scholarly journals First-line management of canine status epilepticus at home and in hospital-opportunities and limitations of the various administration routes of benzodiazepines

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Marios Charalambous ◽  
Holger A. Volk ◽  
Luc Van Ham ◽  
Sofie F. M. Bhatti

AbstractStatus epilepticus (SE) or prolonged epileptic seizure activity is a common neurological emergency with a high mortality rate and, if left untreated, can lead to irreversible cerebral damage and systemic complications. Fast and effective first-line management is of paramount importance, particularly in the at-home management of seizures where drug administration routes are limited. Benzodiazepines (BZDs) have been exclusively used in veterinary medicine for decades as first-line drugs based on their high potency and rapid onset of action. Various administration routes exist in dogs, such as oral, intravenous, intramuscular, rectal, and intranasal, all with different advantages and limitations. Recently, intranasal drug delivery has become more popular due to its unique and favourable characteristics, providing potential advantages over other routes of drug administration in the management of canine SE. This narrative review provides an outline of the management of SE at home and in a hospital setting, discusses considerations and challenges of the various routes of BZD administration, and evaluates the impact of intranasal drug administration (nose-brain pathway) for controlling canine SE at home and within hospital settings.

Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 4046-4046 ◽  
Author(s):  
Angela Huth-Kuehne ◽  
Peter Lages ◽  
Rainer Zimmermann

Abstract Introduction: To investigate the cost-effectinvess of the treatment in patients with hemophilia and inhibitor, the expected number of rebleeds in home treatment is an important factor if one compares different treatment options e.g. APCC or rFVIIa. To evaluate the economic impact in mild to moderate bleeds in home treatment we used a robust established model to compare 1st, 2nd and 3rdline treatment either with rFVIIa or APCC. For the rate of rebleeds we refer to published data on a broad basis. Methods: To compare the economic impact of different treatment regimes, this model refers to an on-demand home treatment of bleeding episodes in adult hemophiliacs (mean body weight 75 kg) and is based on a previously published flow-diagram and calculation formula (Knight 2003). Dosage per bolus: rFVIIa 90μg/kg, aPCC 60 U/kg. Costs for German market were fixed at 1.21 €/IU for APCC, 0.73 €/μg for rFVIIa and 308.98 €/day in hospital. 3 treatment strategies (TS) were calculated: TS 1: APCC at home, followed by in hospital APCC (2nd-line) and rFVIIa (3rd-line) TS 2: APCC at home, followed by in hospital rFVIIa (2nd-line) and rFVIIa (3rd-line) TS 3: rFVIIa at home, followed by in hospital rFVIIa (2nd-line) and rFVIIa (3rd-line) The model was based on published data on dosing and outcome of therapy in each treatment phase. Probability of failure to control bleeding or rebleeding after first-line home treatment was set at 23.5% with APCC and 9.1% with rFVIIa. Results: Median costs for TS 1 are 23,521 Euro per bleeding episode as compared to 21,963 Euro for TS 2 and 14,328 Euro for TS 3. The difference is caused by costs for first attempt to control bleeding at home (APCC 16,335 Euro as compared to rFVIIa 11,333 Euro) and costs at later stages of treatment. Further analyses show, that favorable result for TS 3 is robust to changes of different parameters such as patients’ weight. Conclusions: First line treatment with rFVIIa in case of on demand treatment seems to be the most cost effective option in inhibitor treatment in a home treatment setting or in-hospital treatment. Local prices have to be taken into consideration.


2006 ◽  
Vol 23 (2) ◽  
pp. 129-133 ◽  
Author(s):  
B. A. Khalil ◽  
P. A. Corbett ◽  
M. O. Jones ◽  
C. T. Baillie ◽  
Kevin Southern ◽  
...  

2021 ◽  
Vol 38 (9) ◽  
pp. A16.3-A17
Author(s):  
David Fish ◽  
Fiona Bell ◽  
Clare O’Connell ◽  
Alison Walker ◽  
Laura Evans ◽  
...  

