RESUMEN
PURPOSE: Internal iliac artery (IIA) embolisation is commonly performed prior to endovascular aneurysm repair (EVAR) of aortoiliac aneurysms to prevent type 2 endoleaks via the internal iliac arteries. The safety of this procedure is controversial due to the high incidence of pelvic ischaemic complications. METHODS: We undertook a retrospective review of all patients undergoing IIA embolisation before EVAR from 2002 to 2012, to determine incidence of, and factors associated with pelvic ischaemia. RESULTS: Eight of 25 patients (32 %) experienced new-onset ischaemia, including erectile dysfunction (4 %), and buttock claudication (28 %) that persisted >6 months in only four patients (16 %). Both bilateral IIA embolisation and a shorter time interval to EVAR correlate with increased risk (p = 0.006 and p = 0.044). No co-morbidities or demographic factors were predictive. CONCLUSIONS: We conclude that IIA embolisation remains a beneficial procedure, however, to minimise the risk of buttock claudication we advise against both bilateral IIA embolisation and short time intervals between embolisation and subsequent EVAR.
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Embolización Terapéutica/métodos , Aneurisma Ilíaco/cirugía , Arteria Ilíaca/cirugía , Anciano , Embolización Terapéutica/efectos adversos , Femenino , Humanos , Arteria Ilíaca/patología , Masculino , Estudios Retrospectivos , Factores de Tiempo , Resultado del TratamientoRESUMEN
BACKGROUND: Controversies exist around predictive testing (PT) programmes in neurodegenerative disorders. AIMS: This study sets out to answer the following questions relating to Huntington disease (HD) and other neurodegenerative disorders: differences between these patients in their PT journeys, why and when individuals withdraw from PT, and decision-making processes regarding reproductive genetic testing. METHODS: A case series analysis of patients having PT from the multidisciplinary Western Australian centre for PT over the past 20 years was performed using internationally recognised guidelines for predictive gene testing in neurodegenerative disorders. RESULTS: Of 740 at-risk patients, 518 applied for PT: 466 at risk of HD, 52 at risk of other neurodegenerative disorders - spinocerebellar ataxias, hereditary prion disease and familial Alzheimer disease. Thirteen percent withdrew from PT - 80.32% of withdrawals occurred during counselling stages. Major withdrawal reasons related to timing in the patients' lives or unknown as the patient did not disclose the reason. Thirty-eight HD individuals had reproductive genetic testing: 34 initiated prenatal testing (of which eight withdrew from the process) and four initiated pre-implantation genetic diagnosis. There was no recorded or other evidence of major psychological reactions or suicides during PT. CONCLUSIONS: People withdrew from PT in relation to life stages and reasons that are unknown. Our findings emphasise the importance of: (i) adherence to internationally recommended guidelines for PT; (ii) the role of the multidisciplinary team in risk minimisation; and (iii) patient selection.
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Pruebas Genéticas/métodos , Pruebas Genéticas/normas , Enfermedad de Huntington/diagnóstico , Enfermedad de Huntington/genética , Enfermedades Neurodegenerativas/diagnóstico , Enfermedades Neurodegenerativas/genética , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Toma de Decisiones , Femenino , Humanos , Enfermedad de Huntington/epidemiología , Masculino , Persona de Mediana Edad , Enfermedades Neurodegenerativas/epidemiología , Valor Predictivo de las Pruebas , Estudios Retrospectivos , Australia Occidental/epidemiología , Adulto JovenRESUMEN
INTRODUCTION: Angiomyolipomas (AML) are rare benign renal tumours which are associated with aneurysms that can cause haemorrhage. Embolisation of AML greater than 4 cm with a variety of embolic agents is now the first-line treatment in these cases. METHODS: This was a retrospective analysis of all patients who underwent AML embolisation at Beaumont Hospital from 2000 to 2006 to review the efficacy of embolisation in the treatment of AMLs. RESULTS: There were six patients in total (n = 6). One patient (16%) had a background of tuberous sclerosis. Half of the patients presented acutely with bleeding and abdominal pain (50%) while the other half were found incidentally. There were no mortalities overall and three patients (50%) developed post embolisation syndrome. Five patients (83%) had a good response to embolisation with no further growth or regression of the AML. CONCLUSION: Embolisation is a safe and effective method for treating patients with AML.
