Updated: Oct 27, 2009
Testicular torsion is a true urologic emergency and must be differentiated from other complaints of testicular pain because a delay in diagnosis and management can lead to loss of the testicle. Though testicular torsion can occur at any age, including the prenatal and perinatal periods, it most commonly occurs in adolescent males, and testicular torsion is the most frequent cause of testicle loss in that population.
The testicle is covered by the tunica vaginalis, a potential space that encompasses the anterior two thirds of the testicle and where fluid from a variety of sources may accumulate. The tunica vaginalis attaches to the posterolateral surface of the testicle and allows for little mobility of the testicle within the scrotum.
In patients who have an inappropriately high attachment of the tunica vaginalis, the testicle can rotate freely on the spermatic cord within the tunica vaginalis (intravaginal testicular torsion). This congenital anomaly, called the bell clapper deformity, can result in the long axis of the testicle being oriented transversely rather than cephalocaudal. This congenital abnormality is present in approximately 12% of males, 40% of whom have the abnormality in the contralateral testicle as well.1 The bell clapper deformity allows the testicle to twist spontaneously on the spermatic cord. Torsion occurs as the testicle rotates between 90° to 1080° causing compromised blood flow to the testicle.
Complete torsion usually occurs when the testicle twists 360° or more and incomplete or partial torsion when the twisting is less than this. The twisting causes venous occlusion and engorgement as well as arterial ischemia and infarction of the testicle. How tightly the testicle is twisted and how many turns seem to correlate with how quickly the testicle becomes nonviable from ischemia.
In the neonatal age group, the testicle frequently has not yet descended into the scrotum, where it becomes attached within the tunica vaginalis. This mobility of the testicle predisposes it to torsion (extravaginal testicular torsion). Inadequate fusion of the testicle to the scrotal wall typically occurs within the first 7-10 days of life.
Incidence of torsion in males younger than 25 years is approximately 1 in 4000.2 Torsion more often involves the left testicle.
Of the cases of testicular torsion that occur in the neonatal population, 70% occur prenatally and 30% occur postnatally.
This urologic emergency requires prompt diagnosis, immediate urologic consultation, and rapid definitive operative treatment for salvage of the testicle.
A salvage rate of 90-100% is found in patients who undergo detorsion within 6 hours of pain; the viability rate fell to between 20% and 50% after 12 hours; and 0 to 10% viability if detorsion is delayed greater than 24 hours.3,2
Testicular torsion affects males only.
Testicular torsion most often is observed in males younger than 30 years, with most aged 12-18 years. The peak age is 14 years, although a smaller peak also occurs during the first year of life.
| Appendicitis, Acute | Pediatrics, Appendicitis |
| Epididymitis | Scrotal Trauma |
| Fournier Gangrene | Spermatocele |
| Henoch-Schonlein Purpura | Testicular Choriocarcinoma |
| Hernias | Testicular Seminoma |
| Hydrocele | Testicular Trauma |
| Idiopathic Testicular Infarction | Testicular Tumors: Nonseminomatous |
| Orchitis | Varicocele |
Traumatic rupture
Traumatic hematoma
Torsion of testicular appendage (appendix testis)
If the clinical diagnosis of torsion is suspected, early urologic consultation is mandatory since definitive treatment is surgery for detorsion and orchiopexy or possible orchiectomy.
Administer pain relief judiciously and cautiously after the diagnosis of testicular torsion is made. Some urologists prefer no analgesics be administered so their evaluation and examination of the patient are not prejudiced.
Pain control is essential to quality patient care. It ensures patient comfort, promotes pulmonary toilet, and enables physical therapy regimens. Most analgesics have sedating properties, which are beneficial for patients who have sustained painful trauma.
DOC for narcotic analgesia due to reliable and predictable effects, safety profile, and ease of reversibility with naloxone.
Various IV doses are used; commonly titrated until desired effect obtained.
Starting dose: 0.1 mg/kg IV/IM/SC
Maintenance dose: 5-20 mg/70 kg IV/IM/SC q4h
Neonates: 0.05-0.2 mg/kg dose IV/IM/SC q2-4h prn; not to exceed 15 mg/dose
Children: 0.1-0.2 mg/kg dose IV/IM/SC q2-4h prn
Phenothiazines may antagonize analgesic effects of opiate agonists; TCAs, MAOIs, and other CNS depressants may potentiate adverse effects of morphine
Documented hypersensitivity; hypotension; potentially compromised airway with uncertain rapid airway control; respiratory depression; nausea; emesis; constipation; urinary retention
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
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
These agents are used to prevent nausea and vomiting.
Selective 5-HT3-receptor antagonist that blocks serotonin both peripherally and centrally. Prevents nausea and vomiting associated with emetogenic cancer chemotherapy (eg, high-dose cisplatin), and complete body radiotherapy.
4 mg IV or PO (orally disintegrating tablet) q4-6h prn nausea and vomiting
6 months to 18 years: 0.15 mg/kg IV q4-6h prn nausea and vomiting
Orally disintegrating tablet: 4 mg PO q4-6h prn nausea and vomiting
Although there is potential for cytochrome P-450 inducers (barbiturates, rifampin, carbamazepine, and phenytoin) to change half-life and clearance of ondansetron, dosage adjustment is not usually required
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
May cause headache
These agents are used to reduce anxiety.
Modulates postsynaptic effects of GABA-A transmission, resulting in an increase in presynaptic inhibition. Appears to act on part of the limbic system, the thalamus, and hypothalamus, to induce a calming effect. Also has been found to be an effective adjunct for the relief of skeletal muscle spasm caused by upper motor neuron disorders.
Rapidly distributes to other body fat stores. Twenty minutes after initial IV infusion, serum concentration drops to 20% of Cmax.
Individualize dosage and increase cautiously to avoid adverse effects.
2-10 mg PO/IM/IV q3-4h, repeat q2-4h prn; not to exceed 30 mg in 8 h
0.05-0.3 mg/kg/dose IV over 2-3 min or IM; repeat in 2-4 h prn
Alternatively, 0.12-0.8 mg/kg/d PO divided q6-8h; not to exceed 10 mg/dose
Phenothiazines, barbiturates, alcohols, and MAO inhibitors increase CNS toxicity when administered concurrently
Documented hypersensitivity; narrow-angle glaucoma; reversal agents (eg, flumazenil) contraindicated when lorazepam used for life-threatening conditions (eg, control of intracranial pressure or status epilepticus)
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Caution with other CNS depressants, low albumin levels, or hepatic disease (may increase toxicity)
Complications of testicular torsion may include the following:
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Timothy J Rupp, MD, FACEP, Associate Medical Director, Physicians Emergency Care Associates, Methodist Health System, Dallas, Texas; Staff Physician, Innovative Emergency Medicine, Frisco, Texas; Staff Physician, Department of Emergency Medicine, Children's Medical Center of Dallas, Dallas, Texas
Timothy J Rupp, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Gay and Lesbian Medical Association, Society for Academic Emergency Medicine, and Texas Medical Association
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Mark Zwanger, MD, MBA is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and American Medical Association
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Richard S Krause, MD, Senior Faculty, Department of Emergency Medicine, State University of New York at Buffalo School of Medicine
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John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
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Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School
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