BackgroundStudies have found that pre-hospital and emergency department (ED) analgesia for children is sub-optimal. In the pre-hospital setting, barriers include limited parenteral routes, education or clinical experience and practice legislation restricting the use of opioids by paramedics. Ketamine is safe and effective with multiple administration routes. It is not bound by the controlled drugs limitations in the pre-hospital setting, and is familiar to pre-hospital and ED practitioners.MethodsQuestionnaires were sent to all UK Ambulance Service Medical Directors and Paediatric Major Trauma Centres to establish current use of parenteral analgesics, and acceptability of alternatives in pre-hospital care such as ketamine. Descriptive analysis was undertaken.ResultsIntranasal opiates were the first line parenteral analgesics in injured children in all EDs. Frequent shortages of IN diamorphine resulted in more variability of second line choices, with 40% opting for another opioid. 96% of EDs would support the use of ketamine by pre-hospital clinicians, although concerns regarding inappropriate (IV) use and use by technician crews were raised. Most ED clinicians were unaware of the limited analgesic choices available to paramedics, with many suggesting alternative opiates as well as ketamine.All ambulance service directors recognised the need for alternative analgesics being made available. Without legislative changes, inhaled/IN agents or oral opiates were the only current options. All services were supportive of research to explore the use of ketamine by paramedics for injured children.ConclusionsThere is support for the addition of IN ketamine into paramedics’ repertoire of analgesics and recognition of potential benefit. However, there is a lack of experience and evidence around its use, thus warranting research to consider the impact on analgesic timeliness, adequacy and effectiveness. An analgesia ‘system of care’ which integrates pre- and in-hospital practice would be facilitated by the use of medicines effective in managing pain and familiar to practitioners in both settings.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 281-281
Author(s):  
Christopher E. Jensen ◽  
Hillary M. Heiling ◽  
Konan E. Beke ◽  
Allison M. Deal ◽  
Ashley Leak Bryant ◽  
...  