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Angiomiolipoma/terapia , Ablación por Catéter , Embolización Terapéutica , Neoplasias Renales/terapia , Esclerosis Tuberosa/terapia , Enfermedad Aguda , Adulto , Angiomiolipoma/complicaciones , Femenino , Hemorragia/etiología , Hemorragia/terapia , Humanos , Neoplasias Renales/complicaciones , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Resultado del TratamientoRESUMEN
AIMS: The purpose of this study was to review indications, source of haemorrhage, method of embolisation and clinical outcome in patients referred to Interventional Radiology for the emergency management of acute arterial haemorrhage. METHODS: Retrospective review of patients undergoing emergency percutaneous embolisation over 4 years. Clinical details, computed tomographic findings, embolisation procedure details and clinical outcome are outlined. RESULTS: Patients (n = 41) were included with various clinical indications for embolisation [haemoptysis (n = 8), iatrogenic (n = 7), traumatic pseudoaneurysm (n = 3), retroperitoneal bleed (n = 3), GI bleed (n = 6), splenic rupture (n = 1), renal laceration (n = 1), epistaxis (n = 12)]. Embolisation material consisted of coils, embospheres, glue, and covered stents. Technical success was achieved in 100% of cases. One patient died 2 days after embolisation secondary to myocardial infarction. CONCLUSION: Emergency arterial embolisation is a potentially life-saving treatment. Although it is technically challenging, indications are becoming increasingly varied and outcomes are more successful because of the availability of microcatheters and effective embolisation materials.
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Embolización Terapéutica , Hemoptisis/terapia , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Aneurisma Falso/terapia , Embolización Terapéutica/métodos , Servicios Médicos de Urgencia , Epistaxis/terapia , Femenino , Hemorragia Gastrointestinal/terapia , Hemoptisis/diagnóstico por imagen , Humanos , Masculino , Persona de Mediana Edad , Radiografía Intervencional , Estudios Retrospectivos , Adulto JovenRESUMEN
Arterial wall disruption, as a consequence of inflammation/infection, trauma (penetrating or blunt), or iatrogenic causes, may result in pseudoaneurysm formation. Currently, iatrogenic causes are increasing as a result of the growth of endovascular intervention. The frequency of other causes also seems to be increasing, but this may simply be the result of increased diagnosis by better imaging techniques, such as multidetector contrast-enhanced computed tomography. Clinically, pseudoaneurysms may be silent, may present with local or systemic signs, or can rupture with catastrophic consequences. Open surgical repair, previously the mainstay of treatment, has largely been replaced by image-guided occlusion methods. On the basis of an experience of over 100 pseudoaneurysms, treatments at various anatomical sites, imaging modalities used for accurate diagnosis, current changing therapeutic options for pseudoaneurysm management, approved embolization agents, and clinical follow-up requirements to ensure adequate treatment will be discussed. Image-guided direct percutaneous and endovascular embolization of pseudoaneurysms are established treatment options with favorable success rates and minimal morbidity. The pendulum has now swung from invasive surgical repair of pseudoaneurysms to that of image-guided interventional radiology.
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Aneurisma Falso/diagnóstico , Aneurisma Falso/terapia , Aneurisma Falso/etiología , Angiografía de Substracción Digital , Humanos , Imagen por Resonancia Magnética Intervencional , Radiografía Intervencional , Tomografía Computarizada por Rayos X , Ultrasonografía IntervencionalRESUMEN
T-fastener gastropexy is widely performed as part of gastrostomy insertion. The current literature recommends removal of T-fasteners at 2 weeks. We present a series of patients in whom T-fasteners were removed at 2 days with no major complications. We removed T-fasteners in 109 patients (male-to-female ratio 59:50, age range 18 to 88 years, mean age 62 years) at 2 days after gastrostomy insertion. Indications for gastrostomy included amytrophic lateral sclerosis, cerebrovascular accidents, head and neck carcinoma, multiple sclerosis, and others, including brain tumours and chronic inflammatory demyelinating polyneuropathy. No peritubal leaks or other major complications were seen in the study population. In the study group, 15 minor complications were recorded (14%), including localised infection and pain, both of which resolved on removal of T-fasteners. We conclude that it is feasible and safe to remove T-fasteners at 2 days.
