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2.
Eur J Pediatr ; 183(7): 2921-2933, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38619569

ABSTRACT

Evaluation of guidelines in actual practice is a crucial step in guideline improvement. A retrospective evaluation of the Dutch guideline for children with fever without an apparent source (FWS) showed 50% adherence in young infants. We prospectively evaluated adherence to the Dutch guideline and its impact on management in current practice. Prospective observational multicenter cross-sectional study, including children 3 days to 16 years old presented for FWS at one of seven emergency departments in participating secondary and tertiary care hospitals in the Netherlands. Adherence to the Dutch FWS guideline, adapted from the National Institute for Health and Care Excellence (NICE) guideline, was evaluated, and patterns in non-adherence and the impact of non-adherence on clinical outcomes and resource use were explored. Adherence to the guideline was 192/370 (52%). Adherence was lowest in patients categorized as high risk for severe infection (72/187, 39%), compared to the low-risk group (64/73, 88%). Differences in adherence were significant between risk categories (P < 0.001) but not between age categories. In case of non-adherence, less urinalysis, fewer bacterial cultures (blood, urine, and cerebral spinal fluid), and less empirical antibiotic treatment were performed (P < 0.050). Clinical outcomes were not significantly different between the non-adherence and the adherence group, particularly regarding missed severe infections. CONCLUSIONS: We found a high non-adherence rate of 48%, which did not lead to unfavorable clinical outcomes. This substantiates the need for a critical reevaluation of the FWS guideline and its indications for bacterial cultures, viral testing, and antibiotic treatment. WHAT IS KNOWN: • Despite the development of national guidelines, variation in practice is still substantial in the assessment of febrile children to distinguish severe infection from mild self-limiting disease. • Previous retrospective research suggests low adherence to national guidelines for febrile children in practice. WHAT IS NEW: • In case of non-adherence to the Dutch national guideline, similar to the National Institute for Health and Care Excellence (NICE) guideline from the United Kingdom, physicians have used fewer resources than the guideline recommended without increasing missed severe infections.


Subject(s)
Fever of Unknown Origin , Guideline Adherence , Practice Guidelines as Topic , Humans , Guideline Adherence/statistics & numerical data , Netherlands , Infant , Male , Female , Child, Preschool , Adolescent , Prospective Studies , Cross-Sectional Studies , Child , Infant, Newborn , Fever of Unknown Origin/drug therapy , Fever of Unknown Origin/etiology , Emergency Service, Hospital/statistics & numerical data , Anti-Bacterial Agents/therapeutic use
3.
Ned Tijdschr Geneeskd ; 1672023 02 07.
Article in Dutch | MEDLINE | ID: mdl-36752661

ABSTRACT

BACKGROUND: Diaper dermatitis in children is common and usually harmless. Often the cause is irritation, a secondary candida infection or eczema, for which treatment is simple and effective. In this paper we show that a therapy resistant diaper dermatitis can be the diagnostic clue to the rare but important diagnosis Langerhans cell histiocytosis (LCH). CASE DESCRIPTION: We saw a 14 months old girl with therapy resistant diaper dermatitis, skin abnormalities on the hairy scalp, fever, otorrhea and extensive lymphadenopathy. After a long period of doctor visits, skin biopsies confirmed the diagnosis of LCH. CONCLUSION: LCH is a rare condition that often manifests in the skin. LCH can manifest in different organs. Although skin involvement is sometimes considered as less relevant, cutaneous manifestations can be an important diagnostic clue. In this paper we show that diaper dermatitis is not always harmless: it can be a symptom of LCH.


Subject(s)
Diaper Rash , Eczema , Histiocytosis, Langerhans-Cell , Child , Female , Humans , Infant , Diaper Rash/diagnosis , Diaper Rash/etiology , Diaper Rash/pathology , Skin/pathology , Scalp/pathology , Histiocytosis, Langerhans-Cell/diagnosis
4.
Pediatr Infect Dis J ; 39(12): 1075-1080, 2020 12.
Article in English | MEDLINE | ID: mdl-32858646

ABSTRACT

BACKGROUND: The Dutch fever without an apparent source (FWS) guidelines were published to timely recognize and treat serious infections. We determined the adherence to the Dutch FWS guidelines and the percentage of serious infections in infants younger than 3 months of age. Second, we identified which clinical criteria, diagnostic tests, and management were associated with nonadherence to the guidelines. METHODS: A retrospective cohort study was performed in 2 Dutch teaching hospitals. We assessed the charts of all infants with FWS who presented at the emergency departments from September 30, 2017, to October 1, 2019. Diagnostic and therapeutic decisions were compared with the recommendations, as published in the Dutch guidelines. Infants were categorized into the nonadherence group in case 1 or more recommendations were not adhered to. RESULTS: Data on 231 infants were studied; 51.5% of the cases adhered to the Dutch guidelines and 16.0% suffered from a serious infection. The percentage of infants with a serious infection was higher in the adherence compared with the nonadherence group. We observed no relevant differences in clinical outcomes. Univariate regression analysis showed that an abnormal white blood cell count was associated with nonadherence (OR 0.4, P = 0.049). Not obtaining a urine and blood culture and not starting intravenous antibiotic treatment were the most frequent reasons for nonadherence to the guidelines. CONCLUSIONS: Our study indicates that there was nonadherence in a large proportion of FWS cases. The guidelines may need to be adjusted to increase adherence.


Subject(s)
Fever of Unknown Origin , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/therapeutic use , Bacteremia , Fever of Unknown Origin/drug therapy , Fever of Unknown Origin/epidemiology , Fever of Unknown Origin/microbiology , Guideline Adherence , Humans , Infant , Infant, Newborn , Meningitis , Netherlands , Practice Guidelines as Topic , Retrospective Studies , Time-to-Treatment
5.
Expert Rev Gastroenterol Hepatol ; 14(4): 231-242, 2020 Apr.
Article in English | MEDLINE | ID: mdl-32155096

ABSTRACT

Introduction: The presence of D. fragilis in feces is characterized by an asymptomatic carrier ship to a spectrum of gastrointestinal symptoms. However, a causal relationship remains to be elucidated. In this systematic review, we aimed to evaluate the relationship between the eradication of D. fragilis and symptoms to establish the strength of evidence that D. fragilis in symptomatic children warrants antibiotic treatment.Areas covered: This systematic review covers a challenge in daily clinical practice. Is it necessary to test for D. fragilis in children with gastrointestinal symptoms and does a positive fecal PCR test warrant treatment?Expert opinion: Testing for D. fragilis seems justified in a selection of children with persistent unexplained chronic abdominal pain and diarrhea. Treatment of D. fragilis should be withhold until other causes like celiac disease have been excluded. Both microscopic and Real Time-PCR methods (or a combination of the two) can be used for diagnosis. Paromomycin or clioquinol are antibiotics of choice based on their small spectrum of activity, fewer side effects, and better eradication rates than metronidazole. Future randomized studies, with strict inclusion criteria, appropriate diagnostic testing, and doses of antibiotics based on bodyweight are warranted.


Subject(s)
Dientamoebiasis/diagnosis , Dientamoebiasis/drug therapy , Abdominal Pain/drug therapy , Abdominal Pain/etiology , Abdominal Pain/parasitology , Child , Diagnosis, Differential , