ABSTRACT
Objectives To compare the epidemiological, clinical profle, intensive care needs and outcome of children hospitalized with SARS-CoV-2 infection during the frst and second waves of the pandemic. Methods This was a retrospective study of all children between 1 mo and 14 y, admitted to a dedicated COVID-19 hospital (DCH) during the frst (1st June to 31st December 2020) and second waves (1st March to 30th June 2021). Results Of 217 children, 104 (48%) and 113 (52%) were admitted during the frst and second waves respectively. One hundred ffty-two (70%) had incidentally detected SARS-CoV-2 infection, while 65 (30%) had symptomatic COVID-19. Comorbidities were noted in 137 (63%) children. Fifty-nine (27%) and 66 (30%) children required high-dependency unit (HDU) and ICU care respectively. Severity of infection and ICU needs were similar during both waves. High-fow oxygen (n=5, 2%), noninvasive ventilation [CPAP (n=34, 16%) and BiPAP (n=8, 5%)] and invasive ventilation (n=45, 21%) were respiratory support therapies needed. NIV use was more during the second wave (26% vs. 13%; p=0.02). The median (IQR) length (days) of DCH stay among survivors was longer during the frst wave [8 (6–10) vs. 5.5 (3–8); p=0.0001]. Conclusions Disease severity, associated comorbidities, PICU and organ support need and mortality were similar in the frst and second waves of the pandemic. Children admitted during the second wave were younger, had higher proportion of NIV use and shorter length of COVID-19 hospital stay.
ABSTRACT
Abstract The mucopolysaccharidoses (MPS) are a relatively uncommon group of inherited metabolic disorders. MPSs should be suspected in a child with coarse facies, organomegaly, recurrent respiratory tract infections, developmental delay, and hernias. Early diagnosis and treatment can greatly improve the quality of life in these children. In this study we studied 46 MPS patients diagnosed on enzyme and/or DNA testing and we found that the MPS II was the most common type followed by MPS I and MPS IVA. While the mean age of onset of symptoms was 12 months, the mean age at diagnosis was 4.5 years, a significant delay. One of major presenting features was recurrent respiratory problems, more prevalent in MPS II cases. Many patients also had short stature and contractures. Increasing awareness among physicians is of paramount importance for the early diagnosis and optimal treatment and prevention by prenatal testing and counselling.
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Introduction: Upper and lower respiratory diseases are closelyrelated which has been well documented in literature. Eventhough a relationship between upper and lower airway diseasehas been described, altered pulmonary function in patientswith upper airway diseases is still not fully understood. Thepresent study was conducted to assess the effect of chronicnasal obstruction on pulmonary function and to compare thepulmonary function in same patients after surgical relief ofnasal obstruction.Material and methods: The present study was carried outin the Department of ENT and Head and Neck Surgery andDepartment of Respiratory Medicine, Rohilkhand MedicalCollege and Hospital, Bareilly between November 2017to October 2018. 56 patients with chronic nasal obstructiondue to either deviated nasal septum or chronic rhinosinusitiswith or without nasal polyp underwent pulmonary functiontesting pre and post-operatively at 6 weeks and results werecompared.Results: The most common age group affected was less thanthirty years accounting for more than 50%. Mean age of totalsample size was 24.2 ± 6.98 years. Thirty three (58.9%) patientswere males while 23(41.07%) patients were females. Out of56 subjects, 34(60.71%) patients underwent septoplasty, while22(39.28%) patients underwent functional endoscopic sinussurgery. Clinically and statistically significant improvement inFEV1 and FVC was observed irrespective of age, gender orduration of obstruction.Conclusion: Patients with bilateral nasal obstruction hadworse pulmonary function initially and more significantimprovement after surgery, suggesting an association ofbilateral obstruction with bad prognosis.
ABSTRACT
Inflammatory pseudotumor is an unusual quasineoplastic lesion, of uncertain natural history and etiopathogenesis, which consists of inflammatory cells and myofibroblastic spindle cells; and is usually found in children and young adults. Clinical manifestations and radiological feature of this rare entity, can be indistinguishable from a malignant sarcomatous or lymphoproliferative disorders. Here, a case of surgically proven inflammatory pseudotumor of the omentum in a child and its review of literature is presented. Conservative surgery is curative in most cases of inflammatory pseudotumors. Awareness of this lesion is essential for clinicians, radiologists and pathologists, as pre-operative recognition may spare the child from unnecessary radical surgery or harmful chemoradiotherapy.
Subject(s)
Child, Preschool , Granuloma, Plasma Cell/pathology , Granuloma, Plasma Cell/surgery , Humans , Male , Omentum/pathology , Rare Diseases , Treatment OutcomeABSTRACT
Childhood ARDS is mostly caused by pneumonia. Pulmonary pseudocysts are reported in adults recovering from ARDS, usually in non-dependent lung regions. The authors present a 1.5-year-old boy, who survived severe pulmonary ARDS with development of pulmonary giant pseudocysts and other structural abnormalities in dependent lung region. To the best of authors knowledge, it is the first follow up report of pulmonary abnormality in a toddler with ARDS of extreme severity.
Subject(s)
Diagnosis, Differential , Humans , Infant , Male , Plasma Cell Granuloma, Pulmonary/diagnosis , Plasma Cell Granuloma, Pulmonary/etiology , Respiratory Distress Syndrome/complications , Respiratory Distress Syndrome/diagnosis , Respiratory Distress Syndrome/therapyABSTRACT
A 2-year-old girl presented with recurrent cough, wheese and breathing difficulty. Her imaging (CT and virtual bronchoscopy) revealed a foreign body in tracheobronchial tree, that was removed by rigid bronchoscopy.