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1.
Palliat Support Care ; 22(1): 163-168, 2024 Feb.
Article in English | MEDLINE | ID: mdl-36872568

ABSTRACT

OBJECTIVES: Pediatric palliative care services improve the quality of life for children with life-limiting and life-threatening diseases, although little has been published about variation based on cultural and religious factors. This article sets out to describe clinical and cultural characteristics of pediatric end-of-life patients in a majority Jewish and Muslim country with religious and legal constraints around end-of-life care. METHODS: We conducted a retrospective chart review of 78 pediatric patients who died during a 5-year period and could potentially have utilized pediatric palliative care services. RESULTS: Patients reflected a range of primary diagnoses, most commonly oncologic diseases and multisystem genetic disorders. Patients followed by the pediatric palliative care team had less invasive therapies, more pain management and advance directives, and more psychosocial support. Patients from different cultural and religious backgrounds had similar levels of pediatric palliative care team follow-up but certain differences in end-of-life care. SIGNIFICANCE OF RESULTS: In a culturally and religiously conservative context that poses constraints on decision-making around end-of-life care, pediatric palliative care services are a feasible and important means of maximizing symptom relief, as well as emotional and spiritual support, for children at the end of life and their families.


Subject(s)
Palliative Care , Terminal Care , Humans , Child , Palliative Care/psychology , Islam , Jews , Quality of Life , Retrospective Studies , Terminal Care/psychology , Death
3.
Eur J Pediatr ; 176(2): 199-205, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27987102

ABSTRACT

Mesenteric lymphadenitis (ML) is considered as one of the most common alternative diagnosis in a child with suspected acute appendicitis (AA). In this retrospective study, patients diagnosed with ML (n = 99) were compared in terms of demographic, clinical, and laboratory findings to patients diagnosed with AA (n = 102). This comparison was applied for both lymph nodes smaller and larger than 10 mm. When compared to patients with AA, patients with ML had significantly longer duration of symptoms prior to emergency department (ED) presentation (2.4 ± 2.6 vs 1.4 ± 1.4 days, P = 0.002) and multiple ED presentations (1.3 ± 0.7 vs 1.05 ± 0.3, P < 0.001) and had longer duration of stay in the ED (9.2 ± 5.9 vs 5.2 ± 4 h, P < 0.001), respectively. They also had significantly lower WBC (10.16 ± 4.7 × 103/dl vs 15.8 ± 4.4 × 103/dl, P < 0.001) with lymphocyte predominance (24.6 ± 14 vs 13 ± 8.7%, P < 0.001) and lower CRP levels (0.48 vs 1.6 mg/dl). Migration of pain (28 vs 7%), vomiting (62 vs 34%), and classic abdominal findings of AA (72 vs 20%) were all significantly more common for children with AA. When comparing lymph node size, no significant difference was found between those presenting with small and large nodes. CONCLUSION: This study highlights multiple clinical and laboratory findings that differentiate ML and AA. Moreover, the absence of any difference with regard to the lymph nodes size might suggest that lymph nodes enlargement is a non-specific finding. What is Known : • Mesenteric lymphadenitis is a very common diagnosis in children with suspected acute appendicitis. • Despite its prevalence, only few studies addressed the clinical characteristics of this clinical entity and their comparison with acute appendicitis. What is New: • Mesenteric lymphadenitis and acute appendicitis could be differentiated by multiple clinical and laboratory parameters. • No significant difference was found between those presenting with small and large lymph nodes.


Subject(s)
Appendicitis/diagnosis , Lymph Nodes , Mesenteric Lymphadenitis/diagnosis , Abdominal Pain/diagnostic imaging , Abdominal Pain/etiology , Acute Disease , Adolescent , Appendicitis/complications , Appendicitis/pathology , Appendicitis/physiopathology , Chi-Square Distribution , Child , Child, Preschool , Diagnosis, Differential , Emergency Service, Hospital , Female , Humans , Lymph Nodes/diagnostic imaging , Lymph Nodes/pathology , Male , Mesenteric Lymphadenitis/complications , Mesenteric Lymphadenitis/pathology , Mesenteric Lymphadenitis/physiopathology , Retrospective Studies , Statistics, Nonparametric , Symptom Assessment , Ultrasonography
4.
Neonatology ; 111(3): 240-246, 2017.
Article in English | MEDLINE | ID: mdl-27898422

