Safe Deep Sedation with Midazolam and Propofol for Cerebral MRI in Young Children with Sickle Cell Disease Is Safe: A Single Center Experience in Belgium

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 1324-1324
Author(s):  
Cécile Callewaert ◽  
Laurence Dedeken ◽  
Françoise De Groote ◽  
Laurence Rozen ◽  
Phu-Quoc Lê ◽  
...  

Abstract Introduction Cerebral angio-MRI is required in children with Sickle Cell Disease (SCD) in case of abnormal blood flow velocities or lack of acoustic window at Trans-Cranial Doppler Echography (TCD) and to screen the presence of silent infarcts. MRI in young children requires deep sedation and could potentially lead to hypoxemia and increase the risk of SCD-related complications. For this reason, we studied whether deep sedation (DS) for cerebral MRI in young children with SCD might be associated with more frequent adverse events during and within 30 days after the procedure. Methods We identified all patients with SCD who were investigated by MRI under DS in our center (Hôpital Universitaire des Enfants Reine Fabiola, Brussels, Belgium) from Augustus 2005 to March 2016. Demographic data as well as data about the anaesthetic procedure and acute clinical events 30 days before and after sedation have been collected retrospectively. The anaesthetic procedure for patient with SCD was based on midazolam as premedication followed by propofol for deep sedation. Supplementary oxygen was added to all children to maintain FiO2 > 40%. No prophylactic red blood cell transfusion/exchange were administered before sedation. Data were analyzed for normality; parametric values were assessed by mean and SD, non-parametric values were assessed as medians and interquartile ranges. Student test was used to analyse continuous variable and Chi-square test for discrete variable. Results Seventy four SCD children were identified in whom 147 procedures were performed. 53% were female; 94% were HbSS or HbSβ0. Most of them have already experienced one or more previous acute clinical event (dactylitis 32.4%, vaso-occlusive crisis [VOC] 45.9%, acute chest syndrome [ACS] 32.4%). Hydroxyurea has been prescribed to 39 patients (52.7%) at a median age of 2.4 years (range: 0.6- 4.9 years) mainly for recurrent VOC/ ACS. Five patients were on chronic transfusion program beginning at a median age of 2.6 years (range: 2.1-4.7 years) for primary and secondary stroke prevention. Median age at procedure was 3.1 years (range: 0.9 - 6.1 years). The median number of MRI under DS per patient was 1.8 (range: 1-5). Seven MRI were associated to an incident linked to the DS: 3 episodes of agitation/irritability, 4 desaturations < 95% (with 1 requiring transient manual mask ventilation). Median saturation during the procedure was 100% (range: 84-100%). 28 clinical events (19%) occurred within the 30 days before DS while 16 (11%) occurred within the 30 days after DS. Considering hospitalisations, the number were 16 (11%) and 11 (7.5%) before and after respectively. Considering only VOC and ACS, the numbers were 8 (5.4%) before and 6 (4%) after DS. Patients developing SCD complications after DS were less frequently treated with hydroxyurea (18.8% vs. 44.3%, P=0.06), had longer procedure while Hb level, WBC count, MCV, HbF and LDH were not significantly different. Discussion Deep sedation with midazolam and propofol for Cerebral angio-MRI in SCD children was safe, with few side-effects and no increase of VOC and ACS within one month of sedation. Only one study analyzed the safety of deep sedation in young children with SCD (Belmont et al. J Pediatr May 2015; 166:1226-32) but reported a possible trend of increased complications after sedation with midazolam, phenobarbital and fentanyl. Compared to the series of Belmont (Table 1), our patients were younger, more often treated with hydroxyurea and had a shorter procedure duration with less deep desaturation. The combination of propofol with midazolam seems to be better tolerated by children with SCD than midazolam, pentobarbital and fentanyl and appears to be safe in very young children. Disclosures No relevant conflicts of interest to declare.

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 841-841
Author(s):  
Carlton Dampier ◽  
Elizabeth Ely ◽  
Leela Aertker ◽  
Darcy Brodecki ◽  
Karen Kesler ◽  
...  

