Utility of Basal Laser Doppler Fluxmetry to Assess Resolution of Acute Vaso-Occlusive Episodes In Sickle Cell Disease

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4809-4809
Author(s):  
Patricia A. Shi ◽  
Olugbenga Olowokure ◽  
Crystal Miller

Abstract Abstract 4809 Currently in the field of sickle cell research there are no widely accepted and easily measured means of assessing resolution of a vaso-occlusive episode other than a patient's pain rating, amount of narcotic usage, or length of hospital stay. An easily applicable method of blood flow measurement would therefore be extremely useful. Laser-Doppler fluxmetry is a non-invasive technology that uses the frequency shift of laser light striking moving blood cells for the determination of blood flow. In previous studies in sickle cell patients using this technology, patient-discomforting provocations such as response to transient ischemia, heating, or cold stimulus have been required to show a difference between sickle cell patients and controls, due to large intra-patient variability seen in basal steady-state readings (Bachir D et al, Microvasc Res 1993). However, this variability may be due to long time intervals (2-3 weeks in previous studies) between basal measurements with no confirmation that measurements were repeated in precisely the same anatomic location. Spatial precision is important since blood flow can differ between areas only 1 cm apart (Rodgers GP et al, N Engl J Med 1984). No study, to our knowledge, has yet used successive laser Doppler measurements, basal or provocative, within a hospitalization for a vaso-occlusive episode in order to correlate with its resolution. In this study, laser Doppler measurements (Periflux Model PF3 or PF5000, Perimed, Stockholm, Sweden) of the skin of the forehead and medial calf were assessed approximately every 8 hours from early in admission until hospital discharge in 8 subjects (6 females, 2 males) with SS or S ßthalassemia ranging in age from 10–35 (average 24, median 24) years enrolled in a Phase I clinical trial assessing intravenous immunoglobulin for treatment of acute vaso-occlusive episodes. Patients were normotensive, non-smoking, had no history of cardiovascular disease, no recent caffeine exposure, and no history of leg ulcers. The medial calf was chosen as a measurement site due to its clinical relevance in regard to leg ulcers and relative hairlessness. The forehead was chosen as a site due to report in the literature (in normal volunteers) of a relatively low (compared to other body sites) intra-individual coefficient of variation of 20% (Sundberg S, Scan J Clin Lab Invest 1984). Measurements over the length of the hospital stay were repeated in the precise same area (using a skin marker), with the subject in the supine position, using a 780 nm wavelength, 0.25 mm fiber separation, 1-cm diameter probe programmed to 34°C (to control for the inability to regulate room temperature in the standard inpatient units). Averaging absolute perfusion or blood cell velocity measurements from all evaluable subjects at each time point (number of measurements evaluable at each time point differed according to the number of patients still hospitalized at that time point), there was no linear trend of improvement in blood flow over time in either body location. When averaging percentage (%) change between two consecutive measurements from all evaluable subjects at each time point, there was also no linear trend in blood flow improvement over time. However, when averaging within each subject the % change between consecutive measurements for the length of that subject's hospital stay, all patients showed a positive % change in blood flow in both body locations. In the medial calf, the average and median improvement was 20% and 11% (range 5–52%). In the forehead, the average and median improvement was 37% and 18% (range 1–194%). We conclude that, despite efforts to mitigate possible circadian (Houben AJ et al, Scand J Clin Lab Invest 1994) and disease-related intra-individual patient variability, it is unlikely that basal laser Doppler flow measurements will be useful for real-time assessment of resolution of acute pain episodes. However, as all subjects showed an average % improvement in blood flow over the length of their hospital stay, basal laser Doppler measurements may still be useful as a research tool to compare the degree of blood flow improvement in a treatment versus control group for acute vaso-occlusive episodes. Its main potential advantage over pain ratings is greater objectivity; over narcotic usage greater independence from operator/provider bias; and over length of hospital stay greater resolution. Disclosures: No relevant conflicts of interest to declare.