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Gastrostomía/instrumentación , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Medios de Contraste , Remoción de Dispositivos , Diseño de Equipo , Estudios de Factibilidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Complicaciones Posoperatorias , Radiografía Intervencional , Factores de Riesgo , Resultado del TratamientoAsunto(s)
Aneurisma de la Aorta Torácica/diagnóstico por imagen , Rotura de la Aorta/diagnóstico por imagen , Trombosis/diagnóstico por imagen , Adulto , Aneurisma de la Aorta Torácica/complicaciones , Enfermedades de la Aorta/diagnóstico por imagen , Rotura de la Aorta/complicaciones , Humanos , Masculino , Trombosis/complicaciones , Tomografía Computarizada por Rayos XRESUMEN
Huntington disease (HD) in indigenous Australians is a poorly analysed and difficult problem. This study addresses the issue of HD in remote indigenous Australian populations in the north-west of Western Australia. Proband identification, clinical assessment, neurogenetic studies and pedigree analysis led to the discovery of HD in the 63-year-old male proband and his family. HD in remote indigenous Australian communities is a challenging diagnostic and management problem compounded by the complexity of distance.
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Enfermedad de Huntington/diagnóstico , Enfermedad de Huntington/genética , Linaje , Australia , Humanos , Masculino , Persona de Mediana Edad , Nativos de Hawái y Otras Islas del Pacífico , Población RuralRESUMEN
To evaluate the safety and efficacy of percutaneous antegrade ureteric stent removal using a rigid alligator forceps. Twenty patients were included in our study. Indications for ureteric stent insertion included stone disease (n = 7), malignancy (n = 8) and transplant anastomotic strictures (n = 5). Stent retrieval was carried out for proximal stent placement/migration in seven patients and encrustation in the remaining 13. Twenty-two stents were successfully retrieved in 20 patients. There was one technical failure (5%). There were no major complications. We had four minor complications, which included nephrostomy site pain (n = 2), periprocedural sepsis (n = 1) and a small urinoma (n = 1). All patients settled with conservative management. Percutaneous radiologically guided antegrade ureteric stent removal with an alligator forceps is safe and effective, particularly when initial surgical removal has failed.
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Remoción de Dispositivos/instrumentación , Remoción de Dispositivos/métodos , Stents , Uréter/diagnóstico por imagen , Uréter/cirugía , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Radiografía , Resultado del TratamientoRESUMEN
BACKGROUND: Recently, interventional radiologists have adopted an increasingly prominent role in the placement and management of hemodialysis catheters, as well as in the research and development of new and better catheters. The purpose of this study was to evaluate the viability and hemodialysis efficiency of the AshSplit catheter and the Permcath catheter. METHODS: 204 consecutive patients requiring radiological insertion of hemodialysis catheters were followed, retrospectively, over a 42-month period. Both hemodialysis catheters were placed using a combination of ultrasonic and fluoroscopic guidance and tunneled appropriately. Information collected included catheter insertion sites, insertion complications, catheter duration, and final outcome. RESULTS: Over the study period of two years, 269 catheters were placed into 204 patients with end stage renal failure. Patients received either an AshSplit (101 patients, 127 catheters) or a Permcath (103 patients, 142 catheters). Vascular access route of choice was the right internal jugular vein (67% AshSplit, 71% Permcath). Insertion complications occurred in 18 patients overall (6.6%), with only 1 requiring further intervention (hemopneumothorax). Flow rates averaged 259 mls/min for AshSplits and 248 mls/min for Permcaths (p < 0.001). Follow-up of catheter viability for 42 months yielded a mean AshSplit catheter duration of 246 days (range 6-932) and 239 days (range 1-1,278) for Permcath (p = 0.46). Reasons for catheter failure and elective catheter removal were similar in both groups; however, Permcaths required significantly more thrombolysis than AshSplits, p < 0.001. CONCLUSION: The AshSplit provides significantly better flow rates and less thrombolysis compared to the Permcath, with similar catheter dwell times.
