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1.
Tijdschr Psychiatr ; 63(1): 70-73, 2021.
Artículo en Holandés | MEDLINE | ID: mdl-33537977

RESUMEN

A 61-year-old woman with suspected schizophrenia has been attending an outpatient geriatrics service for some time, initially with memory complaints and panic attacks. During treatment, the diagnosis schizophrenia was rejected and psychopharmaceuticals were largely phased out, which improved cognitive functions. Eventually, flashbacks of incest experienced in childhood remained together with REM sleep pathology. The flashbacks, nightmares and the REM sleep pathology were responsive to rivastigmine. Rivastigmine use for the treatment of REM sleep pathology is known in the literature, but it has never been described previously that rivastigmine also impacts on flashbacks and nightmares..


Asunto(s)
Sueños/efectos de los fármacos , Alucinaciones/tratamiento farmacológico , Incesto/psicología , Rivastigmina/uso terapéutico , Trastornos del Sueño-Vigilia/tratamiento farmacológico , Sueño REM/efectos de los fármacos , Femenino , Alucinaciones/psicología , Humanos , Persona de Mediana Edad , Trastorno de Pánico/etiología , Trastorno de Pánico/psicología , Sueño REM/fisiología , Resultado del Tratamiento
2.
Tijdschr Gerontol Geriatr ; 42(6): 256-62, 2011 Dec.
Artículo en Holandés | MEDLINE | ID: mdl-22250368

RESUMEN

AIM: To identify geriatric patients' and their surrogate decision makers' experience with regard to discussing cardio pulmonary resuscitation (CPR) policy. METHODS: This is a prospective, observational, explorative survey. During 10 weeks, all patients admitted to a geriatric ward of a general Dutch hospital or their representatives were asked for their experience regarding discussion of the resuscitation policy with the physician in attendance. Discussing this policy is a standard procedure at the first day of admission. We also asked on several factors which could influence their experience and on factors to improve discussing resuscitation policies. The primary outcome was the participant's satisfaction expressed on a scale of 1 to l0 regarding satisfaction with the CPR discussion. RESULTS: Seventy-six participants were included, of which 29 patients and 47 surrogate decision makers. Discussing the resuscitation policy took an average of 4,5 minutes (SD 3.2) to complete. In 70% (n=53) of cases a do-not-resuscitate decision was made. Discussing the resuscitation policy was experienced positive, with an average rate of 7,8 (SD 1.5). A total of 121 positive comments were made, as opposed to 70 negative comments. When they talked about their resuscitation policy, most patients expressed positive emotional responses. As most important improvements were mentioned: a better introduction to discussing this subject (17%), a better explanation of resuscitation and chances of survival (17%) and providing information prior to admission to the ward, so that patient and surrogate decision maker have been informed that the resuscitation policy will be discussed (12%). CONCLUSION: Most patients and relatives in this study wished to discuss their resuscitation policy with physicians. Still, there is room for improvement in several respects. Patients and surrogate decision makers are in favour of discussing the standard resuscitation policy with the doctor, and evaluate this conversation with a 7.8 / 10. In order to improve both discussing the CPR policy preparing the patient and his representatives and communicating more extensively during the interview are recommended.


Asunto(s)
Reanimación Cardiopulmonar/psicología , Toma de Decisiones , Geriatría/métodos , Relaciones Médico-Paciente , Órdenes de Resucitación/psicología , Anciano , Anciano de 80 o más Años , Comunicación , Femenino , Geriatría/normas , Humanos , Masculino , Países Bajos , Estudios Prospectivos
3.
Tijdschr Gerontol Geriatr ; 41(3): 146-50, 2010 Jun.
Artículo en Holandés | MEDLINE | ID: mdl-20593742