Neonatology ◽  
2021 ◽  
pp. 1-9
Author(s):  
Matthias Fröhlich ◽  
Tatjana Tissen-Diabaté ◽  
Christoph Bührer ◽  
Stephanie Roll

<b><i>Introduction:</i></b> In very low birth weight (&#x3c;1,500 g, VLBW) infants, morbidity and mortality have decreased substantially during the past decades, and both are known to be lower in girls than in boys. In this study, we assessed sex-specific changes over time in length of hospital stay (LOHS) and postmenstrual age at discharge (PAD), in addition to survival in VLBW infants. <b><i>Methods:</i></b> This is a single-center retrospective cohort analysis based on quality assurance data of VLBW infants born from 1978 to 2018. Estimation of sex-specific LOHS over time was based on infants discharged home from neonatal care or deceased. Estimation of sex-specific PAD over time was based on infants discharged home exclusively. Analysis of in-hospital survival was performed for all VLBW infants. <b><i>Results:</i></b> In 4,336 of 4,499 VLBW infants admitted from 1978 to 2018 with complete data (96.4%), survival rates improved between 1978–1982 and 1993–1997 (70.8 vs. 88.3%; hazard ratio (HR) 0.20, 95% confidence interval 0.14, 0.30) and remained stable thereafter. Boys had consistently higher mortality rates than girls (15 vs. 12%, HR 1.23 [1.05, 1.45]). Nonsurviving boys died later compared to nonsurviving girls (adjusted mean survival time 23.0 [18.0, 27.9] vs. 20.7 [15.0, 26.3] days). LOHS and PAD assessed in 3,166 survivors displayed a continuous decrease over time (1978–1982 vs. 2013–2018: LOHS days 82.9 [79.3, 86.5] vs. 60.3 [58.4, 62.1] days); PAD 40.4 (39.9, 40.9) vs. 37.4 [37.1, 37.6] weeks). Girls had shorter LOHS than boys (69.4 [68.0, 70.8] vs. 73.0 [71.6, 74.4] days) and were discharged with lower PAD (38.6 [38.4, 38.8] vs. 39.2 [39.0, 39.4] weeks). <b><i>Discussion/Conclusions:</i></b> LOHS and PAD decreased over the last 40 years, while survival rates improved. Male sex was associated with longer LOHS, higher PAD, and higher mortality rates.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 3779-3779
Author(s):  
Julie Makani ◽  
Tolulope Ajala-Agbo ◽  
Godfrey Otieno ◽  
Christopher Olola ◽  
Greg Fegan ◽  
...  

Abstract Background: Sickle cell anemia (SCA) is one of the commonest monogenic disorders, with 90% of the world’s population living in sub-Saharan Africa. Cerebrovascular accident (CVA) is a major cause of morbidity, but its clinical prediction in resource rich countries has allowed effective primary and secondary prevention. Measurements of time-averaged maximum of the mean (TAMM) cerebral blood flow velocity (CBFv) in the internal carotid/middle cerebral (ICA/MCA) arteries by Transcranial Doppler (TCD) ultrasonography and of mean overnight oxyhemoglobin saturation (SpO2) have been useful in predicting CVA. The criteria used in Western populations may not be appropriate to children living in Africa. Aims: The aims of this study were to evaluate the TAMM CBFv in patients with SCA in Kilifi district hospital, Kenya, to assess risk factors associated with high ICA/MCA TAMM CBFv and to examine any association with neurological complications. Study design: This was a cross sectional descriptive study, where TCD ultrasonography was performed on all SCA patients attending the outpatient clinic at CGMR-C, Kilifi, Kenya in 2002. Previous data from 1990 and follow-up data from 2004 were included. Results: In 140 patients with SCA, aged 3 months to 16 years, the median ICA/MCA TAMM CBFv was 116cm/sec (SD 38, range 0–219 cms/s) compared with 97 (SD 24, range 46–190) cm/sec in 142 controls aged 2 months to 14 years (p=0.0001). 28 SCA patients (20%) had TAMM CBFv greater than and 16 (11%) had TAMM CBFv less than 2 standard deviations from the mean for controls in one or both ICA/MCA’s, but only seven (5%) had a velocity above 170 cm/sec (one &gt;200cm/sec), with the highest proportion of patients aged between 5–9 years (p=0.02). In only two of the patients with low velocities, both with previous CVA, was there no ultrasound signal from either side. 45 (32%) SCA patients had a second TCD after 2 years (two after 14 years). Of the 21 restudied who had high TAMM CBFv at baseline, 14 remained high and 2 became low. Of the 15 restudied who had low TAMM CBFv at baseline, 14 remained low and none became high. Patients with abnormal TCD had lower daytime SpO2 oxygen saturation (p=0.01) and hematocrit (p=0.05). Abnormal TCD was also associated with lower haemoglobin level, red blood cell count and higher white cell count, but not significantly. Neurological abnormalities included history of convulsions in 25 (18%) and history of CVA in 5 (4%). Of those with CVA, maximum TAMM CBFv on either side were 157, 156, 108, 0 and 0; the last patient subsequently died. Three patients who had convulsions in the interim attended for follow-up TCD; compared with those without seizures there was a trend for a greater increase in TAMM CBFv in these patients (p=0.06). Conclusion: Compared with the developed world, in Africa a smaller proportion of patients with SCA have conditional or abnormal TCDs or CVA, although convulsions are common. The proportion of those with low velocities, perhaps due to ICA/MCA occlusion with moyamoya, may increase with time. Further population-based studies in a birth cohort will determine whether cerebrovascular disease is rare or lethal and, together with imaging and neuropsychology, will establish whether abnormal TCD predicts neurological events in Africa.


