eMedicine Specialties > Urology > Stones

Pregnancy and Urolithiasis: Treatment & Medication

Author: Robert O Wayment, MD, Resident Physician, Division of Urology, Southern Illinois University School of Medicine
Coauthor(s): Bradley Fields Schwartz, DO, FACS, Professor of Urology, Director, Center for Laparoscopy and Endourology, Department of Surgery, Southern Illinois University School of Medicine
Contributor Information and Disclosures

Updated: Mar 19, 2009

Treatment

Medical Care

The initial management of urolithiasis in pregnancy should be conservative. Intravenous hydration and analgesia have been shown to result in spontaneous passage of symptomatic calculi in 64-84% of patients.6,7 Bed rest, antiemetics, and antibiotics are also important, when indicated.

Some stones may simply become asymptomatic, allowing delay of further treatment. Symptomatic urolithiasis is more likely to resolve when calculi are located in the renal pelvis as opposed to the distal ureter.26

Treatment goals in the remaining patients are to reduce maternal discomfort, to prevent renal damage and sepsis due to obstructing calculi, and to minimize risks to the fetus. If conservative measures fail to relieve clinical symptoms or to pass calculi, appropriate surgical intervention should be undertaken.

  • Urine should be strained to obtain stones when they are passed. Chemical analysis should then be performed to guide postpartum treatment and diet modifications to prevent future stone formation. However, because of the physiologic and electrolytic changes associated with pregnancy, metabolic studies should be postponed until completion of pregnancy.
  • Several narcotics have been tested for use during pregnancy. Morphine sulfate, hydromorphone, butorphanol, meperidine, and acetaminophen provide temporary symptomatic relief without harming the fetus. However, avoid codeine during pregnancy because of its association with fetal defects. Long-term use of narcotics in pregnancy can lead to fetal narcotic addiction and even intrauterine growth retardation (IUGR) or premature labor.27
  • Nonsteroidal anti-inflammatory drugs (NSAIDs) are also contraindicated because of an increased risk of miscarriage when used in the first trimester. In addition, fetal renal anomalies, fetal pulmonary hypertension, and premature closure of the ductus arteriosus are risks when NSAIDS are prescribed close to term.
  • Medical expulsive therapy (MET): Ureteral stone passage may be facilitated by alpha-adrenoceptor blockers. These agents promote relaxation of ureteral smooth muscle and have been found to increase rates of stone passage, to hasten stone passage, and to decrease the amount of pain associated with stone passage.28,29 Although these studies have not addressed the use of alpha-adrenoceptor blockers in pregnant women, the authors have successfully used alpha-blockade as MET therapy in several pregnant patients with ureterolithiasis in conjunction with the attending obstetrician. The authors recommend that consultation with the attending obstetrician is recommended before this therapy is instituted.
  • Medical management for reduction of calcium stone disease is contraindicated.
    • Thiazide diuretics, which markedly reduce calciuria and resultant stone formation, are a viable treatment option for urolithiasis in the general population. However, thiazide diuretics are contraindicated during pregnancy because they may induce fetal thrombocytopenia, hypoglycemia, and hyponatremia. Additionally, diuretics are generally dangerous because they may interfere with the normal extracellular volume expansion of pregnancy.
    • The safest method of medically managing calcium stone disease during pregnancy is to increase fluid intake and to avoid excessive calcium intake (including calcium-fortified prenatal vitamins). Typically, calcium intake should not exceed 1000-1200 mg/d during pregnancy. This treatment may prevent or reduce the risk of urolithiasis during pregnancy. Sodium intake and protein consumption should also be curtailed.
  • In uric acid stone disease, xanthine oxidase inhibitors (eg, allopurinol) prevent uric acid stone formation by inhibiting the final step in human purine metabolism, thereby decreasing both serum and urinary uric acid levels. However, use of xanthine oxidase inhibitors is contraindicated during pregnancy because the effects of the drug on the fetus are unknown. Alternative treatment modalities for uric acid stones during pregnancy include increasing fluid intake, limiting dietary purine intake, and increasing urinary alkalinization.
  • Patients with cystine stone disease often have known cystinuria prior to conception. Despite contraindications to the use of common drug therapy, research has shown that careful medical management can allow women with cystinuria who form stones to safely undergo pregnancy without increased risk.
    • Penicillamine reduces cystine stone formation by interchanging disulfide bonds with cystine residues, thereby separating cystine-cystine bonds and allowing increased cystine solubility. Severe or serious adverse effects occur in about 50% of patients. Because penicillamine has been reported to cause fetal abnormalities in rats, it is contraindicated during pregnancy.
    • Increasing urinary volume to 3000 mL and urine alkalinization to an optimal urinary pH of around 7.5 are alternative means to treat cystinuria during pregnancy. However, patients with high urinary excretion of cystine (ie, >300 mg/24 h) may need low-dose penicillamine treatment. Studies performed by Gregory and Mansell (1983) suggest that the risk of recurrent stone formation may outweigh the theoretical risks of penicillamine exposure in this particular situation.10
    • Alpha-mercaptopropionyl glycine (alpha-MPG) is an alternative to penicillamine. It has the same mechanism of action and is roughly equal in efficacy, with somewhat fewer and milder adverse effects. Like penicillamine, it is contraindicated in pregnancy.

