Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041624.90
J. Patrick, Funck François, Henegariu Viviana, Boireau Amélie, Dagorn Joël, Adalla Dora, B. Michel
Background Chronic Heart failure management is based on ESC recommendations. In most countries, medical therapy is based on a medical examination and despite the improvement of medical therapies; most of CHF patients are not optimally managed. Nurses are more and more implicated in CHF management. Methods We have compared double blind medical prescription of a Heart failure trained Nurse (specific training on CHF, ESC recommendations, BNP use and pathophysiology, patient education) and a heart failure specialised cardiologist in 120 consecutive patients. We focusing on clinical examination, BNP interpretation, treatment evaluation and therapeutic modifications proposed. Results We have included 120 consecutive patients. Mean age was 70.2±5. Mean LVEF was 32±5%. Mean BNP was 230±120 pg/ml NYHA classification was similar in 85% of cases. Treatment evaluation was similar in 89% of the patients and 96% of patients considered as under optimal therapy by the heart failure specialist were identified by the HF nurse. Therapeutic modifications proposed by HF nurse were confirmed by the HF specialist in 85% of the patients. ESC recommendations were followed in 100% of the cases. Differences in prescription between HF nurse and HF specialist are mainly related to spironolactone/Angiotensin II receptor antagonist introduction in addition to ACEI therapy. Conclusion A trained HF nurse could act as first line prescriber in CHF with a low risk profile. Données actuelles La gestion de l'insuffisance cardiaque chronique est basée sur les recommandations de l'ESC. Dans la plupart des pays, le traitement médical repose sur un examen médical et en dépit de l'amélioration des thérapies, la plupart des patients atteints d'ICC ne sont pas géré de façon optimale. Les infirmières sont de plus en plus impliquées dans la gestion de CHF mais ont encore un rôle limité à la prise de cosntantes et de prélèvements. Méthodes Nous avons comparé en double aveugle la prescription médicale d'une infirmière formée spécifiquement à insuffisance cardiaque (formation spécifique sur la maldie, les traitemetns, les bilans et la façon de les interpréter, les recommandations de la société européenne de cardiologie, l'utilisation du BNP et de la physiopathologie, l'éducation des patients) et un cardiologue spécialisé chez 120 patients insuffisants cardiaques consécutifsen nous concentrant sur l'examen clinique, l'interprétation de la BNP, l'évaluation des traitements thérapeutiques et des modifications proposées. Résultats Nous avons inclus 120 patients consécutifs. L'Âge moyen était de 70.2±5. La FEVG moyenne était de 32±5%. Le BNP moyen était de 230±120 pg/ml, la classe NYHA a été similaire dans 85% des cas. Traitement de l'évaluation a été similaire dans 89% des patients et 96% des patients sous traitement considéré comme optimal par le spécialiste en insuffisance cardiaque ont été identifiés comme tels par l'infirmière spécialisée
背景:慢性心力衰竭的管理是基于ESC的建议。在大多数国家,尽管医疗方法有所改进,但医疗仍以医疗检查为基础;大多数慢性心力衰竭患者没有得到最佳治疗。护士越来越多地参与到CHF的管理中。方法:我们比较了一名心衰培训护士(CHF、ESC建议、BNP使用和病理生理学、患者教育方面的专门培训)和一名心衰专科心脏病专家在120例连续患者中的双盲用药处方。我们着重于临床检查、脑钠肽解释、治疗评价和治疗修改建议。结果我们纳入了120例连续患者。平均年龄70.2±5岁。平均LVEF为32±5%。平均BNP为230±120 pg/ml, 85%的病例NYHA分类相似。89%的患者的治疗评价相似,96%的心衰专科医生认为处于最佳治疗状态的患者由心衰护士确定。心衰护理人员提出的治疗方案经心衰专科医生确认为85%的患者。所有病例都遵循了ESC的建议。心衰专科护士与心衰专科医生处方差异主要与ACEI治疗外引入螺旋内酯/血管紧张素II受体拮抗剂有关。结论经过培训的心衰护士可作为心衰患者的一线处方医师,其危险性较低。关于慢性心脏不全症的研究表明,慢性心脏不全症与慢性心脏不全症是一致的。Dans la plupart des pays, le tratrament ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment ment。不确定因素包括不确定因素、不确定因素、不确定因素和不确定因素、不确定因素和不确定因素。方法我们已经比较en双aveugle la处方医学一infirmiere formee specifiquement一insuffisance cardiaque(形成specifique苏尔la maldie les traitemetns les bilans等这样拉·德·莱斯解释器,les recommandations de la法国产品de cardiologie l 'utilisation du BNP et de la physiopathologie,在120例患者中,有1例患者的心血管病病病病,1例患者的心血管病病,1例患者的心血管病病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,1例患者的心血管病,3例患者的心血管病,3例患者的心血管病。该研究包括120名患者。L'Âge moyen samtait de 70.2±5。La FEVG moyenne的比例为32±5%。Le BNP moyen的含量为230±120 pg/ml, la类NYHA的含量为85%。与其他患者相比,有89%的患者和96%的患者认为,与其他患者相比,其他患者认为,与其他患者相比,其他患者认为,与其他患者相比,其他患者认为:与其他患者相比,其他患者认为:与其他患者相比,其他患者认为:与其他患者相比,其他患者认为:与其他患者相比,其他患者认为:修订后的医疗器械和其他医疗器械的医疗器械和其他医疗器械的医疗器械和其他医疗器械的医疗器械的医疗器械和其他医疗器械的医疗器械的医疗器械的医疗器械的医疗器械。[3] [3] [3] [3] [3] [3] [3] [3] [3] [3] [3] [3] [1] [3] [1] [3] [1] [3] [1] [3] [1] [3]结论:1个病状不全的患者,在心脏不全的情况下,不能进行心脏不全的改良,不能进行心脏不全的改良。
{"title":"254 Improving care for congestive heart failure by transfering competency to specialised nurses","authors":"J. Patrick, Funck François, Henegariu Viviana, Boireau Amélie, Dagorn Joël, Adalla Dora, B. Michel","doi":"10.1136/QSHC.2010.041624.90","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041624.90","url":null,"abstract":"Background Chronic Heart failure management is based on ESC recommendations. In most countries, medical therapy is based on a medical examination and despite the improvement of medical therapies; most of CHF patients are not optimally managed. Nurses are more and more implicated in CHF management. Methods We have compared double blind medical prescription of a Heart failure trained Nurse (specific training on CHF, ESC recommendations, BNP use and pathophysiology, patient education) and a heart failure specialised cardiologist in 120 consecutive patients. We focusing on clinical examination, BNP interpretation, treatment evaluation and therapeutic modifications proposed. Results We have included 120 consecutive patients. Mean age was 70.2±5. Mean LVEF was 32±5%. Mean BNP was 230±120 pg/ml NYHA classification was similar in 85% of cases. Treatment evaluation was similar in 89% of the patients and 96% of patients considered as under optimal therapy by the heart failure specialist were identified by the HF nurse. Therapeutic modifications proposed by HF nurse were confirmed by the HF specialist in 85% of the patients. ESC recommendations were followed in 100% of the cases. Differences in prescription between HF nurse and HF specialist are mainly related to spironolactone/Angiotensin II receptor antagonist introduction in addition to ACEI therapy. Conclusion A trained HF nurse could act as first line prescriber in CHF with a low risk profile. Données actuelles La gestion de l'insuffisance cardiaque chronique est basée sur les recommandations de l'ESC. Dans la plupart des pays, le traitement médical repose sur un examen médical et en dépit de l'amélioration des thérapies, la plupart des patients atteints d'ICC ne sont pas géré de façon optimale. Les infirmières sont de plus en plus impliquées dans la gestion de CHF mais ont encore un rôle limité à la prise de cosntantes et de prélèvements. Méthodes Nous avons comparé en double aveugle la prescription médicale d'une infirmière formée spécifiquement à insuffisance cardiaque (formation spécifique sur la maldie, les traitemetns, les bilans et la façon de les interpréter, les recommandations de la société européenne de cardiologie, l'utilisation du BNP et de la physiopathologie, l'éducation des patients) et un cardiologue spécialisé chez 120 patients insuffisants cardiaques consécutifsen nous concentrant sur l'examen clinique, l'interprétation de la BNP, l'évaluation des traitements thérapeutiques et des modifications proposées. Résultats Nous avons inclus 120 patients consécutifs. L'Âge moyen était de 70.2±5. La FEVG moyenne était de 32±5%. Le BNP moyen était de 230±120 pg/ml, la classe NYHA a été similaire dans 85% des cas. Traitement de l'évaluation a été similaire dans 89% des patients et 96% des patients sous traitement considéré comme optimal par le spécialiste en insuffisance cardiaque ont été identifiés comme tels par l'infirmière spécialisée","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"48 1","pages":"A136 - A137"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83505028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041616.12
X. Rébillard, B. Ségui, A. Faix, S. A. Hamid, T. Murez, R. Daniel, N. Riolacci, M. Erbault, A. Desplanques, D. Pierre, P. Coloby