2015 ◽  
Vol 6 (1) ◽  
pp. 9-11
Author(s):  
Md Abid Hossain Mollah ◽  
Khondokar Jahirul Hasan ◽  
M Ekhlasur Rahman ◽  
Shegufta Rahman

Objective : To determine the efficacy of oral prednisolone among children with acute bronchiolitis who have associated family history of atopy.Materials and Methods : This randomized double blind placebo controlled trial was carried out in Dhaka Medical College Hospital during July’08 to June’10. A total of sixty patients (1-24 months) of acute bronchiolitis who had family history of atopy (e.g. allergic rhinitis, allergic conjunctivitis, asthma, eczema) were enrolled. After enrollment, allocation of either prednisolone or placebo to the study subjects were done randomly by lottery method and the researcher remained blind about the allocation. Finally 30 cases received prednisoloneorally at a dose of 2mg/kg/day 8 hourly for 3 consecutive days and 30 cases received placebo (made of flour). In addition, both the groups got same supportive measures. During intervention, study subjects were monitored by Modified Respiratory Distress Assessment Instrument (MRDAI) score twice daily for consecutive 3 days. Duration of oxygen therapy as well as length of hospital stay was also determined. Data were analyzed using appropriate statistical tests and a p value of <0.05 was considered significant.Results : The respiratory rate, accessory muscle use and auscultatory finding scores were significantly declined in Prednisolone group than the placebo group (p<.05). However, cyanosis score though declined in both groups, the difference was not significant (p>.05). Mean duration of oxygen therapy needed in Prednisolone group was significantly lesser than the placebo group (13.7 vs 24.1 hours; P<.01). Similarly, the length of hospital stay was shorter in prednisolone group than in placebo group (3.3 vs 4.6days; p<.01).Conclusions : Three days of oral prednisolone therapy along with supportive measures was found to be significantly useful among children with acute bronchiolitis having family history of atopy in terms of clinical recovery, oxygen requirement and duration of hospital stayNorthern International Medical College Journal Vol.6(1) 2014: 9-11


2021 ◽  
Author(s):  
Martine Bek ◽  
Julia C Berentschot ◽  
Majanka Heijenbrok ◽  
Susanne Huijts ◽  
Michel E van Genderen ◽  
...  

