Kluwer, 2012
Kluwer, 2012
gov/pmc/articles/PMC3313741/
Abstract
Kidney stone is a common clinical problem faced by clinicians. The prevalence of the disease
is increasing worldwide. As the affected population is getting younger and recurrence rates
are high, dietary modifications, lifestyle changes, and medical management are essential.
Patients with recurrent stone disease need careful evaluation for underlying metabolic
disorder. Medical management should be used judiciously in all patients with kidney stones,
with appropriate individualization. This chapter focuses on medical management of kidney
stones.
INTRODUCTION
Urinary tract stones (urolithiasis) are known to the mankind since antiquity.[1] Kidney stone
is not a true diagnosis; rather it suggests a broad variety of underlying diseases. Kidney
stones are mainly composed of calcium salts, uric acid, cysteine, and struvite. Calcium
oxalate and calcium phosphate are the most common types accounting for >80% of stones,
followed by uric acid (8–10%) and cysteine, struvite in remainders.
The incidence of urolithiasis is increasing globally, with geographic, racial, and gender
variation in its occurrence. Epidemiological study (1979) in the western population reveals
the incidence of urolithiasis to be 124 per 100,000 in males and 36 per 100,000 in females.[2]
The lifetime risk of having urolithiasis is higher in the Middle East (20–25%) and western
countries (10–15%) and less common in Africans and Asian population. Stone disease carries
high risk of recurrence after the initial episode, of around 50% at 5 years and 70% at 9 years.
[3,4]
Positive family history of stone disease, young age at onset, recurrent urinary tract infections
(UTIs), and underlying diseases like renal tubular acidosis (RTA) and hyperparathyroidism
are the major risk factors for recurrence. High incidence and recurrence rate add enormous
cost and loss of work days.[1]
Though the pathogenesis of stone disease is not fully understood, systematic metabolic
evaluation, medical treatment of underlying conditions, and patient-specific modification in
diet and lifestyle are effective in reducing the incidence and recurrence of stone disease.[5–8]
Kidney stones are made of organic and inorganic crystals amalgamated with proteins.
Calcium stones are the most frequent type, accounting for up to 80% [Table 1]. Of these,
calcium oxalate, calcium phosphate, struvite, and cystine are radio-opaque stones, while uric
acid, xanthine, and hypoxanthine stones are radiolucent. The risk factors for stone disease are
as shown in Table 2.
Table 1
Types of stones
Table 2
Risk factors for stone disease
Medical management is indicated for clinically stable patients with non-obstructive urinary
stones, recurrent stone formers, and the patients with underlying systemic diseases. Detailed
history of patient illness including family history, drug history, and history of previous
similar illness and previous interventions needs to be recorded. Assessment of risk factors for
stone disease [Table 2] should be carried out. Medical management of stone disease includes
laboratory evaluation and treatment. As the laboratory evaluation of renal calculi has been
discussed by Ranabir, Baruah and Ritu Devi in this issue,[8] we will focus on medical
treatment.
Dietary management
Fluid intake and dietary changes are important measures in preventing recurrence of kidney
stones. Many trials have shown that increasing urine volume to at least 2 L/day OR 2 lit/day
can reduce the recurrence of stone disease by up to 40–50%.[9] Fluid intake mainly should
include water. As tea and coffee contain oxalate, milk (which binds free oxalate) should be
added to them. However, increasing the urine volume has a disadvantage of reducing urinary
citrate.
A small reduction in urinary oxalate has been found to be associated with significant
reduction in the formation of calcium oxalate stones; hence, oxalate-rich foods like
cucumber, green peppers, beetroot, spinach, soya bean, chocolate, rhubarb, popcorn, and
sweet potato should be avoided. Many studies have found calcium restriction to increase the
risk of stone disease; therefore, dietary calcium restriction is not recommended.