Surgical Care

Surgical intervention is required in 20-30% of pregnancies complicated by urolithiasis.4 Surgical treatments are somewhat limited and are used to provide temporizing drainage of an obstructed system with placement of a ureteral stent or percutaneous nephrostomy, to delay treatment until completion of the pregnancy, or to definitively diagnose and treat the stone with ureteroscopic methods.

A broad spectrum of interventions, ranging from ureteral stent placement to open lithotomy, have been used to successfully treat urolithiasis in pregnancy8 ; however, regardless of the mode or invasiveness of the surgical intervention (eg, endoscopic, percutaneous, open), each carries an element of risk to the mother and fetus. Thus, surgical intervention is reserved for pregnant patients in whom conservative management fails or when surgery is otherwise indicated. Admission of these patients by the obstetrician service for consultation with a urologist is not unusual. As a result, most if not all, of these women undergo noninvasive fetal monitoring.

  • Indications for surgical intervention include the following:
    • Ureteral obstruction associated with increasing azotemia
    • Obstruction in a solitary kidney
    • Intractable pain despite maximal conservative measures
    • Urosepsis
    • Renal colic–induced premature labor unresponsive to tocolytics
  • Traditional treatment has consisted of initial placement of a percutaneous nephrostomy tube or insertion of a ureteral stent for temporary drainage.8 Ureteral stents and/or nephrostomy tubes are then changed at periodic intervals until delivery, thus allowing delay of definitive treatment until completion of pregnancy.
  • Ureteroscopy is gaining favor as a first-line approach to urinary calculi that require intervention.17,30,25,19 Improved instruments and increased experience have led to successful outcomes with few complications. Disbanding of supposed limitations (anatomical distortion late in pregnancy) and resolution of many associated concerns (anesthesia, radiation) has resulted in advocacy from previous opponents.31,14 These significant changes represent a paradigm shift in intervention for urolithiasis in pregnancy unresponsive to conservative treatment.
  • Ureteral stent placement: Internal stents are usually placed with ultrasound guidance or limited fluoroscopy with local anesthesia. This minimizes risks of radiation and anesthesia to the fetus. Increasing oral hydration and decreasing calcium intake is recommended to prevent stent encrustation secondary to urinary stasis, hypercalciuria, or infection. Replacing stents every 3-4 weeks and antibiotic prophylaxis are suggested to avoid urinary tract infection and calcification.8 Insertion of percutaneous nephrostomy tubes or ureteral stents is considered a minor procedure, yet repeated insertions or changes may carry risks comparable with those of definitive ureteroscopy in a single setting.19 The obstetrician should be involved for fetal monitoring.
    • Ureteral stents often cause irritative voiding symptoms and chronic discomfort.32 The physiologic hydroureteronephrosis of pregnancy has been found to aggravate that by allowing more frequent stent migration within the dilated system.33 Parulkar and coworkers (1998) studied a group of 70 pregnant patients with urolithiasis; 19 patients required intervention, 15 of whom had ureteral stents placed. They reported that 5 of 15 patients (>30%) required subsequent manipulation because of migration, encrustation, or severe irritative symptoms.6
    • Denstedt and Razvi (1992) recommend limiting ureteral stent placement until after 22 weeks of pregnancy, with use of a percutaneous nephrostomy prior to that point.8 If a ureteral stent is indicated but cannot be placed with ultrasound guidance or if urosepsis is present, a percutaneous nephrostomy tube should be placed instead.
    • Disadvantages to internal ureteral stent include the following:
      • Urinary tract infections and promotion of ascending infections
      • Hematuria
      • Irritative voiding symptoms and renal colic due to stent
      • Stent migration due to hydroureteronephrosis of pregnancy
      • Multiple procedures to change stent to avoid encrustation
      • Need for patient compliance and vigilant follow-up for stent change
  • Percutaneous nephrostomy: Use this treatment modality in patients with urosepsis or pyonephrosis. This procedure can be performed with local anesthesia and ultrasound guidance. Nephrostomy tube placement allows for rapid and adequate decompression of the upper urinary tract, control of pain due to acute obstruction, and resolution of the infected hydronephrosis. Another advantage of placing a percutaneous nephrostomy tube is that it may be used for antegrade irrigation with an antibiotic solution to decrease the risk of infection and tube encrustation.34 Internalization of a double-J stent can be performed after recovery from the original illness. This procedure needs to be performed by a physician experienced in percutaneous procedures. Disadvantages to percutaneous nephrostomy include the following:
    • Bacteruria despite preventive antibiotics
    • Frequent obstruction, requiring change and/or flushing
    • Cumbersome external appliance
    • Risk of bleeding
    • Discomfort
  • Ureteroscopy and stone manipulation: Ureteroscopy allows for complete visualization of the entire ureter and renal pelvis, enabling accurate diagnosis and definitive treatment for urolithiasis. Anatomic distortion near the completion of pregnancy has long been thought to make ureteroscopy impossible; however, ureteroscopy has been found to be safe and effective in all stages of pregnancy.17,30,25,19 They also found that rigid ureteroscopy could be performed on the entire urinary tract, even in advanced pregnancy.25 The above group of series, along with the work of Lemos and associates18 , represent 68 patients who underwent ureteroscopy for diagnosis and/or treatment; no obstetrical complications were reported, and only one ureteral perforation was reported. The one perforation19 was treated successfully with a stent, and the child was born healthy at term.
