DOI: https://doi.org/https://doi.org/10.57187/s.3771
Iron deficiency affects millions of people worldwide. Causes are varied and include restricted food intake, increased blood loss, increased needs or intestinal malabsorption. Patients with previous gastric bypass surgery are at risk of micronutrient malabsorption, especially iron, for which the prevalence is 16–42% [1, 2]. Given that oral absorption is reduced after Roux-en-Y gastric bypass surgery, due to decreased gastric acid secretion and bypass of the proximal small intestine, parenteral iron formulations are often preferred to enteral ones. Ferric carboxymaltose (FCM) is among the most prescribed intravenous iron preparations due to its rapid infusion rate and overall safety profile [3–5]. Despite its attractiveness, FCM was recently associated with new-onset hypophosphataemia [5–10]. Mostly underdiagnosed, hypophosphataemia after FCM infusion is usually transient and asymptomatic with a nadir about two weeks after infusion [7, 8, 11]. A prevalence of FCM-induced hypophosphataemia of up to 92% has been described when systematically sought [4, 6, 7, 11–15]. Increase of the biologically active phosphatonin fibroblast growth factor 23 (FGF23) appears to mediate hypophosphataemia induced by FCM infusion [7, 9, 10, 14, 16]. FGF23 is produced by osteoblasts in response to high levels of plasma 1,25-(OH)2 vitamin D or of plasma phosphate. FGF23 inhibits renal reabsorption of phosphate by downregulating the tubular co-transporters NaPiIIa (SLC34A1) and NaPiIIc (SLC34A3) and by decreasing plasma levels of 1,25-(OH)2-vitamin D. Recent reports suggest that among known iron preparations, FCM is more often linked to hypophosphataemia [5–7, 14] than ferric saccharose [17], ferric isomaltoside [11, 18] or ferric dextran [19]. Most of the patients did not display any symptoms, even though in the presence of persistent and severe hypophosphataemia some of them experienced bone pain, osteomalacia and even fractures [9, 10, 20]. Predictive factors associated with intravenous iron-induced hypophosphataemia have been identified, such as the type of intravenous iron (FCM) [7, 10, 11], low body weight [7, 8], high pre-perfusion haemoglobin concentration [7], normal eGFR [6, 7, 10] or abnormal uterine bleeding [6, 7]. Moreover, cumulative doses of iron were also associated with hypophosphataemia [8, 17]. Here, we performed a retrospective case series study in patients with previous Roux-en-Y gastric bypass receiving FCM infusion, to identify predictive risk factors involved in plasma phosphate lowering.
The study recruited patients with previous Roux-en-Y gastric bypass who received FCM infusion during their routine medical care between January 2018 and September 2019 and had plasma phosphataemia measured within three months before the infusion and up to one month after the infusion. In patients who had received several infusions of FCM with measurements of plasma phosphate levels during the study period (n = 5), the infusion that resulted in the lowest plasma phosphate level was arbitrarily selected.
The single-centre retrospective study included patients who underwent Roux-en-Y gastric bypass at Lausanne University Hospital, Lausanne, Switzerland. Laparoscopic Roux-en-Y gastric bypass was performed by the same surgical team by creating a 15–20 ml gastric pouch, a retrocolic 100–150 cm Roux alimentary limb, a 50 cm biliopancreatic limb, a 21 mm circular stapled gastrojejunostomy and a linear stapled jejunostomy. All patients were followed up for obesity at the outpatient clinic of the hospital and received supplements (daily multivitamins, calcium and vitamin D) according to Swiss guidelines on obesity and post-bariatric treatment [21]. The indication for iron infusion was retained in patients with an established diagnosis of iron deficiency by: ferritin <50 µg/l or serum ferritin ≤100 µg/l and and transferrin saturation ≤30% who have failed to respond to oral iron supplementation, either because of insufficient absorption or because of digestive adverse events leading to discontinuation of oral iron supplementation. Phosphatemia was assessed systematically in this time period for the following reasons: Roux-en-Y gastric bypass patients are at risk of poor bone health due to malabsorption of several micronutrients; several iron infusions per year are commonly required, particularly in premenopausal women with Roux-en-Y gastric bypass; and FCM carries a marked risk of hypophosphataemia.
