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1.
Pediatr Blood Cancer ; 67(5): e28225, 2020 05.
Article in English | MEDLINE | ID: mdl-32065511

ABSTRACT

BACKGROUND: Patients with sickle cell disease (SCD) are at increased risk for osteomyelitis (OM). Diagnosis of OM in SCD is challenging as the clinical presentation is similar to a vasoocclusive crisis (VOC) with no diagnostic gold standard. We report characteristics and outcomes of OM in SCD patients treated at our center over 10-year period. DESIGN/METHOD: We conducted a retrospective analysis of patients with SCD who were treated for OM at our center over a 10-year period (2006-2016). Cases were identified utilizing radiology data mining software. Radiology reports and medical charts of potential OM cases were reviewed. RESULTS: Twenty-eight children with SCD were treated for OM at our institution. Patients treated for OM were largely similar to patients treated for a VOC. However, patients treated for OM had significantly higher C-reactive protein (10 mg/dL vs 5.58 mg/dL, P = 0.03) and erythrocyte sedimentation rate (60 mm/h vs 47 mm/h, P = 0.02). Magnetic resonance imaging (MRI) findings were consistent with OM in 18 (64%) patients and indeterminate in the remaining. Based on clinical, laboratory, and radiological findings, the diagnosis of OM was considered confirmed in 3 patients, probable in 6 patients, and presumed in 19 patients. Nontyphoidal Salmonella was isolated from cultures in 9 (32%) patients, while no organism was identified in 19 (67%) patients. All patients were treated with antibiotics. Six patients (21%) required surgical interventions. CONCLUSIONS: OM continues to pose diagnostic challenges. Most patients are treated for OM without definitive confirmation. Nontyphoidal Salmonella was the only organism identified in our cohort.


Subject(s)
Anemia, Sickle Cell , Magnetic Resonance Imaging , Osteomyelitis , Salmonella Infections , Salmonella/isolation & purification , Adolescent , Anemia, Sickle Cell/complications , Anemia, Sickle Cell/drug therapy , Child , Child, Preschool , Female , Humans , Male , Osteomyelitis/drug therapy , Osteomyelitis/etiology , Osteomyelitis/microbiology , Retrospective Studies , Salmonella/classification , Salmonella Infections/drug therapy , Salmonella Infections/etiology , Salmonella Infections/microbiology
2.
Pediatr Emerg Care ; 36(7): e383-e386, 2020 Jul.
Article in English | MEDLINE | ID: mdl-29596280

ABSTRACT

OBJECTIVES: The objective of this study was to determine whether adolescents in emergency departments (EDs) who report engaging in high-risk sexual behaviors are less likely to identify a primary care provider (PCP) and more likely to access the ED than their sexually inexperienced peers. METHODS: This was a secondary analysis of adolescents presenting to a pediatric ED with non-sexually transmitted infection (STI)-related complaints who completed surveys to assess sexual behavior risk and health care access. We measured differences in self-reported PCP identification, preferential use of the ED, and number of ED visits over a 12-month period by sexual experience. Secondary outcomes included clinician documented sexual histories and STI testing. RESULTS: Of 758 patients meeting inclusion criteria, 341 (44.9%) were sexually experienced, and of those, 129 (37.8%) reported engaging in high-risk behavior. Participants disclosing high-risk behavior were less likely to identify a PCP (adjusted odds ratio, 0.5; 95% confidence interval [CI], 0.3-0.9), more likely to prefer the ED for acute care issues (adjusted odds ratio, 1.6; 95% CI, 1.0-2.6), and had a higher rate of ED visits (adjusted relative risk, 1.2; 95% CI, 1.0-1.3) compared with sexually inexperienced peers. Among patients disclosing high-risk behavior, 10.9% had clinician-documented sexual histories and 2.6% underwent STI testing. CONCLUSION: Adolescents who reported engaging in high-risk sexual behaviors were less likely to identify a PCP, as well as more likely to prefer ED-based care and make more ED visits. However, ED clinicians infrequently obtained sexual histories and performed STI testing in asymptomatic youth, thereby missing opportunities to screen high-risk adolescents who may lack access to preventive care.


Subject(s)
Adolescent Behavior , Emergency Service, Hospital/statistics & numerical data , Sexual Behavior , Adolescent , Cross-Sectional Studies , Female , Health Services Accessibility , Humans , Male , Prevalence , Primary Health Care/statistics & numerical data , Sexually Transmitted Diseases/epidemiology , Surveys and Questionnaires , Unsafe Sex
3.
J Pediatr ; 217: 172-176.e1, 2020 02.
Article in English | MEDLINE | ID: mdl-31761430

