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15414 citation(s) found for "Iv, Michael".

Rumination Syndrome in Children and Adolescents: Diagnosis, Treatment, and Prognosis
Chial, Heather J., Camilleri, Michael , Williams, Donald E., Litzinger, Kristi, Perrault, Jean

Pediatrics | August 14, 2004 | Volume: 111 | Issue: 1 | Pages: 158-162

10.1542/peds.111.1.158 | PMID 12509570 Get It

Objectives. To characterize the clinical features, results of diagnostic testing, and treatment outcomes for children and adolescents with rumination syndrome. Methods. Review of the medical records for all 147 patients ages 5 to 20 diagnosed with rumination syndrome at our institution between 1975 and 2000. Data are presented as mean ± the standard error of the mean. Results. Sixty-eight percent were female. Age at diagnosis was 15.0 ± 0.3 years. Symptom duration before diagnosis was 2.2 ± 0.3 years, 73% missed school/work, and 46% had been hospitalized because of symptoms. Before diagnosis, 16 (11%) underwent surgery for evaluation or management of symptoms. Twenty-four (16%) had psychiatric disorders; 3.4% had anorexia or bulimia nervosa. All patients described postprandial regurgitation after almost every meal (2.7 ± 0.1 meals per day). Weight loss was described by 42.2% (median: 7 kg). Additional symptoms included: abdominal pain, 38%; constipation, 21%; nausea, 17%; and diarrhea, 8%. Structural studies were normal. Gastric emptying of solids at 4 hours was delayed in 26 of 56 patients. Esophageal pH testing in 24 patients showed reflux/regurgitation in 54%. Gastroduodenal manometry in 65 patients showed characteristic rumination-waves in 40%. Outcome data (at median follow-up 10 months) were available for 54 patients. Symptoms resolved in 16 (30%) and improved in 30 (56%). Conclusions. Recognition of the clinical features of rumination syndrome in children and adolescents is essential; the diagnosis is often delayed and associated with morbidity. Extensive diagnostic testing is unnecessary. Early behavioral therapy is advocated, and patient outcomes are generally favorable.
Breath-Holding Spells Associated With Significant Bradycardia: Successful Treatment With Permanent Pacemaker Implantation
Kelly, Amy M., Porter, Co-burn J., McGoon, Michael D., Espinosa, Raúl E. , Osborn, Michael J., Hayes, David L.

Pediatrics | August 13, 2004 | Volume: 108 | Issue: 3 | Pages: 698-702

10.1542/peds.108.3.698 | PMID 11533339 Get It

Objective. To determine whether children with pallid breath-holding spells associated with bradycardia can be treated safely and successfully with permanent pacemaker implantation. Methods. The records of pediatric patients who had apparent breath-holding spells and associated bradycardia and were treated with permanent pacemaker implantation were reviewed. Results. Ten pediatric patients with apparent breath-holding spells associated with bradycardia were treated with a permanent ventricular demand pacemaker at the Mayo Clinic between 1985 and 1995. Patients had onset of symptoms between ages 6 days and 12 months and presented for evaluation between ages 12 months and 5 years. Duration of spells was 15 seconds to 10 minutes. Medications to prevent spells were unsuccessful. Electrocardiograms documented asystolic pauses of 1.7 to 24 seconds (mean: 11.9 seconds). Permanent ventricular demand pacemakers were implanted at 10 months to 5 years of age (median: 14.5 months): 9 endocardial and 1 epicardial. Three patients required pacemaker revision. At follow-up of 38 to 170 months (median: 65.5), 5 patients had complete resolution of spells, 2 had only mild color change without loss of consciousness or seizure activity, and 3 continued to have minor brief spells. Conclusions. Permanent pacemaker therapy for children with pallid breath-holding spells associated with severe bradycardia is safe, efficacious, and warranted.
Diagnostic Accuracy of Screening Electrocardiograms in Long QT Syndrome I
Miller, Misha D., Porter, Co-burn J., Ackerman, Michael J.