The study was approved by the institutional ethics committee (CER-VD, project n° 2019-01064) and conducted in accordance with the ethical standards of the Declaration of Helsinki.
The anthropometric and biological parameters obtained from patient charts and the accredited clinical chemistry laboratory of Lausanne University Hospital were: age (years), sex (M/F), time since bariatric surgery (years), weight (kg), height (m) and dose of FCM (mg). Baseline plasma phosphate (mmol/l), ferritin (µg/l), haemoglobin (g/l) and calcium corrected for albumin (mmol/l) were measured up to three months before the accounted FCM infusion; eGFR (ml/min/1.73 m2) was measured up to six months before FCM infusion; and 25-OH-vitamin D (µg/l) and parathyroid hormone (ng/l) were measured up to one month before FCM infusion. Post-infusion plasma phosphate was considered until one month after FCM infusion and the cumulative dose of FCM was calculated up to one year prior the infusion considered in the study.
The primary outcome was phosphataemia lowering following a single FCM infusion up to one month after that infusion.
Standard descriptive analyses were used to summarise the study variables: means with standard deviations (SD) for approximately normally distributed continuous variables; medians with interquartile ranges (IQR) for continuous variables presenting skewness; and frequencies and percentages for categorical variables. A p-value <0.05 was considered statistically significant. To identify predictors of magnitude of plasma phosphate lowering, we defined delta phosphataemia as the outcome and examined baseline haemoglobin, baseline ferritin, baseline eGFR, BMI, cumulative dose of FCM, dose of FCM and time between FCM infusion and post-FCM phosphataemia measurement as predictor variables [7, 18] using multiple linear regression. The number of covariates was chosen to respect the general rule for linear regression models, which is to include at most as many covariates as the number of study subjects divided by ten. Absolute risk of hypophosphataemia according to baseline phosphate levels was assessed by receiver operating characteristic (ROC) analysis. Outliers were defined as patients with a delta phosphataemia more than 3 standard deviations away from the mean. Outliers were kept for descriptive statistics and removed for multiple linear regression model and ROC analysis.
The analysis was performed by the Biostatistical Platform from UniSanté, using the software R (version 3.5.2) and GraphPad Prism (version 8.01, GraphPad Software, San Diego, California, United States).
Seventy-seven patients (70 females and 7 males) with a mean age (SD) of 43.2 (10.7) and a median BMI of 30.9 kg/m2 (IQR 27.9-36.4) were included in the study. A description of baseline and post-FCM infusion characteristics is shown in table 1. Most patients (88.3%) were prescribed 500 mg FCM at the discretion of the treating physician. A decrease in plasma phosphate was measured in 90.9% of patients within a median of 13 days (IQR 10.0–15.0) after FCM infusion and 63.6% of them developed new-onset hypophosphataemia; 40.8% had mild hypophosphataemia (0.6–0.8 mmol/l), 53.1% severe hypophosphataemia (0.3–0.59 mmol/l) and 6.1% critical hypophosphataemia (<0.3 mmol/l). Five patients were already mildly hypophosphataemic and one patient presented severe hypophosphataemia (0.55 mmol/l) before FCM infusion. The variation in plasma phosphate concentrations pre- and post-FCM infusion are shown in figure 1. Delta phosphataemia was found to be approximately normally distributed, except for a severe outlier in the left part of the distribution (a patient having phosphataemia increased by approximately 1.5 mmol/l). Median delta phosphataemia (IQR) was 0.33 mmol/l (0.14–0.49), with the first quartile rising to 0.17 mmol/l if the outlier is excluded. Nearly one-fifth of patients had received a cumulative dose of FCM greater than 500 mg in the year preceding the iron infusion. Mean eGFR (SD) for the whole cohort was normal at 101.5 ml/min/1.73 m2 (19.2). Median ferritin level was low at 27.5 µg/l (IQR 18.3–43.8; reference range: 30–300 µg/l).
Table 1Characteristics of the participants and treatment. Reference range for phosphataemia: 0.8–1.4 mmol/l. Reference range for ferritin: 30–300 µg/l. Reference range for haemoglobin in women: 117–157 g/l, and in men: 133–177 g/l. Reference range for calcium corrected for albumin: 2.10–2.50 mmol/l. Reference range for 25-OH-vitamin D: 8.4–52.3 µg/l. Reference range for parathyroid hormone: 10–70 ng/l.
