scholarly journals Use of Antimicrobials at the End of Life (EOL): A Retrospective Cohort Study Analyzing Providers’ Reasons for Prescribing Antimicrobials at the EOL—Their Benefits and Adverse Effects (S766)

2020 ◽  
Vol 59 (2) ◽  
pp. 566-567
Author(s):  
Pooja Vyas ◽  
Santiago Lopez
2017 ◽  
Vol 56 (10) ◽  
pp. 1265-1271 ◽  
Author(s):  
Liisa K. Rautakorpi ◽  
Johanna M. Mäkelä ◽  
Fatemeh Seyednasrollah ◽  
Anna M. Hammais ◽  
Tarja Laitinen ◽  
...  

The Lancet ◽  
2011 ◽  
Vol 378 (9800) ◽  
pp. 1408-1413 ◽  
Author(s):  
Alvin C Kwok ◽  
Marcus E Semel ◽  
Stuart R Lipsitz ◽  
Angela M Bader ◽  
Amber E Barnato ◽  
...  

2018 ◽  
Vol 44 (9) ◽  
pp. 505-513 ◽  
Author(s):  
Magnolia Cardona ◽  
Robin M. Turner ◽  
Amanda Chapman ◽  
Hatem Alkhouri ◽  
Ebony T. Lewis ◽  
...  

2016 ◽  
Vol 4 (11) ◽  
pp. 1386-1390
Author(s):  
ShereenElazzazy BSc,Pharm,PharmD ◽  
◽  
AzzaHassan MD ◽  
Pascale Haddad ◽  
◽  
...  

2021 ◽  
Author(s):  
Yang Chen ◽  
Jianjun Jiang ◽  
Wei Peng ◽  
Chuan Zhang

Abstract Background: Palliative sedation is consciously reducing the patient's consciousness to alleviate the refractory symptoms. However, studies on palliative sedation for children are scarce. We aimed to survey the symptom control and risks for children with sedative therapy in end of life.Method: This study was a single center retrospective cohort study. Children who died in the Department of Palliative Medicine were divided into palliative sedation (Group A) and non-palliative sedation group (Group B). The symptoms relief, survival time, and last hospitalization time were compared between two groups. Results: From January 2012 to November 2019, 41 children died in department of palliative care. 24 children were sedated (Group A), meanwhile 17 children were not (Group B). The symptoms in Group A were more complex than Group B (p =0.013). Overall symptom relief in Group A was higher than that in Group B (24/24, 10/15 p =0.041). Pain relief rates(7/7, 20/21 p =0.714), maximum/pre-death opioid dose [30(20, 77.5), 18(9, 45) p =0.175, 30(20, 60), 18(9, 45) p =0.208]and pain intensity difference [5(4,6.5), 4(2,6) p =0.315] were not statistically significant difference in both group. After diagnosis, the survival time of the Group A was longer than the Group B (p =0.047). However, the length of hospitalization before death was similar in two groups (p =0.385).Conclusion: Palliative sedation controls complicated, painful symptoms at the end of life and does not shorten the hospitalization time in children.


2019 ◽  
pp. bmjspcare-2019-001984 ◽  
Author(s):  
Eva Schildmann ◽  
Anna Bolzani ◽  
Sophie Meesters ◽  
Bettina Grüne ◽  
Alina Marheineke ◽  
...  

ObjectivesSedatives are frequently used at the end of life in specialist palliative care. There is scarce information about their use in nursing homes. Therefore, we aimed to assess the use of (1) sedatives generally and (2) ‘sedatives with continuous effect’, based on objective operational criteria, within the last week of life in a nursing home.MethodsThis was a retrospective cohort study of residents who died in a German nursing home between 1/2015 and 12/2017, using the nursing home’s medical records, which contained drug sheets and nurses’ notes. Sedatives analysed were those recommended by guidelines for ‘palliative sedation’: benzodiazepines, levomepromazine, haloperidol (≥5 mg/day) and propofol. Exploratory statistical analysis was conducted using R V.3.6.1.Results46/165 (28%) deceased residents received a sedative during the last week of life, all without use of the term ‘sedation’. 26/165 residents (16%) received ‘sedatives with continuous effect’, for median 4 days (range 1–7). Oral lorazepam was used most frequently, mainly for agitation, anxiety and dyspnoea, but also due to palliative status and patients wish. The median total daily dose of lorazepam within the last week of life was 1.5 mg (range 0.5–7.5). The term ‘palliative’ was significantly more often used for residents receiving sedatives (p=0.001).ConclusionsCompared with published data on continuous deep sedation, moderate or deep sedation was less frequent in this nursing home and never labelled as ‘sedation’. Multicentre mixed-methods research is needed to gain representative and more detailed data on sedation practices at the end of life in nursing homes.


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