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Catéteres de Permanencia , Diálisis Renal , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Cateterismo Venoso Central/instrumentación , Remoción de Dispositivos , Diacetato de Etinodiol , Femenino , Humanos , Venas Yugulares , Fallo Renal Crónico/terapia , Masculino , Persona de Mediana Edad , Radiografía Intervencional , Análisis de SupervivenciaRESUMEN
PURPOSE: In a prospective randomized study a standard dual-tip hemodialysis catheter (PermCath, Sherwood Medical, St. Louis, MO, USA) was compared with a newer split-lumen catheter (Ash Split, Medcomp, Harleysville, PA, USA). METHODS: Sixty-nine patients (42 men, 27 women; mean age 62 years) were randomized to receive either the Ash Split (AS) or the PermCath (PC) catheter. The catheters were inserted into the internal jugular vein. The primary outcome evaluated was blood flow measurements during the first six hemodialysis sessions. Secondary outcomes included: technical difficulties encountered at insertion, early complications and late complications requiring catheter removal or exchange. RESULTS: A total of 69 hemodialysis catheters, 33 AS and 36 PC, were successfully inserted in the internal jugular vein (right 60, left 9) of 69 patients. Mean blood flow during dialysis (Qb) was 270.75 ml/min and 261.86 ml/hr for the AS and PC groups respectively (p = 0.27). Mean duration of catheter use was 111.7 days (range 5.4-548.9 days) and 141.2 days (range 7.0-560.9 days) in the AS and PC groups respectively (p = 0.307). Catheter failures leading to removal or exchange occurred in 20 patients: 14 in the AS group and six in the PC group. Survival curves with censored endpoints (i.e., recovery, arteriovenous fistula formation, peritoneal dialysis and transplantation) showed significantly better outcome with PermCath catheters (p = 0.024). There was no significant difference in ease of insertion or early complication rates. CONCLUSION: The Ash Split catheter allows increased rates of blood flow during hemodialysis but this increase was not significant at the beginning (p = 0.21) or end (p = 0.27) of the first six hemodialysis sessions. The Ash Split catheter is more prone to minor complications, particularly dislodgment, than the PermCath catheter.
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Cateterismo Venoso Central/instrumentación , Catéteres de Permanencia , Diálisis Renal/instrumentación , Velocidad del Flujo Sanguíneo , Femenino , Humanos , Venas Yugulares , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Diseño de Prótesis , Falla de Prótesis , Radiografía Intervencional , Estadísticas no ParamétricasRESUMEN
AIM: To evaluate the experience in our institution with ultrasound-guided transrectal and transvaginal (endocavitary) drainage of pelvic abscesses. MATERIALS AND METHODS: Eighteen patients (four male, 14 female; mean age 55 years, range 30-78 years) presenting with pelvic abscesses were referred to our institution for therapeutic drainage over a 4 year period. Patients received broad-spectrum antibiotics prior to drainage, which was performed by either the transvaginal or transrectal route under ultrasound guidance. Patients were given sedo-analgesia in the form of midazolam and fentanyl and local anaesthesia was also employed. Eight French catheters were inserted into the abscess cavities, and patients were subsequently monitored on a daily basis by a member of the interventional radiology team until such time as it was deemed appropriate to remove the catheter. RESULTS: Eighteen catheters were placed in 17 patients, and transvaginal aspiration alone was performed in one patient. Drainage was successful in 16 of 17 patients, but a transgluteal approach was ultimately required in the remaining patient to enable passage of a larger catheter into an infected haematoma. The mean duration of drainage was 5 days, mean time to defervesce 2 days. Spontaneous catheter dislodgement occurred in four patients associated with straining, but this did not have any adverse effect in three of the four patients. CONCLUSION: Endocavitary drainage is an effective method of treatment for pelvic abscesses. Spontaneous catheter dislodgement does not affect patient outcome.
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Absceso/cirugía , Cateterismo/métodos , Drenaje/métodos , Pelvis , Ultrasonografía Intervencional/métodos , Absceso/diagnóstico por imagen , Absceso/etiología , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
Popliteal and femoral aneurysms can be treated by endoluminal graft stenting, instead of conventional surgery. Results in four cases suggest, however, that long-term results do not justify an endovascular approach.