Age (y), mean (SD) | 43.2 (10.7) | |
Sex, n (%) | 70 F / 7 M (90.9%/9.1%) | |
Time from surgery (years), median (IQR; range) | 4.6 (2.6–10.0; 0.4–18.5) | |
BMI (kg/m2), median (IQR; range) | 30.9 (27.9–36.4; 22.0–46.9) | |
Ferritin (µg/l), median (IQR; range) (n = 72) | 27.5 (18.3–43.8; 5.0–176.0) | |
Haemoglobin (g/l), mean (SD) (n = 62) | 131.0 (12.5) | |
eGFR (ml/min/1.73 m2), mean (SD) (n = 66) | 101.5 (19.2) | |
CKD G1* (eGFR >90 ml/min/1.73 m2), n (%) | 48 (72.8%) | |
CKD G2* (eGFR 60–89 ml/min/1.73 m2), n (%) | 16 (24.2%) | |
CKD G3* (eGFR 30–59 ml/min/1.73 m2), n (%) | 2 (3%) | |
Calcium corrected for albumin (mmol/l), mean (SD) (n = 58) | 2.2 (0.07) | |
25-OH-vitamin D (µg/l), mean (SD) (n = 39) | 38.3 (8.0) | |
Parathyroid hormone (ng/l), mean (SD) (n = 35) | 58.7 (29.7) | |
Pre-FCM phosphataemia (mmol/l), mean (SD) | 1.0 (0.2) | |
Cumulative dose of FCM>500 mg, n (%) | 15 (19.5%) | |
Dose of FCM: 500 mg, n (%) | 68 (88.3%) | |
Dose of FCM: 250 mg, n (%) | 9 (11.7%) | |
Time between FCM infusion and post-FCM phosphataemia (days), median (IQR; range) | 13 (10–15; 0.4–18.5) | |
Post-FCM phosphataemia (mmol/l), mean (SD) | 0.7 (0.3) | |
Delta (pre/post infusion) phosphataemia (mmol/l), median (IQR; range) | 0.33 (0.14–0.49; -0.29 – 1.14) | |
Post-FCM infusion hypophosphataemia (<0.8 mmol/l), n (%) | 49 (63.6%) | |
Mild (0.6 – <0.8 mmol/l), n (%) | 20 (40.8%) | |
Severe (0.3 – <0.6 mmol/l), n (%) | 26 (53.1%) | |
Critical (<0.3 mmol/l), n (%) | 3 (6.1%) |
CKD: chronic kidney disease; eGFR: estimated glomerular filtration rate; FCM: ferric carboxymaltose; KDIGO: Kidney Disease: Improving Global Outcomes.
* Stages of Chronic Kidney Disease according to KDIGO clinical guidelines [34]. Missing data: ferritin (n = 5); haemoglobin (n = 15); eGFR (n = 11); calcium corrected for albumin (n = 19); 25-OH-vitamin D (n = 38); parathyroid hormone (n = 42).
Figure 1Variation of plasma phosphate concentration at baseline and after ferric carboxymaltose (FCM) infusion. Baseline plasma phosphate level was assessed up to three months before FCM infusion. Post-FCM plasma phosphate level was assessed up to one month after FCM infusion. The lower limit of normal plasma phosphate level is indicated by a dotted line.