Background and Objectives In France, prostate cancer is the most common cancer in men (71 000 new cases expected in 2009) and the second cause of mortality from cancer (8600 deaths expected in 2009). About 180 000 biopsies are made each year, enabling diagnosis of the disease when still at a localised stage in 70% of cases. Radical prostatectomy (RP) (about 25 000 per year) is a therapeutic option for localised cancer requiring the management of the risk of incomplete tumour excision as well as of postoperative functional morbidity. In 2009, the French Parliamentary Office for the Assessment of Health Policies underscored inconsistencies in prostate cancer management that impact on functional morbidity and mortality. Our objective was to develop clinical practice indicators (CPIs) for inclusion in a computerised clinical pathway to be able to propose improvements in care, whether with regard to diagnostic or therapeutic decisions. Programme The CPIs were based on clinical practice guidelines selected by a panel of urologists and validated by the French Association of Urologists (AFU). The innovative computer system Normind-diagnosis was used to calculate CPI values from patient records. The feasibility and quality of CPI data collection by Normind-diagnosis was validated in an analysis of records from five urology departments and national or regional databases (multidisciplinary review of medical records, the pathology database of CRISAP-LR, the national ABLATHERM registry, and the FRANCIM 2001 cohort). The criteria for assessing the quality and safety of diagnostic and therapeutic care in RP patients were: Quality of the histology report (compliance with the recommendations of the AFU Cancer Committee (CCAFU) and the French Society of Pathology), Correct selection of patients eligible for surgery (D' Amico risk classification, comorbidities) and safety of surgery (transfusion rate), Efficacy in oncological terms (negative surgical margins, undetectable PSA at 3 months), and Detection of postoperative functional morbidity and assessment of quality of life (continence at 1 year, erectile dysfunction at 2 years). Results A total of 545 patients with prostate cancer diagnosed in 2007–2008 benefited from CPI monitoring. The CPIs could be calculated from 89% of patient records: In 2008, 100% of biopsy histology reports complied with CCAFU criteria versus 67% in 2007. The D'Amico prognostic group was determined in 98% of patients. For 185 patients who underwent RP, the decision was completely in line with all good practice criteria in 89% of cases; 1% of patients had transfusions. Surgical margins were negative in 84% of patients; 97% had undetectable PSA at 3 months. 91% of patients were totally continent at 1 year. Data for erectile dysfunction are not available. Discussion and Conclusion This computerised clinical pathway using CPIs is currently being implemented by eight urology teams in three regions in France within the framework of a quality res
背景和目的在法国,前列腺癌是男性中最常见的癌症(2009年预计有71 000个新病例),也是癌症死亡的第二大原因(2009年预计有8600人死亡)。每年进行约18万次活组织检查,在70%的病例中,在仍处于局部阶段时就能诊断出疾病。根治性前列腺切除术(RP)(每年约25,000例)是局部癌症的一种治疗选择,需要控制肿瘤切除不完全的风险以及术后功能发病率。2009年,法国议会卫生政策评估办公室强调了影响功能性发病率和死亡率的前列腺癌管理的不一致性。我们的目标是开发临床实践指标(cpi),以纳入计算机化的临床路径,以便能够提出诊断或治疗决策方面的护理改进。CPIs是基于临床实践指南,由泌尿科医师小组选择,并由法国泌尿科医师协会(AFU)验证。使用创新的计算机系统Normind-diagnosis从患者记录中计算CPI值。通过对五个泌尿科和国家或地区数据库(医疗记录的多学科审查、CRISAP-LR病理数据库、国家ABLATHERM登记和FRANCIM 2001队列)的记录分析,验证了Normind-diagnosis收集CPI数据的可行性和质量。评估RP患者诊断和治疗护理质量和安全性的标准是:组织学报告的质量(符合AFU癌症委员会(CCAFU)和法国病理学会的建议),手术患者的正确选择(D' Amico风险分类,合并症)和手术的安全性(输血率),肿瘤学方面的疗效(手术切界阴性,3个月时未检测到PSA),术后功能并发症的检测和生活质量的评估(1年的尿失禁,1年的尿失禁,1年的尿失禁,3年的尿失禁,3年的尿失禁。勃起功能障碍(2岁)。结果2007-2008年共545例前列腺癌患者受益于CPI监测。cpi可以从89%的患者记录中计算出来:2008年,100%的活检组织学报告符合CCAFU标准,而2007年为67%。在98%的患者中确定了D'Amico预后组。在185例接受RP的患者中,89%的患者的决定完全符合所有良好实践标准;1%的患者接受了输血。84%的患者手术切缘呈阴性;97%的患者3个月时PSA未检出。91%的患者在1年时完全康复。没有关于勃起功能障碍的数据。在质量研究计划(PREQHOS)的框架内,目前法国三个地区的八个泌尿科团队正在实施使用cpi的计算机化临床途径。接受RP治疗的局部癌症患者是前瞻性的。这个实践注册将使团队能够交换经验并观察他们在实践中的趋势。第一批结果预计将于2010年公布。”“背景资料:法国公共前列腺癌调查问卷(2009年1人患前列腺癌,71 000例)和死亡率调查问卷(2009年1人患前列腺癌,8600例)。约18万例活组织检查诊断为有效的恶性肿瘤和浸润性肿瘤诊断,其中70%为恶性肿瘤。前列腺切除术(约2.5万例)是一种治疗癌症的方法,可以治疗局部肿瘤。癌症治疗的效果,疾病治疗的功能,疾病治疗后的疗效,疾病治疗后的疗效,疾病治疗后的疗效,疾病治疗后的适应症,疾病治疗后的疗效,疾病治疗后的疗效,疾病治疗后的适应症,疾病治疗后的疗效。2009年,圣<s:1> <s:1>政治评估议会办公室负责对<s:1>健康与死亡评估委员会职能进行评估。目标-方案:临床化学信息学,包括临床化学指标(IPC)、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标、临床化学指标。我将允许“客观条件下的质量保证”和“客观条件下的质量保证”,并允许“客观条件下的质量保证”和“客观条件下的质量保证”。国际预防犯罪委员会(IPC)发布了关于健康行为的建议,以及关于泌尿科医生小组和有效的泌尿科医生和社会组织的建议。Le systemmes information - atique innovative Normind-diagnosis calle IPC - party - data information structure(信息结构)、(档案)、(医疗)、(患者)。 简编》的可行性和质量Normind-diagnosis cpi由计算机系统已经得到验证,通过分析病历5泌尿和数据库服务的国家或区域协商会议(多学科(RCP) CRISAP-LR的病理基础,国家登记册Ablatherm和队列FRANCIM 2001)。该方法允许根据以下标准客观评估局部癌症诊断和治疗的质量和安全性:组织学研究的质量记录(记录是否符合建议CCAFU)、病理学和法国社会公正选拔合格的病人做手术(' amico, co-morbidités group)和安全输血的手术治疗(率)、carcinologique (d’exérèse负面边际效率和PSA检测不到3个),确定术后功能后遗症和患者的生活质量(1年失禁率,2年勃起功能障碍)。结果对2007 - 2008年确诊的545例前列腺癌患者进行了临床实践指标监测。医疗记录数据允许计算89%患者的cpi,结果如下:2008年,100%的前列腺活检组织学报告符合CCAFU的质量标准,而2007年为67%。98%的患者确定了amico的预后组。在185例前列腺切除术患者中,89%的患者的决定是完整的,并符合良好实践指南的所有标准。1%的人输血。84%的患者的行距为阴性,97%的患者在3个月时PSA检测不到。91%的患者在1岁时完全消失。目前还没有勃起功能障碍的数据。在一项质量研究计划(PREQHOS)的框架内,目前正在法国3个地区的8个泌尿科医生团队中建立基于IPC的计算机临床路径,其中包括前列腺切除术治疗局部癌症的患者。这个练习日志将允许团队交流他们的练习,并对每个练习进行跟踪,以跟踪他们的练习的发展。第一个结果预计将于2010年公布。
{"title":"276 Improving the quality of prostate cancer diagnosis and treatment using shared clinical practice indicators (CPI) and a computerised clinical pathway","authors":"X. Rébillard, B. Ségui, A. Faix, S. A. Hamid, T. Murez, R. Daniel, N. Riolacci, M. Erbault, A. Desplanques, D. Pierre, P. Coloby","doi":"10.1136/QSHC.2010.041616.12","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041616.12","url":null,"abstract":"Background and Objectives In France, prostate cancer is the most common cancer in men (71 000 new cases expected in 2009) and the second cause of mortality from cancer (8600 deaths expected in 2009). About 180 000 biopsies are made each year, enabling diagnosis of the disease when still at a localised stage in 70% of cases. Radical prostatectomy (RP) (about 25 000 per year) is a therapeutic option for localised cancer requiring the management of the risk of incomplete tumour excision as well as of postoperative functional morbidity. In 2009, the French Parliamentary Office for the Assessment of Health Policies underscored inconsistencies in prostate cancer management that impact on functional morbidity and mortality. Our objective was to develop clinical practice indicators (CPIs) for inclusion in a computerised clinical pathway to be able to propose improvements in care, whether with regard to diagnostic or therapeutic decisions. Programme The CPIs were based on clinical practice guidelines selected by a panel of urologists and validated by the French Association of Urologists (AFU). The innovative computer system Normind-diagnosis was used to calculate CPI values from patient records. The feasibility and quality of CPI data collection by Normind-diagnosis was validated in an analysis of records from five urology departments and national or regional databases (multidisciplinary review of medical records, the pathology database of CRISAP-LR, the national ABLATHERM registry, and the FRANCIM 2001 cohort). The criteria for assessing the quality and safety of diagnostic and therapeutic care in RP patients were: Quality of the histology report (compliance with the recommendations of the AFU Cancer Committee (CCAFU) and the French Society of Pathology), Correct selection of patients eligible for surgery (D' Amico risk classification, comorbidities) and safety of surgery (transfusion rate), Efficacy in oncological terms (negative surgical margins, undetectable PSA at 3 months), and Detection of postoperative functional morbidity and assessment of quality of life (continence at 1 year, erectile dysfunction at 2 years). Results A total of 545 patients with prostate cancer diagnosed in 2007–2008 benefited from CPI monitoring. The CPIs could be calculated from 89% of patient records: In 2008, 100% of biopsy histology reports complied with CCAFU criteria versus 67% in 2007. The D'Amico prognostic group was determined in 98% of patients. For 185 patients who underwent RP, the decision was completely in line with all good practice criteria in 89% of cases; 1% of patients had transfusions. Surgical margins were negative in 84% of patients; 97% had undetectable PSA at 3 months. 91% of patients were totally continent at 1 year. Data for erectile dysfunction are not available. Discussion and Conclusion This computerised clinical pathway using CPIs is currently being implemented by eight urology teams in three regions in France within the framework of a quality res","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"1 1","pages":"A35 - A36"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90334289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041624.6
E. Matthieu, L. Carole, C. Jané, Hitoto Hikombo, Mahaza Chetaou, Kempf Marie, Joly-Guillou Marie-Laure
