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Dive into the research topics where Sean Phipps is active.

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Featured researches published by Sean Phipps.


Journal of Consulting and Clinical Psychology | 2005

Using Problem-Solving Skills Training to Reduce Negative Affectivity in Mothers of Children With Newly Diagnosed Cancer: Report of a Multisite Randomized Trial.

Olle Jane Z. Sahler; Diane L. Fairclough; Sean Phipps; Raymond K. Mulhern; Michael J. Dolgin; Robert B. Noll; Ernest R. Katz; James W. Varni; Donna R. Copeland; Robert W. Butler

Mothers of children with cancer experience significant distress associated with their childrens diagnosis and treatment. The efficacy of problem-solving skills training (PSST), a cognitive-behavioral intervention based on problem-solving therapy, was assessed among 430 English- and Spanish-speaking mothers of recently diagnosed patients. Participants were randomized to usual psychosocial care (UPC; n=213) or UPC plus 8 sessions of PSST (PSST; n=217). Compared with UPC mothers, PSST mothers reported significantly enhanced problem-solving skills and significantly decreased negative affectivity. Although effects were largest immediately after PSST, several differences in problem-solving skills and distress levels persisted to the 3-month follow-up. In general, efficacy for Spanish-speaking mothers exceeded that for English-speaking mothers. Findings also suggest young, single mothers profit most from PSST.


Journal of Clinical Oncology | 2000

Late Effects of Treatment in Survivors of Childhood Acute Myeloid Leukemia

Wing Leung; Melissa M. Hudson; Donald K Strickland; Sean Phipps; Deo Kumar Srivastava; Raul C. Ribeiro; Jeffrey E. Rubnitz; John T. Sandlund; Larry E. Kun; Laura C. Bowman; Bassem I. Razzouk; Prasad Mathew; Patricia Shearer; William E. Evans; Ching-Hon Pui

PURPOSE To investigate the incidence of and risk factors for late sequelae of treatment in patients who survived for more than 10 years after the diagnosis of childhood acute myeloid leukemia (AML). PATIENTS AND METHODS Of 77 survivors (median follow-up duration, 16. 7 years), 44 (group A) had received chemotherapy, 18 (group B) had received chemotherapy and cranial irradiation, and 15 (group C) had received chemotherapy, total-body irradiation, and allogeneic bone marrow transplantation. Late complications, tobacco use, and health insurance status were assessed. RESULTS Growth abnormalities were found in 51% of survivors, neurocognitive abnormalities in 30%, transfusion-acquired hepatitis in 28%, endocrine abnormalities in 16%, cataracts in 12%, and cardiac abnormalities in 8%. Younger age at the time of diagnosis or initiation of radiation therapy, higher dose of radiation, and treatment in groups B and C were risk factors for the development of academic difficulties and greater decrease in height Z: score. In addition, treatment in group C was a risk factor for a greater decrease in weight Z: score and the development of growth-hormone deficiency, hypothyroidism, hypogonadism, infertility, and cataracts. The estimated cumulative risk of a second malignancy at 20 years after diagnosis was 1.8% (95% confidence interval, 0.3% to 11.8%). Twenty-two patients (29%) were smokers, and 11 (14%) had no medical insurance at the time of last follow-up. CONCLUSION Late sequelae are common in long-term survivors of childhood AML. Our findings should be useful in defining areas for surveillance of and intervention for late sequelae and in assessing the risk of individual late effects on the basis of age and history of treatment.


Cancer | 2006

Assessment of health-related quality of life in children with cancer : Consistency and agreement between parent and child reports

Kathryn M. W. Russell; Melissa M. Hudson; B A Alanna Long; Sean Phipps

In pediatric settings, measures of health‐related quality of life (HRQL) are often obtained by proxy, especially from parents, but the correlation between parental report and patient report has not been clearly established. In the current study, the authors examined the agreement between child and parent reports of HRQL in children with cancer (both those receiving treatment and those off treatment) and healthy controls.


Journal of Developmental and Behavioral Pediatrics | 2002

Problem-solving skills training for mothers of children with newly diagnosed cancer: a randomized trial.