Multiple linear regression was applied to analyse the joint influence of baseline haemoglobin, baseline ferritin, baseline eGFR, BMI, cumulative dose of FCM, dose of FCM and time elapsed between FCM infusion and post-FCM phosphataemia assessment, on delta phosphataemia (outcome). An interaction between FCM dose and the time between FCM infusion and post-FCM phosphataemia was also tested and founded to be not significant (not shown). The model’s assumptions (linearity, normality and homogeneity of variance) were verified by inspection of the residuals plotted against the model’s fitted values and the normal probability plot of the residuals. No evidence of assumption violation was detected. Table 2 shows the results of univariate and of multivariable regression models. Effects represent increments in mean phosphate serum lowering (mmol/l) associated with a one-point increase in continuous covariates. For the FCM dose (dichotomous variable), the effect represents the additional mean phosphate serum lowering associated with a dose of 500 mg vs a dose of 250 mg. The dose of FCM infused was significantly associated with the extent of phosphate serum lowering: a higher dose (500 mg vs 250 mg) was associated with a significantly greater mean decrease in phosphataemia (difference of 0.26 mmol/l, p = 0.020). Since the choice of the FCM dose may depend on previous hypophosphataemia post-FCM, we re-estimated the model by adding baseline phosphate level as an additional covariate in the model. We found that the effect of FCM dose remained approximately the same adding baseline phosphate (0.23 mmol/l) as the one obtained in the original model (0.26 mmol/l). Thus, at equal values of baseline phosphate level, a higher dose of FCM will result in a greater drop in phosphate. The interaction between the two variables was also tested and found to be non-significant.We did not identify any other significant predictive factors but observed a trend for eGFR, specifically a protective effect of higher eGFR values on phosphate serum lowering, which can be quantified as an average reduction of 0.02 mmol/l in the phosphate lowering effect for each ten-point increase in eGFR (ml/min/1.73 m2) (p = 0.081).
Table 2Multiple linear regression model with delta phosphataemia as outcome.
Univariate analysis | Multivariable analysis | |||||||
Estimated effect (mmol/l) | 95% CI | p-value | Estimated effect (mmol/l) | 95% CI | p-value | |||
Dose of FCM = 500 mg | 0.258 | 0.064 | 0.452 | 0.010 | 0.253 | 0.042 | 0.464 | 0.020 |
Cumulative dose of FCM >500 mg | 0.055 | –0.109 | 0.219 | 0.505 | 0.104 | –0.101 | 0.309 | 0.313 |
log BMI | –0.277 | –0.647 | 0.094 | 0.141 | -0.248 | –0.702 | 0.207 | 0.279 |
Haemoglobin | –0.003 | –0.009 | 0.003 | 0.293 | -0.004 | –0.010 | 0.002 | 0.174 |
eGFR | –0.002 | –0.006 | 0.001 | 0.185 | -0.003 | –0.007 | 0.000 | 0.081 |
log ferritin | 0.026 | –0.074 | 0.125 | 0.611 | 0.016 | –0.096 | 0.129 | 0.771 |
log time between FCM infusion and post-FCM phosphataemia | –0.001 | –0.215 | 0.213 | 0.992 | -0.005 | –0.025 | 0.014 | 0.587 |
eGFR: estimated glomerular filtration rate; FCM: ferric carboxymaltose.
ROC analysis was performed assessing baseline phosphate levels as the predictor for absolute hypophosphataemia post-FCM infusion, as shown in figure S1 and table S1 (in the appendix). Area under the curve (AUC) was 0.678. A baseline phosphataemia of ≤1.2 mmol/l (table S1) could be identified with Youden index as a risk factor for absolute hypophosphataemia after FCM infusion with a sensitivity of 94%, a specificity of 37% and a positive predictive value of 73%.
In this retrospective case series of Roux-en-Y gastric bypass patients receiving FCM, we found that the dose of iron infused was significantly associated with the decrease in phosphate concentration. Ninety percent of the patients exhibited a decreased phosphate concentration post-iron infusion and 63.6% developed hypophosphataemia within one month after infusion. Most of the patients included were women (91%), as expected. Indeed, females are much more represented in the general gastric bypass population than males [23].
FCM-associated hypophosphataemia is frequent, mostly transient, and asymptomatic, with a nadir two weeks after the FCM infusion [7, 8, 11]. However, in some extreme cases, plasma phosphate concentration can remain low for several weeks to months and may lead to osteomalacia and bone fractures [9]. Identification of patients at risk of developing long-lasting hypophosphataemia following FCM infusion is essential for preventing major health threats.
Risk factors for hypophosphataemia have been sought in several studies [7, 18]. The type of iron infused (FCM), lower body weight, Black ethnicity, higher baseline haemoglobin levels and low baseline plasma phosphate levels have been associated with the risk of developing hypophosphataemia. Other studies identified the cumulative dose of FCM as associated with hypophosphataemia [8, 17]. The way the underlying disease may contribute to the risk of developing post-iron infusion hypophosphataemia or osteomalacia is less clear, with some case reports associated with chronic blood loss [24–26], inflammatory bowel diseases [27–29] or malnutrition [30]. In the study by Wolf et al. [7], iron deficiency due to abnormal uterine bleeding compared to unspecified iron deficiency was more often associated with post-FCM-induced hypophosphataemia.