Background, objective After opening hours, the activity of a clinical microbiology laboratory (CML) is usually limited to the inoculation of specimens sent by clinical wards and gram-stain examinations. A continuous functioning (CF) has been implemented for the last 4 years in the CML of Angers teaching hospital. With the CF, in addition to gram-stain examination and inoculations, urine cultures, blood cultures and cultures from certain fluids (ascitis, articular, pleural, perioperative, cerebrospinal) are monitored two or three times every night. In the case of colony growth, bacterial identifications (BI) and susceptibility to antibiotics testing (SAT) are performed. Concurrently to a geographical grouping of our hospital laboratories expected in 2010, the permanence of the CT is questioned. Therefore, our objective was to assess its interest in order to maintain it. Program: description, implementation, follow-up For each specimen for whom a BI and/or SAT were performed by night, the impact of the CF was assessed in terms of decrease in the delays from the time of sampling to the time at which results became available, and in terms of consequences of this decrease for the management of patient antimicrobial treatments. The delays in the absence of CF were estimated by considering the laboratory opening hours in the absence of CF and delays in incubation necessary for BI and SAT. Two major benefits have been defined: the early implementation of an effective treatment (EIET) and the early change to a reduced-spectrum but still efficient regimen (ECRR). The decrease of the delay was either 24 h or 48 h. Results in terms of clinical impact During the 4 months of the study, a BI and/or a SAT were performed for 430 specimens during the night period. An EIET was reported for 97 samples (22.6%), representing a cumulative gain of 111 days. For 49 patients, this EIET corresponded to the modification of an ineffective treatment, and for the 48 others, it corresponded to the implementation of an effective treatment in a patient not treated. An EIET was observed in 37.9% of blood cultures, 20.8% of urine cultures, and 17.9% of fluid cultures concerned by the night activity. An ECRR was reported for 23 samples accounting for 5.4% of overall specimens and representing 29 days of treatment. Among the nine wards for which the CF was the most profitable in terms of EIET, there were seven medical and two surgical wards. Therefore, there was no intensive care unit (ICU) among those wards. Similarly, the medical ICU was only in fourth position in terms of ECRR. Discussion, conclusion Even though an economical study would have been useful, this system, unique in France, is helpful to improve the proper use of antibiotics. Unlike a classic night functioning for whom the results of gram-stain examinations are reported by night, often in the absence of clinician, the night activity in our CF allows to provide results during the day period (with 24 or 48 h in advance),
{"title":"112 Why perform bacterial identifications and antibiotic sensitivity analyses during night shifts in a bacteriology laboratory in a university medical centre?","authors":"E. Matthieu, L. Carole, C. Jané, Hitoto Hikombo, Mahaza Chetaou, Kempf Marie, Joly-Guillou Marie-Laure","doi":"10.1136/QSHC.2010.041624.6","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041624.6","url":null,"abstract":"Background, objective After opening hours, the activity of a clinical microbiology laboratory (CML) is usually limited to the inoculation of specimens sent by clinical wards and gram-stain examinations. A continuous functioning (CF) has been implemented for the last 4 years in the CML of Angers teaching hospital. With the CF, in addition to gram-stain examination and inoculations, urine cultures, blood cultures and cultures from certain fluids (ascitis, articular, pleural, perioperative, cerebrospinal) are monitored two or three times every night. In the case of colony growth, bacterial identifications (BI) and susceptibility to antibiotics testing (SAT) are performed. Concurrently to a geographical grouping of our hospital laboratories expected in 2010, the permanence of the CT is questioned. Therefore, our objective was to assess its interest in order to maintain it. Program: description, implementation, follow-up For each specimen for whom a BI and/or SAT were performed by night, the impact of the CF was assessed in terms of decrease in the delays from the time of sampling to the time at which results became available, and in terms of consequences of this decrease for the management of patient antimicrobial treatments. The delays in the absence of CF were estimated by considering the laboratory opening hours in the absence of CF and delays in incubation necessary for BI and SAT. Two major benefits have been defined: the early implementation of an effective treatment (EIET) and the early change to a reduced-spectrum but still efficient regimen (ECRR). The decrease of the delay was either 24 h or 48 h. Results in terms of clinical impact During the 4 months of the study, a BI and/or a SAT were performed for 430 specimens during the night period. An EIET was reported for 97 samples (22.6%), representing a cumulative gain of 111 days. For 49 patients, this EIET corresponded to the modification of an ineffective treatment, and for the 48 others, it corresponded to the implementation of an effective treatment in a patient not treated. An EIET was observed in 37.9% of blood cultures, 20.8% of urine cultures, and 17.9% of fluid cultures concerned by the night activity. An ECRR was reported for 23 samples accounting for 5.4% of overall specimens and representing 29 days of treatment. Among the nine wards for which the CF was the most profitable in terms of EIET, there were seven medical and two surgical wards. Therefore, there was no intensive care unit (ICU) among those wards. Similarly, the medical ICU was only in fourth position in terms of ECRR. Discussion, conclusion Even though an economical study would have been useful, this system, unique in France, is helpful to improve the proper use of antibiotics. Unlike a classic night functioning for whom the results of gram-stain examinations are reported by night, often in the absence of clinician, the night activity in our CF allows to provide results during the day period (with 24 or 48 h in advance),","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"2 1","pages":"A52 - A53"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75222436","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041624.46
L. Stephanie, Razafimahefa Hasinirina, Sgaggero Betty, Brosseau Martine
Context Iatrogenic incidents, major public health problem, can be responsible for damage and serious after-effects, particularly in neonates. They would be responsible for complications in 10% of the hospital admittances. Newborn children are particularly exposed to these iatrogenic risks. Several studies showed that these incidents increase significantly the risk of morbi-mortality in paediatric departments. Only few data are available on their incidence and consequences in neonatology. Objective of this work was to determine the epidemiology of iatrogenic risks in neonates, to look for answers to these dysfunctions and to sensitise medical and paramedical professionals to this public health problem. Description of the program A multidisciplinary group called ‘Amélioration des soins à l'enfant’, with monthly medical and paramedical meetings for synthesis and exposition of the results, was created in 2005. The group defined the methodology of the program, set up a continuous statement of adverse events (AE), analysed the data and identified corrective actions to AE. In 2008, this approach was continued with modified objectives and two nurses were associated in the five following domains: respiratory, intravenous, oral tract and skin incidents and incidents concerning the management and the organisation of care. An anonymised form was created in each domain to improve the exhaustiveness of the data. Results In 2005, 171/248 (70%) of the AE concerned the parenteral route, especially central (45%). Twenty cases of catheter removal secondarily to catheter obstruction were collected. Identification of the causes of these obstructions allowed the introduction of corrective actions (reprogramming of pumps, change in use of solutions). Thus, obstructions became less frequent (6) and did not require catheter removal any more. From November 2008 to January 2009, 205 AE were collected. The main problem identified was the presence of water in the respiratory tubes during non-invasive ventilation (30/93 cases of respiratory incidents), responsible for episodes of deep bradycardia and desaturations in children. Contacts with biomedical service, with other neonatal intensive care units and with tube manufacturers demonstrated that the solution was to use another equipment (dual hose heater adaptator for respiratory system) to avoid condensation. An inventory of our equipment followed by the purchase of all the necessary material at the beginning of February 2009 allowed the disappearance of this AE within our department. Discussion Improvement of the tool to collect AE is the principal objective of our group. It will allow a better exhaustiveness and then, a more rapid reaction in the introduction of corrective actions. Other objectives are the information and the knowledge updating of health care workers and the review or the elaboration of new protocols. One limit of this work is the reluctance of health care workers to report AE, as they consider AE as a r