Abstract Introduction The prognosis for older adults with acute myeloid leukemia (AML) is poor. Of approximately 12,000 adults age ≥ 60 diagnosed with AML in the U.S. annually, less than 40% survive 1 year from diagnosis. Prior research has shown that adults with AML feel time at home is a critical consideration in treatment selection. However, to date, no study has adequately described the amount of time older adults can expect to spend at home following initiation of AML therapy. In this study, we aimed to (1) quantify this time and (2) assess the impact of venetoclax (VEN) combination therapy on time at home for older adults with AML. Methods We queried records from University of North Carolina Health to identify individuals age ≥ 60 newly diagnosed with AML from 2015 to 2020. First-line AML therapy was identified, and those receiving azacitidine (AZA) and/or VEN were included. Dates of diagnosis, first remission, death, last follow up, and all oncology clinic / emergency department (ED) / inpatient encounters were captured. Patients with incomplete records were excluded. The primary outcome was proportion of days at home (PDH). PDH was calculated for each patient by subtracting the number of care days (days hospitalized or seen in an ED / oncology clinic / infusion center) from the total days of follow up, divided by total days of follow up. Overall survival (OS) was calculated via the Kaplan-Meier method. Covariates including demographics and disease risk (per European Leukemia Net 2017) were captured. PDH was evaluated via summary statistics for the full cohort and stratified by each categorical variable, both for the full follow up period and on a month-by-month basis among survivors. Associations between PDH and covariates were further assessed via linear regression with adjustment for length of follow up, with significance assessed via Wald Chi-square test. Results From 2015-2020, 137 older adults receiving first-line AZA and/or VEN were identified. 24 were excluded due to incomplete records. Among the remaining 113, mean age was 76 (range 60-99), 80.4% were white, and 43.4% were female. Most received AZA+VEN (51.3%) followed by AZA monotherapy (39.0%) and other VEN-containing combinations (9.7%). The majority had adverse-risk AML (61.3%). Baseline covariates including age and ELN risk were similar across therapy groups. Over the full follow up period, mean PDH was 0.58 (95% confidence interval 0.54-0.63) with a median of 0.63. PDH was similar among those with adverse-risk (mean 0.55, CI 0.49-0.61) and intermediate-risk AML (0.64, CI 0.56-0.72). PDH did not differ among therapy groups: AZA+VEN (0.60, CI 0.54-0.66), AZA alone (0.57, CI 0.49-0.66), and other VEN-containing regimens (0.54, CI 0.40-0.69). When adjusted for length of follow up, no covariate had a significant association with PDH (all p > 0.05). When evaluated month-by-month, the proportion of days at home rose over time among survivors. For example, of patients who survived the full month, mean PDH was 0.51 (CI 0.47-54, n = 105) in month 1 following diagnosis and 0.77 (CI 0.72-0.82, n = 57) in month 6. Figure 1 summarizes person-days at home or engaged in care for 12 months following diagnosis (including contributions from those who did not survive the full month). 34.5% of patients achieved composite complete remission, with higher rates among those receiving AZA+VEN (51.7%) than AZA alone (13.6%) (OR 6.8, p = 0.0002). Median OS was 0.64 years (CI 0.32 - 0.91) and was similar across therapy groups. Conclusion Burden of care for older adults with AML treated with first-line AZA or VEN is high. These individuals spend nearly half (cohort mean 42%) of days following diagnosis engaged in oncology care. In randomized studies, the addition of VEN to AZA improves OS and increases remission rates though results in higher rates of neutropenic fever. Although this study may be underpowered to detect small differences, the superior remission rates with AZA+VEN did not translate to more days at home, perhaps due to increased admissions for neutropenic fever and office/infusion visits. Given the importance of time at home to older adults with AML identified in prior research, these data provide new information to support shared decision making regarding treatment options. Future prospective trials should evaluate burden of care, including time at home, as an endpoint. While awaiting these data, larger analyses of the impact of treatment regimen on burden of care would be useful. Figure 1 Figure 1. Disclosures Bryant: Carevive: Consultancy, Research Funding; Jazz Pharmaceuticals: Consultancy, Research Funding; Servier Pharmaceuticals: Honoraria, Speakers Bureau. Coombs: Alexion Pharmaceuticals: Research Funding; Machaon Diagnostics: Research Funding. Foster: Macrogenics: Research Funding; Rafael Pharmaceuticals: Research Funding; Macrogenics: Consultancy; Daiichi Sankyo: Consultancy; Agios: Consultancy; Bellicum Pharmaceuticals: Research Funding.


2019 ◽  
Author(s):  
William E Oswald ◽  
Katherine E Halliday ◽  
Carlos Mcharo ◽  
Stefan Witek-McManus ◽  
Stella Kepha ◽  
...  

AbstractIntroductionFew studies have simultaneously examined the role of sanitation conditions at the home, school, and community on soil-transmitted helminth (STH) infection. We examined the contribution of each domain that children inhabit (home, village, and school) and estimated the association of sanitation in each domain with STH infection.MethodsUsing data from 4,104 children from Kwale County, Kenya, who reported attending school, we used logistic regression models with cross-classified random effects to calculate measures of general contextual effects and estimate associations of village, school, and household sanitation with STH infection.FindingsWe found reported use of a sanitation facility by households was associated with reduced prevalence of hookworm infection but not with reduced prevalence of T. trichiura infection. School sanitation coverage > 3 toilets per 100 pupils was associated with lower prevalence of hookworm infection. School sanitation was not associated with T. trichiura infection. Village sanitation coverage > 81% was associated with reduced prevalence of T. trichiura infection, but no protective association was detected for hookworm infection. General contextual effects represented by residual heterogeneity between village and school domains had comparable impact upon likelihood of hookworm and T. trichiura infection as sanitation coverage in either of these domains.ConclusionFindings support the importance of providing good sanitation facilities to support mass drug administration in reducing the burden of STH infection in children.Author SummaryInfection by whipworm and hookworm results from either ingestion of eggs or larvae or through skin exposure to larvae. These eggs and larvae develop in suitable soils contaminated with openly-deposited human faeces. Safe disposal of faeces should reduce transmission of these soil-transmitted helminths (STH), yet evidence of the impact of sanitation on STH transmission remains limited. We used data collected during a large, community-wide survey to measure prevalence of STH infections in coastal Kenya in 2015 to examine the relationship between sanitation conditions at home, school, and village and the presence of STH infection among 4,104 children who reported attending schools. We found that sanitation access at home and school sanitation coverage, but not the overall level of village sanitation coverage, was protective against hookworm infection. In contrast, only high village sanitation coverage, but not home or school sanitation, was protective against whipworm infection. Current STH control strategies emphasise periodic deworming through mass drug administration (MDA) of at-risk populations, including school-age children. Our findings highlight the need for continued efforts, alongside MDA, to extend access to good sanitation facilities at homes, schools, and across communities.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1817-1817
Author(s):  
Loretta J. Nastoupil ◽  
Ashish Rai ◽  
Joseph Lipscomb ◽  
Chadi Nabhan ◽  
Jessica N Williams ◽  
...  