It has not been established that the dose of FCM is associated with hypophosphataemia. Wolf et al. [7] identified “lower body weight” as a risk factor and suggested that for a given dose, low body weight would expose the patient to a higher iron concentration and therefore proposed that relative dose may affect the magnitude of the plasma phosphate lowering effect. However, no study confirmed this hypothesis. Our study now demonstrates that FCM infusion dose has an impact on phosphataemia in obese patients (BMI of 30.9 kg/m2) who underwent Roux-en-Y gastric bypass surgery. We used two relatively low doses, 250 mg (about 10% of the patients) and 500 mg of FCM (90%) and showed that the higher the dose of FCM, the greater the probability of developing hypophosphataemia after infusion. This dose-dependent risk is also supported by the fact that all patients receiving FCM 250 mg were those who previously developed hypophosphataemia with FCM 500 mg. The dose effect suggests that the FCM dose should be adjusted in patients at risk. We cannot speculate on higher doses (≥1000 mg) that are often encountered in clinical practice, as these high doses were not used in our clinic.
This study also found a trend between impaired renal function and a decreased risk of hypophosphataemia after FCM infusion. These results are in line with Wolf et al. [7] and are usually explained by resistance to FGF23 action seen in chronic kidney disease. Regarding other risk factors for decreased phosphataemia after FCM infusion, we did not find an association with haemoglobin or ferritin levels nor with BMI or cumulative FCM dose, as previously described. This might be due to the limited size of our cohort or to specificities due to Roux-en-Y gastric bypass.
Patients with Roux-en-Y gastric bypass are at risk of poor bone health. Chronic malabsorption of several micronutrients such as calcium and vitamin D, secondary hyperparathyroidism and lower bone mineralisation are common and increase the risk of bone fracture [31–33]. Correcting iron deficiency with the FCM formulation may add an additional risk factor for bone health by inducing hypophosphataemia and demineralisation. Schoeb et al. [13] conducted a prospective study in this at-risk population and found that almost 30% of patients with previous Roux-en-Y gastric bypass receiving a single dose of 500 mg of FCM developed hypophosphataemia. However, no bone parameters were studied. We urge clinicians to carefully investigate bone parameters in patients receiving iron infusions.
We found a median delta phosphataemia of 0.33 mmol/l, similar to what Schoeb et al. found (0.3 mmol/l), but lower compared to the study by Wolf et al. (0.49 mmol/l) [7]. In the latter study, the FCM dose was three times higher (1500 mg). This is in line with the dose-response effect we observed in this study and is likely to explain the stronger effect on phosphataemia.
The weak association between low baseline phosphataemia (≤1.2 mmol/l) and post-FCM hypophosphataemia does not justify changes to clinical management and will need additional confirmatory studies.
This study has some limitations. Firstly, it was retrospective and by definition is limited to the available data. Indeed, there were missing data for baseline ferritin (n = 5), haemoglobin (n = 15), eGRF (n = 11), calcium corrected for albumin (n = 19), 25-OH-vitamin D (n = 38) and parathyroid hormone (n = 42). However, the set of data gathered here allowed the establishment of a multiple logistic regression model with significant results, indicating sufficient power. Secondly, we did not measure FGF23 at baseline and after FCM infusion, as this parameter is rarely assessed in routine clinical practice. This means that we cannot confirm the involvement of FGF23 in the dose-dependent effect of FCM on the degree of hypophosphataemia. Thirdly, our study did not examine the symptoms of hypophosphataemia or other hard endpoints on bone or muscle strength. This should be done in future prospective studies. Fourth, females were overrepresented in our study compared to men (only 9%). However, this high proportion of women is representative of the general gastric bypass population. Fifth, we focused only on patients with previous Roux-en-Y gastric bypass with a recorded phosphataemia before and after FCM infusion. Indeed, patients without data on phosphataemia were not included. Finally, the design of our study induced a selection bias due to the selection of the lowest phosphataemia after FCM infusion for individuals who had several infusions. Due to the limited number of such cases (n = 5), a sensitivity analysis could not be performed. However, the aim of this study was not to determine the exact incidence of FCM-associated hypophosphataemia but rather to identify risk factors. The strengths of our study are the real-world context and the analysis carried out in a precisely defined population, after Roux-en-Y gastric bypass surgery, and requiring frequent iron infusions.