{"title":"149 Follow-up of adverse events in a neonatal intensive care unit","authors":"L. Stephanie, Razafimahefa Hasinirina, Sgaggero Betty, Brosseau Martine","doi":"10.1136/QSHC.2010.041624.46","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041624.46","url":null,"abstract":"Context Iatrogenic incidents, major public health problem, can be responsible for damage and serious after-effects, particularly in neonates. They would be responsible for complications in 10% of the hospital admittances. Newborn children are particularly exposed to these iatrogenic risks. Several studies showed that these incidents increase significantly the risk of morbi-mortality in paediatric departments. Only few data are available on their incidence and consequences in neonatology. Objective of this work was to determine the epidemiology of iatrogenic risks in neonates, to look for answers to these dysfunctions and to sensitise medical and paramedical professionals to this public health problem. Description of the program A multidisciplinary group called ‘Amélioration des soins à l'enfant’, with monthly medical and paramedical meetings for synthesis and exposition of the results, was created in 2005. The group defined the methodology of the program, set up a continuous statement of adverse events (AE), analysed the data and identified corrective actions to AE. In 2008, this approach was continued with modified objectives and two nurses were associated in the five following domains: respiratory, intravenous, oral tract and skin incidents and incidents concerning the management and the organisation of care. An anonymised form was created in each domain to improve the exhaustiveness of the data. Results In 2005, 171/248 (70%) of the AE concerned the parenteral route, especially central (45%). Twenty cases of catheter removal secondarily to catheter obstruction were collected. Identification of the causes of these obstructions allowed the introduction of corrective actions (reprogramming of pumps, change in use of solutions). Thus, obstructions became less frequent (6) and did not require catheter removal any more. From November 2008 to January 2009, 205 AE were collected. The main problem identified was the presence of water in the respiratory tubes during non-invasive ventilation (30/93 cases of respiratory incidents), responsible for episodes of deep bradycardia and desaturations in children. Contacts with biomedical service, with other neonatal intensive care units and with tube manufacturers demonstrated that the solution was to use another equipment (dual hose heater adaptator for respiratory system) to avoid condensation. An inventory of our equipment followed by the purchase of all the necessary material at the beginning of February 2009 allowed the disappearance of this AE within our department. Discussion Improvement of the tool to collect AE is the principal objective of our group. It will allow a better exhaustiveness and then, a more rapid reaction in the introduction of corrective actions. Other objectives are the information and the knowledge updating of health care workers and the review or the elaboration of new protocols. One limit of this work is the reluctance of health care workers to report AE, as they consider AE as a r","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"28 1","pages":"A92 - A93"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77097056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041608.9
J. Pépin, G. Huchon, Y. Grillet, M. Sapéne, A. Vicente, B. Housset, Au Nom Des Membres De L'osfp
Background and Objectives The national French Registry to evaluate sleep breathing disorders (OSFP Registry: Observatoire sommeil de la Fédération de Pneumologie) is intended to collect updated information about current practices of respiratory physicians managing sleep apnoea patients. Methods, Program Description and Follow-up The main goal of the Internet-based registry (www.osfp.fr) is to improve clinical management quality by offering respiratory physicians a complete and systematically organised online evaluation of patients referred for sleep disorders. The content of the registry addresses four goals: (1) to improve physician's knowledge not only of sleep apnoea but also of alternative diagnosis by the systematic use of validated clinical scales for sleepiness, fatigue, depression and restless legs syndrome, (2) to increase awareness of comorbidities and cardio-metabolic risk associated with sleep apnoea, by suggesting measurements of waist circumference, blood pressure, fasting lipids and fasting glucose, (3) to identify subgroups of at-risk patients (ie obesity hypoventilation and a combination of chronic obstructive pulmonary disease and sleep apnoea, the so-called overlap syndrome), and (4) to suggest appropriate follow-up and treatments for these specific subgroups of patients according to national guidelines. Information from the database is available at anytime and data can be extracted for statistical analysis. Participating physicians can compare their practices with others’ in the registry and with the guidelines established with the French High Health authority (HAS: Haute Autorité de Santé). Results in terms of clinical impact More than 560 centres were involved and between January 2007 and November 2009, more than 22 000 suspected sleep apnoea patients were enrolled. These centres included varied clinical practices, reflecting real life sleep apnoea clinical management in France. The majority of centres were private practices (74% of the patients) whilst others were public hospital practices, either teaching university hospitals (4% of the patients) or district hospitals (22% of the patients). Patients from all regions of France were included and constitute a representative sample in terms of places of residence, rural/urban ratio and socio-professional groups. Sleep apnoea was diagnosed in 80% of referred patients and CPAP prescribed in 70% of them, with a mean CPAP usage of 5.7 h/night which is higher than the usually reported compliance in clinical studies (Cochrane 2009: 5.5 h/night). Significant improvement occurred with reduction in the sleepiness, fatigue and depression scales (from 12 to 8, 14 to 9 and 6 to 4.5, respectively). Appropriate characterisation of the patients at baseline allowed the identification of cardiovascular comorbidities in 45% of the patients. A significant percentage of patients (11%) were referred to cardiologist or other specialists after associated or alternative diagnosis had been appropr
{"title":"159 Sleep apnoea: clinical impact of a quality improvement program using an Internet-based registry","authors":"J. Pépin, G. Huchon, Y. Grillet, M. Sapéne, A. Vicente, B. Housset, Au Nom Des Membres De L'osfp","doi":"10.1136/QSHC.2010.041608.9","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041608.9","url":null,"abstract":"Background and Objectives The national French Registry to evaluate sleep breathing disorders (OSFP Registry: Observatoire sommeil de la Fédération de Pneumologie) is intended to collect updated information about current practices of respiratory physicians managing sleep apnoea patients. Methods, Program Description and Follow-up The main goal of the Internet-based registry (www.osfp.fr) is to improve clinical management quality by offering respiratory physicians a complete and systematically organised online evaluation of patients referred for sleep disorders. The content of the registry addresses four goals: (1) to improve physician's knowledge not only of sleep apnoea but also of alternative diagnosis by the systematic use of validated clinical scales for sleepiness, fatigue, depression and restless legs syndrome, (2) to increase awareness of comorbidities and cardio-metabolic risk associated with sleep apnoea, by suggesting measurements of waist circumference, blood pressure, fasting lipids and fasting glucose, (3) to identify subgroups of at-risk patients (ie obesity hypoventilation and a combination of chronic obstructive pulmonary disease and sleep apnoea, the so-called overlap syndrome), and (4) to suggest appropriate follow-up and treatments for these specific subgroups of patients according to national guidelines. Information from the database is available at anytime and data can be extracted for statistical analysis. Participating physicians can compare their practices with others’ in the registry and with the guidelines established with the French High Health authority (HAS: Haute Autorité de Santé). Results in terms of clinical impact More than 560 centres were involved and between January 2007 and November 2009, more than 22 000 suspected sleep apnoea patients were enrolled. These centres included varied clinical practices, reflecting real life sleep apnoea clinical management in France. The majority of centres were private practices (74% of the patients) whilst others were public hospital practices, either teaching university hospitals (4% of the patients) or district hospitals (22% of the patients). Patients from all regions of France were included and constitute a representative sample in terms of places of residence, rural/urban ratio and socio-professional groups. Sleep apnoea was diagnosed in 80% of referred patients and CPAP prescribed in 70% of them, with a mean CPAP usage of 5.7 h/night which is higher than the usually reported compliance in clinical studies (Cochrane 2009: 5.5 h/night). Significant improvement occurred with reduction in the sleepiness, fatigue and depression scales (from 12 to 8, 14 to 9 and 6 to 4.5, respectively). Appropriate characterisation of the patients at baseline allowed the identification of cardiovascular comorbidities in 45% of the patients. A significant percentage of patients (11%) were referred to cardiologist or other specialists after associated or alternative diagnosis had been appropr","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"27 1","pages":"A11 - A12"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84701478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041608.21
