Search PubMed⌕ Search

Biomedical subjects

N W Todd

Publications and source records attributed to N W Todd.

At least 37 records · Page 2Linked to original sources

Observer agreement about laryngoscopic assessment of papilloma.

BACKGROUND: Observer bias may confound the assessment of therapies utilized for recurrent respiratory papilloma, a recidivistic fluctuating disease. Any convincing change in a patient's disease must exceed the imprecision of the measuring system. MATERIALS AND METHODS: Videotapes of ten children, who had airway endoscopy for care of laryngeal papilloma, were edited. The videotapes were independently reviewed by six otolaryngologists, of whom five repeated their assessments 5 to 20 weeks later. The 'reference standard' was the operating surgeon's categorization of his patient's videotape. Agreement was calculated by the kappa statistic, the observed proportions of positive and negative agreement, and the proportion categorized as exact opposites, for each of twelve anatomic sites. RESULTS: Moderate agreement was found for both (a) the operative findings versus the later-determined 'reference standard', and (b) the 'reference standard' versus categorizations by other otolaryngologists. Intra-observer agreements were better than inter-observer agreements. Agreement as to whether or not papilloma involved each of twelve sites was within about 20% for the five pediatric otolaryngologists vs the 'reference standard', and within about 10% for the same reviewer. CONCLUSION: Videotapes may add objectivity to the assessment of laryngeal papilloma. For changes to be considered significant, an observer should identify a 10% change in the number of sites involved, or a 30% change in the extent of overall airway obstruction. For different observers, changes would have to be even greater to be meaningful.

Child↗

Autoimmune hypothesis of acquired subglottic stenosis: lack of support at time of surgical repair in children.

Numerous mechanisms have been suggested for the development of subglottic stenosis. This study sought serum antibody and cricoid cartilage immunohistologic evidence of an autoimmune process. The autoimmune hypothesis is that subglottic inflammation may extend into the cricoid cartilage, degrade the extracellular matrix and expose normally-sequestered type II collagen to the afferent arm of the immune system. The resultant anti-collagen antibodies are hypothesized to contribute to further injury and scarring. Specimens were obtained from 10 patients. Immunofluorescent stains for antibodies in histologic specimens, and serum antibodies to type II and type IX collagen were sought. No evidence for an autoimmune process was found in these specimens with the techniques used. The negative findings may be attributable to the autoimmune process being inactive at the mature stage of the disease in the patients studied.

Adolescent↗

Conotruncal cardiac anomalies and otitis media.

BACKGROUND: The neural crest influences the differentiation of the branchial arches, including the precursor tissue of the cardiac outflow tract and the eustachian tubes. Abnormal eustachian tubes are associated with otitis media. We hypothesized a relationship between conotruncal anomalies and eustachian tube anomalies. METHODS: We surveyed 115 nonsyndromic patients, aged 5 to 20 years, attending a state-run pediatric cardiology clinic. The cardiac anomalies were conotruncal (transposition of the great arteries, tetralogy of Fallot, or aortic stenosis) or nonconotruncal (atrial septal defect, tricuspid atresia, atrioventricular canal). Tympanic membrane photographs were categorized independently by two physicians as to normal, abnormal (scarred or other indication of otitis proneness), or indeterminate. RESULTS: For the 37 patients who had both ears categorized as normal or abnormal by both physicians, 20 of the 26 with a conotruncal anomaly had evidence of otitis media. In contrast, only 4 of 11 with nonconotruncal cardiac anomaly had evidence of otitis (p < 0.03; relative risk [conotruncal vs nonconotruncal], 5.83; 95% confidence interval, 1.26 to 26.95). CONCLUSION: The concept is supported that a neural crest determined branchial field defect influences the development of the cardiac outflow tract and the eustachian tubes. Children with congenital cardiac conotruncal anomalies are otitis media prone.

Adolescent↗

Management of nasopharyngeal and oropharyngeal stenosis in children.

Nasopharyngeal stenosis and oropharyngeal stenosis are rare and challenging problems in the pediatric population. The most common etiology is currently the surgical trauma associated with adenotonsillectomy. Stenosis can vary from a thin band to a complete obstructing cicatrix. Presenting symptoms range from mild hyponasal speech to severe airway obstruction. We present a series of eight children with varying degrees of stenosis and associated symptoms. Choice of treatment varied with the severity of disease. In our series, successful interventions included triamcinolone acetonide injection, lysis of adhesions, rotational and advancement mucosal flaps, and jejunal free flap. Preoperative evaluation and individualized surgical repair are essential for successful treatment.

