Teresa Diez

Dr. Teresa Diez

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 February 2013 in Therapeutic Advances in Psychopharmacology
Verified
Journal Article
Open access
KHKyoko Higashi
Kyoko Higashi
GMGoran Medic
Goran Medic
KLKavi J. Littlewood
Kavi J. Littlewood
TDTeresa Diez
Teresa Diez
OGOla Granström
Ola Granström
MHMarc De Hert
Marc De Hert
Background: Nonadherence to medication is a recognized problem and may be the most challenging aspect of treatment. Methods: We performed a systematic review of factors that influence adherence and the consequences of nonadherence to the patient, healthcare system and society, in patients with schizophrenia. Particular attention was given to the effect of nonadherence on hospitalization rates, as a key driver of increased costs of care. A qualitative systematic literature review was conducted using a broad search strategy using disease and adherence terms. Due to the large number of abstracts identified, article selection was based on studies with larger sample sizes published after 2001. Thirty-seven full papers were included: 15 studies on drivers and 22 on consequences, of which 12 assessed the link between nonadherence and hospitalization. Results: Key drivers of nonadherence included lack of insight, medication beliefs and substance abuse. Key consequences of nonadherence included greater risk of relapse, hospitalization and suicide. Factors positively related to adherence were a good therapeutic relationship with physician and perception of benefits of medication. The most frequently reported driver and consequence were lack of insight and greater risk of hospitalization respectively. Conclusions: Improving adherence in schizophrenia may have a considerable positive impact on patients and society. This can be achieved by focusing on the identified multitude of factors driving nonadherence.

15 January 2005 in The Journal of Clinical Psychiatry
Verified
Journal Article
Closed access
JSJerónimo Saiz-Ruiz
Jerónimo Saiz-Ruiz
CBCarlos Blanco
Carlos Blanco
AIAngela Ibáñez
Angela Ibáñez
XMXavier Masramon
Xavier Masramon
MGMargarita M. Gómez
Margarita M. Gómez
TDTeresa Diez
Teresa Diez
Several open-label and double-blind studies have suggested that selective serotonin reuptake inhibitors may be useful in the treatment of pathological gambling. The purpose of this study was to evaluate the efficacy of sertraline in the treatment of pathological gambling. Sixty patients meeting the DSM-IV criteria for pathological gambling were treated for 6 months in a double-blind, flexible-dose, placebo-controlled study of sertraline 50 to 150 mg/day. Data were collected from November 1998 to January 2001. The primary outcome measure assessing change in clinical status was the responder rate with respect to the Criteria for Control of Pathological Gambling Questionnaire (CCPGQ). Secondary measures included the Clinical Global Impressions scale (CGI) (Severity of Illness and Improvement subscales), and Visual Analogue Scales assessing gambling frequency, severity, amount, and improvement. Concomitant medication and psychotherapy were not allowed during the study. At the end of the study, 23 sertraline-treated subjects (74%) and 21 placebo-treated subjects (72%) were considered as responders on the CCPGQ (p = .9). Similar results were obtained when the CGI-Improvement scale limited to symptoms of pathological gambling was used as an outcome measure. Sertraline was well tolerated throughout the study. Sertraline was not statistically significantly superior to placebo in the overall sample. The power of the study was limited by the high placebo-response rate and the small sample size.

1 February 2008 in Schizophrenia Research
Verified
Journal Article
Closed access
OPOscar Pino
Oscar Pino
GGGeorgina Guilera
Georgina Guilera
JRJ. Emilio Rojo
J. Emilio Rojo
JGJuana Gómez-Benito
Juana Gómez-Benito
MBMiquel Bernardo
Miquel Bernardo
JRJavier Rejas
Javier Rejas

1 February 2012 in Comprehensive Psychiatry
Verified
Journal Article
Closed access
SMSusana Majadas
Susana Majadas
JOJose Olivares
Jose Olivares
JGJaime Galan
Jaime Galan
TDTeresa Diez
Teresa Diez