Introduction: A large proportion of patients experiences a wide range of sequelae after acute COVID-19 infection, especially after severe illness. The long-term health sequelae need to be assessed. Our objective was to longitudinally assess persistence of symptoms and clusters of symptoms up to 12 months after hospitalization for COVID-19, and to assess determinants of the main persistent symptoms. Methods: In this multicenter prospective cohort study patients with COVID-19 are followed up for 2 years with measurements at 3, 6, 12, and 24 months after hospital discharge. Here, we present interim results regarding persistent symptoms up to 12 months. Symptoms were clustered into physical, respiratory, cognitive and fatigue symptoms. Results: We included 492 patients; mean age was 60.2 years, 335 (68.1%) males, median length of hospital stay 11 days. At 3 months after discharge 97.0% of the patients had at least 1 persisting symptom, this declined to 95.5% and 92.0% at 6 and 12 months, respectively (p=0.010). Muscle weakness, exertional dyspnea, fatigue, and memory and concentration problems were the most prevalent symptoms with rates over 50% during follow-up. Over time, muscle weakness, hair loss, and exertional dyspnea decreased significantly (p<0.001), while other symptoms, such as fatigue, concentration and memory problems, anosmia, and ageusia persisted. Symptoms from the physical and respiratory cluster declined significantly over time, in contrast to symptoms from the fatigue and cognitive clusters. Female gender was the most important predictor of persistent symptoms and co-occurrence of symptoms from all clusters. Shorter hospital stay and treatment with steroids were related with decreased muscle weakness; comorbidity and being employed were related with increased fatigue; and shorter hospital stay and comorbidity were related with memory problems. Conclusion: The majority of patients experienced COVID-19 sequelae up to 12 months after hospitalization. Whereas physical and respiratory symptoms showed slow gradual decline, fatigue and cognitive symptoms did not evidently resolve over time. This finding stresses the importance of finding the underlying causes and effective treatments for post-COVID condition, beside adequate COVID-19 prevention.


2021 ◽  
Vol 7 (2) ◽  
pp. 67-71
Author(s):  
Bithi Debnath ◽  
Sajani Islam ◽  
Nazmul Haque

Background: Bronchiolitis is the most common reason for hospitalization among children younger than 2 years. Objective: The aim of the study was to assess the possibility that the associated risk factors in children suffering from bronchiolitis could predict the length of hospital stay and also to observe the immediate outcome. Methodology: This prospective study was conducted in a district hospital of Bangladesh in a period of two years from January 2011 to December 2012. Patients aged 2 years or less fulfilling inclusion criteria for bronchiolitis and required admission were enrolled in this study. Patients having comorbidities and who were discharged before fulfilling the study criteria for discharge were excluded from the study. Treatment was given according to National Guidelines for the Management of Bronchiolitis. All demographic, clinical and laboratory data were recorded in a prefixed questionnaire and analyzed. Results: Among 100 patients, 60% cases were hospitalized for 4 days or more. Mean duration of hospital stay was 4.37±1.93 days. Patients of male sex (67%), younger than 6 months of age (71%), preterm birth (21%), weight-for-age was either ≥2SD (60%) or ≤3SD (23%) were hospitalized for longer duration. Length of hospitalization was also increased in patients with family history of asthma (37%), smoking (75%), using wood-burning stoves for cooking (89%) and no previous history of respiratory distress (81%). Exclusively breastfed infants (41%) stayed hospital for shorter duration than those who fed partially (53%) or not at all (6%). All patients were improved in this case series (100%). Conclusion: Bronchiolitis patients having male sex, age less than 6 months, preterm born, partially breast fed , family history of asthma, exposure to smoking and wood-burning stoves were deduced to be significant risk factors for prolongation of length of hospitalization. Further research is needed to determine how these risk factors contribute to the development of the disease and prolong the length of hospital stay. Bangladesh Journal of Infectious Diseases 2020;7(2):67-71


2016 ◽  
Vol 31 (2) ◽  
pp. 20-23 ◽  
Author(s):  
Melanie Grace Y. Cruz ◽  
Natividad A. Almazan