Abstract Abstract 841 Pain is the hallmark symptom of vaso-occlusion in sickle cell disease (SCD), but has not been well studied, particularly in children. Previous studies of pain in very young children with SCD have largely been limited to episodes sufficiently severe as to require acute care visits or hospitalizations. Our previous studies in school-aged children and adolescents (Dampier CD et al. J Pediatr Hematol Oncol 2004), as well as those in adults (Smith W et al Ann Inter Med 2009) suggest that vaso-occlusive pain is frequently managed at home outside of acute care medical settings. We sought to obtain similar data about the home pain experience of infants and young children with SCD as reported by parents or guardians, and to explore the relationship between the pain experience and hematological biomarkers. Enrollment and data collection was conducted from Jan 1999-Mar 2008 at the Marian Anderson Sickle Cell Center as part of the Comprehensive Sickle Cell Centers program. Families with SCD infants identified by newborn screening were first approached about the study after completion of confirmatory diagnosis and initial SCD-related education, usually between 4 to 6 months of age. After informed consent, parents/guardians were trained in pain assessment and daily reporting. When sickle cell related pain events occurred, parents/guardians reported pain occurrence, location, associated symptoms and the treatment that they provided. Daily paper diaries were generally used in the first year of life to familiarize families with pain assessment and reporting. Subsequently a novel daily pager system was used to provide a method allowed daily reporting, but with reduced participant burden. A monthly telephone system in conjunction with a daily calendar was used for those families unable to effectively comply with providing daily reports. All pain reports were adjudicated by consensus of study staff and PI/Co-PI. Children were removed from the study for any period of chronic transfusion for clinical events (splenic sequestration, recurrent acute chest syndrome, surgery). Over the study period, 103 children (58% male) were enrolled beginning at a median age of 7.3 months (range 1.5, 65.2 months). This represented about 50% of SCD children referred to the Center by newborn screening during these time periods; the most common reasons for refusal were inability to complete daily reporting and geographic distance from the Center. An SS genotype was present in 50 children (48.5%), SC in 32 (31.1%), SB0thalassemia in 6 (5.8%), SB+thalassemia in 15 (14.6%). Children were actively followed for a median of 3.8 years (range 0.3–7.6 years). The total number of days children were assessed for pain was 141,197 days with an additional 28,079 days of missing data (16%). The total number of days that children had reported pain was 2,288 days (1.6%), which represented 768 distinct episodes of pain. Over 80% of children reported to have pain in the 0–12 month age interval had pain locations (hands/feet) and characteristics (swelling or tenderness) consistent with dactylitis, which became progressively less prevalent in older age intervals. Significantly more SS/SB0 patients (58%) had >2 days of average dactylitis pain during 0–12 months or 12–24 months (53%) intervals compared to SC/SB+ patients (0%) (p=0.04). The timing of the first reported dactylitis event (<2 years or ≥2 years) significantly predicted the frequency of SCD pain events per person year, with earlier onset associated with more frequent pain events during the study period (p=0.02), for both the SS/SB0 and SC/SB+ (P=0.03) groups. Our study demonstrates the feasibility of initial recruitment and subsequent daily reporting of clinical events by families of infants and young children with SCD over many years, particularly when careful consideration is given to enhance family support and minimizing respondent burden. The onset of an initial dactylitis episode prior 2 years of age, even if treated at home, was associated with more frequent pain throughout childhood, irrespective of hemoglobinopathy type. Such children may be appropriate for interventions, such as oral hydroxyurea, that reduce excessive pain frequency. Supported by NIHHL-051495 and HL-083705. Disclosures: Dampier: Anthera Pharmaceuticals Inc:; Glycomimetics Inc: .


2015 ◽  
Vol 166 (5) ◽  
pp. 1226-1232 ◽  
Author(s):  
Ami P. Belmont ◽  
Fadi Nossair ◽  
Donald Brambilla ◽  
Marjorie Friedman ◽  
Jan Boswinkel ◽  
...  

2011 ◽  
Vol 4 ◽  
pp. OJCS.S8032 ◽  
Author(s):  
Taysir Garadah ◽  
Saleh Gabani ◽  
Mohamed Al Alawi ◽  
Ahmed Abu-Taleb