Olle Jane Z. Sahler; James W. Varni; Diane L. Fairclough; Robert W. Butler; Robert B. Noll; Michael J. Dolgin; Sean Phipps; Donna R. Copeland; Ernest R. Katz; Raymond K. Mulhern

ABSTRACT. Mothers of children with serious illnesses have lower levels of well-being than mothers in the general population. Problem-solving therapy (PST), a cognitive-behavioral intervention, has been shown to be effective in treating negative affectivity (depression, anxiety) and other manifestations of reduced well-being. This report describes a problem-solving skills training (PSST) intervention, based on problem-solving therapy, for mothers of newly diagnosed pediatric cancer patients. Ninety-two mothers were randomly assigned to receive PSST or to receive standard psychosocial care (Control Group). After the 8-week intervention, mothers in the PSST Group had significantly enhanced problem-solving skills and significantly decreased negative affectivity compared with controls. Analysis revealed that changes in self-reports of problem-solving behaviors accounted for 40% of the difference in mood scores between the two groups. Interestingly, PSST had the greatest impact on improving constructive problem solving, whereas improvement in mood was most influenced by decreases in dysfunctional problem solving. The implications of these findings for refinement of the PSST intervention and for extension to other groups of children with serious illnesses are discussed.


Journal of Clinical Oncology | 2000

Cognitive and Academic Functioning in Survivors of Pediatric Bone Marrow Transplantation

Sean Phipps; Maggi Dunavant; Deo Kumar Srivastava; Laura C. Bowman; Raymond K. Mulhern

PURPOSE To evaluate cognitive and academic functioning in survivors of pediatric bone marrow transplants (BMTs) at 1 and 3 years after a BMT. PATIENTS AND METHODS In a prospective, longitudinal design, patients underwent a comprehensive battery of neurocognitive measures before admission for transplantation and at 1, 3, and 5 years after a BMT. This article describes a cohort of 102 survivors with follow-up data available for 1 year after a BMT, including 54 survivors with follow-up available for 3 years. This represents the largest cohort of pediatric BMT survivors yet reported in a prospective study. RESULTS In the cohort as a whole, there were no significant changes on global measures of intelligence (intelligence quotient [IQ]) and academic achievement at either 1 or 3 years after a BMT, despite adequate power to detect an IQ change of three points or greater. Likewise, performance on specific tests of neuropsychologic function remained stable. No significant differences were observed between patients whose conditioning regimen included total-body irradiation (TBI) and those whose did not. The primary predictor of neurocognitive outcome was patient age, with younger patients more likely to show declines over time. The subset of patients who were less than 3 years of age at the time of transplantation seemed to be particularly vulnerable to cognitive sequelae. CONCLUSION The use of BMTs with or without TBI entails minimal risk of late neurocognitive sequelae in patients who are 6 years of age or older at the time of transplantation. However, patients who are less than 6 years of age at the time of transplantation, and particularly those less than 3 years of age, seem to be at some risk of cognitive declines.


Pediatric Blood & Cancer | 2005

Symptoms of post-traumatic stress in children with cancer and their parents: Effects of informant and time from diagnosis

Sean Phipps; Alanna Long; Melissa M. Hudson; Shesh N. Rai

Post‐traumatic stress disorder (PTSD) has been put forth as a model for understanding the adjustment of children with cancer and their parents, but findings in the literature regarding the prevalence of post‐traumatic stress symptoms (PTSS) have been mixed. This study examined PTSS levels in both patients and parents as a function of time elapsed from diagnosis, and by use of parent versus child reports for assessing patient PTSS.


Psychosomatic Medicine | 2002

Repressive adaptive style in children with chronic illness

Sean Phipps; Ric G. Steele

Objective The primary objectives of this study were 1) To assess whether previously reported findings of high levels of repressive adaptation in children with cancer are unique to the cancer population or are generally characteristic of children with serious chronic illness and 2) to assess the utility of including a new measure of anger expression in the adaptive style measurement paradigm. Methods Measures of defensiveness, trait anxiety, and anger expression were obtained from three groups of children: those with cancer (N = 130), those with chronic illnesses (diabetes, cystic fibrosis, and juvenile rheumatoid disorders;N = 121), and healthy control participants (N = 368). Based on their self-reports, participants were categorized according to the adaptive style paradigm as either high anxious, low anxious, defensive high anxious, or repressor. The prevalence of these categories was compared across groups. Results Children in the cancer and chronic illness groups both reported significantly higher levels of defensiveness and lower levels of anxiety than did the healthy control participants. Application of the adaptive style paradigm produced a significantly higher percentage of children identified as repressors in the both cancer and chronic illness groups relative to healthy children. Children classified as repressors also reported significantly less expression of anger than did nonrepressors. Conclusions An increased prevalence of repressive adaptation is not unique to children with cancer, but may be generally characteristic of children with serious chronic illness. Use of anger in place of anxiety as the repressed affect produced a similar distribution of adaptive styles in the study populations.


International Journal of Cancer | 1999

Assessment of health-related quality of life in acute in-patient settings: use of the BASES instrument in children undergoing bone marrow transplantation.