RESUMEN

OBJECTIVES: Since January 2008 in The Netherlands, two cholinesterase inhibitors, oral galantamine and rivastigmine transdermal patch, are registered as a one-day symptomatic treatment for Alzheimer's disease. As no head to head study was performed yet, the objective of this study was to describe the daily practice of oral galantamine and rivastigmine transdermal patch in a real life population of a memory clinic of a suburban teaching hospital in The Netherlands. METHODS: A randomized open label study in 84 ambulant Alzheimer's patients with at least 6 months follow-up and treated either with oral galantamine (group G) or rivastigmine transdermal patch (group R). Data collection included patients' demographic and disease variables. Adverse events were collected and, in case of interruption of the primary treatment, the alternative treatment was registered. RESULTS: Serious adverse events did not occur. In group G respectively group R adverse events occurred in 20 patients (50%) and 18 patients (41%). No difference occurred in the frequency of nausea or vomiting. In group R more patients noted dermatological adverse events. In group G respectively group R medication was stopped in 12 patients (30%) and 14 patients (32%). However, compared to group G after stopping the treatment in group R more patients received a new anti-dementia medication (respectively 11 patients (79%) and 4 patients (33%)) (chi2(1) = 5.418, p = .026). CONCLUSION: Despite different forms, the use of oral galantamine and rivastigmine transdermal patch showed neither difference in the frequency of adverse events neither in the frequency of stopping primary treatment. However, compared to oral galantamine use, rivastigmine transdermal patch resulted in more dermatological adverse events and after stopping rivastigmine transdermal patch, new anti-dementia medication or form was more often started. More research is urgently needed.


Asunto(s)
Enfermedad de Alzheimer/tratamiento farmacológico , Inhibidores de la Colinesterasa/uso terapéutico , Galantamina/uso terapéutico , Fenilcarbamatos/uso terapéutico , Administración Cutánea , Administración Oral , Anciano , Anciano de 80 o más Años , Inhibidores de la Colinesterasa/administración & dosificación , Inhibidores de la Colinesterasa/efectos adversos , Femenino , Galantamina/administración & dosificación , Galantamina/efectos adversos , Humanos , Masculino , Memoria/efectos de los fármacos , Persona de Mediana Edad , Fenilcarbamatos/administración & dosificación , Fenilcarbamatos/efectos adversos , Rivastigmina , Resultado del Tratamiento
4.
Tijdschr Gerontol Geriatr ; 41(6): 231-40, 2010 Dec.
Artículo en Holandés | MEDLINE | ID: mdl-21229776

RESUMEN

OBJECTIVE: The MoCA is a new screening test to detect Mild Cognitive Impairment (MCI). Purpose of this study is validating the Dutch version (MoCA-D). METHOD: We administered the MoCA-D to healthy control subjects and to elderly with MCI or dementia from a memory disorder outpatient clinic and a geriatric (outpatient) clinic (n = 30, 32, 37 respectively, age > or = 60). Neuropsychological testing was part of the standard procedure for patients to diagnose MCI. Sensitivity, specificity and predictive values (positive: PPV and negative: NPV) of the MoCA-D were assessed. RESULTS: A significant effect of group was found on MoCA-D total score (F (2.95) =67.9; p < 0.01). With a cutoff score of < or = 25, sensitivity and specificity to detect MCI in relation to healthy controls were 72% and 73%, respectively. PPV and NPV were 84% and 56%, respectively. With a cut-off score of < or = 20, sensitivity to detect dementia in relation to MCI was 100% for severe dementia and 75% for mild dementia. Specificity for dementia was 81%, PPV 94% and NPV 55%. CONCLUSION: The MoCA-D distinguishes between healthy elderly, MCI patients and dementia patients. However, in this study, insufficient sensitivity and poor specificity were found. For the present, applying a broader and flexible screening procedure in order to detect MCI seems a more useful method than the interpretation of one test result in particular.