Background The prevalence and epidemiological data of atrial fibrillation (AF) among multi-ethnic populations is less well studied worldwide. Aim Evaluation of the prevalence and predisposing factors of AF in patients who were admitted to acute medical emergencies (ER) in Bahrain over the period of one year. Methods Two hundred and fifty three patients with onset of AF were studied. The mean difference of biochemical data and clinical characteristics between Middle Eastern (ME) and sub continental (SC) patients was evaluated. The odds ratio of different predisposing factors for the development of clinical events in AF patients was assessed using multiple logistic regression analysis. Results Out of 7,450 patients that were admitted to ER over one year, 253 had AF based on twelve leads Electrocardiogram (ECG), with prevalence of 3.4%. In the whole study, the mean age was 59.45 ± 18.27 years, with 164 (65%) male. There were 150 ME patients (59%), and 107 (41%) SC, 55 (22%) were Indian (IND) and 48 (19%) were South Asian (SA). In the whole study clinical presentation was of 48% for palpitation, pulmonary edema was of 14%, angina pectoris on rest of 12%, 10% had embolic phenomena, 6% had dizziness, and 7% were asymptomatic. The odds ratio of different variables for occurrence of clinical events in the study was positive of 2.2 for history of hypertension, 1.8 for sickle cell disease, 1.2 for high body mass index (BMI) >30, 1.1 for mitral valve disease. The ME patients, compared with SC, were older, had significantly higher body mass index, higher history of rheumatic valve disease, sickle cell disease with high level of uric acid and lower hemoglobin. The history of hypertension, DM and smoking was higher among the SC patients. The rate of thyroid disease was equal in both groups. Conclusion The prevalence of atrial fibrillation was 3.4% with male predominance of 65%. Patients of sub continental origin were younger with a significantly high history of hypertension and ischemic heart disease. The patients of Middle Eastern origin had significantly high rate of rheumatic heart disease, and sickle cell disease. The history of hypertension was the most important independent clinical predictor of adverse events in patients presented with AF.


2020 ◽  
Vol 67 (5) ◽  
Author(s):  
Corinna L. Schultz ◽  
Trudy Tchume‐Johnson ◽  
Tannoa Jackson ◽  
Henrietta Enninful‐Eghan ◽  
Marilyn M. Schapira ◽  
...  

2019 ◽  
Vol 105 (6) ◽  
pp. 575-579 ◽  
Author(s):  
Lisa van Geyzel ◽  
Michele Arigliani ◽  
Baba Inusa ◽  
Bethany Singh ◽  
Wanda Kozlowska ◽  
...  

IntroductionSickle cell disease (SCD) is one of the most common inherited diseases worldwide. It is associated with lifelong morbidity and reduced life expectancy. Hydroxyurea (HU) has been shown to reduce the frequency and severity of vaso-occlusive episodes in SCD. Hypoxaemia and intermittent nocturnal oxygen desaturations occur frequently in children with SCD and contribute to the associated morbidity, including risk of cerebrovascular disease.ObjectiveTo evaluate the effect of HU on oxygen saturation (SpO2) overnight and on daytime SpO2 spot checks in children with SCD.MethodsA retrospective review of children with SCD and respiratory problems who attended two UK tertiary sickle respiratory clinics and were treated with HU. Longitudinal data were collected from 2 years prior and up to 3 years after the commencement of HU.ResultsForty-three children, 23 males (53%) with a median age of 9 (range 1.8–18) years were included. In the 21 children who had comparable sleep studies before and after starting HU, mean SpO2 was higher (95.2% from 93.5%, p=0.01) and nadir SpO2 was higher (87.2% from 84.3%, p=0.009) when taking HU. In 32 of the children, spot daytime oxygen saturations were also higher (96.3% from 93.5%, p=0.001).ConclusionChildren with SCD had higher oxygen saturation overnight and on daytime spot checks after starting HU. These data suggest HU may be helpful for treating persistent hypoxaemia in children with SCD pending more evidence from a randomised clinical trial.


Blood ◽  
1995 ◽  
Vol 86 (2) ◽  
pp. 776-783 ◽  
Author(s):  
FM Gill ◽  
LA Sleeper ◽  
SJ Weiner ◽  
AK Brown ◽  
R Bellevue ◽  
...  