Abstract Background The oldest old constitute a large proportion of the total patient (pt) population with FL. Therapeutic decision making in this group is limited by comorbidities, adverse disease and pts' characteristics, potential treatment toxicity, and limited life expectancy. Further, randomized clinical trials have rarely included this pt population. Whether current practice patterns for these pts affect their outcome remains unanswered. Therefore, we aimed to determine treatment selections, patterns of care, prognostic factors, and survival outcomes of first-line management strategies in a large United States (US) based cohort of the oldest old (pts aged > 80 years at diagnosis). Methods We used the linked Surveillance, Epidemiology, and End Results -Medicare database to identify 1,878 FL cases in pts > 80 years diagnosed between 1995 and 2009 and focused on the period when rituximab (R) claims occurred. We ascertained first-line management strategies from Medicare claims made within 90 days of diagnosis. We used multiple variable logistic regression models to evaluate the relationship between pt characteristics and the use of two common first-line management strategies—observation (obs) and treatment with R, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). We used Kaplan-Meier estimators stratified by stage to evaluate survival functions for first-line management strategies and Cox proportional hazards models adjusted for pt demographics, comorbidity index, disease characteristics, and year of diagnosis to compare the impact of first-line management strategies on survival. Results Of the 1,878 oldest adult pts, 63% were female, 95% were white, 2% were African American, 52% had stage III/IV FL, 17% had grade 3 FL, 5 % had B-symptoms, 35% had extranodal involvement, and 14% had a comorbidity index ≥ 2. Common first-line management strategies were: obs, 46%; R, 17%; chemotherapy (chemo) plus R, 11%; chemo, 11%; and radiotherapy (XRT), 11%. In the cohort of pts diagnosed between 1995 and 2009, obs was more commonly associated with urban pts (ref. less urban/rural pts; OR 1.91; 95% CI 1.15-3.18), and comorbidity index of ≥ 1 (ref. index=0; OR 1.28; 95% CI 1.00-1.64). Obs was less commonly associated with stage III/IV FL (ref. stage I/II; OR 0.67; 95% CI 0.54-0.84), grade 3 FL (ref. grade 1/2; OR 0.35; 95% CI 0.26-0.47), and year of diagnosis (ref. year 1995; OR for 1997 0.23; 95% CI 0.07-0.75; steady decrease thereafter). In the cohort of pts diagnosed between 1999 and 2009, the use of R-CHOP was associated with grade3 FL (ref. grade 1/2; OR 8.20; 95% CI 3.83-17.55) and presence of B-symptoms (ref. absent; OR 4.18; 95% CI 1.81-9.62). R-CHOP use did not vary with year of diagnosis. The table displays median survival and hazard ratios (HRs) for first-line management strategies. Most favorable outcomes were associated with first-line R-Chemo. Among stage III/IV cases, the least favorable outcomes were observed in the group that received chemo without R. The HRs did not vary with more recent years of diagnosis. Conclusion In this largest retrospective analysis of the oldest old US-based FL pts, we demonstrate that first-line R-Chemo is associated with improved survival. Confirmatory prospective studies specifically designed for this pt population are warranted. CVP-cyclophosphamide, vincristine, prednisone; CHOP- cyclophosphamide, doxorubicin, vincristine, prednisone; R-CVP- rituximab, cyclophosphamide, vincristine, prednisone. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1805-1805
Author(s):  
Ashish Rai ◽  
Loretta J. Nastoupil ◽  
Joseph Lipscomb ◽  
Kevin Ward ◽  
David H. Howard ◽  
...  