1 January 2013 in Neuropsychiatric Disease and Treatment
Verified
Journal Article
Open access
PDF file
GMGoran Medic
Goran Medic
KHKyoko Higashi
Kyoko Higashi
KLKavi J Littlewood
Kavi J Littlewood
TDTeresa Diez
Teresa Diez
OGOla Granström
Ola Granström
RKRené S Kahn
René S Kahn
Background: The purpose of this study was to investigate the impact of dosing frequency on adherence in severe chronic psychiatric and neurological diseases. Methods: A systematic literature review was conducted for articles in English from medical databases. Diseases were schizophrenia, psychosis, epilepsy, bipolar disorder, and major depressive disorder. Results: Of 1420 abstracts screened, 12 studies were included. Adherence measures included Medication Event Monitoring System (MEMS®), medication possession ratio, medication persistence, and refill adherence. Three schizophrenia and one epilepsy study used MEMS, and all showed a trend towards higher adherence rates with less frequent dosing regimens. Three depression and one schizophrenia study used the medication possession ratio; the pooled odds ratio of being adherent was 89% higher (ie, 1.89, 95% credibility limits 1.71–2.09) on once-daily versus twice-daily dosing. Two studies in depression and one in all bupropion patients assessed medication persistence and refill adherence. The pooled odds ratio for the two depression studies using medication persistence was 2.10 (95% credibility limits 1.86–2.37) for once-daily versus twice-daily dosing. For refill adherence after 9 months, 65%–75% of patients on once-daily versus 56% on twice-daily dosing had at least one refill. In all but one of the studies using other measures of adherence, adherence rates were higher with once-daily dosing compared with more frequent dosing regimens. No relevant studies were identified for bipolar disorder or psychosis. Conclusion: Differences in study design and adherence measures used across the studies were too large to allow pooling of all results. Despite these differences, there was a consistent trend of better adherence with less frequent dosing.

1 April 2009 in Health and Quality of Life Outcomes
Verified
Journal Article
Open access
PDF file
GGGeorgina Guilera
Georgina Guilera
OPOscar Pino
Oscar Pino
JGJuana Gómez-Benito
Juana Gómez-Benito
JRJ Emilio Rojo
J Emilio Rojo
Eduard VietaEduard Vieta
Eduard Vieta
TFthe Spanish Working Group in Cognitive Function
the Spanish Working Group in Cognitive Function
Background: The relevance of persistent cognitive deficits to the pathogenesis and prognosis of bipolar disorders (BD) is understudied, and its translation into clinical practice has been limited by the absence of brief methods assessing cognitive status in Psychiatry. This investigation assessed the psychometric properties of the Spanish version of the Screen for Cognitive Impairment in Psychiatry (SCIP-S) for the detection of cognitive impairment in BD. Methods: After short training, psychiatrists at 40 outpatient clinics administered the SCIP three times over two weeks to a total of 76 consecutive type I BD admissions. Experienced psychologists also administered a comprehensive battery of standard neuropsychological instruments to clinical sample and 45 healthy control subjects. Results: Feasibility was supported by a brief administration time (approximately 15 minutes) and minimal scoring errors. The reliability of the SCIP was confirmed by good equivalence of forms, acceptable stability (ICC range 0.59 to 0.87) and adequate internal consistency (Chronbach's alpha of 0.74). Construct validity was granted by extraction of a single factor (accounting 52% of the variance), acceptable correlations with conventional neuropsychological instruments, and a clear differentiation between bipolar I and normal samples. Efficiency was also provided by the adequate sensitivity and specificity. Limitations: The sample size is not very large. The SCIP and the neurocognitive battery do not cover all potentially relevant cognitive domains. Also, sensitivity to change remains unexplored. Conclusion: With minimal training, physicians obtained a reliable and valid estimate of cognitive impairment in approximately 15 minutes from an application of the SCIP to type I BD patients.