Adenoidectomy↗

Upper airway obstruction in children with Down syndrome.

OBJECTIVES: To analyze the complex nature of upper airway obstruction (UAO) and the response to surgery in children with Down syndrome. DESIGN: Retrospective medical chart review of all patients with Down syndrome who had UAO during a 5-year period. SETTING: Academic tertiary care children's hospital. PATIENTS: Seventy-one pediatric patients with Down syndrome who had significant UAO. Thirty-four patients had pulmonary artery hypertension; 44 patients had multiple sites of airway obstruction. The obstructive problems included lymphoid hyperplasia, macroglossia, narrow nasopharynx, laryngomalacia, congenital subglottic stenosis, tracheobronchomalacia, and tracheal stenosis. INTERVENTIONS: Children with Down syndrome and UAO underwent surgical procedures including tonsillectomy, adenoidectomy, tonsillar pillar plication, uvulopalatopharyngoplasty, anterior tongue reduction, tonguehyoid suspension, laryngotracheoplasty, and tracheotomy. MAIN OUTCOME MEASURES: Postoperative symptoms found on medical chart review, or parental telephone survey, or both, and results of postoperative diagnostic tests. Patients were grouped as "improved" or having "significant residual symptoms." RESULTS: Twenty-seven of the 55 surgical patients had mild obstructive symptoms, and most improved after tonsil or adenoid surgery, or both. The remaining patients were younger and had more severe symptoms, multiple sites of obstruction, and a high incidence of cardiac disease. Eleven (39%) of the 28 patients in this group had significant residual symptoms after surgery. Four children are tracheotomy-dependent. Five deaths occurred; 3 were attributable to the upper airway. CONCLUSIONS: Upper airway obstruction in children with Down syndrome often is a complex process with multifocal causes. Residual symptoms of airway obstruction are common after surgery. A comprehensive and individualized approach is important in the management of UAO in Down syndrome.

Adenoidectomy↗

Cisplatin in children: hearing loss correlates with iris and skin pigmentation.

Pigmentation is reported to affect cisplatin-induced ototoxicity in adult humans. The hearing loss is worse in people with brown irises, than in those with blue irises. We assessed the hypothesis that cisplatin-treated children with dark irises suffer more deterioration in auditory thresholds than do those with less pigmentation. For the 19 children whose data met the requirements of this observational retrospective study, we found a weak correlation (Spearman's r = 0.50; p < 0.05) of high frequency hearing loss (at 4000 Hz) and pigmentation. Blue or hazel-eyed children averaged 2.9 dB worsening at 4000 Hz, in contrast to 14.2 dB worsening for brown or black-eyed children. Pigmentation may account for some of the individual susceptibility to cisplatin ototoxicity. We suggest that iris colour be included in future reports of cisplatin-related hearing loss.

Adolescent↗

Neck flexion and extension in children with Down syndrome: a somatosensory study.

The cervical spine in Down syndrome patients is often lax, at least at radiographic imaging, and the risk of spinal cord embarrassment is increased. This study was performed to obtain information that would help identify patients at risk for this problem and reduce the risk of endotracheal intubation and other surgical procedures in patients with Down syndrome. Somatosensory evoked potential studies were performed in 15 consecutive children who were undergoing elective otolaryngic surgery. None had neurologic symptoms or the physical examination finding of cervical spinal cord embarrassment, and their cervical spines were considered normal by plain radiographs obtained in the neutral, flexed, and extended positions. No significant change in latency (P = .16) or amplitude (P = .19) was found when the anesthetized children had their necks placed in either full flexion or full extension. With more than 90% certainty, the authors believe that children with Down syndrome who have "normal" plain cervical spine radiographs are exposed to no extra risks from neck flexion or extension during surgery.

Analysis of Variance↗

Oil-on-water: proposed method for intraoperative identification of perilymphatic fistula.