Pediatrics | August 13, 2004 | Volume: 108 | Issue: 1 | Pages: 8-12

10.1542/peds.108.1.8 | PMID 11433047 Get It

Objective. Inherited long QT syndrome (LQTS) may present with syncope, seizures, and/or sudden death as a result of ventricular tachyarrhythmias. Identification of family members who are at risk because they harbor the genetic substrate for LQTS is critical. Presently, such identification relies on the 12-lead electrocardiogram (ECG). The purpose of this study was to evaluate the efficacy of the automated ECG as a screening tool for LQTS. Method. Molecular testing of a proband and 22 additional family members for the KVLQT1 mutation and symptomatic status facilitated the classification of each family member into the following patient groups: noncarriers (13), asymptomatic carriers (5), and symptomatic carriers (5). Each individual had a standard 12-lead ECG from which the computer and manual (lead II) corrected QT interval were determined. In addition, we determined the accuracy of the computer ECG diagnostic interpretation for each patient group. Results. With the use of a corrected QT interval of ≥460 ms as a diagnostic cutoff, the positive and negative predictive values for identifying at-risk individuals were 100%. Despite this, the computer-generated ECG diagnostic interpretation erroneously classified 6 of 23 family members. Moreover, half of the family members, proved to have the ion channel defect, received the diagnostic interpretation “normal ECG.” Conclusion. Reliance on the computer-generated ECG diagnostic interpretation alone will fail to identify many at-risk family members. It is suggested that all first-degree relatives of an identified LQTS proband have a 12-lead ECG that is reviewed independently by a physician who is familiar with LQTS in an effort to improve screening for this potentially lethal syndrome.electrocardiogram, long QT syndrome, QT interval, sudden death.
Parental Knowledge and Attitudes of Minnesota Laws Concerning Adolescent Medical Care
Cutler, Ellen M., Bateman, Michael D., Wollan, Peter C. , Simmons, Patricia S.

Pediatrics | August 13, 2004 | Volume: 103 | Issue: 3 | Pages: 582-587

10.1542/peds.103.3.582 | PMID 10049960 Get It

Objective. To determine parents' knowledge and attitudes of medicolegal issues affecting adolescent medical care. Design. An anonymous, mailed survey with 16 questions concerning Minnesota consent and confidentiality laws that affect adolescents' medical care. Setting. A community of >70 000 in rural, southeastern Minnesota. Participants. Parents of 600 randomly selected 7th- through 12th-grade public school students. Results. Two hundred eighty-eight (48%) parents returned the surveys. Parents achieved a median score of 18.8% (range, 0%–93.8%) correct on a test of knowledge. Opinion was a median of +0.3 on a scale where −1 signified “a bad law,” 0 signified “neither a good nor bad law,” and +1 signified “a good law.” Four questions, however, generated a more intense response. Seventy-seven percent of parents reported that, as a whole, the laws in the survey had no effect on them and/or their children. Conclusions. These results suggest that parents are not knowledgeable of Minnesota laws that affect adolescent medical care. Overall opinion of these laws was mildly positive, with notable exceptions. Parents also lack a sense of impact of laws affecting adolescent medical care. Lack of knowledge and the presence of certain attitudes allow for identification of issues that clinicians should address by incorporating medicolegal education into the care of adolescents and their families. These results are especially timely in light of the Parental Rights and Responsibilities Act under consideration in Congress, which would provide parents greater authority over their children's medical care.
Cortical Microvascular Remodeling in the Stenotic Kidney
Zhu, Xiang-Yang, Chade, Alejandro , Rodriguez‐Porcel, Martin , Bentley, Michael D., Ritman, Erik L., Lerman, Lilach O. , Lerman, Amir

Arteriosclerosis, Thrombosis, and Vascular Biology | August 13, 2004 | Volume: 24 | Issue: 10 | Pages: 1854-1859

10.1161/01.atv.0000142443.52606.81 | PMID 15308558 Get It

Objective— Mechanisms of renal injury distal to renal artery stenosis (RAS) remain unclear. We tested the hypothesis that it involves microvascular remodeling consequent to increased oxidative stress. Methods and Results— Three groups of pigs (n=6 each) were studied after 12 weeks of RAS, RAS+antioxidant supplementation (100 IU/kg vitamin E and 1 g vitamin C daily), or controls. The spatial density and tortuousity of renal microvessels (<500 μm) were tomographically determined by 3D microcomputed tomography. The in situ production of superoxide anion and the expression of vascular endothelial growth factor (VEGF), its receptor VEGFR-2, hypoxia-inducible-factor (HIF)-1α, von Hippel-Lindau (VHL) protein, and NAD(P)H oxidase (p47phox and p67phox subunits) were determined in cortical tissue. RAS and RAS+antioxidant groups had similar degrees of stenosis and hypertension. The RAS group showed a decrease in spatial density of cortical microvessels, which was normalized in the RAS+antioxidant group, as was arteriolar tortuousity. RAS kidneys also showed tissue fibrosis (by trichrome and Sirius red staining), increased superoxide anion abundance, NAD(P)H oxidase, VHL protein, and HIF-1α mRNA expression. In contrast, expression of HIF-1α, VEGF, and VEGFR-2 protein was downregulated. These were all significantly improved by antioxidant intervention. Conclusions— Increased oxidative stress in the stenotic kidney alters growth factor activity and plays an important role in renal microvascular remodeling, which can be prevented by chronic antioxidant intervention.
RE: RENAL VEIN OR INFERIOR VENA CAVAL EXTENSION IN PATIENTS WITH RENAL CORTICAL TUMORS: IMPACT OF TUMOR HISTOLOGY
Cheville, John C. , Frank, Igor, Leibovich, Bradley C. , Lohse, Christine M. , Blute, Michael L.

