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Featured researches published by Ingrid H. Valdez.


The New England Journal of Medicine | 1993

Oral Pilocarpine for Post-Irradiation Xerostomia in Patients with Head and Neck Cancer

Jonas T. Johnson; Gerald A. Ferretti; W. James Nethery; Ingrid H. Valdez; Philip C. Fox; David Ng; Muscoplat Cc; Susan C. Gallagher

BACKGROUND AND METHODS We evaluated pilocarpine hydrochloride for the treatment of radiation-induced xerostomia, a common complication of irradiation of the head and neck. A prospective, randomized, double-blind, placebo-controlled trial was undertaken to test the safety and efficacy of pilocarpine, particularly in reversing the decrease in the production of saliva and other manifestations of xerostomia. Patients received either placebo or pilocarpine (5 mg or 10 mg orally three times a day) for 12 weeks and were evaluated at base line and every 4 weeks. RESULTS We studied 207 patients who had each received > or = 4000 cGy of radiation to the head and neck. In the patients receiving the 5-mg dose of pilocarpine, oral dryness improved in 44 percent, as compared with 25 percent of the patients receiving placebo (P = 0.027). There was overall improvement in 54 percent of the 5-mg group as compared with 25 percent of the placebo group (P = 0.003), and 31 percent of the 5-mg group had improved comfort of the mouth and tongue, as compared with 10 percent of the placebo group (P = 0.002). Speaking ability improved in 33 percent of the 5-mg group as compared with 18 percent of the placebo group (P = 0.037). Saliva production was improved, but it did not correlate with symptomatic relief. There were comparable improvements in the group receiving the 10-mg dose. The primary adverse effect was sweating, in addition to other minor cholinergic effects. Six and 29 percent of the patients in the 5-mg and 10-mg groups, respectively, withdrew from the study because of adverse effects. There were no serious adverse effects related to pilocarpine. CONCLUSIONS Pilocarpine improved saliva production and relieved symptoms of xerostomia after irradiation for cancer of the head and neck, with minor side effects that were predominantly limited to sweating.


International Journal of Radiation Oncology Biology Physics | 1993

MAJOR SALIVARY GLAND FUNCTION IN PATIENTS WITH RADIATION- INDUCED XEROSTOMIA: FLOW RATES AND SIALOCHEMISTRY

Ingrid H. Valdez; Jane C. Atkinson; Jonathan A. Ship; Philip C. Fox

Radiation therapy for cancer of the head and neck region often causes salivary gland dysfunction and xerostomia. Several reports suggest that the submandibular/sublingual (SM/SL) glands may be less radiosensitive than the parotid. The purpose of this study was to evaluate differential radiation effects on the major salivary glands. Fifty patients with radiation-induced xerostomia were evaluated (33 males, 17 females; mean age 52.7). The average total tumor dose was 6034 cGy. Major salivary gland function was compared with that of 50 non-irradiated controls. Salivary flow rates included unstimulated and stimulated flows of both the parotid and SM/SL glands. Sialochemical analyses included total protein, lysozyme, lactoferrin, sodium, chloride, and potassium. All four measures of salivary flow were significantly reduced in patients as compared to controls (p = .0001). Like the parotid, submandibular/sublingual gland dysfunction appears to be radiation dose- and field-dependent. Patients in the lowest radiation dose quartile (< or = 5000 cGy) had significantly increased salivary flow compared to those in the highest dose quartile (> or = 6800 cGy; p = .025). Glands that were partially irradiated were more likely to have some residual function than fully irradiated glands (p = .003). Lactoferrin content was increased in parotid saliva of radiation patients (p = .0001). Chloride content was significantly increased also (p = .0001). The SM/SL glands are clearly dysfunctional in post-irradiation xerostomia patients compared to controls, in terms of both flow rates and sialochemistry.


Cancer | 1993

Use of pilocarpine during head and neck radiation therapy to reduce xerostomia and salivary dysfunction.

Ingrid H. Valdez; Andy Wolff; Jane C. Atkinson; Alice A. Macynski; Philip C. Fox

Background. Salivary gland hypofunction commonly develops during radiation therapy to the head and neck region. This study evaluated whether the sialogogue pilocarpine given during radiation therapy may reduce the severity of xerostomia and salivary dysfunction.


Critical Reviews in Oral Biology & Medicine | 1993

Diagnosis and Management of Salivary Dysfunction

Ingrid H. Valdez; Philip C. Fox

Salivary gland dysfunction may occur as a result of common medications, cancer therapy, or Sjögrens syndrome. Affected patients may develop significant oral, dental, and upper gastrointestinal sequelae. This article reviews the basic elements in diagnosis of salivary dysfunction, including initial evaluation and specialized diagnostic procedures. Patient management depends primarily on the severity of salivary dysfunction. More severe permanent forms of dysfunction, such as radiation-induced and Sjögrens syndrome, require long-term care, with preventive measures to maintain the dentition and therapeutic attempts to increase oral fluids.


