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Compliance in patients with dietary hyperoxaluria: A cohort study and systematic review |
Derek B. Hennesseya,b,*(),Ned Kinnearb,Gilbert Ricea,David Currya,Siobhan Woolseya,Brian Duggana,c
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a.Department of Urology, Belfast City Hospital, Belfast, United Kingdom; b.Department of Urology, Austin Hospital, Melbourne, Australia; c.Department of Urology, Ulster Hospital, Belfast, United Kingdom |
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Abstract Objective Hyperoxaluria leads to calcium oxalate crystal formation and subsequent urolithiasis. This study aims to analyse the effect of treatment compliance in hyperoxaluria, firstly by analysis of patients with non-primary hyperoxaluria and secondly via systematic review in patients with any hyperoxaluria.Methods In a retrospective cohort study, adults with non-primary hyperoxaluria managed with dietary counselling in 2013 were enrolled. Twenty-four-hour (24 h) urine collections initially and at 6 months were obtained. Compliance was assessed by self-reported dietary compliance and 24 h urinary volume >2 L. Patients were followed for 24 months. Primary outcomes were urinary oxalate and calcium 24 h load at 6 months, and urolithiasis-related procedural rates at 24 months. A Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)-compatible systematic review of compliance among hyperoxaluric patients was performed.Results In the cohort study, of 19 eligible patients (4 female) with median age 52 years, 10 (53%) were considered compliant. Compared with the non-compliant group, these patients had significantly increased subsequent 24 h urinary volume (2250 mL vs. 1600 mL; p = 0.008) and lower procedural rates (10% vs. 56%; p = 0.033). Subsequent 24 h urinary oxalate load was non-significantly lower in compliant patients. Systematic review regarding compliance in hyperoxaluric patients revealed five studies. Only one utilised dietary counselling or analysed compliant vs. non-compliant patients, finding no difference. None examined the effect of compliance on procedural rates.Conclusion Hyperoxaluria is an important cause of recurrent urolithiasis. Increasing fluid intake and reducing dietary oxalate reduce the risk of operative intervention and remain fundamental to the treatment of hyperoxaluria.
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Received: 02 April 2017
Available online: 29 March 2018
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Corresponding Authors:
Derek B. Hennessey
E-mail: derek.hennessey@gmail.com
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Characteristics | Values | Total number | 19 | Age (year)a | 52 (45-60) | Sex | Male | 15 (79%) | Female | 4 (21%) | Lithogenic medical conditions (n = 14) | Diabetes mellitus | 1 (7.25%) | Hypercalcaemia | 1 (7.25%) | Hyperuricaemia | 2 (12.751%) | Recurrent UTI | 2 (12.75%) | Malabsorptive disorders | 4 (28.5%) | Renal anatomical abnormalities | 4 (28.5%) | Non-operative treatment compliance | Self-reported reduced dietary oxalate | 16 (84%) | Increased fluid intake | 12 (63%) | Both dietary and fluid measures | 10 (53%) | Thiazide diuretics (n = 4) | 4 (100%) | Stone analysis (n = 15) | Calcium oxalate | 4 (26%) | Calcium oxalate/apatate | 7 (47%) | Calcium oxalate/apatate/magnesium phosphate | 3 (20%) | Calcium oxalate/magnesium phosphate | 1 (7%) |
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Patient characteristics.
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Parameter | Values | Indications for 24 h collection, n (%) | | Paediatric onset | 4 (21) | Family history | 2 (11) | Recurring stone disease | 7 (36) | Bilateral stones | 2 (11) | Medical disorder | 4 (21) | 24 h urine collection, median (IQR) | | Volume (mL) | 1550 (1400-2000) | Oxalate (mmol/L) | 0.54 (0.49-0.68) | Calcium (mmol/L) | 5.69 (2.64-9.76) | Citrate (mmol/L) | 3.47 (1.6 0-5.15) | Phosphate (mmol/L) | 30.13 (20.25-43.65) | Urate (mmol/L) | 3.26 (2.34-4.57) | Creatinine (mmol/L) | 13.45 (7.45-16.10) | pH | 6.50 (5.675-6.80) | Sodium (mmol/L) | 138.00 (78.00-208.50) | Potassium (mmol/L) | 85.00 (53.75-109.50) | Chloride (mmol/L) | 130.00 (84.00-193.50) | Protein (mmol/L) | 0.08 (0.04-0.14) |
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First 24 h collection indications and findings.