The intraoperative diagnosis of a perilymphatic fistula is usually subjective and controversial. Unless there is profuse gushing of fluid, there is no reliable, objective, intraoperative indicator of a perilymphatic fistula. The authors suggest a technique for the real-time determination of the existence and location of a perilymphatic fistula: visualization of clear perilymphatic fluid beneath a layer of mineral oil. Mineral oil is transparent to visible light, hydrophobic, and lighter than perilymphatic fluid. The oil traps the aqueous fluid, and tends to keep it contained in a droplet. With standard otomicroscopic viewing, a droplet of less than 1 microL of fluid is readily visible through the oil. In vitro temporal bone studies showing the utility and objectivity of identifying the aqueous fluid in the mesotympanum are reported. Mineral oil floats on saline and is readily removed with suction-irrigation techniques. The authors consider the oil-on-water technique to increase the resolution of identifying minute aqueous droplets and recommend in vivo study in patients.

Cochlear Aqueduct↗

Mastoid pneumatization in patients with unilateral aural atresia.

Debate continues regarding theories of the control of temporal bone pneumatization. The "hereditary theory" holds that mastoid size is independent of status of the mesotympanum. The "environmental theory" holds that the size of the mastoid air cell system is determined by the degree of pathological involvement of the middle ear during childhood: that is, an abnormal middle ear prompts a small mastoid. This report concerns the volume of temporal bone pneumatization in patients with unilateral aural atresias, involving a malformed mesotympanum and absence of the external ear canal. Computed tomograms of the temporal bones were available for 16 patients. The mastoid pneumatization volumes of the atretic/non-atretic sides were approximately equal (Spearman's r = 0.80, P < 0.01) but not symmetrical. In 12 patients, the atretic side had less pneumatization than did the non-atretic side; in 3, the atretic side had more pneumatization; and, in 1 patient, neither mastoid had any pneumatization. Such a non-symmetrical pattern is unlikely by chance (P < 0.04). These data can be interpreted to endorse both the hereditary and environmental theories of temporal bone pneumatization.

Adolescent↗

At-risk populations for hearing impairment in infants and young children.

The epidemiologic patterns of childhood hearing loss are ill-defined. Patterns found in prospective observations of newborns in intensive care nurseries are quite different from the patterns apparent in retrospective studies of hearing-impaired children. High-risk registers, at least those prior to the 1990 reformulation, missed about half of children subsequently identified as having hearing loss. Items comprising high-risk registers carry unequal weight. Children with sensorineural hearing loss have a disproportionately increased occurrence of otitis media, with its conductive hearing loss. Sensorineural hearing loss can be progressive. Case-control studies of children with hearing loss are needed. Efforts for the early diagnosis of hearing loss in children must take into practical consideration the uncertainties of available epidemiologic data, and the clinical nuances.

Child↗

Three-dimensional magnetic resonance imaging evaluation of pediatric tracheobronchial tree.

Magnetic resonance imaging (MRI) of the airway has recently emerged as a diagnostic tool for evaluating tracheobronchial obstruction in pediatric patients. Computer-assisted reconstructions of transaxial images have enabled three-dimensional reconstructions of the airway to be manipulated in any plane and visualized in relation to adjacent anatomical structures. Eight patients in whom magnetic resonance imaging was used to diagnose a variety of airway obstructive lesions are presented. A protocol for the evaluation of pediatric tracheobronchial obstruction is presented, with the role of three dimensionally reconstructed MR imaging emphasized.

Airway Obstruction↗

Common congenital anomalies of the neck. Embryology and surgical anatomy.

A good knowledge of embryology and surgical anatomy allows for the anticipation of intraoperative findings, and, hence, for safer and more efficient care of patients with congenital anomalies of the neck. Presumptive thyroglossal anomalies that are at or above the level of the hyoid mandate extra vigilance: the patient may not have sufficient thyroid tissue in the usual thyroid location. The discontinuous character of thyroglossal tracts, related to ontogenesis, ordains dissection to the lingual mucosa. First branchial cleft cysts and fistulas require knowledge of facial nerve anatomy; in some of these cases, the facial nerve is best identified in the temporal bone. Branchial cysts, sinuses, and fistulas only can be assigned to a specific pouch-cleft by their anatomic relations to cervical structures.

Branchial Region↗

Pulmonary drug toxicity in patients with primary breast cancer treated with high-dose combination chemotherapy and autologous bone marrow transplantation.