    • Most ureteroscopies are performed in the absence of radiation. In the above studies, radiation was used sparingly in only a few patients; furthermore, Ulvik et al (1995)19 and Scarpa et al (1996)25 used no radiation. Physiologic hydroureteronephrosis of pregnancy allows entry of the ureteroscope under direct vision without dilation of the ureteral orifice; dilation is rarely performed.4,25,19
    • General anesthesia is rarely used. The vast majority of procedures have been performed with epidural or spinal analgesia with an element of sedation. Scarpa and coworkers (1996) performed ureteroscopies in 5 patients without anesthesia and used only neuroleptic anesthesia (fentanyl or propofol and atropine) in 10.25 Ulvik et al (1995) reports the use of sedation analgesia and feel that it may be preferred to spinal or general anesthesia.19 Both rigid and flexible scopes have been used successfully.
    • Kavoussi and associates (1998) suggest that definitive ureteroscopy may be preferable to stenting in select patients (particularly patients >6 wk prior to term).33 Ulvik and associates (1995)19 found a significant decrease in hospital stay among ureteroscopy patients (mean, 2.7 d) compared with ureteral stent patients (mean, 7 d) of Stothers and Lee (1992)7 .
    • Stone retrieval via ureteroscopy has been performed successfully in many forms.35,17,25,19 These include holmium YAG Laser, pulsed dye laser, ballistic lithotriptor, ultrasonic lithotriptor, basket retrieval, and forceps crush and retrieval; all were used successfully without known complications. The holmium YAG laser, with less than 1 mm of penetration, has been used most frequently in the more recent studies.35,17,30 Ulvik and coworkers (1995) recommended against the use of the ultrasonic lithotriptor until further data can prove its safety in fear that the high-pitched noise may result in hearing injury to the fetus.19
    • Akpinar and associates (2006) presented the most recent experience of ureteroscopy in 7 patients.35 The holmium laser was used with success in 6 patients and no stone was found in the seventh. They compared postoperative pain with or without a ureteral stent. They recommend routine stent placement with a string for 72 hours postoperation in order to reduce pain and analgesic requirements.
    • Contraindications to ureteroscopy include the following:4
      • Stones larger than 1 cm
      • Multiple calculi
      • Sepsis
      • Transplanted kidney
      • Ureteroscopic inexperience or inadequate instruments
      • Absence of general obstetrical services or high-risk obstetrical services
  • Open surgery: In the past, pregnant patients who required intervention for urolithiasis underwent open lithotomy or blind stone manipulation under general anesthesia, similar to the general population. However, more modern procedures used to surgically treat urolithiasis are performed without anesthesia or radiation and carry lower morbidity rates while maintaining equal or greater success rates. Consequently, open surgery is now used as a last resort. Open surgery is used if a stone must be removed before delivery because of complications of conservative or invasive management of urolithiasis, or if contraindications to ureteroscopy are present.
  • Percutaneous nephrolithotomy (PCNL), when indicated, is best postponed until postpartum because of the risks to the fetus of anesthesia and radiation.4
  • Extracorporeal shockwave lithotripsy (ESWL) is frequently used in the nongravid population; however, it requires frequent use of ionizing radiation, and the potential adverse effects of energy dispersion on the fetus are unknown. At this time, ESWL is contraindicated during pregnancy.36
  • Surgical risk: Physiologic organ system changes increase specific perioperative risk factors in the pregnant patient. Special attention to these risk factors can help prevent associated morbidity to the mother and fetus.
    • Venous thromboembolism (VTE) and pulmonary embolism (PE): Pregnancy-related changes in the cardiovascular and hematologic systems create a hypercoagulable state and place the patient at increased risk of VTE and PE. The risk of venous thromboembolism is progressive throughout gestation and, in the third trimester, is estimated to be 5-6 times greater than that of a nongravid female.14
    • The increasing size of the gravid uterus changes the hemodynamics in the lower extremities. Compression of the great vessels by the uterus reduces the velocity of venous blood return, increases pressure, and increases the risk of stasis in the lower extremities.14 Hematologic changes include increased plasma levels of clotting factors VII, VIII, and X and fibrinogen27 , as well as a decrease in fibrinolytic activity14 .
    • Low-dose heparin is considered safe and effective by some researchers and is recommended in patients with a history of thromboembolism.37
    • Aspiration: Pregnancy-related changes in gastrointestinal function and relative anatomy increase the risk of inadvertent perioperative aspiration. These changes include compromised integrity of the gastroesophageal sphincter, decreased gastrointestinal motility, and a decrease in the pH of gastric secretions.27 Intravenous proton pump inhibitors provide acid suppression and may be used in the perioperative period as prophylaxis for acid aspiration syndrome during induction of anesthesia.38
  • Fetal risks of anesthesia: Inhalation anesthetics readily cross the placenta because of their lipid solubility. These agents have been shown to increase risk of teratogenicity. General anesthesia should be avoided during the first trimester, after which the risk is minimal.4