Sean Phipps; Maggi Dunavant; Deepthi Jayawardene; Deo Kumar Srivastiva

The Behavioral, Affective and Somatic Experiences Scale (BASES) represents a set of tools for assessing aspects of health‐related quality of life (HRQL) in patients undergoing active, intensive therapy. Separate versions have been developed for parent, nurse and patient reports. The scales were constructed to be sensitive to change and appropriate for repeated measures in longitudinal designs. We report preliminary results with these measures from a sample of 105 children undergoing bone marrow transplantation (BMT). Adequate reliability of the instruments is documented through measures of both internal consistency and cross‐informant consistency. Several analyses provide evidence of the clinical validity of the measures. Repeated‐measures ANOVAs indicated reliable patterns of change over time, with trajectories that conformed to a priori predictions. Discriminative validity was demonstrated through detection of significant differences in the predicted direction between patients undergoing allogeneic and autologous BMT. Additional evidence for validity comes from the very similar symptom trajectories in parent, nurse and patient reports. Differences between the BASES and other measures of HRQL are identified and alternative uses of the instruments are discussed. Int. J. Cancer Suppl. 12:18–24, 1999. ©1999 Wiley‐Liss, Inc.


Medicine | 2007

A prospective cohort study of late sequelae of pediatric allogeneic hematopoietic stem cell transplantation.

Wing Kwan Leung; Hyunah Ahn; Susan R. Rose; Sean Phipps; Teresa Smith; Kwan Gan; Madeline O'Connor; Gregory A. Hale; Kimberly A. Kasow; Raymond C. Barfield; Renee Madden; Ching-Hon Pui

As survivors of pediatric allogeneic hematopoietic stem cell transplantations (HSCTs) increase in number, it is increasingly important to evaluate their well-being. We conducted this prospective cohort study to evaluate the cumulative incidence and risk factors for late sequelae of HSCT. Comprehensive surveillance tests were performed annually on every participant, regardless of signs and symptoms, to obtain accurate information on the time-of-onset of each late event to allow hazard function analyses. All participants included in this report had been followed for at least 3 years after HSCT. With a median follow-up of 9 years and a current age of 18.5 years, only 20 of the 155 participants (13%) had no late sequelae; 18 survivors (12%) had 1 chronic health condition, 71 (46%) had 2-4 conditions, and 46 (30%) had 5-9 conditions. Risk factors for increasing number of chronic conditions included young age at the time of HSCT, female sex, high radiation dose, and history of chronic graft-versus-host disease. The cumulative incidence at 10 years for common late events was as follows (ordered by the median time-of-onset): osteonecrosis 13.8%, chronic renal insufficiency 26.8%, hypothyroidism 45.1%, growth hormone deficiency 31.2%, female hypogonadism 57.4%, osteopenia 47.7%, cataracts 43.4%, pulmonary dysfunction 63.2%, and male hypogonadism 20.3%. Coexistence of multiple late sequelae was common in HSCT survivors. Our findings provide a basis for more effective patient counseling, optimal surveillance, and early intervention. Abbreviations: ACTH = adrenocorticotropin, CI = confidence intervals, DLCO = diffusing capacity of carbon monoxide, FEV1 = forced expiratory volume in 1 second, FSH = follicle-stimulating hormone, FT4 = free thyroxine, FVC = forced vital capacity, GVHD = graft-versus-host disease, HSCTs = hematopoietic stem cell transplantations, IGFBP3 = insulin-like growth factor binding protein-3, LH = luteinizing hormone, OR = odds ratio, PFT = pulmonary function test, TBI = total body irradiation, TLC = total lung capacity, TSH = thyroid stimulating hormone.


Psycho-oncology | 2012

Perceived Positive Impact of Cancer Among Long-term Survivors of Childhood Cancer: a report from the Childhood Cancer Survivor Study

Brad Zebrack; Margaret L. Stuber; Kathleen Meeske; Sean Phipps; Kevin R. Krull; Qi Liu; Yutaka Yasui; Carla Parry; Rachel Hamilton; Leslie L. Robison; Lonnie K. Zeltzer

Investigations examining psychosocial adjustment among childhood cancer survivors have focused primarily on negative effects and psychopathology. Emergent literature suggests the existence of positive impact or adjustment experienced after cancer, as well. The purpose of this study is to examine the distribution of Perceived Positive Impact (PPI) and its correlates in young adult survivors of childhood cancer.

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Alanna Long

St. Jude Children's Research Hospital

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Robert B. Noll

University of Pittsburgh

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Ernest R. Katz

University of Southern California

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Shesh N. Rai

University Of Tennessee System

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Victoria W. Willard

St. Jude Children's Research Hospital

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Diane L. Fairclough

University of Colorado Denver

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Raymond K. Mulhern

St. Jude Children's Research Hospital

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Alanna M. Long

St. Jude Children's Research Hospital

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