Journal of Urology | August 12, 2004 | Volume: 172 | Issue: 3 | Pages: 1196-1196

10.1097/01.ju.0000134623.05472.bd | PMID 15311069 Get It

Evaluation of the TRUGENE HCV 5′NC Genotyping Kit with the New GeneLibrarian Module 3.1.2 for Genotyping of Hepatitis C Virus from Clinical Specimens
Germer, Jeffrey J., Rosser, Michael, Thompson, Amber , Mitchell, P. Shawn, Smith, Thomas F., Elagin, Slava, Yao, Joseph D. , Majewski, David

Journal of Clinical Microbiology | August 5, 2004 | Volume: 42 | Issue: 8 | Pages: 3911-3911

10.1128/jcm.42.8.3911.2004 Get It

Clinical Evaluation and Management Strategy for Sexual Dysfunction in Men and Women
Hatzichristou, Dimitrios , Rosen, Raymond C., Broderick, Gregory A. , Clayton, Anita H. , Cuzin, B. , Derogatis, Leonard R. , Litwin, Mark S. , Meuleman, Eric, O’Leary, Michael P. , Quirk, Frances , Sadovsky, Richard, Seftel, Allen D.

The Journal of Sexual Medicine | August 4, 2004 | Volume: 1 | Issue: 1 | Pages: 49-57

10.1111/j.1743-6109.2004.10108.x | PMID 16422983 Get It

ABSTRACT Introduction The optimal approach for identification and evaluation of the sexual problems in men and women in primary care or general medicine practice has not been consensed. Aim To provide recommendations/guidelines concerning state-of-the-art knowledge for clinical evaluation and management strategies in the evaluation and treatment of sexual dysfunction in men and women, emphasizing evidence-based medicine and a patient-centered framework. Methods An International Consultation in collaboration with the major urology and sexual medicine associations assembled over 200 multidisciplinary experts from 60 countries into 17 committees. Committee members established specific objectives and scopes for various male and female sexual medicine topics. The recommendations concerning state-of-the-art knowledge in the respective sexual medicine topic represent the opinion of experts from five continents developed in a process over a 2-year period. Concerning the Clinical Evaluation and Management Strategies Committee, there were 12 experts from five countries. Main Outcome Measure Expert opinion was based on grading of evidence-based medical literature, widespread internal committee discussion, public presentation and debate. Results Three concepts underlie sexual medicine management: (i) adoption of a patient-centered framework for evaluation and treatment; (ii) application of the principles of evidence-based medicine in diagnostic and treatment planning; and (iii) use of a unified management approach in men and women. When taken together, these three principles provide a balanced and integrated approach to sexual dysfunction management. Common algorithms for diagnosis and management of men and women with sexual dysfunction, brief sexual symptom checklists, basics in history and physical examination, indications for specialized referral and development of a follow-up strategy are presented. Conclusions More research is needed in understanding the role of evidence-based and patient-centered medicine in the clinical evaluation and management strategies of men and women with sexual dysfunction.
Hemangioblastoma of the Optic Nerve
Kerr, Daniel J., Scheithauer, Bernd W., Miller, Gary M. , Ebersold, Michael J., McPhee, Thomas J.

Neurosurgery | July 30, 2004 | Volume: 36 | Issue: 3 | Pages: 573-581

10.1097/00006123-199503000-00017 Get It

Coexisting Corticotroph and Lactotroph Adenomas
Wynne, Alan, Scheithauer, Bernd W., Kovács, Kálmán, Ebersold, Michael J., Horváth, Éva , Young, William F.

Neurosurgery | July 30, 2004 | Volume: 30 | Issue: 6 | Pages: 919-922

10.1097/00006123-199206000-00018 Get It