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| Compliant | Non-compliant | p-Value | Initial Collection | Volume (mL) | 1643 (1250-1938) | 1400 (1400-1800) | 1 | Oxalate (mmol/L) | 0.55 (0.51-0.63) | 0.53 (0.49-0.68) | 0.97 | Citrate (mmol/L) | 3.17 (2.69-4.93) | 4.07 (1.38-6.08) | 1 | Calcium (mmol/L) | 5.09 (2.46-6.38) | 7.28 (3.44-9.76) | 0.45 | Subsequent collection | Volume (mL) | 2250 (2000-2400) | 1600 (1200-1700) | 0.008 | Oxalate (mmol/L) | 0.41 (0.34-0.46) | 0.53 (0.43-0.55) | 0.066 | Citrate (mmol/L) | 2.92 (2.13-3.61) | 3.95 (2.22-5.17) | 0.55 | Calcium (mmol/L) | 4.21 (2.91-6.81) | 7.14 (4.96-7.77) | 0.35 |
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Comparison of initial and subsequent 24 h urine collection results between compliant and non-compliant groups, median (IQR).
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Impact of compliance on 24 h urinary oxalate excretion. (A) Non complaint (n = 9); (B) Complaint patients (n = 10).
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Effect at 6 months of thiazide diuretics on 24 h urinary oxalate and calcium excretion. (A) Urinary oxalate 24 h excretion; (B) Urinary calcium 24 h excretion.
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PRISMA flow diagram of citations reviewed in the course of systematic review of compliance to intervention in patients with hyperoxaluria. PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses.
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Year | Author | Nation | Population | Methods | N | Outcomes | 2013 | Schwen et al. [19] | USA | Adults with idiopathic hyperoxaluria, renal stones, at least two 24 h urine collections >30 days apart and non-operative management | Retrospective cohort study with contemporary controls. Oxalate-avoidant dietary counselling was given. Compliance was measured by self-reporting, improvement in urine volume and ability to keep follow-up appointments. | 149 | 132/149 (89%) compliant. Overall, mean UrOx was significantly reduced (p < 0.001), however no difference between compliant and non-compliant UrOx (p = 0.84). | 2011 | Hoppe et al. [20] | Germany | Children and adults with primary hyperoxaluria | Double-blind randomised placebo-controlled trial. Oral Oxalobacter formigenes (107 colony forming units) twice daily for 24 weeks. Compliance self-reported. | 42 | 37/42 (88%) compliant. Overall vs. placebo, no significant change in mean UrOx (p = 0.62). Compliant vs. non-compliant UrOx not compared. | 1995 | Leumann et al. [21] | Switzerland | Children with primary hyperoxaluria | Prospective interventional study with no controls. Oral sodium citrate (0.10-0.15 g/kg) daily, long term (mean 4 years). Compliance measured by variability in urinary pH and citrate load. | 7 | 3/5 (60%) compliant (other two lost to follow-up). Overall, significant decrease in mean UrOx (p = 0.02). Compliant vs. non-compliant UrOx not compared. | 1991 | Edwards et al. [22] | UK | Adults with no disease, primary hyperoxaluria or mild metabolic hyperoxaluria | Prospective interventional study with healthy controls. Oral pyridoxine of various dosage. Compliance measured by urinary 4-pyridoxic acid. | 15 | 15/15 (100%) compliant. Compared to those with healthy patients, patients with mild metabolic hyperoxaluria, patients (p < 0.01) but not with primary hyperoxaluria displayed lower serum pyridoxal phosphate levels. No measurement of UrOx. No non-compliant patients for comparison. | 1989 | D'Cruz et al. [23] | UK | Adults with enteric hyperoxaluria due to Crohn's disease+/-bowel resection | Prospective interventional study with no controls. Comparison of 24 h urine collection before and after 2 weeks of oral allopurinol 300 mg daily. Compliance measured by fall in plasma uric acid. | 8 | 8/8 (100%) patient compliant. Overall, no change in mean UrOx (p = n/s). No non-compliant patients for comparison. |
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Eligible studies resulting from systematic review of intervention compliance among patients with hyperoxaluria.
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