A protocol consisting of standard-dose adjuvant chemotherapy, high-dose combination alkylating agent chemotherapy, and autologous bone marrow transplant (ABMT) used at our institution for patients with primary breast cancer and extensive axillary lymph node involvement has been associated with a clinical syndrome of pulmonary drug toxicity in 23 of 59 patients (39%). In 10 patients in whom open-lung biopsies or transbronchial lung biopsies were obtained, we correlated the pulmonary pathology with the clinical features of the syndrome. These 10 patients presented with dyspnea, cough, fever, and hypoxemia at a mean time of 48 +/- 14 days after initiation of high-dose chemotherapy. Chest radiographs and CT scans showed interstitial and alveolar opacities. Pulmonary function tests revealed restrictive lung disease and reduced diffusing capacities. Open-lung and transbronchial lung biopsies showed alveolar septal thickening with fibrosis, atypical Type II pneumocytes, and pulmonary endothelial cell injury characteristic of drug toxicity. Corticosteroid therapy resulted in clinical improvement in 7 of 10 patients, but significant pulmonary function abnormalities remained. Local radiation therapy to the chest wall and regional lymph nodes appeared to exacerbate preexisting pulmonary drug toxicity in 4 patients. Two agents in the protocol, cyclophosphamide and carmustine (BCNU), can be implicated in the pathogenesis of this syndrome, and these agents most likely act synergistically to deplete reduced glutathione and impair antioxidant defenses. Since these drugs appear to contribute to the protocol in prolonging disease-free survival, prophylactic therapy of the lung should be investigated to reduce the high incidence of pulmonary toxicity.

Adult↗

Effects of inhibition and induction of cytochrome P-450 isozymes on hyperoxic lung injury in rats.

Pulmonary oxygen toxicity most likely results from excessive production of reactive oxygen species. The role of the cytochromes P-450 in this process is controversial because these enzymes have been reported both to enhance hyperoxic lung injury and to protect from the damaging effects of 100% oxygen. We sought to further determine the role of the cytochromes P-450 in hyperoxic lung injury by inhibiting and inducing pulmonary cytochrome P-450 isozymes in rats. Treatment with the cytochrome P-450 inhibitor cimetidine or 8-methoxypsoralen did not improve survival or reduce lung edema in rats exposed to 100% oxygen. The activity of cytochrome P-450IIB1, the major pulmonary cytochrome P-450 isozyme in rats, was clearly inhibited by 8-methoxypsoralen. beta-Naphthoflavone (beta NF), a selective inducer of cytochrome P-450IA1, was administered in two-dose and five-dose regimens. The two-dose regimen produced significant and sustained induction of cytochrome P-450IA1 activity, but survival in these rats was not improved when exposed to 100% oxygen. In rats treated with five doses of beta NF, a small increase in survival time was found from 71.1 +/- 8.7 to 88.0 +/- 20.2 h; however, there was no difference in the induction of cytochrome P-450IA1 activity between this five-dose regimen and the two-dose regimen. The small improvement in survival after five doses of beta NF is thus unrelated to cytochrome P-450IA1 induction. We conclude that neither inhibition of cytochrome P-450IIB1 activity nor induction of cytochrome P-450IA1 activity protects adult rats against hyperoxic lung injury.

Animals↗

Minuscule submucous cleft palate. Cadaver study.

Otitis media is almost universal in cleft palate patients, at least during infancy. A lesser cleft manifestation, the occult submucous cleft palate, is identifiable in living patients by surgical dissection or flexible fiberoptic nasopharyngoscopy. We addressed the hypothesis that an even more subtle form of submucous cleft palate, involving both an abnormal musculus levator veli palatini and an abnormal musculus uvulae, is associated with otitis media. We studied 35 adult human cadaver specimens for histologic and infrared photographic transillumination evidence of what we have identified as the minuscule submucous cleft palate. None of the specimens had evidence of clinical otitis media, or clinical abnormality of the palate. Approximately one fifth of the specimens had evidence of minuscule submucous cleft palate: minimal bulk of the musculus uvulae and haphazard organization of the fibers of the musculus levator veli palatini. These data support the nasopharyngoscopic inference that in occult submucous cleft palate, there is both hypoplasia of the musculus uvulae and abnormal orientation of the fibers of the musculus levator veli palatini. Although not significant statistically, a trend was suggested for minuscule submucous cleft palate to be associated with indicators of prior otitis media.

Adult↗