A. Desplanques-Leperre, N. Riolacci-Dhoyen, M. Erbault, L. Banaeï-Bouchareb, C. Chan-Chee, J. Deligne, V. Corre, P. Ricordeau, B. Lavallart
Background and Objectives Neuroleptics (NL) are often prescribed to patients with Alzheimer's disease (AD), mainly for behaviour disorders and during episodes of confusion. However, these drugs are known to have frequent and severe iatrogenic effects: treating 1000 patients with behaviour disorders receiving NL for 12 weeks would result in 10 additional deaths, 18 strokes (half of which were severe), additional 58 to 94 cases of gait disorders and only 91 to 200 decrease in behaviour disorders. In fact, all AD patients will present behaviour disorders at some time or other. The French Alzheimer public health plan aims to reduce the avoidable iatrogenic effects of NL. Program The national cooperative group for the optimisation of the prescription of psychotropic drugs in the elderly was established at the initiative of HAS. Its members include nurses, patients, insurers and institutions. A problem-solving approach centred on the patient pathway that included three quality dimensions (Efficacy (E), Safety (S) and Access to best care (A)) was used to develop and implement the tools to achieve an integrated programme going ‘from practice improvement to clinical impact measurement’. The practice improvement part which is aimed at reducing the iatrogenic effects of NL in AD patients includes: (1) identification of AD patients with NL (local warning signal=percentage of AD patients taking NL). This indicator is easy to measure in all care sectors and comes with a good practice indicator ‘absence of daytime sedation’ and monitoring of prescriptions for other psychotropic drugs to prevent drug switching, (2) review of prescriptions for identified AD patients in order to correct inappropriate prescriptions (local indicator for risk containment=percentage of prescriptions reviewed for AD patients), and (3) two new guidelines on behaviour disorders in AD patients and on confusion in the elderly that describe proper use of NL and other psychotropic drugs (E, S) as well as new nondrug techniques of care (A). Reduction of exposure to NL before and after prescription is based on these guidelines. Clinical impact is given by the national rate of exposure of AD patients to NL and is measured in the French AD patient population covered by the three main sickness funds. Results The first national measures in 2007 on 400 000 AD patients showed that exposure to NL in AD patients was five times higher (16.95%) than in the general population of the same age (2.9%). One year after the Alzheimer plan was launched and after raising the awareness of families and health professionals to the risks of NL, exposure had fallen slightly to 16.1% (equivalent to 3500 fewer cases of exposure). The above programme is in the process being implemented. Results for the national warning signal have been widely diffused. The programme is supported by training initiatives and information campaigns aimed at the general public, the families of AD patients, and health professionals. These are
{"title":"282 Reducing the iatrogenicity of neuroleptics in patients with Alzheimer's disease","authors":"A. Desplanques-Leperre, N. Riolacci-Dhoyen, M. Erbault, L. Banaeï-Bouchareb, C. Chan-Chee, J. Deligne, V. Corre, P. Ricordeau, B. Lavallart","doi":"10.1136/QSHC.2010.041608.21","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041608.21","url":null,"abstract":"Background and Objectives Neuroleptics (NL) are often prescribed to patients with Alzheimer's disease (AD), mainly for behaviour disorders and during episodes of confusion. However, these drugs are known to have frequent and severe iatrogenic effects: treating 1000 patients with behaviour disorders receiving NL for 12 weeks would result in 10 additional deaths, 18 strokes (half of which were severe), additional 58 to 94 cases of gait disorders and only 91 to 200 decrease in behaviour disorders. In fact, all AD patients will present behaviour disorders at some time or other. The French Alzheimer public health plan aims to reduce the avoidable iatrogenic effects of NL. Program The national cooperative group for the optimisation of the prescription of psychotropic drugs in the elderly was established at the initiative of HAS. Its members include nurses, patients, insurers and institutions. A problem-solving approach centred on the patient pathway that included three quality dimensions (Efficacy (E), Safety (S) and Access to best care (A)) was used to develop and implement the tools to achieve an integrated programme going ‘from practice improvement to clinical impact measurement’. The practice improvement part which is aimed at reducing the iatrogenic effects of NL in AD patients includes: (1) identification of AD patients with NL (local warning signal=percentage of AD patients taking NL). This indicator is easy to measure in all care sectors and comes with a good practice indicator ‘absence of daytime sedation’ and monitoring of prescriptions for other psychotropic drugs to prevent drug switching, (2) review of prescriptions for identified AD patients in order to correct inappropriate prescriptions (local indicator for risk containment=percentage of prescriptions reviewed for AD patients), and (3) two new guidelines on behaviour disorders in AD patients and on confusion in the elderly that describe proper use of NL and other psychotropic drugs (E, S) as well as new nondrug techniques of care (A). Reduction of exposure to NL before and after prescription is based on these guidelines. Clinical impact is given by the national rate of exposure of AD patients to NL and is measured in the French AD patient population covered by the three main sickness funds. Results The first national measures in 2007 on 400 000 AD patients showed that exposure to NL in AD patients was five times higher (16.95%) than in the general population of the same age (2.9%). One year after the Alzheimer plan was launched and after raising the awareness of families and health professionals to the risks of NL, exposure had fallen slightly to 16.1% (equivalent to 3500 fewer cases of exposure). The above programme is in the process being implemented. Results for the national warning signal have been widely diffused. The programme is supported by training initiatives and information campaigns aimed at the general public, the families of AD patients, and health professionals. These are","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"26 1","pages":"A22 - A23"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82865853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041624.37
J. Breaud, Griffet Jacques, Julie Manuel, Bensaid Ronny, M. Carine, J. Quaranta
Background and objectives For Morbidity Monitoring Staff (MMS) meetings to be efficient, they need to include all patient files concerned with medical failures or logistics failures. The major difficulty is selecting all relevant files. Our objective was to develop a computer application that would select the files that need to be discussed in order to identify medical failures and logistics failures that need remedying. Programme The computer application for automatic file selection is based on a comparison of the actual length of hospital stay with the predicted length of stay for a given disease and/or surgical procedure. Every 2 months, all selected files are reviewed to determine which files are incomplete, which relate to medical failures, and which to logistics failures. Results During the 30-month period from January 2006 to April 2009, 8540 children underwent surgery in our department. A total of 1364 (16%) medical files were automatically selected for review by MMS. A total of 51 cases (0.6%) of medical failure and 16 cases (0.19%) of logistics failure were identified and analysed. Three improvement actions ensued: (i) the development of a specific multidisciplinary medical file for ASA III patients, (ii) routine bacteriological analysis in cases of appendectomy in order to fight antibiotic-resistant infections better, (iii) changes in the organisation of day-care surgery (phone-call the day before and after surgery, changes in the timetable…) Conclusion The automated procedure for the selection of medical files for review by MMS helped us identify medical failures (0.6% rate) and initiate specific actions in order to improve health care delivery in our department. Our tool may be useful for MMS in all cases of scheduled hospitalisation or elective surgery. Introduction l'amélioration des pratiques professionnelles repose entre autre sur la réalisation au sein des équipes médicales et paramédicales de RMM. Toutefois, la sélection des dossiers à analyser dépend le plus souvent d'une évaluation individuelle de la survenue d'un évènement porteur de risque ou d'une complication et n'est pas toujours exhaustive. Afin de pallier à cette situation, nous avons développé un système automatique de sélection des dossiers à analyser, basé sur la durée du séjour hospitalier et le caractère complet ou nom du dossier (présence de résumé d'activité médicale et de compte rendu opératoire). Ce mode de sélection nous permettant d'extraire les dossiers incomplets et de les finaliser, mais aussi de mettre en exergue les complications médicales et les problèmes organisationnels. Matériel et méthodes Une application informatique développée sur le logiciel ACCESS (microsoft*) permet, pour chaque patient opéré dans le service, de comparer la durée de l'hospitalisation effectuée à la durée prévisible de l'hospitalisation pour la pathologie et le geste chirurgical concerné. Ainsi, tout patient dont la durée dépasse la d
