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Urinary bicarbonate and metabolic alkalosis during exacerbations in cystic fibrosis

Giulia Spoletini, Giles Fitch, Lindsey Gillgrass, Christine Etherington, Ian Clifton, Daniel G. Peckham
ERJ Open Research 2022 8: 00669-2021; DOI: 10.1183/23120541.00669-2021
Giulia Spoletini
1The Leeds Regional Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds Teaching Hospital NHS Trust, Leeds, UK
2Leeds Institute of Medical Research, University of Leeds, Leeds, UK
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  • ORCID record for Giulia Spoletini
  • For correspondence: giulia.spoletini@nhs.net
Giles Fitch
3North West Midlands Adult Cystic Fibrosis Centre, University Hospital of North West Midlands NHS Trust, Stoke on Trent, UK
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Lindsey Gillgrass
1The Leeds Regional Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds Teaching Hospital NHS Trust, Leeds, UK
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Christine Etherington
1The Leeds Regional Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds Teaching Hospital NHS Trust, Leeds, UK
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Ian Clifton
1The Leeds Regional Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds Teaching Hospital NHS Trust, Leeds, UK
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Daniel G. Peckham
1The Leeds Regional Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds Teaching Hospital NHS Trust, Leeds, UK
2Leeds Institute of Medical Research, University of Leeds, Leeds, UK
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Tables

  • TABLE 1

    Baseline characteristics, and serum and urinary electrolyte data from the two cohorts

    CasesControlsp-value
    Subjects, n1516
    Age, years31 (26–35)45 (33–59)0.002
    Males10 (66.7)7 (43.8)0.2
    BMI, kg·m−222.5 (17.4–24.9)27.8 (23–32)0.007
    FEV1 %36 (27–45)61 (55–99)<0.001
    Emergency hospital admission013 (81.3)<0.001
    Diagnosis<0.01
     CF15 (100)
      F/F9 (60)
      F/MF3 (20)
      F/RF3 (20)
     Asthma9 (56.25)
     Non-CF bronchiectasis3 (18.75)
     Pneumonia3 (18.75)
     ILD1 (6.25)
    Comorbidities
     Cardiovascular1 (6.7)5 (31.3)0.083
     Liver disease10 (66.7)1 (6.3)0.002
     Diabetes4 (26.7)1 (6.3)0.061
    ABG
     pH7.46 (7.41–7.49)7.43 (7.42–7.49)0.953
     PaCO2 mmHg#5.25 (4.88–5.73)4.49 (4.26-4.68)<0.001
     PaO2, mmHg9.6 (9–10.2)11.29 (8.19–13.87)0.281
     HCO3−, mmol·L−127.8 (26.3–30)23.4 (22.9–24.5)<0.001
     BE, mmol·L−13 (2–7)−0.85 (−2.75–0.17)<0.001
    Serum HCO3−, mmol·L−128 (25.5–28.5)24 (22.5–24)0.001
    Serum chloride, mmol·L−1101 (97.5–104)105 (102.5–106.5)0.067
    Serum sodium, mmol·L−1138 (137.5–140.5)141 (138.5–141.5)0.108
    Serum potassium, mmol·L−14.1 (3.9–4.3)4.0 (3.8–4.2)0.892
    Urea, mmol·L−14.2 (3.2–6.4)5.5 (3.25–5.6)1.0
    Creatinine, μmol·L−161 (45.5–91)58 (53–64)0.650
    Urinary pH (lab)6.0 (5.75–6.5)6.0 (5.25–6.87)0.918
    Urinary HCO3−, mmol·L−13.5 (1.22–5)2.5 (0–9.75)0.982
    Urinary chloride, mmol·L−1133 (65.25–174.75)49.5 (37.5–117)0.070
    Urinary sodium, mmol·L−199 (65.75–157.75)51.5 (29–91)0.056
    Urinary creatinine, mmol·L−111 (5.27–12.25)10.7 (4.72–16.96)0.711
    Fractional excretion
     Chloride, %0.65 (0.42–1.05)0.73 (0.21–1.08)0.713
     HCO3−, %0.094 (0.04–0.29)0.076 (0–1.08)0.974
     Sodium, %0.54 (0.33–0.7)0.57 (0.089–0.75)0.533

    Data are presented as n (%) and median (interquartile range), unless otherwise stated. BMI: body mass index; FEV1: forced expiratory volume in 1 s; CF: cystic fibrosis; F/F: homozygous for the F508del-CFTR mutation; F/MF: heterozygous for the F508del-CFTR mutation and a minimal function CFTR mutation; F/RF: heterozygous for the F508del-CFTR mutation and a residual function CFTR mutation; ILD: interstitial lung disease; ABG: arterial blood gas; PaCO2: arterial carbon dioxide tension; PaO2: arterial oxygen tension; HCO3–: bicarbonate; BE: base excess. #: data presented as median (25th–75th percentile).

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    Urinary bicarbonate and metabolic alkalosis during exacerbations in cystic fibrosis
    Giulia Spoletini, Giles Fitch, Lindsey Gillgrass, Christine Etherington, Ian Clifton, Daniel G. Peckham
    ERJ Open Research Apr 2022, 8 (2) 00669-2021; DOI: 10.1183/23120541.00669-2021

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    Urinary bicarbonate and metabolic alkalosis during exacerbations in cystic fibrosis
    Giulia Spoletini, Giles Fitch, Lindsey Gillgrass, Christine Etherington, Ian Clifton, Daniel G. Peckham
    ERJ Open Research Apr 2022, 8 (2) 00669-2021; DOI: 10.1183/23120541.00669-2021
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