Consultations

Management of pregnant patients with urolithiasis should always involve the obstetrician. When treatment beyond conservative measures is indicated, for the fetus' safety, coordinated care with a neonatologist, an anesthesiologist, and even a radiologist is appropriate.

Diet

Dietary modification is the cornerstone of preventing urolithiasis. General recommendations include dietary moderation of high-oxalate foods and purines with an increase in fluid intake. Salt and sodium intake should also be moderated because of their tendency to increase fluid retention and hypercalciuria. Low-calcium diets frequently cause a paradoxical rise in calcium stone formation and are discouraged.

  • Specific long-term dietary changes should ideally be based on objective information from the stone composition analysis and 24-hour urine chemistry determinations.
  • A low-oxalate diet tends to prevent calcium oxalate stone formation. Common foods that are high in oxalate include chocolate, nuts, green leafy vegetables, coffee, spinach, beets, and tea. Moderation and proportionate reductions are suggested rather than complete avoidance of high-oxalate foods that the patient enjoys.
  • While excessively high calcium ingestion is discouraged, unusually low-calcium diets can also increase stone production by allowing increased oxalate absorption from the gastrointestinal tract. Low calcium intake may also lead to a decrease in calcium bone deposition with associated osteopenia and osteoporosis. In general, one calcium meal per day is suggested. If a calcium supplement is being used by the patient, calcium citrate seems to be the least likely to increase calcium stone production because of a compensatory increase in urinary citrate excretion with this particular supplement.
  • Drinking at least 2 qt of water per day decreases the risk of stone formation. Actually, recommending a fluid intake sufficient to generate a 24-hour urine volume of 2000 mL per day may be better. A patient guide to maintaining an increased urinary volume developed by Stephen W. Leslie, MD, FACS, may be helpful. This recommendation includes stones of all types. In patients unable to drink the required amount of water, lemonade is a reasonable substitute. Lemon juice is high in citrate, which is a natural inhibitor of kidney stone formation.
  • A low-methionine diet has been reported to decrease the risk of cystine stone formation. Methionine is a dietary precursor of cystine. However, this diet is unpalatable, and patient compliance is poor.
  • Diets that are high in purines and green vegetables may increase the likelihood of stone formation. A low-purine diet decreases the risk of both uric acid and calcium stone formation. This diet requires avoidance of red meats, beef, chicken, fish and peanuts.

Medication

The goals of pharmacotherapy are to reduce morbidity and to prevent complications.

Nonsteroidal anti-inflammatory drugs are not recommended during the first 20 weeks of pregnancy. They have been shown to be associated with an 80% increased risk of miscarriage over non-use in a study of 1055 women.39 NSAID use is also linked to renal congenital abnormalities and fetal pulmonary hypertension40 and may cause premature closure of the ductus arteriosus41 .

Narcotic analgesics

These agents are used to treat pain and provide patient comfort.


Butorphanol (Stadol)

Mixed agonist-antagonist narcotic with central analgesic effects for moderate to severe pain. Causes less smooth muscle spasm and respiratory depression than morphine or meperidine. Weigh advantages against increased cost of butorphanol.

Adult

0.5-2.9 mg IV q3-4h prn; 1-4 mg IM q3-4h prn

Pediatric

Not established

Toxicity increases with guanabenz, MAOIs, CNS depressants, phenothiazines, barbiturates, and skeletal muscle relaxants

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in hepatic or renal insufficiency; respiratory limitations (eg, bronchial asthma, obstructive respiratory conditions, cyanosis); may increase CSF pressure and cardiac overload; causes respiratory depression


Meperidine (Demerol)

Analgesic with multiple actions similar to those of morphine but may produce less constipation, smooth muscle spasm, and depression of cough reflex than similar analgesic doses of morphine.