背景和目的发病率监测工作人员(MMS)会议要有效率,他们需要包括所有与医疗失败或后勤失败有关的患者档案。主要的困难是选择所有相关的文件。我们的目标是开发一个计算机应用程序,它可以选择需要讨论的文件,以确定需要补救的医疗故障和后勤故障。程序自动选择文件的计算机应用程序是基于对给定疾病和/或外科手术的实际住院时间与预测住院时间的比较。每2个月审查所有选定的文件,以确定哪些文件不完整,哪些与医疗故障有关,哪些与后勤故障有关。结果2006年1月至2009年4月30个月间,我科共收治患儿8540例。MMS共自动选择1364份(16%)医疗文件进行审查。共发现和分析医疗故障51例(0.6%)和后勤故障16例(0.19%)。随后采取了三项改进措施:(i)为ASA III患者建立特定的多学科医疗档案;(ii)阑尾切除术病例的常规细菌学分析,以便更好地对抗抗生素耐药性感染;(III)改变日间护理手术的组织(术前和术后的一天电话通话);结论MMS自动选择医疗文件进行审查的程序帮助我们识别医疗事故(0.6%),并采取具体措施,以提高我科的医疗服务质量。我们的工具可能是有用的MMS在所有情况下,计划住院或择期手术。引言职业实践的职业生涯和职业生涯的职业生涯和职业生涯的职业生涯和职业生涯的职业生涯和职业生涯。最后,将所有的数据汇总起来,将所有的数据汇总起来,将所有的数据汇总起来,将所有的数据汇总起来,将所有的数据汇总起来,将所有的数据汇总起来。在较不稳定的情况下,目前的情况是,我们的系统自动收集和分析了所有的数据,我们的系统自动收集和分析了所有的数据,我们的系统自动收集和分析了所有的数据,我们的系统自动收集和分析了所有的数据,完成了所有的数据。这些模数都是由不同的模数组成的,它们都是由不同的模数组成的,它们都是由不同的模数组成的。matriel et msamthodes Une application informatique danalys ys (microsoft*) permission (logiciel ACCESS) permission, pour chque patient opsamro . dansle service, de compare la dursamro . de l'hospitalisation效果,la dursamro . pracro . datos病理,以及其他一些外科问题。在印度,病人不要用“a dursame”代替“a dursame”,而是用“a dursame”代替“a dursame”。我将分析多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科、多学科。30 mois(2006年1月至2009年6月)8540个婴儿使用了()和()服务。在RMM中,有1364个档案(16%)是由材料和材料组成的,包括材料和材料组成的。51份档案(0.6%)涉及到职业健康组织和职业健康组织和职业健康组织(19%)。为了分析回顾des档案有的生几个次准备倒拉撬en电荷des病人告诉问:la宪法d一个档案病人multidisciplinaire pre等post-operatoire倒les病人ASA三世。laremationationd 'une分析bactsamriologique en cas d' appendicatique afin de faire face, '幻影'幻影de germerisistants aux抗生素通常。病人流动医疗机构的变更(上诉:taccel tsamelsamoniques La veille et le lendemain de l'intervention, horaire d'admission…)。结论:采用“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”、“利用”。让所有人都知道,所有的人都有自己的生活方式,例如,所有的人都有自己的生活方式,所有的人都有自己的生活方式。
{"title":"291 Improved management of surgical paediatric patients by computerised selection of medical files for analysis in morbidity monitoring staff meetings","authors":"J. Breaud, Griffet Jacques, Julie Manuel, Bensaid Ronny, M. Carine, J. Quaranta","doi":"10.1136/QSHC.2010.041624.37","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041624.37","url":null,"abstract":"Background and objectives For Morbidity Monitoring Staff (MMS) meetings to be efficient, they need to include all patient files concerned with medical failures or logistics failures. The major difficulty is selecting all relevant files. Our objective was to develop a computer application that would select the files that need to be discussed in order to identify medical failures and logistics failures that need remedying. Programme The computer application for automatic file selection is based on a comparison of the actual length of hospital stay with the predicted length of stay for a given disease and/or surgical procedure. Every 2 months, all selected files are reviewed to determine which files are incomplete, which relate to medical failures, and which to logistics failures. Results During the 30-month period from January 2006 to April 2009, 8540 children underwent surgery in our department. A total of 1364 (16%) medical files were automatically selected for review by MMS. A total of 51 cases (0.6%) of medical failure and 16 cases (0.19%) of logistics failure were identified and analysed. Three improvement actions ensued: (i) the development of a specific multidisciplinary medical file for ASA III patients, (ii) routine bacteriological analysis in cases of appendectomy in order to fight antibiotic-resistant infections better, (iii) changes in the organisation of day-care surgery (phone-call the day before and after surgery, changes in the timetable…) Conclusion The automated procedure for the selection of medical files for review by MMS helped us identify medical failures (0.6% rate) and initiate specific actions in order to improve health care delivery in our department. Our tool may be useful for MMS in all cases of scheduled hospitalisation or elective surgery. Introduction l'amélioration des pratiques professionnelles repose entre autre sur la réalisation au sein des équipes médicales et paramédicales de RMM. Toutefois, la sélection des dossiers à analyser dépend le plus souvent d'une évaluation individuelle de la survenue d'un évènement porteur de risque ou d'une complication et n'est pas toujours exhaustive. Afin de pallier à cette situation, nous avons développé un système automatique de sélection des dossiers à analyser, basé sur la durée du séjour hospitalier et le caractère complet ou nom du dossier (présence de résumé d'activité médicale et de compte rendu opératoire). Ce mode de sélection nous permettant d'extraire les dossiers incomplets et de les finaliser, mais aussi de mettre en exergue les complications médicales et les problèmes organisationnels. Matériel et méthodes Une application informatique développée sur le logiciel ACCESS (microsoft*) permet, pour chaque patient opéré dans le service, de comparer la durée de l'hospitalisation effectuée à la durée prévisible de l'hospitalisation pour la pathologie et le geste chirurgical concerné. Ainsi, tout patient dont la durée dépasse la d","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"134 7‐8","pages":"A83 - A84"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91418797","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041608.17
F. Woimant, R. Simon-Prel, M. Neveux, M. Degrave
Context and Objectives Numerous studies and metaanalysis showed the efficiency of Stroke Units (SU). Organised care has been proven to decrease morbidity and mortality after stroke. In Ile-de-France, there are 16 SU, and among them 10 were created since 2003. The implementation of the SU and of their networks are regularly evaluated on behalf of the regional hospitalisation agency (ARH-IF), with information feedback to multidisciplinary stroke teams and hospital administrators to optimise the quality of care of stroke patients. Description of the Program Two types of indicators are collected. Epidemiological data such as number of hospital admissions for stroke in the region and by territory and establishment and demographic data of stroke patients are analysed. Since 2000, they are collected from the national hospital discharge database, according to a protocol of extraction defined by the professionals. Other indicators concern the hospital management of stroke patients such as proportion of patients admitted in SU vs other nondedicated units, the type of stroke (transient ischaemic attacks, infarction and haemorrhage), the stroke severity, the treatments (including rehabilitation), the complications, the length of hospital stay and the outcome. Time indicators are important to assess the organisation of the care: delay of hospitalisation, of admission within the SU, of access to the neurological expertise, to the brain imaging, to the physiotherapist and speech therapist evaluation and to the stroke rehabilitation unit. These data are prospectively collected from surveys regularly realised on 30 to 50 consecutive patients admitted in SU and stroke rehabilitation wards. A web-based tool was used to collect data from sites. The analysis is realised by the pole ‘Affaires hospitalières de la CRAMIF’. The results of these evaluations are presented during an ARH-IF plenary session to the neurologists, the rehabilitation physicians and the hospital administrators of the concerned establishments, and then within each establishment with all the medical and non-medical multidisciplinary team and the directors. Results These evaluations permit to estimate, in an iterative way, the professional practices and to suggest actions to improve organisation of stroke care, measured in particular on patients' proportion admitted in SU, on the decrease of pre-and intra-hospital delays allowing more patients to have access to the thrombolytic therapy. Within Ile-de-France”, the number of stroke patients admitted in establishments with SU increased from 22% to 48.5% between 2003 and 2008; the median age of stroke patients did not modify in the region (71 years), but the age of stroke patients admitted in establishments with SU increased from 63 to 67 years. The in-hospital stroke mortality decreased from 15.8% to 10.5% and the SU- mortality from 12.5% to 8.6%. The number of patients evaluated within the first 48 h by a physiotherapist and/or a speech therapist incr