ABSTRACT

OBJECTIVE: To evaluate adherence to annual transcranial Doppler ultrasound (TCD) screening to prevent stroke among patients with sickle cell anemia (SCA) seen in the emergency department (ED). STUDY DESIGN: This retrospective chart review included patients with SCA seen at a large pediatric ED over 64 weeks. Patients who did not need a TCD (age <2 or ≥16 years, on chronic transfusions, history of an inadequate TCD) or were not followed at the study institution were excluded. Patients who had received a TCD in the last 12 months (TCD adherent) were compared with patients who had not (TCD nonadherent). RESULTS: During the study period, 257 patients with SCA in need of an annual TCD were identified and 63 patients (25%) had not received an annual TCD, including 19 patients (7%) who had never had a TCD. All TCD adherent patients had a clinic visit in the last year compared with 75% of TCD nonadherent patients, P < .0001. The mean interval time since the last hematology clinic appointment from the ED encounter was greater for the TCD nonadherent group: 70 vs 270 days, P < .0001. Demographics including markers of socioeconomic status were not significantly different between the 2 groups. CONCLUSIONS: Patients with SCA who present to the ED and are nonadherent to TCD screening guidelines are less likely to have had a recent hematology clinic visit. Future interventions to improve screening for stroke in SCA should target this patient population seen in the ED but not clinic.


Subject(s)
Anemia, Sickle Cell/complications , Cerebrovascular Circulation/physiology , Emergency Service, Hospital , Mass Screening/methods , Patient Compliance , Stroke/diagnosis , Ultrasonography, Doppler, Transcranial/methods , Adolescent , Anemia, Sickle Cell/diagnosis , Child , Child, Preschool , District of Columbia/epidemiology , Female , Follow-Up Studies , Humans , Incidence , Male , Retrospective Studies , Stroke/epidemiology , Stroke/etiology
4.
Int J Lab Hematol ; 40(6): 704-709, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30152174

ABSTRACT

INTRODUCTION: Sickle cell disease (SCD) is a multisystemic disorder, the pathology being driven by recurrent inflammation particularly during a vaso-occlusive crisis. GlycA, a composite measure of protein glycation, is a sensitive biomarker for disorders associated with vascular inflammation. We determined the utility of GlycA as a biomarker of inflammation in SCD. METHODS: Stored plasma samples from patients with SCD recruited to two clinical studies were analyzed. One study encompasses 488 patient samples with SCD (HbSS, HbSß0 and HbSC) at steady state and 52 race-matched, healthy controls. The other study included paired plasma samples during steady state and acute pain crisis from (HbSS) patients with SCD. Plasma GlycA was measured using a proton NMR on the Vantera® Clinical Analyzer. We performed analysis comparing patients with SCD, healthy controls, and paired samples analysis. RESULTS: The mean plasma GlycA level was lower in SCD compared with healthy controls (324.6 ± 70.4 µmol/L vs. 386.3 ± 74.6 µmol/L, P < 0.0001). Within the same patient, mean plasma GlycA during acute pain crisis was lower than steady state, although the difference was not significant (300.5 ± 36.3 µmol/L vs 314.2 ± 34.8 µmol/L, P = 0.020). Plasma GlycA correlated inversely with serum LDH (P = 0.009). CONCLUSION: GlycA is not a suitable biomarker of inflammation in SCD. We surmise that its signal is confounded by hemolysis leading to a depletion of haptoglobin, one of the major plasma proteins included in the composite NMR signal. Hemolysis is further exacerbated during an acute pain crisis, hence the lower GlycA levels in crisis compared to steady state.


Subject(s)
Anemia, Sickle Cell/blood , Glycation End Products, Advanced/blood , Nuclear Magnetic Resonance, Biomolecular , Adult , Biomarkers/blood , Female , Humans , Inflammation/blood , Male , Middle Aged
5.
Clin Pediatr (Phila) ; 51(3): 254-9, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21903621

ABSTRACT

INTRODUCTION: The supine sleep position is recommended to reduce sudden infant death syndrome risk. Swaddling may improve adherence with supine placement. AIM: To assess knowledge, attitudes, and practice regarding swaddling among adult caregivers of 0- to 3-month-old infants. METHODS: Cross-sectional descriptive survey. RESULTS: All 103 adults interviewed had swaddled their infant. Common reasons for swaddling included infant comfort and warmth. Almost 80% of those who swaddled their infant found it effective, 80% believed it to be comfortable, and ~90% believed swaddling to be safe. Parents who routinely used swaddling were more likely to find it effective and to place their infant supine when swaddled (P < .01). CONCLUSIONS: Parents often use swaddling to comfort the infant, and most find it effective. Parents who routinely use swaddling are more likely to place their infant supine if swaddled. Swaddling may be a strategy for parents of infants who have difficulty sleeping in the supine position.


Subject(s)
Bedding and Linens , Health Knowledge, Attitudes, Practice , Infant Care/methods , Parents/psychology , Sleep , Sudden Infant Death/prevention & control , Supine Position , Adolescent , Adult , Cross-Sectional Studies , Female , Health Surveys , Humans , Infant , Infant Care/instrumentation , Infant Care/statistics & numerical data , Infant, Newborn , Male , Young Adult
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