Asunto(s)
Trastornos del Conocimiento/diagnóstico , Evaluación Geriátrica , Encuestas y Cuestionarios/normas , Anciano , Estudios de Casos y Controles , Trastornos del Conocimiento/epidemiología , Femenino , Humanos , Masculino , Países Bajos , Valor Predictivo de las Pruebas , Prevalencia , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Índice de Severidad de la Enfermedad , Traducciones
5.
Tijdschr Gerontol Geriatr ; 40(3): 133-7, 2009 Jun.
Artículo en Holandés | MEDLINE | ID: mdl-19731749

RESUMEN

Progressive supranucleair palsy (PSP) is a serious neurologic disease which is seldom diagnosed due to its complexity. In 1996 international diagnostic criteria were developed by a group of experts, the diagnosis remains complicated. We describe three cases, which were followed in the period 2001-2008. In these case reports we elaborate on the therapeutic use of rivastigmine. During off-label rivastigmine use, patients showed minimal further cognitive decline, specifically with respect to frontal defects. However, larger studies and trials are necessary to explore the effects of rivastigmine in patients with PSP.


Asunto(s)
Inhibidores de la Colinesterasa/uso terapéutico , Fenilcarbamatos/uso terapéutico , Parálisis Supranuclear Progresiva/tratamiento farmacológico , Anciano , Trastornos del Conocimiento/etiología , Trastornos de Deglución/etiología , Diagnóstico Diferencial , Resultado Fatal , Femenino , Humanos , Masculino , Persona de Mediana Edad , Rivastigmina , Parálisis Supranuclear Progresiva/diagnóstico , Parálisis Supranuclear Progresiva/fisiopatología , Resultado del Tratamiento
6.
Tijdschr Gerontol Geriatr ; 40(1): 24-8, 2009 Feb.
Artículo en Holandés | MEDLINE | ID: mdl-19326699

RESUMEN

PURPOSE: This study aimed to examine a triage system for non-urgent ambulant frail elderly. METHODS: Three months prospective evaluation of patients, admitted for an out-hospital evaluation on a geriatric ward of an non-academic teaching hospital and not suitable for a memory clinic or falls clinic. A maximum of four patients entered the triage system at the same moment and a nurse and a physiotherapist investigated these patients separately during 30 minutes in total. After these investigations, triage consensus was reached and immediately thereafter, 2 patients were admitted to a fall clinic, 1 patient was admitted to a consultant and 1 patient was admitted to a resident. For each admission, there were positive and negative reasons defined. RESULTS: During 22 moments of triage, 68 patients were admitted to the different out-hospital evaluations. In 90% positive reasons for triage were used. CONCLUSIONS: A triage system for non-urgent ambulant frail elderly seems to be effective. However, more research is needed.


Asunto(s)
Anciano Frágil , Evaluación Geriátrica , Admisión del Paciente , Triaje/organización & administración , Accidentes por Caídas/estadística & datos numéricos , Actividades Cotidianas , Anciano , Anciano de 80 o más Años , Trastornos del Conocimiento/terapia , Toma de Decisiones , Femenino , Necesidades y Demandas de Servicios de Salud , Humanos , Masculino , Selección de Paciente , Estudios Prospectivos
7.
Tijdschr Gerontol Geriatr ; 40(4): 168-72, 2009 Sep.
Artículo en Holandés | MEDLINE | ID: mdl-20088343

RESUMEN

Dementia with Lewy Bodies (DLB) is a well-described clinical entity. DLB patients can be treated with acetylcholinesterase inhibitors (AChEI's). However, should we also treat patients who have but part of the symptoms and who are currently described as MCI-DLB? Will these MCI-DLB patients benefit from AChEI's in terms of direct effect on cognition and behaviour and final outcome? Two cases are presented to demonstrate the clinical features of MCI-DLB and the effect of treatment with rivastigmine (AChEI). The discussion then focuses on the possible value of diagnosing MCI-DLB and if this diagnosis should result in a different medication treatment than the diagnosis MCI-AD, for which AChEI medication is not recommended.