Hypocitraturia is a proven risk factor for stone formation and is found in about 16–63% of
calcium stone formers.[10,11] Oral potassium citrate (Kcit) has been shown to be useful in
increasing urinary citrate and reducing the stone recurrence. Dietary replacement with high
citrate as a substitute to Kcit has been studied. Lemon juice when delivered as a lemonade
therapy was found to increase urinary citrate.[12] Odvina found orange juice to increase urine
pH and urinary citrate.[13] Kang et al. compared 11 patients taking Kcit with 11 matched
patients on lemonade therapy and found both the therapies to increase urinary citrate.
However, the effect with Kcit was significantly better than the effect with lemonade.[14]
Yilmaz et al. studied tomato, orange, lemon, and mandarin juice for nutritional content.[15]
Surprisingly, fresh tomato juice was found to have the highest citrate and low oxalate content.
Reduction of animal protein intake is suggested in both calcium oxalate and uric acid stone
formers.
Stone-specific therapies
In patients with idiopathic hypercalciuria, thiazide diuretics have shown to reduce the
recurrence rates by up to 70%.[9] It is the only medical therapy directed at reducing urinary
calcium.[16] Citrate supplements as detailed earlier are useful. Pyridoxine sometimes can be
useful in patients with primary hyperoxaluria, but not in idiopathic hyperoxaluria.
[17] Oxalobacter formigenes is an oxalate degrading bacterium found in human
gastrointestinal tract. It is thought that increased colonization of the gut might lead to
decreased absorption of dietary oxalate and decrease in urinary oxalate excretion.
Colonization with O. formigenes showed benefit in uncontrolled studies;[18,19] however, a
prospective, randomized, placebo control, double-blind trial refuted such benefits.[20]
The aim of treatment in uric acid stones is to increase the solubility of uric acid in urine. It is
achieved by increasing the urine volume and by alkali therapy. Allopurinol is a useful adjunct
to the therapy.
Struvite stones
Struvite stones form in alkaline urine from infection with urea-splitting microorganisms.
Antibiotics are the mainstay of the therapy with occasional use of acetohydroxamic acid.[17]
Cystine stones
This is a rare stone type. The aim of treatment is to reduce the concentration of free cystine
and increase its solubility in urine. A high fluid intake up to 4-5 L/day OR 4-5 lit/day and
alkalinization of urine with target urine pH >7 is desirable. Chelating agents like D-
penicillamine or tiopronin are indicated when 24-hour urine cystine concentration exceeds
2000 μmol/l.[17]
MET is treatment with combination of drugs which facilitates the spontaneous passage of
ureteric calculi. Ureteric colic is an emergency and management depends upon the severity of
obstruction and degree of renal function deterioration. Approximately 90% of stones <5 mm
and 15% of stones between 5 and 8 mm pass spontaneously within 4 weeks, while 95% of
those larger than 8 mm require urological intervention.[21] The American Urology
Association Nephrolithiasis Clinical Guidelines panel in its recent guidelines have found
MET to facilitate and accelerate the spontaneous passage of ureteric stones and the stone
fragments generated by shock wave lithotripsy.[22]
In a recent prospective, randomized study which compared three drugs as MET for distal
ureteral calculi, patients with symptomatic distal ureteral stones >4 mm were randomly
assigned to three treatment groups : p0 hloroglucinol and corticosteroid, tamsulosin and
corticosteroid, and nifedipine and corticosteroid.[23] Tamsulosin and corticosteroid was the
most efficacious combination – stones passed more quickly and the need for analgesics was
reduced.[23] A randomized, controlled, prospective study has also shown tamsulosin to be a
useful addition to shock wave lithotripsy.[1,23]
Alpha adrenergic receptors are densely located in the smooth muscles of ureter. Alpha-1a-
receptors predominate in bladder outlet, prostate, and proximal urethra, whereas alpha-1d-
receptors are seen in lower ureter and detrussor muscle of bladder.[24] Drugs which block
these receptors cause smooth muscle relaxation and inhibits peristalsis and relieves spasm.