Objective: To review cases of adult acute epiglottitis in a tertiary government hospital and describe the clinical presentations, diagnostics performed, management and outcomes. Methods: Study Design:            Retrospective Chart Review Setting:                       Tertiary Government Hospital Subjects: Records of patients admitted by or referred to the Department of Otolaryngology Head and Neck Surgery with a diagnosis of acute epiglottitis from January 2008 to August 2014 were identified from the department census and charts were retrieved from the Hospital Record Section and evaluated according to inclusion and exclusion criteria.  Information regarding demographic data, clinical features, laboratory and other diagnostic examinations, medical management, and length of hospital stay were collected. Results: There were 20 cases in seven years and eight months. Most were male, 18 to 37-years-old, presenting with dysphagia, odynophagia and a swollen epiglottis on laryngoscopy. Abnormal soft-tissue lateral radiographs of the neck and leukocytosis were seen in 73 % and 83% respectively. Intravenous antibiotics and corticosteroids were administered in all cases, and mean hospital stay was 11.2 days. Conclusion: Adult acute epiglottitis should be highly suspected in patients presenting with dysphagia, odynophagia, and muffling of the voice even with a normal oropharyngeal examination. History of respiratory infection, co-morbidities, smoking and alcohol intake, concomitant laryngeal pathology and supraglottic structure insults contribute to development of the disease.  Laryngoscopy is still the gold standard in diagnosis. Airway protection is mandatory but prophylactic intubation or tracheostomy are not advised.  Intravenous antibiotics are necessary and corticosteroids may be of benefit.  Keywords: epiglottitis, supraglottitis, epiglottis, adult, Philippines


2020 ◽  
Author(s):  
Yunwei Ou ◽  
Xiaofan Yu ◽  
Xiaojuan Liu ◽  
Qian Jing ◽  
Baiyun Liu ◽  
...  

Abstract Background: Clinical features in chronic subdural hematomas (CSDH) patients with and without history of head trauma are not clear. Here, we seek to investigate difference of clinical characteristics in CSDH patients with and without head trauma.Methods: Retrospectively collected clinical characteristics of CSDH patients, who were performed exhaustive drainage strategy in burr-hole craniostomy from August 2011 to May 2019. Divided patients into trauma and no trauma groups. Chi-square test or t-test was used to analyze differences of clinical characteristics between two groups. Multiple linear regression analysis was performed to analyze relationships between clinical characteristics and reduction of hematoma cavity and length of hospital stay in CSDH patients with trauma.Results: 1,307 CSDH patients were collected. 805 patients occurred history of head trauma, 502 patients without it. Mean age of patients with trauma was 64.0 ± 16.1 years, while 61.5 ± 17.9 years in patients without trauma (p=0.010). More patients occurred hypertension in without trauma group than trauma group (40.2% vs 32.9%, p=0.007). Dizziness occurred in 29.2% patients with trauma, 23.1% in patients without trauma (p=0.016). Reduction of hematoma cavity after surgery in patients without trauma was less than ones with trauma (p=0.002). Length of hospital stay in patients with trauma was 7.9 ± 4.5 days, which was longer than patients without trauma (7.3 ± 3.7 days, p=0.016). No significantly different densities of hematoma on CT, complications, mortality, recurrence rate and outcome were found between two groups.Conclusion: Pathogenesis and some clinical characteristics occur differences in CSDH patients with and without trauma, but if we choose an optimal treatment method, such as our exhaustive drainage, and we can achieve the same effect.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 3647-3647
Author(s):  
Azada Ibrahimova ◽  
Bruce Bernstein ◽  
Rida Abid ◽  
Nataly Apollonsky