Asunto(s)
Inhibidores de la Colinesterasa/uso terapéutico , Enfermedad por Cuerpos de Lewy/diagnóstico , Enfermedad por Cuerpos de Lewy/tratamiento farmacológico , Fenilcarbamatos/uso terapéutico , Anciano de 80 o más Años , Diagnóstico Precoz , Femenino , Humanos , Pronóstico , Rivastigmina , Resultado del Tratamiento
8.
Neth J Med ; 77(3): 109-115, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-31012428

RESUMEN

BACKGROUND: The seasonal influenza epidemic poses a significant burden on hospitals, both in terms of capacity and costs. Beds that are occupied by isolated influenza patients result in hospitals temporary being closed to admissions and elective operations being cancelled. Improving hospital and emergency department (ED) patient flow during the influenza season could solve these problems. Microbiological point-of-care-testing (POCT) could reduce unnecessary patient isolation by providing a positive/negative result before admission, but has not yet broadly been implemented. METHODS: A clinical pathway for patients with acute respiratory tract infection presenting at the ED was implemented, including a PCR-based POCT for influenza, operated by nurses and receptionists. In parallel, a temporary ward equipped with 15 beds for influenza-positive patients was established. In this retrospective observational study, we describe the results of implementing this pathway by comparison with the previous epidemic. RESULTS: Clinical performance of the POCT within the clinical pathway was good with strongly decreased time from ED presentation to sample collection (194 vs 47 min) and time from sample collection to result (1094 vs 62 min). Hospital patient flow was improved by a decreased percentage of admitted influenza-positive patients (91% vs 73%) and shorter length of subsequent stay (median 5.86 vs 4.61 days) compared to the previous influenza epidemic. In addition, 430 patient-days of unnecessary isolation have been prevented within a time span of 18 weeks. Roughly estimated savings were almost 400,000 euros. CONCLUSION: We recommend that hospitals explore possibilities for improving patient flow during an influenza epidemic.


Asunto(s)
Vías Clínicas/estadística & datos numéricos , Servicio de Urgencia en Hospital/estadística & datos numéricos , Gripe Humana/diagnóstico , Pruebas en el Punto de Atención , Infecciones del Sistema Respiratorio/diagnóstico , Adulto , Anciano , Anciano de 80 o más Años , Epidemias , Femenino , Implementación de Plan de Salud , Hospitalización/estadística & datos numéricos , Humanos , Gripe Humana/epidemiología , Masculino , Persona de Mediana Edad , Países Bajos/epidemiología , Estudios Retrospectivos
9.
Ned Tijdschr Geneeskd ; 151(30): 1681-5, 2007 Jul 28.
Artículo en Holandés | MEDLINE | ID: mdl-17725257

RESUMEN

OBJECTIVE: Inventarisation and evaluation of the incidence, risk factors, and prognosis of postoperative delirium in patients with a fractured hip admitted to a surgical ward. DESIGN: Descriptive study of patient records. METHOD: All patients with a fractured hip admitted to the surgical ward of the Jeroen Bosch Hospital, Den Bosch, the Netherlands, in 2004 were included and evaluated. Active multidisciplinary interventions for the recognition and treatment of delirium by non-pharmacological and pharmacological means take place in this surgical ward. The records of all patients from the surgical and geriatric wards were evaluated and the data were analysed statistically by means of univariate and multivariate logistic 'step-forward' regression analysis. RESULTS: 114 patients were included. The incidence of postoperative delirium was 37%. Older age was a significant risk factor for the development of delirium in both the univariate and the multivariate analysis after correcting for overestimation (p < 0.01). Several other factors, including sex, type of surgery, and medical history, had no effect on the risk of delirium. CONCLUSION: Delirium after a hip fracture is not rare; the most important risk factor is older age.