Adult

50-150 mg PO/IV/IM/SC q3-4h prn
50 mg PO q4h or 25 mg IM q4h in elderly patients

Pediatric

Not established

Monitor for increased respiratory and CNS depression with co-administration of cimetidine; hydantoins may decrease effects of meperidine; avoid with protease inhibitors; may aggravate adverse effects of isoniazid; MAOIs, fluoxetine, and other SSRIs greatly potentiate the effects of meperidine; CNS depressants, tricyclic antidepressants, and phenothiazines may potentiate effects

Documented hypersensitivity; MAOIs; upper airway obstruction or significant respiratory depression; during labor when delivery of premature infant is anticipated

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in patients with head injuries because meperidine may increase respiratory depression and CSF pressure (use only if absolutely necessary); caution when using postoperatively and with history of pulmonary disease (suppresses cough reflex); substantially increased dose levels because of tolerance may aggravate or cause seizures even if no prior history of convulsive disorders exists; monitor closely for morphine-induced seizure activity in patients with prior seizure history


Morphine sulfate (Oramorph, MS Contin, Duramorph)

Criterion standard for relief of acute severe pain; may be administered in various ways; commonly titrated until desired effect obtained. IV morphine demonstrates half-life of 2-3 h; however, half-life may be 50% longer in elderly patients.

Adult

Loading dose: 0.1 mg/kg IV/IM/SC
Maintenance dose: 5-20 mg/70 kg IV/IM/SC q4h
Relatively hypovolemic patients: Start with 2 mg IV/IM/SC and reassess hemodynamic effects of dose

Pediatric

0.11-0.2 mg/kg/dose IV; then titrate carefully to adequate pain relief

Phenothiazines may antagonize analgesic effects; tricyclic antidepressants, MAOIs, and other CNS depressants may potentiate adverse effects

Documented hypersensitivity; hypotension; potentially compromised airway in which establishing rapid airway control would be difficult

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Avoid in hypotension, respiratory depression, nausea, emesis, constipation, and urinary retention; caution in atrial flutter and other supraventricular tachycardias; has vagolytic action and may increase ventricular response rate


Hydromorphone (Dilaudid)

A hydrogenated ketone of morphine. Hydromorphone is a narcotic analgesic. Analgesic action of parenterally administered Dilaudid is apparent within 15 min and usually remains in effect for >5 h.

Adult

1-2 mg IV q2-4h

Pediatric

Not recommended

Hydantoins may decrease effects; phenothiazines, CNS depressants, and tricyclic antidepressants may increase toxicity

Documented hypersensitivity; obstetrical analgesia; increased intracranial pressure; respiratory depression; ulcerative colitis; Crohn disease; abdominal cramping and distention

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in patients with head injuries because may increase respiratory depression and CSF pressure (use only if absolutely necessary); caution postoperatively and with history of pulmonary disease (suppresses cough reflex); increased dosing levels, because of tolerance, may aggravate or cause seizures (even without prior history); adjust dose in renal insufficiency (do not use in severe renal dysfunction); normeperidine metabolite accumulation may induce CNS toxicity; monitor closely for morphine-induced seizure activity if prior seizure history

Analgesics

These agents are used to treat pain and to provide patient comfort.


Acetaminophen (Tylenol)

Inhibits prostaglandin synthesis in the CNS and peripherally blocks pain impulse generation. Produces antipyresis from inhibition of hypothalamic heat-regulating center.

Adult

325-650 mg PO q4-6h; 1000 mg tid/qid; not to exceed 4 g/d

Pediatric

Not established

Rifampin can reduce analgesic effects of acetaminophen; coadministration with barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity

Documented hypersensitivity; known G-6-P deficiency

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Overdose may cause severe hepatic toxicity; use with caution in patients with alcoholic liver disease

Alpha-adrenergic blocking agent, oral

These agents relax smooth muscle to facilitate ureteral stone passage.


Tamsulosin (Flomax)

This alpha-1 selective blocker is indicated for the treatment of lower urinary tract symptoms due to prostatic enlargement. An off-label use, as discussed above, is to facilitate passage of ureteral stones. Only short-term therapy (10 d) should be considered for this indication.

Adult

0.4 mg tab PO qd

Pediatric

Not established

Cimetidine may significantly increase plasma concentrations; tamsulosin may increase toxicity of warfarin

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Not for use as antihypertensive drug; may cause orthostasis; avoid situations that may result in injuries if syncope occurs; rule out presence of carcinoma or cancer before initiating treatment

More on Pregnancy and Urolithiasis

Overview: Pregnancy and Urolithiasis
Differential Diagnoses & Workup: Pregnancy and Urolithiasis
Treatment & Medication: Pregnancy and Urolithiasis
Follow-up: Pregnancy and Urolithiasis
Multimedia: Pregnancy and Urolithiasis
References

References

  1. Folger GK. Pain and pregnancy; treatment of painful states complicating pregnancy, with particular emphasis on urinary calculi. Obstet Gynecol. Apr 1955;5(4):513-8. [Medline].

  2. Rodriguez PN, Klein AS. Management of urolithiasis during pregnancy. Surg Gynecol Obstet. Feb 1988;166(2):103-6. [Medline].