Digestive Diseases | 1991

Interactions of the Salivary and Gastrointestinal Systems

Ingrid H. Valdez; Philip C. Fox

Salivary gland dysfunction is uniformly detrimental to the oral cavity. Its effects on the GI tract have begun to be explored. Dry mouth is a common complaint among older adults, probably due to systemic disease and its therapy rather than the aging process per se. Evaluation of complaints of dry mouth should include medical history, sialometry and physical examination. Numerous medications can elicit drug-induced xerostomia. Patients who have received radiation therapy to the head and neck region often have permanent radiation-induced xerostomia, which has been linked to esophagitis. SS is an autoimmune systemic exocrinopathy resulting in irreversible salivary gland dysfunction. SS has numerous GI manifestations, including dysphagia, temporal defects of deglutition, esophageal dysmotility, gastritis, pancreatitis and liver disease. Management of salivary hypofunction is directed toward preserving the dentition and improving patient comfort. Drug-induced xerostomia is often correctable by altering the therapeutic modality.


Physiology & Behavior | 1993

Taste intensity performance in patients irradiated to the head and neck

Lisa K. Schwartz; James M. Weiffenbach; Ingrid H. Valdez; Philip C. Fox

Decrements in taste-detection thresholds during radiotherapy and subsequent recovery in the months after therapy are well documented. However, few studies have explored suprathreshold taste intensity perception in radiation patients. This cross-sectional study compared taste function in 15 men postradiation with a group of 23 healthy, nonirradiated male volunteers. A direct-scaling procedure was used to assess taste intensity perception of the four basic taste qualities. Patients performed nearly as well as control subjects on objective measures of suprathreshold functioning. Postradiation intensity judgments of salty (sodium chloride), sweet (sucrose), and bitter (quinine sulfate) solutions were not significantly reduced. Subtle, age-related taste impairments were identified for sour perception (citric acid) postradiotherapy. Younger patients judged citric acid to be more intense than did age-appropriate control subjects, whereas older patients judged it to be less intense. Moreover, younger patients were likely to be midly dysgeusic, whereas older patients appeared to be hypogeusic for citric acid. This study provides evidence for near normal suprathreshold taste intensity perception in patients who have received head and neck irradiation.


Oral Surgery, Oral Medicine, Oral Pathology | 1991

Xeroderma pigmentosum: Review and report of a case

Lauren L. Patton; Ingrid H. Valdez

Xeroderma pigmentosum is a rare inherited dermatosis that provides insight into the basic mechanism of carcinogenesis. It is a model disorder linking defective DNA repair with clinical abnormalities and neoplasia. UV light-induced damage to the skin begins early and results in multiple benign and malignant skin tumors, especially in sun-exposed areas of the head and neck. Oral cancers, primarily squamous cell carcinomas of the anterior third of the tongue, occur with greatly increased frequency. A patient with multiple facial neoplasia and oral manifestations of xeroderma pigmentosum is presented. The role of the dentist in surveillance of oral and perioral structures is emphasized. The dentist is advised against the use of UV light-curing units in these patients because UV-induced epithelial damage may cause dysplasia when DNA repair mechanisms are dysfunctional.


Oral Surgery, Oral Medicine, Oral Pathology | 1990

Premature alveolar bone loss in Erdheim-Chester disease

Ingrid H. Valdez; Ronald W. Katz; William D. Travis

Erdheim-Chester disease is a rare histiocytosis also known as lipoid granulomatosis. Oral findings have not been reported previously to our knowledge. This case report documents evidence of oral sequelae of Erdheim-Chester disease. A patient whose course was followed for 10 years at the National Institutes of Health had premature alveolar bone resorption. He underwent full-mouth extraction at age 29 years because of severe periodontitis. Histopathologic evidence of Erdheim-Chester disease was demonstrated in the periodontal soft tissues. In the ensuring years, accelerated resorption of the residual ridges precluded the use of conventional dentures. We recommend early preventive dental management for patients with Erdheim-Chester disease.


JAMA Internal Medicine | 1991

Pilocarpine Treatment of Salivary Gland Hypofunction and Dry Mouth (Xerostomia)

Philip C. Fox; Jane C. Atkinson; Alice A. Macynski; Andy Wolff; David S. Kung; Ingrid H. Valdez; William L. Jackson; Robert A. Delapenha; Jeffrey Shiroky; Bruce J. Baum


Special Care in Dentistry | 1991

Radiation‐induced salivary dysfunction: clinical course and significance

Ingrid H. Valdez

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Philip C. Fox

Carolinas Medical Center

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Jane C. Atkinson

National Institutes of Health

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Alice A. Macynski

National Institutes of Health

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Andy Wolff

National Institutes of Health

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Lauren L. Patton

National Institutes of Health

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Bruce J. Baum

National Institutes of Health

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David Ng

National Institutes of Health

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James M. Weiffenbach

National Institutes of Health

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Jeffrey Shiroky

National Institutes of Health

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