{"title":"259 Measure of the impact of the implementation of organised stroke care in the region lle-de-France","authors":"F. Woimant, R. Simon-Prel, M. Neveux, M. Degrave","doi":"10.1136/QSHC.2010.041608.17","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041608.17","url":null,"abstract":"Context and Objectives Numerous studies and metaanalysis showed the efficiency of Stroke Units (SU). Organised care has been proven to decrease morbidity and mortality after stroke. In Ile-de-France, there are 16 SU, and among them 10 were created since 2003. The implementation of the SU and of their networks are regularly evaluated on behalf of the regional hospitalisation agency (ARH-IF), with information feedback to multidisciplinary stroke teams and hospital administrators to optimise the quality of care of stroke patients. Description of the Program Two types of indicators are collected. Epidemiological data such as number of hospital admissions for stroke in the region and by territory and establishment and demographic data of stroke patients are analysed. Since 2000, they are collected from the national hospital discharge database, according to a protocol of extraction defined by the professionals. Other indicators concern the hospital management of stroke patients such as proportion of patients admitted in SU vs other nondedicated units, the type of stroke (transient ischaemic attacks, infarction and haemorrhage), the stroke severity, the treatments (including rehabilitation), the complications, the length of hospital stay and the outcome. Time indicators are important to assess the organisation of the care: delay of hospitalisation, of admission within the SU, of access to the neurological expertise, to the brain imaging, to the physiotherapist and speech therapist evaluation and to the stroke rehabilitation unit. These data are prospectively collected from surveys regularly realised on 30 to 50 consecutive patients admitted in SU and stroke rehabilitation wards. A web-based tool was used to collect data from sites. The analysis is realised by the pole ‘Affaires hospitalières de la CRAMIF’. The results of these evaluations are presented during an ARH-IF plenary session to the neurologists, the rehabilitation physicians and the hospital administrators of the concerned establishments, and then within each establishment with all the medical and non-medical multidisciplinary team and the directors. Results These evaluations permit to estimate, in an iterative way, the professional practices and to suggest actions to improve organisation of stroke care, measured in particular on patients' proportion admitted in SU, on the decrease of pre-and intra-hospital delays allowing more patients to have access to the thrombolytic therapy. Within Ile-de-France”, the number of stroke patients admitted in establishments with SU increased from 22% to 48.5% between 2003 and 2008; the median age of stroke patients did not modify in the region (71 years), but the age of stroke patients admitted in establishments with SU increased from 63 to 67 years. The in-hospital stroke mortality decreased from 15.8% to 10.5% and the SU- mortality from 12.5% to 8.6%. The number of patients evaluated within the first 48 h by a physiotherapist and/or a speech therapist incr","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"11 1","pages":"A18 - A19"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83583950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/QSHC.2010.041624.31
A. Eichenberger, G. Haller, B. Walder
Introduction The aim of the study was to assess the impact of a clinical pathway implemented in a post-anaesthesia care unit (PACU) on postoperative outcomes. Methods A patient clinical pathway which includes a nurse-driven fast track program (FTP) for uncomplicated patients and minor interventions and a medical-driven slow track program (STP) for complicated patients were implemented over a period of 2 months. A retrospective cohort study based on electronic patient records was performed to assess the effectiveness of this program on PACU and hospital length of stay (LOS) and in-hospital mortality and unplanned admission to the intensive care unit (ICU). We compared the period before and after implementation of the program. Statistical analysis was performed using the Student t test, χ2, Wilcoxon-rank test. Multivariate analysis using linear and logistic regression was performed to adjust for differences in patient demographic characteristics, co-morbidities, type of surgery and anaesthesia and emergency status between the two periods. A p≤0.05 was considered significant. Results Patients characteristics, ASA scores, type of anaesthesia and surgery were similar before and after implementation of the clinical pathways. We observed a decrease in PACU median length of stay for all patients from 163 min (IQR, 103–291) to 148 min (IQR, 96–270 min) (p<0.001). In ASA 1-2 patients median LOS in PACU decreased from 152 min (IQR, 102–249 min) to 135 min (IQR 91–227 min) in ASA 1-2 patients (p<0.001). Hospital LOS however remained unchanged. Overall in-hospital mortality after pathway implementation decreased for all patients from 1.7 to 0.9% (adjusted OR 0.36 (95%CI 0.22 to 0.59), p value<0.01). The number of unplanned admissions to ICU decreased also from 113 (2.8%) to 91 (2.1%) (adjusted OR 0.73 (95%CI 0.53 to 0.99); p value 0.04). Conclusion A significant reduction of LOS in PACU, in-hospital mortality and unplanned admission to ICU was observed after implementation of a clinical pathway in the PACU. Introduction La phase postopératoire est une phase risquée pour le patient en terme de complications. La mortalité postopératoire actuelle, tous actes chirurgicaux confondus, se situe entre 1.2 et 2.6%, alors que la morbidité est supérieure à 11%. Dans notre salle de surveillance post-interventionnel (SSPI), nous avons un flux important de patients en bonne santé habituelle ayant bénéficié d'un acte chirurgical mineur et des patients polymorbides ayant bénéficié d'une chirurgie majeure. Nous avons mis en application un programme de prise en charge des patients permettant de libérer rapidement ceux en bonne santé habituelle sur la base de critères cliniques standardisés de manière à libérer les ressources de soins nécessaires pour la prise en charge des patients à haut risque de complications. But de l’étude Le but de cette étude était d’évaluer les bénéfices d'un programme de qualité incluant deux itinéraires cliniques distin
本研究的目的是评估在麻醉后护理单位(PACU)实施的临床路径对术后结果的影响。方法采用为期2个月的患者临床路径,对病情简单的患者实施护士驱动的快速通道方案(FTP)和轻微干预措施,对病情复杂的患者实施医疗驱动的慢通道方案(STP)。一项基于电子病历的回顾性队列研究评估了该方案对PACU、住院时间(LOS)、住院死亡率和非计划入住重症监护病房(ICU)的有效性。我们比较了项目实施前后的情况。统计学分析采用Student t检验、χ2、wilcox -rank检验。使用线性和逻辑回归进行多变量分析,以调整患者人口统计学特征、合并症、手术类型和麻醉以及两个时期的急诊状态的差异。A p≤0.05被认为是显著的。结果实施临床路径前后患者特征、ASA评分、麻醉方式及手术方式相似。我们观察到所有患者PACU的中位住院时间从163分钟(IQR, 103-291)减少到148分钟(IQR, 96-270分钟)(p<0.001)。ASA 1-2患者PACU的中位LOS从152 min (IQR, 102-249 min)降至135 min (IQR, 91-227 min) (p<0.001)。然而,医院LOS保持不变。实施路径后,所有患者的住院总死亡率从1.7%降至0.9%(校正OR 0.36 (95%CI 0.22 ~ 0.59), p值<0.01)。非计划入住ICU的人数也从113例(2.8%)下降到91例(2.1%)(调整OR 0.73 (95%CI 0.53 ~ 0.99);P值0.04)。结论在PACU实施临床路径后,可显著降低PACU的LOS、住院死亡率和非计划入院率。一期手术后的患者和一期手术后的患者均出现并发症。死亡统计数据(死亡统计数据)、疾病统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)、死亡统计数据(死亡统计数据)等。在介入后监测中(SSPI),我们注意到一些重要的因素,如患者在手术过程中是否存在不可抗力,如习惯性的不可抗力,或是否存在不可抗力,或是否存在多病性的不可抗力。目前的情况是,在应用程序中,对病人进行收费,对病人进行渗透,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对并发症,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费,对病人的收费。但是,在所有的电子表格中,所有的电子表格和电子表格都包含了电子表格和电子表格,包括电子表格和电子表格,电子表格和电子表格,电子表格和电子表格,电子表格和电子表格,电子表格和电子表格,电子表格和电子表格,电子表格和电子表格,电子表格和电子表格。描述方案和m - ims - ms - ims - ms - ms - ms - ms - ms - ms - ms - ms - ms - ms - ms第一阶段的<s:1>医疗器械和医疗器械的<s:1>医疗器械和医疗器械的<s:1>医疗器械和医疗器械的医疗器械(FTP:快速通道);在第二阶段,如“多病合并”、“不可抗力合并”、“不可抗力合并”、“不可抗力合并”、“不可抗力合并”。目前的研究对象包括:成年(≥18岁)患者和成年(≥18岁)患者,均采用SSPI治疗,但不能采用单纯的手术治疗,也不能采用单纯的手术治疗,也不能采用单纯的麻醉治疗。《关于薪金和其他方面的信息原则》是关于薪金和其他方面的资料,关于薪金和其他方面的资料是关于薪金和其他方面的。Les p10.1.2007和2008年1月1日分别于2007年1月1日和2007年7月31日(avant l' implicationdu programme)和2008年1月1日和2008年7月31日(apr<s:1> l' implicationdu programme)。在收集申诉者、管理和利用申诉者的基础上(DPI)和利用和利用申诉者的基础上(DPI),关于申诉和利用申诉者的注意事项的说明,说明了申诉和利用申诉者的情况。不能用其他的形式来代替其他的形式。将有身份的和有身份的、有身份的、有身份的和有身份的。<s:1> <s:1> <s:1> <s:1> <s:1> <s:1> <s:1> <s:1> <s:1> <s:1> <s:1> - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -在2007年10月1日(148分钟),在2008年(96分钟),在2008年4月1日(148分钟),在2008年1月1日(148分钟),在2007年1月1日(148分钟),在2008年1月1日(148分钟),在2008年1月1日(p<0。