  3. Drago JR, Rohner TJ, Chez RA. Management of urinary calculi in pregnancy. Urology. Dec 1982;20(6):578-81. [Medline].

  4. Biyani CS, Joyce AD. Urolithiasis in pregnancy. II: management. BJU Int. May 2002;89(8):819-23. [Medline].

  5. Swanson SK, Heilman RL, Eversman WG. Urinary tract stones in pregnancy. Surg Clin North Am. Feb 1995;75(1):123-42. [Medline].

  6. Parulkar BG, Hopkins TB, Wollin MR, Howard PJ Jr, Lal A. Renal colic during pregnancy: a case for conservative treatment. J Urol. Feb 1998;159(2):365-8. [Medline].

  7. Stothers L, Lee LM. Renal colic in pregnancy. J Urol. Nov 1992;148(5):1383-7. [Medline].

  8. Denstedt JD, Razvi H. Management of urinary calculi during pregnancy. J Urol. Sep 1992;148(3 Pt 2):1072-4; discussion 1074-5. [Medline].

  9. Glowacki LS, Beecroft ML, Cook RJ, Pahl D, Churchill DN. The natural history of asymptomatic urolithiasis. J Urol. Feb 1992;147(2):319-21. [Medline].

  10. Gregory MC, Mansell MA. Pregnancy and cystinuria. Lancet. Nov 19 1983;2(8360):1158-60. [Medline].

  11. Boridy IC, Maklad N, Sandler CM. Suspected urolithiasis in pregnant women: imaging algorithm and literature review. AJR Am J Roentgenol. Oct 1996;167(4):869-75. [Medline].

  12. Waltzer WC. The urinary tract in pregnancy. J Urol. Mar 1981;125(3):271-6. [Medline].

  13. Wolff JM, Jung PK, Adam G, Jakse G. Non-traumatic rupture of the urinary tract during pregnancy. Br J Urol. Nov 1995;76(5):645-8. [Medline].

  14. Loughlin KR, McAleer SJ. Management of Urological Problems in Pregnancy: A Rationale and Strategy. AUA Update Series. 2005;24: Lesson 5.

  15. American College of Obstetricians and Gynecologists (ACOG). ACOG Committee Opinion. Number 299, September 2004 (replaces No. 158, September 1995). Guidelines for diagnostic imaging during pregnancy. Obstet Gynecol. Sep 2004;104(3):647-51. [Medline].

  16. Srirangam SJ, Hickerton B, Van Cleynenbreugel B. Management of urinary calculi in pregnancy: a review. J Endourol. May 2008;22(5):867-75. [Medline].

  17. Lifshitz DA, Lingeman JE. Ureteroscopy as a first-line intervention for ureteral calculi in pregnancy. J Endourol. Feb 2002;16(1):19-22. [Medline].

  18. Lemos GC, El Hayek OR, Apezzato M. Rigid ureteroscopy for diagnosis and treatment of ureteral calculi during pregnancy. Int Braz J Urol. Jul-Aug 2002;28(4):311-5; discussion 316. [Medline].

  19. Ulvik NM, Bakke A, Høisaeter PA. Ureteroscopy in pregnancy. J Urol. Nov 1995;154(5):1660-3. [Medline].

  20. Laing FC, Benson CB, DiSalvo DN, Brown DL, Frates MC, Loughlin KR. Distal ureteral calculi: detection with vaginal US. Radiology. Aug 1994;192(2):545-8. [Medline].

  21. Loughlin KR, Ker LA. The current management of urolithiasis during pregnancy. Urol Clin North Am. Aug 2002;29(3):701-4. [Medline].

  22. Shokeir AA, Abdulmaaboud M. Resistive index in renal colic: a prospective study. BJU Int. Mar 1999;83(4):378-82. [Medline].

  23. White WM, Zite NB, Gash J, Waters WB, Thompson W, Klein FA. Low-dose computed tomography for the evaluation of flank pain in the pregnant population. J Endourol. Nov 2007;21(11):1255-60. [Medline].

  24. Rittenberg MH, Bagley DH. Ureteroscopic diagnosis and treatment of urinary calculi during pregnancy. Urology. Nov 1988;32(5):427-8. [Medline].

  25. Scarpa RM, De Lisa A, Usai E. Diagnosis and treatment of ureteral calculi during pregnancy with rigid ureteroscopes. J Urol. Mar 1996;155(3):875-7. [Medline].

  26. Houshiar AM, Ercole CJ. Urinary calculi during pregnancy. When are they cause for concern?. Postgrad Med. Oct 1996;100(4):131-8. [Medline].

  27. Barron WM. Medical evaluation of the pregnant patient requiring nonobstetric surgery. Clin Perinatol. Oct 1985;12(3):481-96. [Medline].

  28. Lipkin M, Shah O. The use of alpha-blockers for the treatment of nephrolithiasis. Rev Urol. 2006;8 Suppl 4:S35-42. [Medline].

  29. Parsons JK, Hergan LA, Sakamoto K, Lakin C. Efficacy of alpha-blockers for the treatment of ureteral stones. J Urol. Mar 2007;177(3):983-7; discussion 987. [Medline].