Asunto(s)
Delirio/epidemiología , Fracturas de Cadera/cirugía , Complicaciones Posoperatorias/epidemiología , Factores de Edad , Anciano , Anciano de 80 o más Años , Femenino , Hospitalización , Humanos , Incidencia , Modelos Logísticos , Masculino , Análisis Multivariante , Países Bajos/epidemiología , Pronóstico , Estudios Retrospectivos , Factores de Riesgo
10.
Tijdschr Gerontol Geriatr ; 37(3): 117-20, 2006 Jul.
Artículo en Holandés | MEDLINE | ID: mdl-16886519

RESUMEN

We report three cases of patients with Parkinson's disease without dementia, admitted to our hospital because of hallucinations. The anti-Parkinson medication was adapted and the patients started with rivastigmine. As a result, hallucinations no longer occurred. A 79 years old man also required short-term quetiapine because of agitation and anti-Parkinson doses were without side effects, as a result of which mobility improved. An 84 years old woman reported mild side effects of rivastigmine, without consequences, whereas her mobility appeared to be good. A 72 years old woman reported mild memory problems upon admission, which improved during admission, as did her mobility after increasing the anti-Parkinson medication doses. Treatment of rivastigmine can be useful in the therapeutic dilemma in the treatment of hallucinations in patients with Parkinson's disease (start anti-psychotic or reduce anti-Parkinson medication). In addition to adapting anti-Parkinson doses and sometimes short-term treating with an anti-psychotic, treatment with rivastigmine appears to be a quick improvement, without serious side effects. Also, mobility can improve, due to the possibility of increasing the anti-Parkinson doses, if necessary. Because of the many remaining questions, prospective randomised trials are needed.


Asunto(s)
Alucinaciones/tratamiento farmacológico , Fármacos Neuroprotectores/uso terapéutico , Enfermedad de Parkinson/complicaciones , Fenilcarbamatos/uso terapéutico , Anciano , Anciano de 80 o más Años , Antiparkinsonianos/uso terapéutico , Relación Dosis-Respuesta a Droga , Femenino , Alucinaciones/etiología , Humanos , Masculino , Fenilcarbamatos/efectos adversos , Rivastigmina , Resultado del Tratamiento
11.
Ned Tijdschr Geneeskd ; 160: D151, 2016.
Artículo en Holandés | MEDLINE | ID: mdl-27438389

RESUMEN

OBJECTIVE: To describe the extent to which the essential changes in the new Dutch delirium guideline for adults and the elderly, published in April 2014, have been incorporated in local hospital protocols, so as to estimate the consequences this could have for patients. DESIGN: Quantitative study. METHOD: Dutch hospital protocols were collected for two periods: before (September to December 2012) and after publication of the guideline (March to July 2015). Protocols were compared with respect to basic delirium care (screening, diagnostic approach, therapy and follow-up care) and organisation of care. RESULTS: Of the 80 Dutch hospitals approached, we were able to include 57 (71%) protocols in this study. 16 hospitals (28%) had adapted their protocols to the new guideline. Screening for the risk of delirium using the questions from the Dutch safety management system (Veiligheidsmanagementsysteem) was described in 29 (51%) of the protocols. Use of the Delirium Observation Screening Scale was reported in 52 (91%) protocols. A policy of moderation regarding antipsychotic therapy was described in 12 of 53 (23%) protocols, but in 21/53 (40%) the haloperidol dosages were higher than advised by the guideline. Follow-up care is described in 40 (70%) of the protocols. Organisation of delirium care, for example restriction of consultation of an expert to complex cases, was advised in 33/57 (58%) protocols. CONCLUSION: 15 months after publication, only just over a quarter of the protocols incorporated the guideline. In terms of the treatment of patients with delirium, this may have led to unnecessary treatment with antipsychotics. Furthermore, basic delirium care is apparently still not considered as the responsibility of every medical specialist in the hospital.