Tamsulosin is effective in expulsion therapy as it increases the passage rate and reduces the
passage time for stones up to 10 mm.[25,26] In a study of tamsulosin in renal colic, 100%
expulsion rate was seen in the treatment group and 70% in the control group. The mean
expulsion time in the treatment group was 65.7 h (range 2–288 h) compared with 111.1 h for
the control group (range 12–240 h).[25] In this study, the mean stone size was 6.7 (SD 2.1)
mm in the treatment group, compared with 5.8 mm in control subjects (P=0.047). A recent
study using sustained release alfuzosin 10 mg once daily was found to be effective in
enhancing the ureteral stone spontaneous passage rate, particularly for upper ureteral stones.
The patients treated with alfuzosin required fewer analgesics and less surgical interventions
like ureteroscopic lithotripsy and/or extracorporeal shock wave lithotripsy.[27]
Calcium channel blockers (CCBs) cause inhibition of calcium channels in distal ureter and
decrease the contraction and spasm caused by distal ureter calculus.[28] A study of
combination therapy with nifedepine and deflazacort in distal ureter stone resulted in stone
expulsion in 79% of the treatment group and in only 35% of control subjects. The average
stone size was 5.8 mm (range 3.5–10 mm) for the treatment group and 5.5 mm (range 3–10
mm) for the control group. CCBs can facilitate spontaneous passage for stones up to 10 mm,
though no correlation was found between stone size and expulsion time in the treatment
group.[29]
A comparative study between nifedepine and tamsulosin reveals a better stone expulsion rate
of 97.1% in tamsulosin versus 77.1% in nifedepine group. Average expulsion times were 72
h and 120 h (P<0.001) in the two groups, respectively, despite the presence of larger stones in
the tamsulosin group (tamsulosin 7.2 mm vs. nifedepine 6.2 mm; P=0.002).[21,29,30]
Steroids are also found to be useful as medical expulsive agents in distal ureteric stones.
Calculus in distal ureter causes inflammation and submucosal edema which further
aggravates the obstruction due to the stone per se. Being anti-inflammatory agents, steroids
reduce the inflammation and neutrophil-induced damage. This class of drug, in combination
with other agents described earlier, improves stone passage and reduces stone expulsion time.
[30,31]
Patients receiving MET, who do not pass their stones within 4 weeks, should be reffered to a
urologist since delay in definitive management may increase the rate of complications,
including renal dysfunction, urosepsis, and intractable pain.[32] Side effect profile should be
considered before initiation, and during therapy.
CONCLUSIONS
Kidney stones present as an important and challenging clinical problem. Medical therapy,
when used judiciously in conjunction with dietary measures, can help in preventing
recurrence and in expulsion of small size (<10 mm) stones. Awareness of the advantages and
limitations of different modalities of medical therapy is necessary in order to provide the
correct treatment to pateints presenting with this common complaint.
Footnotes
Source of Support: Nil
Article information
Indian J Endocrinol Metab. 2012 Mar-Apr; 16(2): 236–239.
doi: 10.4103/2230-8210.93741
PMCID: PMC3313741
PMID: 22470860
Shriganesh R. Barnela, Sachin S. Soni,1,2 Sonali S. Saboo,1 and Ashish S. Bhansali3
Department of Nephrology, Kamalnayan Bajaj Hospital, Aurangabad, Maharashtra, India
1
Department of Nephrology, Manik Hospital, Aurangabad, Maharashtra, India
2
Department of Nephrology, Mahatma Gandhi Mission Medical College, Aurangabad,
Maharashtra, India
3
Department of Medicine, Bhansali Hospital, Paratwada, Maharashtra, India
Corresponding Author: Dr. Sachin S. Soni, Department of Nephrology, Manik Hospital,
Near Jawahar Nagar Police Station, Aurangabad - 431 005, Maharashtra, India. E-
mail: moc.oohay@inosnihcas_rd
Copyright : © Indian Journal of Endocrinology and Metabolism
This is an open-access article distributed under the terms of the Creative Commons
Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use,
distribution, and reproduction in any medium, provided the original work is properly cited.