  30. Watterson JD, Girvan AR, Beiko DT, Nott L, Wollin TA, Razvi H. Ureteroscopy and holmium:YAG laser lithotripsy: an emerging definitive management strategy for symptomatic ureteral calculi in pregnancy. Urology. Sep 2002;60(3):383-7. [Medline].

  31. Loughlin KR. Management of urologic problems during pregnancy. Urology. Aug 1994;44(2):159-69. [Medline].

  32. Evans HJ, Wollin TA. The management of urinary calculi in pregnancy. Curr Opin Urol. Jul 2001;11(4):379-84. [Medline].

  33. Kavoussi LR, Jackman SV, Bishoff JT. Re: Renal colic during pregnancy: a case for conservative treatment. J Urol. Sep 1998;160(3 Pt 1):837-8. [Medline].

  34. Kavoussi LR, Albala DM, Basler JW, Apte S, Clayman RV. Percutaneous management of urolithiasis during pregnancy. J Urol. Sep 1992;148(3 Pt 2):1069-71. [Medline].

  35. Akpinar H, Tüfek I, Alici B, Kural AR. Ureteroscopy and holmium laser lithotripsy in pregnancy: stents must be used postoperatively. J Endourol. Feb 2006;20(2):107-10. [Medline].

  36. Streem SB. Contemporary clinical practice of shock wave lithotripsy: a reevaluation of contraindications. J Urol. Apr 1997;157(4):1197-203. [Medline].

  37. Kakkar VV. The current status of low-dose heparin in the prophylaxis of thrombophlebitis and pulmonary embolism. World J Surg. Jan 1978;2(1):3-18. [Medline].

  38. Pisegna JR. Switching between intravenous and oral pantoprazole. J Clin Gastroenterol. Jan 2001;32(1):27-32. [Medline].

  39. Li DK, Liu L, Odouli R. Exposure to non-steroidal anti-inflammatory drugs during pregnancy and risk of miscarriage: population based cohort study. BMJ. Aug 16 2003;327(7411):368. [Medline].

  40. Boubred F, Vendemmia M, Garcia-Meric P, Buffat C, Millet V, Simeoni U. Effects of maternally administered drugs on the fetal and neonatal kidney. Drug Saf. 2006;29(5):397-419. [Medline].

  41. Koren G, Florescu A, Costei AM, Boskovic R, Moretti ME. Nonsteroidal antiinflammatory drugs during third trimester and the risk of premature closure of the ductus arteriosus: a meta-analysis. Ann Pharmacother. May 2006;40(5):824-9. [Medline].

  42. Khoo L, Anson K, Patel U. Success and short-term complication rates of percutaneous nephrostomy during pregnancy. J Vasc Interv Radiol. Dec 2004;15(12):1469-73. [Medline].

  43. Armstrong SJ, Witcombe JB. Calcified hydronephrosis in pregnancy. Br J Radiol. Oct 1991;64(766):966-8. [Medline].

  44. Asgari MA, Safarinejad MR, Hosseini SY. Extracorporeal shock wave lithotripsy of renal calculi during early pregnancy. BJU Int. Oct 1999;84(6):615-7. [Medline].

  45. Butler EL, Cox SM, Eberts EG. Symptomatic nephrolithiasis complicating pregnancy. Obstet Gynecol. Nov 2000;96(5 Pt 1):753-6. [Medline].

  46. Cass AS, Smith CS, Gleich P. Management of urinary calculi in pregnancy. Urology. Nov 1986;28(5):370-2. [Medline].

  47. Fabrizio MD, Gray DS, Feld RI. Placement of ureteral stents in pregnancy using ultrasound guidance. Tech Urol. Fall 1996;2(3):121-5. [Medline].

  48. Fligelstone LJ, Datta SN, Evans C. Problematic renal calculi presenting during pregnancy. Ann R Coll Surg Engl. Mar 1996;78(2):142-5. [Medline].

  49. Gana BM, Taube M. Extracorporeal shock wave lithotripsy of renal calculi during early pregnancy. BJU Int. Feb 2000;85(3):384. [Medline].

  50. Gorton E, Whitfield HN. Renal calculi in pregnancy. Br J Urol. Jul 1997;80 Suppl 1:4-9. [Medline].

  51. Hendricks SK, Ross SO, Krieger JN. An algorithm for diagnosis and therapy of management and complications of urolithiasis during pregnancy. Surg Gynecol Obstet. Jan 1991;172(1):49-54. [Medline].

  52. Horowitz E, Schmidt JD. Renal calculi in pregnancy. Clin Obstet Gynecol. Jun 1985;28(2):324-38. [Medline].

  53. Kroovand RL. Stones in pregnancy and in children. J Urol. Sep 1992;148(3 Pt 2):1076-8. [Medline].

  54. Leslie S. Increasing urinary volume. Personal communication. Used with permission. 2001.

  55. Leslie S. The IRS plan for increasing urinary volume. In: Savitz G, Leslie S, eds. The Kidney Stones Handbook. 2nd ed. Roseville, Calif: Four Geez Press; 1999:141-4.