Patients with Roux-en-Y gastric bypass are at risk of iron deficiency and therefore receive repeated parenteral iron infusions, mostly FCM. We found that single doses of FCM are followed by mild to critical hypophosphataemia in this at-risk population and that the dose of FCM infused was associated with delta phosphataemia. We thus recommend monitoring plasma phosphate levels in patients with Roux-en-Y gastric bypass receiving FCM infusions or to switch to other iron formulations much less associated with hypophosphataemia, such as ferric saccharose or ferric isomaltoside.
Further studies evaluating long-term consequences of iron-induced hypophosphataemia on target organs (heart, muscles, bone, …) are warranted.
The authors would like to thank the patients and the staff of the outpatient clinic for obesity of Lausanne University Hospital. Dr O. Lamy is acknowledged for his review of the Master thesis work of CPP.
Authors’ contribution: CPP designed the study, collected data, analysed and interpreted data, and wrote the manuscript. OB designed the study, analysed and interpreted data, and wrote the manuscript. IL performed statistical analysis, analysed and interpreted data and revised the manuscript. LF was in charge of patient care, designed the study, analysed and interpreted data and revised the manuscript. All authors read and approved the submitted version of the manuscript.
OB’s research is supported by grants from the Swiss National Science Foundation 310030-182312 and 51NF40-183774 (NCCR Kidney.CH).
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. CPP and IL declare that they have no conflict of interest. OB did receive consultancy honorarium from CSL Vifor, Switzerland. OB and LF did receive an investigator-initiated research grant from Pierre Fabre.
1. Enani G, Bilgic E, Lebedeva E, Delisle M, Vergis A, Hardy K. The incidence of iron deficiency anemia post-Roux-en-Y gastric bypass and sleeve gastrectomy: a systematic review. Surg Endosc. 2020 Jul;34(7):3002–10.
2. Engebretsen KV, Blom-Høgestøl IK, Hewitt S, Risstad H, Moum B, Kristinsson JA, et al. Anemia following Roux-en-Y gastric bypass for morbid obesity; a 5-year follow-up study. Scand J Gastroenterol. 2018 Aug;53(8):917–22.
3. Rognoni C, Venturini S, Meregaglia M, Marmifero M, Tarricone R. Efficacy and Safety of Ferric Carboxymaltose and Other Formulations in Iron-Deficient Patients: A Systematic Review and Network Meta-analysis of Randomised Controlled Trials. Clin Drug Investig. 2016 Mar;36(3):177–94.
4. Schaefer B, Meindl E, Wagner S, Tilg H, Zoller H. Intravenous iron supplementation therapy. Mol Aspects Med. 2020 Oct;75:100862.
5. Blumenstein I, Shanbhag S, Langguth P, Kalra PA, Zoller H, Lim W. Newer formulations of intravenous iron: a review of their chemistry and key safety aspects - hypersensitivity, hypophosphatemia, and cardiovascular safety. Expert Opin Drug Saf. 2021;20(7):757-69. Epub 20210515. doi: . PubMed PMID: 33993818.
6. Schaefer B, Tobiasch M, Viveiros A, Tilg H, Kennedy NA, Wolf M, et al. Hypophosphataemia after treatment of iron deficiency with intravenous ferric carboxymaltose or iron isomaltoside-a systematic review and meta-analysis. Br J Clin Pharmacol. 2021;87(5):2256-73. Epub 20201207. doi: . PubMed PMID: 33188534; PubMed Central PMCID: PMC8247006.
7. Wolf M, Chertow GM, Macdougall IC, Kaper R, Krop J, Strauss W. Randomized trial of intravenous iron-induced hypophosphatemia. JCI Insight. 2018 Dec;3(23):e124486.
8. Rosano G, Schiefke I, Göhring UM, Fabien V, Bonassi S, Stein J. A Pooled Analysis of Serum Phosphate Measurements and Potential Hypophosphataemia Events in 45 Interventional Trials with Ferric Carboxymaltose. J Clin Med. 2020;9(11). Epub 20201106. doi: . PubMed PMID: 33172157; PubMed Central PMCID: PMC7694774.
