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1.
Pediatr Radiol ; 31(4): 247-50, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11321741

ABSTRACT

BACKGROUND: While sedation is necessary for much pediatric imaging, there are new alternatives that may help patients hold still without medication. OBJECTIVE: We examined the effect of an audio/visual system consisting of video goggles and earphones on the need for sedation during magnetic resonance imaging (MRI). MATERIALS AND METHODS: All MRI examinations from May 1999 to October 1999 performed after installation of the MRVision 2000 (Resonance Technology, Inc.) were compared to the same 6-month period in 1998. Imaging and sedation protocols remained constant. Data collected included: patient age, type of examination, use of intravenous contrast enhancement, and need for sedation. The average supply charge and nursing cost per sedated patient were calculated. RESULTS: The 955 patients from 1998 and 1,112 patients from 1999 were similar in demographics and examination distribution. There was an overall reduction in the percent of patients requiring sedation in the group using the video goggle system from 49 to 40% (P < 0.001). There was no significant change for 0-2 years (P = 0.805), but there was a reduction from 53 to 40% for age 3-10 years (P < 0.001) and 16 to 8% for those older than 10 years (P < 0.001). There was a 17% decrease in MRI room time for those patients whose examinations could be performed without sedation. Sedation costs per patient were $80 for nursing and $29 for supplies. CONCLUSION: The use of this video system reduced the number of children requiring sedation for MRI examination by 18%. In addition to reducing patient risk, this can potentially reduce cost.


Subject(s)
Audiovisual Aids , Conscious Sedation , Magnetic Resonance Imaging , Pediatrics , Conscious Sedation/economics , Conscious Sedation/nursing , Humans , Magnetic Resonance Imaging/economics , Magnetic Resonance Imaging/nursing , Videotape Recording
2.
Kidney Int ; 59(5): 1654-62, 2001 May.
Article in English | MEDLINE | ID: mdl-11318935

ABSTRACT

BACKGROUND: Although many case reports describe manifestations of autosomal-dominant polycystic kidney disease (ADPKD) in children, no longitudinal studies have examined the natural progression or risk factors for more rapid progression in a large number of children from ADPKD families. METHODS: Since 1985, we have studied 312 children from 131 families with a history, a physical examination, blood and urine chemistries, an abdominal ultrasonography, and gene linkage analysis. One hundred fifteen of 185 affected children were studied multiple times for up to 15 years. Renal volumes were determined by ultrasound imaging. Graphs of mean renal volumes according to age were compared between affected and unaffected children, ADPKD children with and without early severe disease, and children with and without high blood pressure. RESULTS: Affected children had faster renal growth than unaffected children. ADPKD children with severe renal enlargement at a young age continued to experience faster renal growth than those with mild enlargement or normal kidney size for their age, and affected children with high blood pressure had faster renal growth than those with lower blood pressure. Glomerular filtration rate did not decrease in any children except for two with unusually severe early onset disease. CONCLUSIONS: The progression of ADPKD clearly occurs in childhood and manifests as an increase in cyst number and renal size. This study identifies children at risk for rapid renal enlargement who may benefit the most from future therapeutic interventions.


Subject(s)
Polycystic Kidney, Autosomal Dominant/etiology , Adolescent , Adult , Age of Onset , Blood Pressure , Child , Female , Humans , Kidney/pathology , Kidney Failure, Chronic/etiology , Longitudinal Studies , Male , Polycystic Kidney, Autosomal Dominant/pathology , Polycystic Kidney, Autosomal Dominant/physiopathology , Risk Factors
14.
Pediatr Radiol ; 30(8): 533-7; discussion 537-9, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10993537

ABSTRACT

BACKGROUND: Determination of the presence of pulmonary metastases in children with Wilms' tumor is an important part of staging and treatment. We sought to compare the efficacy of chest radiography (CXR) and chest CT in the evaluation for pulmonary metastases in patients with Wilms' tumor. MATERIALS AND METHODS: This retrospective study included 83 children with Wilms' tumor diagnosed between 1980 and 1993. All patients with pulmonary nodules (n = 12) as well as 14 Wilms' tumor patients without pulmonary metastases (control group) had blinded review of the CXR and chest CTs by three pediatric radiologists. Presence, size, and certainty of metastatic diagnosis were recorded. Medical records were reviewed. The remaining 57 patients had review of their medical and imaging records to confirm the absence of pulmonary metastases. RESULTS: Ten of the 12 with pulmonary masses had imaging available for review. Eight had both positive CXR and chest CT examinations. Two patients had pulmonary nodules seen by CT only: one had a right cardiophrenic angle mass and died as a result of liver metastases. The other had a solitary nodule, which proved to be a plasma-cell granuloma. Overall, the CXR and chest CT data concur in 79/81 (98%). CONCLUSION: CXR alone appears adequate for the diagnosis or exclusion of pulmonary metastases in patients with Wilms' tumor.