  56. Powell CR, Stoller ML, Schwartz BF. Impact of body weight on urinary electrolytes in urinary stone formers. Urology. Jun 2000;55(6):825-30. [Medline].

  57. Rosenfeld JA. Renal disease and pregnancy. Am Fam Physician. Apr 1989;39(4):209-12. [Medline].

  58. Savitz G, Leslie S. Water, Water Everywhere. In: Savitz G, Leslie S, eds. The Kidney Stones Handbook. 2nd ed. Roseville, Calif: Four Geez Press; 1999:131-40.

  59. Shokeir AA, Mahran MR, Abdulmaaboud M. Renal colic in pregnant women: role of renal resistive index. Urology. Mar 2000;55(3):344-7. [Medline].

  60. Thompson T, Kelly JD, Keane PF. Problematic renal calculi presenting during pregnancy. Ann R Coll Surg Engl. Jul 1996;78(4):399. [Medline].

  61. Wolf MC, Hollander JB, Salisz JA. A new technique for ureteral stent placement during pregnancy using endoluminal ultrasound. Surg Gynecol Obstet. Dec 1992;175(6):575-6. [Medline].

Further Reading

Keywords

urolithiasis in pregnancy, kidney stones, ureteral stones, bladder stones, urolithiasis, calculi, calculus, urosepsis, urinary tract infection, stone formation, uric acid stone disease, calcium stone disease, cystinuria, uric acid stone formation, calcium oxalate stone formation, calcium phosphate stone formation, crystalluria, struvite stones, renal calculi, nephrolithiasis, hypercalcemia, hypercalciuria, hydroureteronephrosis

Contributor Information and Disclosures

Author

Robert O Wayment, MD, Resident Physician, Division of Urology, Southern Illinois University School of Medicine
Robert O Wayment, MD is a member of the following medical societies: American Medical Association and American Urological Association
Disclosure: Nothing to disclose.

Coauthor(s)

Bradley Fields Schwartz, DO, FACS, Professor of Urology, Director, Center for Laparoscopy and Endourology, Department of Surgery, Southern Illinois University School of Medicine
Bradley Fields Schwartz, DO, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Association of Military Osteopathic Physicians and Surgeons, Endourological Society, Society of Laparoendoscopic Surgeons, and Society of University Urologists
Disclosure: Nothing to disclose.

Medical Editor

Jeffrey B Garris, MD, Chief, Assistant Professor, Department of Obstetrics and Gynecology, Division of Urogynecology and Reconstructive Pelvic Surgery, Tulane University School of Medicine
Jeffrey B Garris, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Institute of Ultrasound in Medicine, American Medical Association, American Urological Association, Association of Professors of Gynecology and Obstetrics, Louisiana State Medical Society, Royal Society of Medicine, and Sigma Xi
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Eleanor Lederer, MD, Consulting Staff, Louisville VA Hospital; Professor of Medicine, Director of Nephrology Training Program, Kidney Disease Program, University of Louisville School of Medicine; Director, Metabolic Stone Clinic
Eleanor Lederer, MD is a member of the following medical societies: American Association for the Advancement of Science, American Federation for Medical Research, American Society for Biochemistry and Molecular Biology, American Society for Bone and Mineral Research, American Society of Nephrology, American Society of Transplantation, International Society of Nephrology, Kentucky Medical Association, National Kidney Foundation, and Phi Beta Kappa
Disclosure: Nothing to disclose.

CME Editor

J Stuart Wolf Jr, MD, FACS, David A Bloom Professor of Urology, Director of Division of Minimally Invasive Urology, Department of Urology, University of Michigan
J Stuart Wolf Jr, MD, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Catholic Medical Association, Endourological Society, Society for Urology and Engineering, Society of Laparoendoscopic Surgeons, Society of University Urologists, and Society of Urologic Oncology
Disclosure: Terumo Corporation Consulting fee Consulting; Omeros Corporation Consulting fee Consulting

Chief Editor

Bradley Fields Schwartz, DO, FACS, Professor of Urology, Director, Center for Laparoscopy and Endourology, Department of Surgery, Southern Illinois University School of Medicine
Bradley Fields Schwartz, DO, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Association of Military Osteopathic Physicians and Surgeons, Endourological Society, Society of Laparoendoscopic Surgeons, and Society of University Urologists
Disclosure: Nothing to disclose.

 
 
HONcode

We subscribe to the
HONcode principles of the
Health On the Net Foundation

All material on this website is protected by copyright, Copyright© 1994- by Medscape.
This website also contains material copyrighted by 3rd parties.

DISCLAIMER: The content of this Website is not influenced by sponsors. The site is designed primarily for use by qualified physicians and other medical professionals. The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The information provided here is for educational and informational purposes only. In no way should it be considered as offering medical advice. Please check with a physician if you suspect you are ill.