9. Zoller H, Schaefer B, Glodny B. Iron-induced hypophosphatemia: an emerging complication. Curr Opin Nephrol Hypertens. 2017 Jul;26(4):266–75.
10. Glaspy JA, Wolf M, Strauss WE. Intravenous Iron-Induced Hypophosphatemia: An Emerging Syndrome. Adv Ther. 2021;38(7):3531-49. Epub 20210530. doi: . PubMed PMID: 34053011; PubMed Central PMCID: PMC8279965.
11. Wolf M, Rubin J, Achebe M, Econs MJ, Peacock M, Imel EA, et al. Effects of Iron Isomaltoside vs Ferric Carboxymaltose on Hypophosphatemia in Iron-Deficiency Anemia: Two Randomized Clinical Trials. JAMA. 2020 Feb;323(5):432–43.
12. Favrat B, Balck K, Breymann C, Hedenus M, Keller T, Mezzacasa A, et al. Evaluation of a single dose of ferric carboxymaltose in fatigued, iron-deficient women—PREFER a randomized, placebo-controlled study. PLoS One. 2014 Apr;9(4):e94217.
13. Schoeb M, Räss A, Frei N, Aczél S, Brändle M, Bilz S. High Risk of Hypophosphatemia in Patients with Previous Bariatric Surgery Receiving Ferric Carboxymaltose: A Prospective Cohort Study. Obes Surg. 2020 Jul;30(7):2659–66.
14. Kassianides X, Bhandari S. Hypophosphataemia, fibroblast growth factor 23 and third-generation intravenous iron compounds: a narrative review. Drugs Context. 2021;10. Epub 20210119. doi: . PubMed PMID: 33519940; PubMed Central PMCID: PMC7819638.
15. Bager P, Hvas CL, Dahlerup JF. Drug-specific hypophosphatemia and hypersensitivity reactions following different intravenous iron infusions. Br J Clin Pharmacol. 2017;83(5):1118-25. Epub 20170118. doi: . PubMed PMID: 27859495; PubMed Central PMCID: PMC5401972.
16. Coppolino G, Nicotera R, Cernaro V, Calimeri S, Leonardi G, Cosentino S, et al. Iron Infusion and Induced Hypophosphatemia: The Role of Fibroblast Growth Factor-23. Ther Apher Dial. 2020;24(3):258-64. Epub 20191025. doi: . PubMed PMID: 31483921.
17. Hardy S, Vandemergel X. Intravenous iron administration and hypophosphatemia in clinical practice. Int J Rheumatol. 2015;2015:468675.
18. Schaefer B, Würtinger P, Finkenstedt A, Braithwaite V, Viveiros A, Effenberger M, et al. Choice of High-Dose Intravenous Iron Preparation Determines Hypophosphatemia Risk. PLoS One. 2016 Dec;11(12):e0167146.
19. Wolf M, Koch TA, Bregman DB. Effects of iron deficiency anemia and its treatment on fibroblast growth factor 23 and phosphate homeostasis in women. J Bone Miner Res. 2013 Aug;28(8):1793–803.
20. Schaefer B, Tobiasch M, Wagner S, Glodny B, Tilg H, Wolf M, et al. Hypophosphatemia after intravenous iron therapy: Comprehensive review of clinical findings and recommendations for management. Bone. 2021;154:116202. Epub 20210915. doi: . PubMed PMID: 34534708.
21. SMOB. Directives pour le traitement chirurgical de l’obésité. 2021.
22. Jepsen P, Tapper EB, Deleuran T, Kazankov K, Askgaard G, Sorensen HT, et al. Risk and Outcome of Venous and Arterial Thrombosis in Patients With Cirrhosis: A Danish Nation-wide Cohort Study. Hepatology. 2021;74(5):2725-34. Epub 20210909. doi: . PubMed PMID: 34137045; PubMed Central PMCID: PMC8542589.
23. Young MT, Phelan MJ, Nguyen NT. A Decade Analysis of Trends and Outcomes of Male vs Female Patients Who Underwent Bariatric Surgery. J Am Coll Surg. 2016;222(3):226-31. Epub 20151217. doi: . PubMed PMID: 26782151.