Asunto(s)
Delirio/diagnóstico , Delirio/tratamiento farmacológico , Adhesión a Directriz/estadística & datos numéricos , Guías de Práctica Clínica como Asunto , Antipsicóticos/uso terapéutico , Hospitales , Humanos , Países Bajos
13.
Tijdschr Gerontol Geriatr ; 36(4): 156-163, 2005 Aug.
Artículo en Holandés | MEDLINE | ID: mdl-23203515

RESUMEN

Fear of falling in a fall clinic for geriatric patients: a pilot study Objective. In this pilot study we wantto determine how often fear of falling occurs in geriatric patients visiting a fall clinic and to study the characteristics of fear of falling and its consequences.Design. Retrospective study of patient's records.Method. A random sample of 100 medical records of geriatric patients of the fall clinic of the Jeroen Bosch Ziekenhuis in Den Bosch was systematical examined.Results. The mean age of the patients was 79.8 ± 6 years. Before visiting the fall clinic, the patients had a history of falling during 34.6 months, and 62% of them visited a hospital due to the consequences of falling. In the fall clinic a mean number of 2.5 probable causes per fall was diagnosed.In this study 31% of the patients had fear of falling. The demographic characteristics and the causes of falling of the patients with or without fear of falling, were almost the same. Patients with fear of falling had a hip prothesis in 26%, whereas patients without fear of falling only in 7% had a hip prothesis (P<0.05). In patients with fear of falling, in 90% extra diagnostic investigation was needed, whereas in patients without fear of falling extra diagnostic investigation only occurred in 53% (P<0.01). Finally, patients with fear of falling needed 1.8 more times physical therapy compared to patients without fear of falling (P<0.01).Conclusion. After a fall, fear of falling occurs often in geriatric patients. In this study, no causes for fear of falling could be determinated, although hip prothesis are associated with fear of falling. In patients with fear of falling more medical consumption occurs. In medical practice as in science fear of falling needs more attention.

14.
Tijdschr Gerontol Geriatr ; 36(4): 138-45, 2005 Sep.
Artículo en Holandés | MEDLINE | ID: mdl-16194060

RESUMEN

OBJECTIVE: In this pilot study we want to determine how often fear of falling occurs in geriatric patients visiting a fall clinic and to study the characteristics of fear of falling and its consequences. DESIGN: Retrospective study of patient's records. METHOD: A random sample of 100 medical records of geriatric patients of the fall clinic of the Jeroen Bosch Ziekenhuis in Den Bosch was systematical examined. RESULTS: The mean age of the patients was 79.8 +/- 6 years. Before visiting the fall clinic, the patients had a history of falling during 34.6 months, and 62% of them visited a hospital due to the consequences of falling. In the fall clinic a mean number of 2.5 probable causes per fall was diagnosed. In this study 31% of the patients had fear of falling. The demographic characteristics and the causes of falling of the patients with or without fear of falling, were almost the same. Patients with fear of falling had a hip prothesis in 26%, whereas patients without fear of falling only in 7% had a hip prothesis (P < 0.05). In patients with fear of falling, in 90% extra diagnostic investigation was needed, whereas in patients without fear of falling extra diagnostic investigation only occurred in 53% (P < 0.01). Finally, patients with fear of falling needed 1.8 more times physical therapy compared to patients without fear of falling (P < 0.01). CONCLUSION: After a fall, fear of falling occurs often in geriatric patients. In this study, no causes for fear of falling could be determinated, although hip prothesis are associated with fear of falling. In patients with fear of falling more medical consumption occurs. In medical practice as in science fear of falling needs more attention.


Asunto(s)
Accidentes por Caídas , Miedo/psicología , Prevención de Accidentes , Anciano , Anciano de 80 o más Años , Femenino , Geriatría , Prótesis de Cadera/psicología , Humanos , Masculino , Proyectos Piloto , Estudios Retrospectivos , Factores de Riesgo
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