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* 1. What is your dialysis program (province, city, name of dialysis program/affiliated hospital and/or university)?

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* 2. What hemodialysis machine does your program use (i.e., make/model)

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* 3. Is bicarbonate delivery performed at the level of the individual hemodialysis machine (vs. centralized delivery system)?

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* 4. What bicarbonate product does your program use?

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* 5. Does your program adjust the dialysate bicarbonate concentration regularly (i.e., weekly or monthly) based on individual patient factors, such as pre-dialysis serum bicarbonate concentration?

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* 6. For chronic dialysis patients, does your program use a different dialysate bicarbonate concentration in the inpatient/acute setting compared to the outpatient setting?

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* 7. Does your program prescribe the same dialysate bicarbonate concentration for >90% of patients?

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* 8. What is the dialysate bicarbonate concentration prescribed for most patients in your program?

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* 9. For the purposes of a trial examining the impact of different dialysate bicarbonate concentrations on patient outcomes, what is the lowest concentration you would be willing to randomize patients to?

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* 10. For the purposes of a trial examining the impact of different dialysate bicarbonate concentrations on patient outcomes, what is the highest concentration you would be willing to randomize patients to?

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* 11. Does your program prescribe oral sodium bicarbonate to chronic hemodialysis patients?

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* 12. Would your dialysis program be willing to participate in a national, cluster randomized pragmatic trial that compares two different standard dialysate bicarbonate concentrations to one another?

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