Abstract Splenic complications are often seen in pediatric patients with sickle cell disease and could lead to an increase in morbidity and mortality. The most common splenic event is acute splenic sequestration crisis (ASSC) which has been often managed with surgical splenectomy. Although splenectomy has been the treatment of choice for years, the long term complications of splenectomy on vascular events has not been broadly assessed. It has been reported that splenectomy could lead to vascular complications and increased risk of thrombosis in chronic hemolytic conditions. As it was proposed, it could be partially due to the shift form extravascular hemolysis to intravascular leading to the scavenging of nitric oxide (Kato et al, 2007). In terms of cerebral vasculopathy in children with sickle cell disease, screening is usually done by measuring blood flow velocity in the main cerebral arteries using Transcranial Doppler Ultrasonography (TCD). In 2014 Peter Soh and Abdul Siddiqui reported an increased risk of cerebrovascular complications in splenectomized patients with sickle cell disease (3), but it has not been confirmed by other publications. The aim of our study is to evaluate how splenectomy affects cerebral blood flow measured by TCD in patients with homozygous HbS. The secondary aim is to evaluate if Hydroxyurea (HU) has a protective effect on the development of cerebral vasculopathy in splenectomized patients. We performed a retrospective chart review of patients with sickle cell disease Hb SS and Hb S beta thalassemia followed at the Marian Anderson Center at St. Christopher's Hospital for Children, Philadelphia between 1999 and 2016. In the final analysis we included TCD data on 153 patients, of which 36 had undergone splenectomy. A total of 516 TCD studies were collected, of which 145 patients had a history of splenectomy. Of the 516 TCD assessments in this sample, 70 (13.6%) patients were on HU of which 21 had undergone splenectomy. Pearson correlations were calculated to explore linear associations of mean cerebral blood flow velocities (CBFV) with age at the time of TCD assessment, time since splenectomy, and TCD values. Associations of CVFV with splenectomy and with HU administration for splenectomy patients were analyzed with analysis of covariance (ANCOVA). The association of time elapsed since splenectomy to TCD measure, adjusting for age at TCD assessment, was explored with multiple linear regression models. Statistical analysis was conducted with SPSS ver. 24.0. Age at the time of TCD was significantly correlated with mean right cerebral artery (RMCA) (r = -.199, p < .001), LMCA (r = -.181, p < .001), RDICA (r = -.110, p = .047), LDICA (r = -.142, p = .01) and Basilar (r = -.186, p = < .001) velocities. Tables 1 and 2 present estimated mean TCD values (calculated adjusting for age at the time of TCD). In analysis of all TCDs, the estimated mean (RMCA) velocity was significantly higher in patients with history of splenectomy than in patients without splenectomy, (Table 1). There was also significant difference in LDICA, RDICA and right posterior cerebral artery (RPCA) velocities, all of which were higher in splenectomized patients (Table 1). When analyzing the velocities according to time since splenectomy, there were significant associations between years since splenectomy (0-5, 5-10 and >10years) and with both RMCA and LMCA abnormalities. Analysis of TCD results in splenectomized patients on HU versus non-HU, indicates all estimated mean TCDs except for RPCA, are lower for the patients on HU (Table 1), with RMCA and LMCA statistically significant. Based on our analysis we conclude that in patients with homozygous HbS disease history of surgical splenectomy increases the risk for cerebral vasculopathy. It remains unclear if cerebral vasculopathy develops as a result of splenectomy or if there is a preexisting factor leading to the development of both complications. The other important finding of our study is a protective effect of hydroxyurea on the development of cerebral vasculopathy in splenectomized patients. Disclosures No relevant conflicts of interest to declare.


2021 ◽  
Vol 9 ◽  
Author(s):  
Zhu Li ◽  
Li Xiao ◽  
Lin Yang ◽  
Shaojun Li ◽  
Liping Tan

Objective: Acute poisoning in children is characterized by regional differences. This study described the basic situation of childhood poisoning in southwest China based on hospitalized cases.Data and Methods: A total of 1,076 acute poisoning cases among hospitalized children admitted to Children's Hospital of Chongqing Medical University from January 2012 to December 2020 were included in this study. Clinical data such as gender, age, living environment, poisonous substance, and cause of poisoning were statistically described. Trends of length of hospital stay, population distribution, poisonous substances, and causes of acute poisoning in the hospitalized children were compared over time.Results: The cohort comprised 588 males and 488 females; 811 cases lived in rural areas and the rest resided in urban areas. Most cases were between early childhood and school age. Poisoning usually occurred at home (973 cases, 90.4%). Pesticides (381 cases, 35.4%) and drugs (275 cases, 25.6%) were the two most common poisonous substances. Two main causes of poisoning were accidental taking (755 cases, 70.2%) and suicide (177 cases, 16.4%). The results of univariate analysis of suicide showed significant correlations among gender, place of residence, age, poisonous substance, and place of suicide (P &lt; 0.001), while living environment (town), age (adolescence), and poisonous substance (pesticide, drug) were independent risk factors (P &lt; 0.05). There was no significant change in the length of hospital stay for poisoning over time. The overall number of hospitalizations presented a decreasing trend, while the number of urban children gradually increased. The proportion of adolescent poisoned children and suicidal children increased in the last 3 years.Conclusion: Optimizing the package and distribution channels of pesticides and drugs, raising safety awareness of children to avoid accidental injuries, and paying attention to children's mental health are measures that are necessary to prevent poisoning in children.


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