ABSTRACT

BACKGROUND: The American Academy of Pediatrics (AAP) recently narrowed the indications for respiratory syncytial virus (RSV) prophylaxis, while in Israel the guidelines have not changed. OBJECTIVE: To compare the prevalence and severity of RSV infection among preterm infants born earlier than 340/7 weeks of gestation (PI), late preterm infants born at 340/7-366/7 weeks (LPTI), and term infants born after 370/7 weeks of gestation (TI) and to determine whether the results support a change in local policy. METHODS: Data of all children aged 0-14 years hospitalized with PCR-positive RSV in a single tertiary center from 2010 to 2014 were collected. A total of 793 children were included and divided into 3 groups: 637 were TI, 105 were LPTI, and 50 were PI. These groups were compared regarding incidence of hospitalization due to RSV infection, intensive care unit (ICU) hospitalization, and length of hospitalization. RESULTS: The hospitalization rate due to RSV infection was 5.2, 3.5, and 1.3% among PI, LPTI, and TI, respectively (p < 0.01). The hospitalization rate in the ICU was 24, 7.6, and 3% among PI, LPTI, and TI, respectively (p < 0.001). The length (days) of hospitalization was significantly longer among PI compared with LPTI and TI (p < 0.001). Overall, the hospitalization rate and disease severity were significantly higher for infants born earlier than 35 weeks of gestation compared with more maturely born infants. CONCLUSION: RSV infection remains a major cause of morbidity among children born prematurely even after RSV prophylaxis and would probably be greater were prophylaxis curtailed. Our results do not support applying the current AAP guidelines in Israel. Further local studies are needed to optimize prophylaxis for both PI and LPTI.


Subject(s)
Hospitalization/statistics & numerical data , Infant, Premature , Respiratory Syncytial Virus Infections/therapy , Female , Gestational Age , Humans , Infant , Infant, Newborn , Intensive Care Units , Israel , Male , Practice Guidelines as Topic , Respiratory Syncytial Viruses , Retrospective Studies , Severity of Illness Index , Tertiary Care Centers
5.
Acta Derm Venereol ; 97(4): 489-492, 2017 Apr 06.
Article in English | MEDLINE | ID: mdl-27868144

ABSTRACT

Erythema multiforme (EM) is an immune-mediated reaction presenting as acrofacial target lesions. Most studies utilize the outdated classification, which includes EM, Stevens-Johnson syndrome and toxic epidermal necrolysis as related entities. We describe here epidemiological, aetiological, clinical, laboratory and treatment characteristics of paediatric EM. This is a retrospective single-centre study, performed between 2000 and 2013. Of 119 children given a diagnosis of EM, only 30 met clinical criteria and were included in this study. Most misdiagnosed cases were non-specific eruptions and urticaria multiforme. Mean age was 11.3 years. Fifty percent had mucosal involvement. An aetiology was observed in half of the patients. Seventy percent of patients were admitted to hospital, 46.7% were treated with systemic steroids. Sixteen percent had recurrent EM. The most common identified infectious agent associated with EM in this study was Mycoplasma pneumonia and the cases associated with this infection may represent the recent entity, mycoplasma-induced rash and mucositis. Association with herpes simplex virus was not observed. Despite being a benign, self-limiting condition, children were over-treated in terms of hospitalization and therapy.


Subject(s)
Erythema Multiforme/diagnosis , Erythema Multiforme/epidemiology , Adolescent , Age of Onset , Child , Child, Preschool , Diagnosis, Differential , Diagnostic Errors , Erythema Multiforme/classification , Erythema Multiforme/therapy , Female , Hospitalization , Humans , Israel/epidemiology , Male , Medical Overuse , Pneumonia, Mycoplasma/diagnosis , Pneumonia, Mycoplasma/epidemiology , Predictive Value of Tests , Retrospective Studies , Risk Factors , Terminology as Topic , Treatment Outcome
6.
J Pediatr Endocrinol Metab ; 28(7-8): 943-6, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25741940

ABSTRACT

Antenatal type I Bartter syndrome (ABS) is usually identified by the presence of polyhydramnios, premature delivery, hypokalemia, metabolic alkalosis, hypercalciuria, and nephrocalcinosis caused by mutations in the Na-K-2Cl cotransporter (NKCC2)-encoding SLC12A1 gene. In this report, we describe a novel presentation of this syndrome with hypercalcemic hypercalciuric hyperparathyroidism, and review the literature of the variable atypical presentations of ABS.


Subject(s)
Bartter Syndrome/diagnosis , Hypercalciuria/diagnosis , Hyperparathyroidism/diagnosis , Hypokalemia/diagnosis , Mutation/genetics , Solute Carrier Family 12, Member 1/genetics , Bartter Syndrome/complications , Bartter Syndrome/genetics , Diagnosis, Differential , Humans , Hypercalciuria/complications , Hypercalciuria/genetics , Hyperparathyroidism/complications , Hyperparathyroidism/genetics , Hypokalemia/complications , Hypokalemia/genetics , Infant , Male , Phenotype , Prognosis
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