phase, the variation in strong ion difference is mainly due to sodium variations and is not paralleled by modifications of standard base excess. In the chronic setting, strong ion difference changes are due to chloride variations and are mirrored by standard base excess.
- MeSH
- acidobazická rovnováha * MeSH
- chloridy farmakologie MeSH
- hydrogenuhličitany * MeSH
- koncentrace vodíkových iontů MeSH
- lidé MeSH
- psi MeSH
- sodík farmakologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- psi MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
The authors present the cases of monozygotic male twins with right-sided Legg-Calvé-Perthes disease (LCPD) with different formation of the lumbosacral junction. This is likely the fi rst description of a lumbosacral junction formation disorder associated with identical twins who were both treated for LCPD as children. The disease began at 6 and 9 years of age and during treatment as well as in adulthood signifi cantly different bone formation of the lumbosacral transitional vertebra, was observed in both brothers. Twin A has a unilateral right-sided fusion of the enlarged L5 transverse process with the ipsilateral sacral ala, twin B has a complete sacralization of the fi fth lumbar vertebra. The LCPD treatment outcomes in the twins were consistent with the results from large studies, i.e., age at the time of LCPD onset is the main factor infl uencing the prognosis, however the morphological difference in the transitional vertebrae in these monozygotic twins was signifi cantly. Key words: lumbosacral transitional vertebra, lumbosacral junction formation, sacralization of lumbar vertebra, megatransverse of vertebra L5.
- MeSH
- bederní obratle diagnostické zobrazování MeSH
- dítě MeSH
- dvojčata monozygotní MeSH
- křížová kost diagnostické zobrazování MeSH
- lidé MeSH
- nemoci páteře * MeSH
- Perthesova nemoc * MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- přehledy MeSH
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1. elektronické vydání 1 online zdroj (354 stran)
This textbook for medical students include an overview of essential information on etiology, pathogenesis, clinical picture, diagnostics and treatment of developmental and acquired orthopedic diseases and disorders, including musculoskeletal injuries. It also includes an overview of essential conservative and surgical procedures used in orthopedics and traumatology of the musculoskeletal system in adult and child patients. As this textbook is intended as an aid for the preparation of the final state exam in surgical fields for the students at the Third Faculty of Medicine, Charles University, the chapters are arranged according to questions taken from the "pool" of Orthopedics and Traumatology used in this exam. However, we believe that this textbook can help students from other medical faculties of Charles University as a tool for quick and easy reference to a range of orthopedic diseases and injuries to the musculoskeletal system.
- Klíčová slova
- Chirurgie, ortopedie, traumatologie,
- MeSH
- ortopedie MeSH
- traumatologie MeSH
- NLK Obory
- ortopedie
- traumatologie
- MeSH
- acidobazická rovnováha * MeSH
- krevní proteiny * MeSH
- Publikační typ
- dopisy MeSH
- komentáře MeSH
- práce podpořená grantem MeSH
- MeSH
- acidobazická rovnováha * MeSH
- koncentrace vodíkových iontů MeSH
- Publikační typ
- dopisy MeSH
- komentáře MeSH
- MeSH
- axiální spondyloartritida diagnóza komplikace terapie MeSH
- lidé MeSH
- nemoci páteře * diagnóza etiologie komplikace terapie MeSH
- páteř abnormality diagnostické zobrazování patologie MeSH
- Scheuermannova nemoc diagnóza etiologie terapie MeSH
- skolióza diagnóza etiologie terapie MeSH
- spondylóza diagnóza etiologie komplikace terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- přehledy MeSH