{"title":"133 Clinical pathways in post-anaesthesia care unit to reduce length of stay, mortality and unplanned intensive care unit admission","authors":"A. Eichenberger, G. Haller, B. Walder","doi":"10.1136/QSHC.2010.041624.31","DOIUrl":"https://doi.org/10.1136/QSHC.2010.041624.31","url":null,"abstract":"Introduction The aim of the study was to assess the impact of a clinical pathway implemented in a post-anaesthesia care unit (PACU) on postoperative outcomes. Methods A patient clinical pathway which includes a nurse-driven fast track program (FTP) for uncomplicated patients and minor interventions and a medical-driven slow track program (STP) for complicated patients were implemented over a period of 2 months. A retrospective cohort study based on electronic patient records was performed to assess the effectiveness of this program on PACU and hospital length of stay (LOS) and in-hospital mortality and unplanned admission to the intensive care unit (ICU). We compared the period before and after implementation of the program. Statistical analysis was performed using the Student t test, χ2, Wilcoxon-rank test. Multivariate analysis using linear and logistic regression was performed to adjust for differences in patient demographic characteristics, co-morbidities, type of surgery and anaesthesia and emergency status between the two periods. A p≤0.05 was considered significant. Results Patients characteristics, ASA scores, type of anaesthesia and surgery were similar before and after implementation of the clinical pathways. We observed a decrease in PACU median length of stay for all patients from 163 min (IQR, 103–291) to 148 min (IQR, 96–270 min) (p<0.001). In ASA 1-2 patients median LOS in PACU decreased from 152 min (IQR, 102–249 min) to 135 min (IQR 91–227 min) in ASA 1-2 patients (p<0.001). Hospital LOS however remained unchanged. Overall in-hospital mortality after pathway implementation decreased for all patients from 1.7 to 0.9% (adjusted OR 0.36 (95%CI 0.22 to 0.59), p value<0.01). The number of unplanned admissions to ICU decreased also from 113 (2.8%) to 91 (2.1%) (adjusted OR 0.73 (95%CI 0.53 to 0.99); p value 0.04). Conclusion A significant reduction of LOS in PACU, in-hospital mortality and unplanned admission to ICU was observed after implementation of a clinical pathway in the PACU. Introduction La phase postopératoire est une phase risquée pour le patient en terme de complications. La mortalité postopératoire actuelle, tous actes chirurgicaux confondus, se situe entre 1.2 et 2.6%, alors que la morbidité est supérieure à 11%. Dans notre salle de surveillance post-interventionnel (SSPI), nous avons un flux important de patients en bonne santé habituelle ayant bénéficié d'un acte chirurgical mineur et des patients polymorbides ayant bénéficié d'une chirurgie majeure. Nous avons mis en application un programme de prise en charge des patients permettant de libérer rapidement ceux en bonne santé habituelle sur la base de critères cliniques standardisés de manière à libérer les ressources de soins nécessaires pour la prise en charge des patients à haut risque de complications. But de l’étude Le but de cette étude était d’évaluer les bénéfices d'un programme de qualité incluant deux itinéraires cliniques distin","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"13 1","pages":"A78 - A78"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85897084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-04-01DOI: 10.1136/qshc.2010.041632.26
A. Vitoux, F. Farsi, C. Grenier
Context and Objectives The disclosure protocol, defined in the first French cancer plan, is intended to benefit patients, giving them better conditions for disclosing their illness and the treatment plan proposed, and this throughout its management. This protocol relies on a multidisciplinary management involving primarily physicians (medical time) and paramedics (accompanying time) and aims to inform and accompany the patients and their family. The quality of patient information is considered as a crucial point for quality of care. Our program has been set up to improve its modalities. The objectives of this program are the following: Description of the current situation, Feedback on experiences Implementation of improvement projects Demonstration of the progress made Programme Six Comprehensive Cancer Centers (CCCs) were involved in a voluntary program. First, the most important aspects of the disclosure protocol were identified. Six valid, reproductible and discriminative quality indicators (QIs) were developed. Each of these QIs includes several items. The relative weight of each item was defined from the quotation of items by participants and experts in terms of relative importance. Each QI was quoted on a scale from 0 to 1. In the CCCs involved in the program, an audit (September 2008) was performed using medical records of 60 new patients who were under treatment (surgery, chemotherapy and/or radiotherapy) for a new cancer. This retrospective audit was used to establish the state of practices. Professional practices were benchmarked between the different CCCs and weaknesses were identified. Improvement actions to be implemented have been discussed and a specific quality plan has been set up in each CCC. Results The assessed QIs were respectively: the disclosure process: mean score=0.63, range: 0.53–0.76 continuity of care: mean score=0.61, range: 0.00–0.75 consideration of patient needs: mean score=0.46, range: 0.26–0.68, information delivered to the patient: mean score=0.28, range 0.25–0.30, patient feelings: mean score=0.27, range 0.09–0.37 needs of relatives for support: mean score=0.26, range 0.02–0.44 Even if the lack of traceability may explain a large part of measured quality defaults, professionals also identified the need to precise the good practices, to disseminate them and to structure the modalities of the disclosure process for each patient. This process has been standardised in each center. A systematic production of a personalised care program for each patient is still ongoing. Some skills have already been developed by professionals (e.g. information delivered to the patient, information process, adaptation to patient singular choices, information check list) and shared between CCCs. Conclusion The second audit will be conducted in February 2010 and the comparison of results for each hospital may demonstrate the progress made. Thus, consistency of such programs can be discussed in April 2010. Such an approach is required i
{"title":"148 Patient information: definition of indicators on the quality of disclosures to patients","authors":"A. Vitoux, F. Farsi, C. Grenier","doi":"10.1136/qshc.2010.041632.26","DOIUrl":"https://doi.org/10.1136/qshc.2010.041632.26","url":null,"abstract":"Context and Objectives The disclosure protocol, defined in the first French cancer plan, is intended to benefit patients, giving them better conditions for disclosing their illness and the treatment plan proposed, and this throughout its management. This protocol relies on a multidisciplinary management involving primarily physicians (medical time) and paramedics (accompanying time) and aims to inform and accompany the patients and their family. The quality of patient information is considered as a crucial point for quality of care. Our program has been set up to improve its modalities. The objectives of this program are the following: Description of the current situation, Feedback on experiences Implementation of improvement projects Demonstration of the progress made Programme Six Comprehensive Cancer Centers (CCCs) were involved in a voluntary program. First, the most important aspects of the disclosure protocol were identified. Six valid, reproductible and discriminative quality indicators (QIs) were developed. Each of these QIs includes several items. The relative weight of each item was defined from the quotation of items by participants and experts in terms of relative importance. Each QI was quoted on a scale from 0 to 1. In the CCCs involved in the program, an audit (September 2008) was performed using medical records of 60 new patients who were under treatment (surgery, chemotherapy and/or radiotherapy) for a new cancer. This retrospective audit was used to establish the state of practices. Professional practices were benchmarked between the different CCCs and weaknesses were identified. Improvement actions to be implemented have been discussed and a specific quality plan has been set up in each CCC. Results The assessed QIs were respectively: the disclosure process: mean score=0.63, range: 0.53–0.76 continuity of care: mean score=0.61, range: 0.00–0.75 consideration of patient needs: mean score=0.46, range: 0.26–0.68, information delivered to the patient: mean score=0.28, range 0.25–0.30, patient feelings: mean score=0.27, range 0.09–0.37 needs of relatives for support: mean score=0.26, range 0.02–0.44 Even if the lack of traceability may explain a large part of measured quality defaults, professionals also identified the need to precise the good practices, to disseminate them and to structure the modalities of the disclosure process for each patient. This process has been standardised in each center. A systematic production of a personalised care program for each patient is still ongoing. Some skills have already been developed by professionals (e.g. information delivered to the patient, information process, adaptation to patient singular choices, information check list) and shared between CCCs. Conclusion The second audit will be conducted in February 2010 and the comparison of results for each hospital may demonstrate the progress made. Thus, consistency of such programs can be discussed in April 2010. Such an approach is required i","PeriodicalId":20849,"journal":{"name":"Quality and Safety in Health Care","volume":"24 1","pages":"A171 - A172"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90803090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}