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Aneurisma/cirugía , Implantación de Prótesis Vascular/métodos , Arteria Femoral , Arteria Poplítea , Stents , Anciano , Aneurisma/diagnóstico por imagen , Aneurisma/mortalidad , Angiografía/métodos , Humanos , Masculino , Persona de Mediana Edad , Procedimientos Quirúrgicos Mínimamente Invasivos/métodos , Pronóstico , Medición de Riesgo , Muestreo , Sensibilidad y Especificidad , Índice de Severidad de la Enfermedad , Tasa de Supervivencia , Resultado del Tratamiento , Grado de Desobstrucción Vascular/fisiologíaRESUMEN
PURPOSE: T-fastener gastropexy is used by many interventional radiologists during percutaneous radiologic gastrostomy (PRG) placement. Whether gastropexy is a prerequisite to safe gastrostomy placement is uncertain. We evaluated the use of T-fastener gastropexy versus no gastropexy for PRG in a prospective, randomized study. METHODS: Of 90 consecutive patients referred for PRG, 48 were randomly selected to receive T-fastener gastropexy (M:F, 35:13; mean age 62 years, range 20-90 years) and 42 to receive no gastropexy (M:F, 31:11; mean age 63 years, range 40-90 years). Technical difficulties and fluoroscopy times were recorded for both groups and all patients were followed up for postprocedural complications. T-fasteners were removed between 3 and 7 days after gastrostomy insertion. RESULTS: A major complication was encountered in four patients from the non-gastropexy group (10%). In these cases the guidewire and dilator "flipped" out of the stomach into the peritoneal cavity. This resulted in misplacement of the gastrostomy tube in the peritoneal cavity in two of the patients. This was discovered at the end of the procedure when a test injection of contrast medium was performed. In three of these patients the procedure was rescued and completed radiologically. One patient underwent endoscopic gastrostomy placement. Five of 48 patients (10%) who received a gastropexy had pain associated with the T-fastener sites. Six patients (13%) had skin excoriation at the T-fastener sites. No skin complications were seen in the non-gastropexy group. No statistical difference in fluoroscopy time was observed between the two groups. CONCLUSION: Our experience of PRG without T-fastener gastropexy involved a 10% incidence of serious technical complications. We suggest that T-fastener gastropexy should be performed routinely for all PRG procedures. T-fastener gastropexy has an associated minor complication of pain and skin excoriation at the gastrostomy site which resolves on removing the T-fasteners.
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Gastrostomía/métodos , Radiografía Intervencional , Pared Abdominal/cirugía , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Fluoroscopía , Gastrostomía/efectos adversos , Gastrostomía/instrumentación , Humanos , Intubación Gastrointestinal , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Estómago/diagnóstico por imagen , Estómago/cirugíaRESUMEN
AIM: The purpose of this study was to evaluate the usefulness of gadolinium enhanced 3D magnetic resonance (MR) angiography (CE MRA) as an alternative to translumbar or brachial angiography in the pre-operative work-up of patients with aortoiliac occlusion. MATERIALS AND METHODS: Nineteen patients (14 men and five women; age range 45-77 years; mean 62 years), not suitable for perfemoral angiography (aortoiliac occlusion, n = 18; infected femoro-femoral graft with femoral artery pseudoaneurysm, n = 1), underwent pre-operative CE MRA and catheter angiography (translumbar, n = 5; brachial, n = 14). CE MRA was performed using a 3D fast spoiled gradient-recalled pulse sequence during the intravenous injection of 40 ml of gadolinium DTPA and a 32-s breath-hold. All patients subsequently underwent surgical (n = 13) or percutaneous transluminal (n = 6) treatment for their vascular disease. The accuracy of CE MRA was determined compared with the findings at catheter angiography taken as the gold standard. RESULTS: CE MRA gave accurate information about the occlusion, inflow and distal run-off in the majority of patients. CE MRA revealed occlusions with an accuracy of 94.7% in the aortic segment, 98.7% in the iliac segment, and 100% in the common femoral segment. The arterial segments distal to the common femoral artery were not completely visualized in four patients but CE MRA provided sufficient information to plan either surgical or percutaneous transluminal therapy in all but one patient. CONCLUSION: CE MRA is highly accurate in showing the presence and extent of aortoiliac occlusions. In our study group, CE MRA gave sufficient information in the pre-operative evaluation of aortoiliac occlusion.