Subject(s)
Kidney Neoplasms , Lung Neoplasms/diagnostic imaging , Lung Neoplasms/secondary , Radiography, Thoracic , Tomography, X-Ray Computed , Wilms Tumor , Adolescent , Child , Child, Preschool , Humans , Retrospective Studies
15.
Pediatr Radiol ; 30(2): 90-3, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10663519

ABSTRACT

BACKGROUND: Surveillance imaging of the brain and spinal neuraxis in patients with posterior fossa malignant tumors is commonly performed, with the assumption that early detection of tumor recurrence will improve outcome. However, the benefit of this imaging has not been proven. PURPOSE: To evaluate the usefulness of spinal surveillance imaging in children with nonmetastatic (at diagnosis, M0) posterior fossa ependymoma and medulloblastoma. MATERIALS AND METHODS: This retrospective study included 65 children (3 months to 16 years, mean 5.7 years) treated between 1985 and 1997 for ependymoma (22) and medulloblastoma (43). Medical records were reviewed for pathology and treatment data. Serial imaging of the head and spine was reviewed for evidence of tumor recurrence. RESULTS: Twenty-four patients (37 %) had tumor recurrence, including 13 with ependymoma and 11 with medulloblastoma. Of the 17/24 recurrent patients initially diagnosed as M0 (6 medulloblastoma and 11 ependymoma), 13 (76 %) had a cranial recurrence only, and 4 (24 %) presented with concomitant cranial and spinal recurrence. No M0 patient presented solely with spinal metastases at recurrence. CONCLUSION: This study suggests that spinal surveillance imaging in patients with posterior fossa ependymoma or medulloblastoma initially staged as M0 may not be useful, as these patients initially recur intracranially. Thus, until an intracranial recurrence is detected, these patients may be spared the time, expense and sedation risk necessary for spinal imaging.


Subject(s)
Brain Neoplasms/pathology , Ependymoma/pathology , Medulloblastoma/pathology , Adolescent , Brain Neoplasms/mortality , Child , Child, Preschool , Ependymoma/mortality , Female , Humans , Infant , Magnetic Resonance Imaging , Male , Medulloblastoma/mortality , Neoplasm Recurrence, Local , Retrospective Studies , Spinal Neoplasms/pathology , Tomography, X-Ray Computed
16.
Am J Kidney Dis ; 34(4): 639-45, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10516343

ABSTRACT

Although for decades autosomal dominant polycystic kidney disease (ADPKD) was considered a disease of adults, our recent longitudinal studies on children from ADPKD families have shown that the disease is evident by ultrasound imaging in approximately 75% of children who are carriers of the ADPKD1 gene, the most common form of ADPKD. Here we report that, in contrast to adults, the disease appears to be unilateral initially in approximately 17% of children. Asymmetric enlargement of the kidneys is also frequently observed. This renal asymmetry can be extreme and lead to diagnostic confusion. We present 2 unusual cases of asymmetric renal involvement that we have observed during the last 10 years. The first is a 14-year-old boy who was scheduled for a nephrectomy to relieve pain and whose family requested a second opinion. The second is a 10-year-old girl who was diagnosed with ADPKD in utero by prenatal ultrasound. After birth, 1 kidney progressively developed cysts and enlarged, whereas the other had only a few tiny cysts and remained normal in size. A review of the literature shows that presentations like these often lead to a nephrectomy or surgical biopsy. A carefully obtained family history and examination of both parents with ultrasound can help to avoid unnecessary invasive procedures. If pain is a prominent symptom, it can be treated by cyst aspiration if there are only a few cysts or a single dominant cyst. The molecular mechanism for extremely asymmetric renal disease remains to be elucidated.