This article has been cited by other articles in PMC.
Articles from Indian Journal of Endocrinology and Metabolism are provided here courtesy
of Wolters Kluwer -- Medknow Publications
REFERENCES
1. Miller NL, Lingeman JE. Management of kidney stones. BMJ. 2007;334:468–72. [PMC
free article] [PubMed] [Google Scholar]
2. Johnson CM, Wilson DM, O’Fallon WM, Malek RS, Kurland LT. Renal stone
epidemiology : A0 25-year study in Rochester, Minnesota. Kidney Int. 1979;16:624–
31. [PubMed] [Google Scholar]
3. Williams RE. Long term survey of 538 patients with upper urinary tract stone. Br J
Urol. 1963;35:416–37. [PubMed] [Google Scholar]
4. Prezioso D, Di Martino M, Galasso R, Iapicca G. Laboratory assessment. Urol
Int. 2007;79(Suppl 1):20–5. [PubMed] [Google Scholar]
5. Lotan Y, Cadeddu JA, Pearle MS. International comparison of cost effectiveness of
medical management strategies for nephrolithiasis. Urol Res. 2005;33:223–
30. [PubMed] [Google Scholar]
6. Heilberg IP, Schor N. Renal stone disease : C0 auses, evaluation and medical
treatment. Arq Bras Endocrinol Metabol. 2006;50:823–31. [PubMed] [Google Scholar]
7. Levy FL, Adams-Huet B, Pak CY. Ambulatory evaluation of nephrolithiasis : A0 n update
of a 1980 protocol. Am J Med. 1995;98:50–9. [PubMed] [Google Scholar]
8. Ranabir S, Baruah M, Ritu Devi K. Nephrolitiasis: Endocrine evaluation. Indian J
Endocrinol Metab. 2012 [In Press] [Google Scholar]
9. Borghi L, Meschi T, Amato F, Briganti A, Novarini A, Giannini A. Urinary volume, water
and recurrences in idiopathic calcium nephrolithiasis : A0 5-year randomized prospective
study. J Urol. 1996;155:839–43. [PubMed] [Google Scholar]
10. Hamm LL, Hering-Smith KS. Pathophysiology of hypocitraturic nephrolithiasis.
(8).Endocrinol Metab Clin North Am. 2002;31:885–93.[PubMed] [Google Scholar]
11. Pak CY. Medical management of urinary stone disease. Nephron Clin
Pract. 2004;98:c49–53. [PubMed] [Google Scholar]
12. Seltzer MA, Low RK, McDonald M, Shami GS, Stoller ML. Dietary manipulation with
lemonade to treat hypocitraturic calcium nephrolithiasis. J Urol. 1996;156:907–
9. [PubMed] [Google Scholar]
13. Odvina CV. Comparative value of orange juice versus lemonade in reducing stone-
forming risk. Clin J Am Soc Nephrol. 2006;1:1269–74. [PubMed] [Google Scholar]
14. Kang DE, Sur RL, Haleblian GE, Fitzsimons NJ, Borawski KM, Preminger GM. Long-
term lemonade based dietary manipulation in patients with hypocitraturic nephrolithiasis. J
Urol. 2007;177:1358–62. discussion 1362; quiz 1591. [PubMed] [Google Scholar]
15. Yilmaz E, Batislam E, Basar M, Tuglu D, Erguder I. Citrate levels in fresh tomato juice:
A possible dietary alternative to traditional citrate supplementation in stone-forming
patients. Urology. 2008;71:379–83.discussion 383-4. [PubMed] [Google Scholar]
16. Moe OW, Pearle MS, Sakhaee K. Pharmacotherapy of urolithiasis : E0 vidence from
clinical trials. Kidney Int. 2011;79:385–92. [PMC free article][PubMed] [Google Scholar]
17. Johri N, Cooper B, Robertson W, Choong S, Rickards D, Unwin R. An update and
practical guide to renal stone management. Nephron Clin Pract. 2010;116:c159–
71. [PubMed] [Google Scholar]