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Enfermedades de la Aorta/diagnóstico , Arteriopatías Oclusivas/diagnóstico , Arteria Ilíaca/fisiopatología , Angiografía por Resonancia Magnética , Anciano , Enfermedades de la Aorta/diagnóstico por imagen , Enfermedades de la Aorta/terapia , Aortografía , Arteriopatías Oclusivas/diagnóstico por imagen , Arteriopatías Oclusivas/terapia , Medios de Contraste , Femenino , Gadolinio DTPA , Humanos , Arteria Ilíaca/diagnóstico por imagen , Procesamiento de Imagen Asistido por Computador , Masculino , Persona de Mediana Edad , Estudios ProspectivosRESUMEN
PURPOSE: Percutaneous endoscopic gastrostomy (PEG) is not possible or fails in some patients. We aimed to categorize the reasons for PEG failure, to study the success of percutaneous radiologic gastrostomy (PRG) in these patients, and to highlight the associated technical difficulties and complications. METHODS: Forty-two patients (28 men, 14 women; mean age 60 years, range 18-93 years) in whom PEG failed or was not possible, underwent PRG. PEG failure or unsuitability was due to upper gastrointestinal tract obstruction or other pathology precluding PEG in 15 of the 42 patients, suboptimal transillumination in 22 of 42 patients, and advanced cardiorespiratory decompensation precluding endoscopy in five of 42 patients. T-fastener gastropexy was used in all patients and 14-18 Fr catheters were inserted. RESULTS: PRG was successful in 41 of 42 patients (98%). CT guidance was required in four patients with altered upper gastrointestinal anatomy. PRG failed in one patient despite CT guidance. In the 16 patients with high subcostal stomachs who failed PEG because of inadequate transillumination, intercostal tube placement was required in three and cephalad angulation under the costal margin in six patients. Major complications included inadvertent placement of the tube in the peritoneal cavity. There was one case of hemorrhage at the gastrostomy site requiring transfusion and one case of superficial gastrostomy site infection requiring tube removal. Minor complications included superficial wound infection in six patients, successfully treated with routine wound toilette. CONCLUSION: We conclude that PRG is a safe, well-tolerated and successful method of gastrostomy and gastrojejunostomy insertion in the technically difficult group of patients who have undergone an unsuccessful PEG. In many such cases optimal clinical evaluation will suggest primary referral for PRG as the preferred option.
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Endoscopía del Sistema Digestivo , Enfermedades Gastrointestinales/cirugía , Gastrostomía/métodos , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Constricción Patológica/diagnóstico por imagen , Constricción Patológica/cirugía , Contraindicaciones , Femenino , Fluoroscopía , Enfermedades Gastrointestinales/diagnóstico por imagen , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Tomografía Computarizada por Rayos X , Insuficiencia del TratamientoRESUMEN
The Yale-New Haven Hospital (YNHH) clinical workstation came into existence in 1993 to provide a simple menu-driven interface to high use information systems that would be easily accessible on the wards and in the intensive care units. Direct Internet access, advances in Web-based software, and greater cooperation between Yale-New Haven Hospital and Yale School of Medicine network technology groups have enabled the clinical workstations to become an integral tool for providing clinical care. The workstation provides bedside access to an expanding array of internal and external resources to support patient care and has the potential to become the basis for an interface that will be utilized throughout the multi-location Yale-New Haven Healthcare System.
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Centros Médicos Académicos/organización & administración , Sistemas de Apoyo a Decisiones Clínicas/organización & administración , Sistemas de Información en Hospital/organización & administración , Internet , Connecticut , Humanos , Almacenamiento y Recuperación de la Información , Desarrollo de Programa , Interfaz Usuario-ComputadorRESUMEN
The purpose of our study was to evaluate the accuracy of MR myelography in depicting disc herniation in the lumbar spine when compared with conventional MRI in patients presenting with clinical evidence of disc herniation. One hundred patients referred for conventional MR imaging of the lumbar spine also had coronal MR (TR 9000 ms, TE 272 ms eff, NEX 3, echo train length 32) myelography performed. Three experienced observers compared magnetic resonance myelography (MRM) with conventional lumbar spine MR using the following variables: visibility of thecal sac and nerve roots, and the presence, location and severity of disc herniation. Disc protrusions were seen at 110 disc space levels on conventional MR images as opposed to 93 on MRM. However, only 72 % of lesions seen on conventional MR were diagnosed by MRM. Similarly, only 63.8 % of nerve root compression abnormalities seen at conventional MR were visualized when compared with conventional MRM. The sensitivity, specificity and accuracy of MRM when compared with conventional MR was 72, 93 and 85 %, respectively. The MRM technique yields images that resemble conventional myelography and may be used to help confirm abnormalities seen on conventional MR in selected cases; however, the large number of false-positive and false-negative examinations indicates that caution should be used in interpreting MRM images.