Abstract Background Therapeutic decision making for patients with low-grade (grade 1 and 2) FL involves deciding whether to treat, when to treat, and which among the numerous treatment modalities to administer. The lack of trials comparing outcomes of these treatment modalities makes it a complex process. This study seeks to examine the evolving treatment paradigm and evaluate the outcomes of first-line management strategies for low-grade FL in adults aged ≥ 66. Methods We used the linked Surveillance, Epidemiology, and End Results (SEER)-Medicare database to identify 4,233 low grade FL patients (pts) aged 66 years and older diagnosed between 1995 and 2009. We ascertained first-line management strategies from Medicare claims made within 90 days of diagnosis. We used Kaplan-Meier estimators stratified by stage to evaluate survival functions for first-line management strategies. We used multivariate Cox proportional hazards models—stratified by stage and adjusted for patient demographics, comorbidity index, and year of diagnosis—to compare the impact of first-line management strategies on overall survival (OS). Results Of the 4,233 pts, 57% were female, 3% were African American, 93% were White, 51% resided in big metropolitan areas, 70% were diagnosed after 2000, 44% had stage III/IV disease, and 38% had extranodal involvement. The median age at diagnosis was 74 years (interquartile range 70-80). Common first-line management strategies were: observation (obs), 47%; chemotherapy (chemo) plus rituximab (R), 20%; chemo alone, 12%; R alone, 9%; and radiotherapy (XRT) alone, 9%. Among pts receiving chemo plus R (R-chemo), the most commonly used regimens were: R-CHOP (R, cyclophosphamide, doxorubicin, vincristine, and prednisone; 36%), R-CVP (R, cyclophosphamide, vincristine, and prednisone; 47%), R-Fludarabine based (9%), and R-other (7%). The table displays median survival and hazard ratios (HRs) for first-line management strategies. Among stage I/II cases, most favorable outcomes were observed in cases receiving XRT alone, whereas among stage III/IV cases most favorable outcomes were observed in the group that received R-chemo. In the subset of stage III/IV pts that received R-chemo, R-CHOP was associated with the most favorable outcomes. HRs decreased steadily with increasing years of diagnosis. Conclusion First-line R-chemo is commonly used in older adults with low-grade FL in the United States and is associated with most favorable survival outcomes. XRT is associated with very favorable outcomes in stage I/II pts. Outcomes have improved steadily in the past 10 years. CVP–cyclophosphamide, vincristine, prednisone; CHOP- cyclophosphamide, doxorubicin, vincristine, prednisone Disclosures: No relevant conflicts of interest to declare.


1998 ◽  
Vol 13 (1_suppl) ◽  
pp. S23-S26 ◽  
Author(s):  
Elizabeth Martina Bebin

The pharmacologic interventions for treatment of acute repetitive seizures and those for treatment of status epilepticus are similar. The choice of treatment should be based on the drug's onset of action, spectrum of anticonvulsant activity, route and ease of administration, elimination half-life, therapeutic margin of safety, and redistribution from the central nervous system. Treatment should be initiated early in patients who are prone to seizure clusters or prolonged partial seizures that may generalize or progress to status epilepticus. Benzodiazepines have become first-line drugs for treatment of acute seizures and status epilepticus, followed by phenytoin/fosphenytoin and phenobarbital. Short-acting benzodiazepines, including diazepam, lorazepam, clonazepam, and midazolam, can decrease the frequency of emergency department visits if given at the appropriate times. The recently approved intravenous formulation of valproate may be of use in children receiving oral valproate who develop breakthrough seizures caused by subtherapeutic plasma levels that are secondary to missed doses or an inability to tolerate oral valproate. (J Child Neurol 1998;13(Suppl 1):S23-S26).


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