18. Kaufman DW, Kelly JP, Curhan GC, Anderson TE, Dretler SP, Preminger GM, et al.
Oxalobacter formigenes may reduce the risk of calcium oxalate kidney stones. J Am Soc
Nephrol. 2008;19:1197–203. [PMC free article][PubMed] [Google Scholar]
19. Campieri C, Campieri M, Bertuzzi V, Swennen E, Matteuzzi D, Stefoni S, et al.
Reduction of oxaluria after an oral course of lactic acid bacteria at high
concentration. Kidney Int. 2001;60:1097–105. [PubMed] [Google Scholar]
20. Goldfarb DS, Modersitzki F, Asplin JR. A randomized, controlled trial of lactic acid
bacteria for idiopathic hyperoxaluria. Clin J Am Soc Nephrol. 2007;2:745–
9. [PubMed] [Google Scholar]
21. Liu M, Henderson SO. Myth: Nephrolithiasis and medical expulsive therapy. Can J
Emerg Med. 2007;9:463–5. [PubMed] [Google Scholar]
22. Preminger GM, Tiselius HG, Assimos DG, Alken P, Buck C, Gallucci M, et al. 2007
guideline for the management of ureteral calculi. J Urol. 2007;178:2418–
34. [PubMed] [Google Scholar]
23. Gravina GL, Costa AM, Ronchi P, Galatioto GP, Angelucci A, Castellani D, et al.
Tamsulosin treatment increases clinical success rate of single extracorporeal shock wave
lithotripsy of renal stones. Urology. 2005;66:24–8.[PubMed] [Google Scholar]
24. Cervenakov I, Fillo J, Mardiak J, Kopecny M, Smirala J, Lepies P. Speedy elimination of
ureterolithiasis in lower part of ureters with the alpha 1-blocker–Tamsulosin. Int Urol
Nephrol. 2002;34:25–9. [PubMed] [Google Scholar]
25. Dellabella M, Milanese G, Muzzonigro G. Efficacy of tamsulosin in the medical
management of juxtavesical ureteral stones. J Urol. 2003;170:2202–5.[PubMed] [Google
Scholar]
26. De Sio M, Autorino R, Di Lorenzo G, Damiano R, Giordano D, Cosentino L, et al.
Medical expulsive treatment of distal-ureteral stones using tamsulosin: A single-center
experience. J Endourol. 2006;20:12–6. [PubMed] [Google Scholar]
27. Chau LH, Tai DC, Fung BT, Li JC, Fan CW, Li MK. Medical expulsive therapy using
alfuzosin for patient presenting with ureteral stone less than 10 mm: A prospective
randomized controlled trial. Int J Urol. 2011;18:510–4.[PubMed] [Google Scholar]
28. Borghi L, Meschi T, Amato F, Novarini A, Giannini A, Quarantelli C, et al. Nifedipine
and methylprednisolone in facilitating ureteral stone passage : A0 randomized, double-blind,
placebo-controlled study. J Urol. 1994;152:1095–8.[PubMed] [Google Scholar]
29. Porpiglia F, Destefanis P, Fiori C, Fontana D. Effectiveness of nifedipine and deflazacort
in the management of distal ureter stones. Urology. 2000;56:579–82. [PubMed] [Google
Scholar]
30. Dellabella M, Milanese G, Muzzonigro G. Randomized trial of the efficacy of tamsulosin,
nifedipine and phloroglucinol in medical expulsive therapy for distal ureteral calculi. J
Urol. 2005;174:167–72. [PubMed] [Google Scholar]
31. Cooper JT, Stack GM, Cooper TP. Intensive medical management of ureteral
calculi. Urology. 2000;56:575–8. [PubMed] [Google Scholar]
32. Hubner WA, Irby P, Stoller ML. Natural history and current concepts for the treatment of
small ureteral calculi. Eur Urol. 1993;24:172–6. [PubMed] [Google Scholar]