24. Callejas-Moraga EL, Casado E, Gomez-Nuñez M, Caresia-Aroztegui AP. Severe osteomalacia with multiple insufficiency fractures secondary to intravenous iron therapy in a patient with Rendu-Osler-Weber syndrome. Bone Rep. 2020 Aug;13:100712.
25. Sangrós Sahún MJ, Goñi Gironés E, Camarero Salazar A, Estébanez Estébanez C, Lozano Martínez ME. Symptomatic hypophosphataemic osteomalacia secondary to the treatment with iron carboxymaltose detected in bone scintigraphy. Rev Esp Med Nucl Imagen Mol. 2016;35(6):391–3. 10.1016/j.remnie.2016.09.002
26. Moore KL, Kildahl-Andersen O, Kildahl-Andersen R, Tjønnfjord GE. Uncommon adverse effect of a common medication. Tidsskr Nor Laegeforen. 2013 Jan;133(2):165.
27. Bartko J, Roschger P, Zandieh S, Brehm A, Zwerina J, Klaushofer K. Hypophosphatemia, Severe Bone Pain, Gait Disturbance, and Fatigue Fractures After Iron Substitution in Inflammatory Bowel Disease: A Case Report. J Bone Miner Res. 2018 Mar;33(3):534–9.
28. Klein K, Asaad S, Econs M, Rubin JE. Severe FGF23-based hypophosphataemic osteomalacia due to ferric carboxymaltose administration. BMJ Case Rep. 2018 Jan;2018:bcr2017222851.
29. Schaefer B, Glodny B, Zoller H. Blood and Bone Loser. Gastroenterology. 2017 May;152(6):e5–6.
30. Fierz YC, Kenmeni R, Gonthier A, Lier F, Pralong F, Coti Bertrand P. Severe and prolonged hypophosphatemia after intravenous iron administration in a malnourished patient. Eur J Clin Nutr. 2014 Apr;68(4):531–3.
31. Axelsson KF, Werling M, Eliasson B, Szabo E, Näslund I, Wedel H, et al. Fracture Risk After Gastric Bypass Surgery: A Retrospective Cohort Study. J Bone Miner Res. 2018 Dec;33(12):2122–31.
32. Yu EW, Kim SC, Sturgeon DJ, Lindeman KG, Weissman JS. Fracture Risk After Roux-en-Y Gastric Bypass vs Adjustable Gastric Banding Among Medicare Beneficiaries. JAMA Surg. 2019 Aug;154(8):746–53.
33. Fashandi AZ, Mehaffey JH, Hawkins RB, Schirmer B, Hallowell PT. Bariatric surgery increases risk of bone fracture. Surg Endosc. 2018 Jun;32(6):2650–5.
34. Summary of Recommendation Statements. Kidney Int Suppl (2011). 2013;3(3):263-5. doi: . PubMed PMID: 25018998; PubMed Central PMCID: PMC4089618.
Figure S1Receiver operating characteristic (ROC) curve of the absolute risk of hypophosphataemia as a function of baseline phosphate level. AUC: area under the curve.
Table S1Cutoffs of baseline phosphataemia as a risk factor for post-ferric carboxymaltose hypophosphataemia according to ROC analysis.
Cutoffs | Positive* | Negative** | Likelihood ratio | 95% CI |
0.4–0.8 | 5 | 1 | 2.755 | 0.339–22.388 |
0.8–1.0 | 21 | 7 | 1.653 | 0.809–3.379 |
1.0–1.2*** | 20 | 9 | 1.224 | 0.651–2.302 |
1.2–1.4 | 2 | 8 | 0.138 | 0.0315–0.603 |
1.4–2.0 | 1 | 2 | 0.276 | 0.0262–2.901 |
Total | 49 | 27 | ||
Sensitivity*** | 94% | |||
Specificity*** | 37% | |||
PPV*** | 73% | |||
NPV | 78% |
CI: confidence interval; NPV: negative predictive value; PPV: positive predictive value.
* Disease = 1
** Disease = 0
*** A baseline phosphataemia of ≤1.2 mmol/l could be identified with Youden index as a risk factor for absolute hypophosphataemia after FCM infusion with a sensitivity of 94%, a specificity of 37%, a positive predictive value of 73% and a negative predictive value of 78%.