Within the Cooperative Study of Sickle Cell Disease, 694 infants with confirmed sickle cell disease were enrolled at less than 6 months of age. Information about the nature and frequency of complications was collected prospectively over a 10-year period. Painful crises and acute chest syndrome were the most common sickle cell-related events in homozygous sickle cell anemia (SS), hemoglobin SC disease (SC), and S beta thalassemia patients (overall incidence in SS patients of 32.4 and 24.5 cases per 100 person-years, respectively). Bacteremia occurred most frequently in SS children under 4 years of age and in SC patients less than 2 years of age. The mortality rate was low in this cohort compared with that found in previous reports. Twenty children, all with Hb SS, died (1.1 deaths per 100 person-years among SS patients). Infection, most commonly with Streptococcus pneumoniae and Hemophilus influenzae, caused 11 deaths. Two children died of splenic sequestration, 1 of cerebrovascular accident, and 6 of unclear causes. Two patients underwent cholecystectomies, and 17 underwent splenectomies after one or more splenic sequestration crises. The experience of this cohort should reflect closely the true clinical course of those children with Hb SS and Hb SC disease who are observed in sickle cell centers in the United States.


Blood ◽  
2010 ◽  
Vol 115 (17) ◽  
pp. 3447-3452 ◽  
Author(s):  
Charles T. Quinn ◽  
Zora R. Rogers ◽  
Timothy L. McCavit ◽  
George R. Buchanan

Abstract The survival of young children with sickle cell disease (SCD) has improved, but less is known about older children and adolescents. We studied the Dallas Newborn Cohort (DNC) to estimate contemporary 18-year survival for newborns with SCD and document changes in the causes and ages of death over time. We also explored whether improvements in the quality of medical care were temporally associated with survival. The DNC now includes 940 subjects with 8857 patient-years of follow-up. Most children with sickle cell anemia (93.9%) and nearly all children with milder forms of SCD (98.4%) now live to become adults. The incidence of death and the pattern of mortality changed over the duration of the cohort. Sepsis is no longer the leading cause of death. All the recent deaths in the cohort occurred in patients 18 years or older, most shortly after the transition to adult care. Quality of care in the DNC has improved over time, with significantly more timely initial visits and preventive interventions for young children. In summary, most children with SCD now survive the childhood years, but young adults who transition to adult medical care are at high risk for early death.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 2328-2328
Author(s):  
A. Kyle Mack ◽  
Roberto F. Machado ◽  
Vandana Sachdev ◽  
Mark T. Gladwin ◽  
Gregory J. Kato

Abstract Patients with sickle cell disease have decreased nitric oxide bioavailability, and studies from several groups have confirmed a blunted response to various NO donors in humans and mice with sickle cell disease. Recently published studies show that nitrite induces vasodilation in humans, apparently mediated by conversion of nitrite to NO. This study is designed to determine the potential therapeutic effect of intra-arterial nitrite infusion to restore nitric oxide dependent blood flow in the forearms of patients with sickle cell disease. Venous occlusion strain gauge plethysmography is used to measure the change of forearm blood flow in patients with sickle cell disease, before and after sequential brachial artery infusions of increasing doses of sodium nitrite. In addition, NO responsiveness before and after nitrite infusion is measured by test doses of the NO donor sodium nitroprusside (SNP). Six patients have completed the study and enrollment is continuing. These data indicate that nitrite promotes regional blood flow in patients with sickle cell disease, albeit with a blunted response compared to our healthy control subjects, in whom we previously have found increased blood flow up to 187% with comparable dosing. The significant but blunted response is consistent with the state of nitric oxide resistance to NO donors that has been seen by several groups in patients and mice with SCD. Additionally, we find in these patients that nitrite partially restores SNP responsiveness, with baseline maximal SNP responses more than doubling on average following nitrite infusion, although this finding is preliminary. No adverse effects of nitrite were seen in these six patients. Our early results support a role for nitrite as an NO donor effective in restoring NO-dependent blood flow in patients with sickle cell disease. Additional translational studies are warranted to evaluate the therapeutic effects of systemic nitrite dosing. Table 1. Forearm Blood Flow Response to Nitrite Infusion Nitrite Dose (micromole/min) Sickle Cell Disease Historical Controls P&lt; .0001 (ANOVA) 0.4 5 +/−7.2% N=6 22 +/−3.2% N=10 4 15 +/− 11% N=6 Not infused 40 49 +/− 8.9% N=6 187 +/− 16%N=18 Table 2. Nitrite Effect on Nitroprusside Responsiveness SNP Dose (micrograms/min) Pre-Nitrite Post-Nitrite P= .02 (RM-ANOVA) N=6 0.8 +21 +/− 5.6% +33 +/− 8.3% 1.6 +15 +/− 5.9% +62 +/− 15.1% 3.2 +29 +/− 6.3% +67 +/− 11.5%


Sign in / Sign up

Export Citation Format

Share Document