Subject(s)
Polycystic Kidney, Autosomal Dominant/genetics , Adolescent , Adult , Child , Female , Genetic Carrier Screening , Genetic Predisposition to Disease/genetics , Humans , Kidney Function Tests , Male , Phenotype , Polycystic Kidney, Autosomal Dominant/diagnostic imaging , Pregnancy , Prognosis , Risk , Ultrasonography, Prenatal
17.
Otolaryngol Head Neck Surg ; 120(3): 328-34, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10064633

ABSTRACT

Chronic sinusitis in children is a common and vexing disease for clinicians and the public. There are insufficient data in the literature to develop an evidence-based clinical guideline. Experience in managing pediatric chronic sinusitis has been gained through a multidisciplinary clinic at our institution during the past 3 years. A panel of experts was formed, and with the guidance of a guideline methodologist, the development of a rigorous outcome-based guideline was undertaken. Symptom-improvement and recurrence estimates for a variety of medical and surgical treatments were assessed. Wide probability estimates were made by the panelists in most cases. Although we refrained from making specific recommendations, we developed a ranked series of practical treatment options taking into account side effects and costs.


Subject(s)
Practice Guidelines as Topic , Sinusitis/therapy , Anti-Bacterial Agents/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Child , Child, Preschool , Chronic Disease , Combined Modality Therapy , Evidence-Based Medicine , Female , Humans , Male , Nasal Decongestants/therapeutic use , Otorhinolaryngologic Surgical Procedures , Patient Selection , Recurrence , Retrospective Studies , Sinusitis/diagnosis , Sinusitis/etiology , Steroids , Treatment Outcome
18.
Pediatr Neurosurg ; 31(5): 246-50, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10681679

ABSTRACT

We report successful use of bleomycin in a low-grade astrocytoma tumor cyst of the tectal plate. A 6-year-old male underwent subtotal resection of a low-grade astrocytoma of the tectal plate followed by chemotherapy and proton beam radiation at age 2 and a half. Despite resolution of the solid portion of the tumor, serial MRI showed enlargement of a bilobar tumor cyst 3 years after the original diagnosis. The patient developed progressive ataxia, short-term memory loss and dysconjugate gaze. Following stereotactic placement of an Ommaya reservoir into the cyst, Isovue contrast and CT scan were used to confirm the integrity of the cyst. Five consecutive daily doses of 3.0 mg of bleomycin were instilled into the cyst after removal of cyst fluid. The therapy was well tolerated in the outpatient setting, and the clinical findings resolved. Subsequent CT and MRI at 4 months and 2 years after bleomycin confirmed no recurrence of the tumor or cyst.


Subject(s)
Antibiotics, Antineoplastic/administration & dosage , Astrocytoma/complications , Bleomycin/administration & dosage , Brain Diseases/drug therapy , Brain Neoplasms/complications , Cysts/drug therapy , Brain Diseases/etiology , Child , Child, Preschool , Cysts/etiology , Humans , Injections, Intralesional , Instillation, Drug , Male
20.
Pediatr Radiol ; 27(9): 743-7, 1997 Sep.
Article in English | MEDLINE | ID: mdl-9285736

ABSTRACT

BACKGROUND: Child abuse specialists rely heavily on diagnostic neuroimaging. OBJECTIVES: Study objectives were: (1) to compare the frequencies of six specific intracranial CT abnormalities in accidental and non-accidental pediatric head trauma, and (2) to assess interobserver agreement regarding these CT findings. MATERIALS AND METHODS: Three pediatric radiologists blindly and independently reviewed cranial CT scans of pediatric patients who sustained closed head trauma between 1991 and 1994. All patients were less than 4 years of age. Study cases included thirty-nine (50 %) with non-accidental head trauma and thirty-nine (50 %) with accidental head trauma. Each scan was evaluated for the presence or absence of the following six intracranial findings: (1) interhemispheric falx hemorrhage, (2) subdural hemorrhage, (3) large (non-acute) extra-axial fluid, (4) basal ganglia edema, (5) posterior fossa hemorrhage, and (6) frontal-parietal shearing tear(s). Interobserver agreement was calculated as the percentage of total cases in which all reviewers agreed a specific CT finding was present or absent. Diagnosis required independent agreement by all three pediatric radiologists. The frequencies of these six intracranial CT abnormalities were compared between the two study groups by Chi-square analysis and Fisher's exact test. RESULTS: Interobserver agreement between radiologists was greater than 80 % for all lesions evaluated, with the exception of frontal-parietal shearing tear(s). Interhemispheric falx hemorrhage, subdural hemorrhage, large (non-acute) extra-axial fluid, and basal ganglia edema were discovered significantly more frequently in non-accidental trauma (P

Subject(s)
Brain Injuries/diagnostic imaging , Child Abuse/diagnosis , Tomography, X-Ray Computed , Accidents , Brain Injuries/physiopathology , Chi-Square Distribution , Craniocerebral Trauma/diagnostic imaging , Craniocerebral Trauma/physiopathology , Female , Humans , Infant , Infant, Newborn , Male , Observer Variation , Retrospective Studies
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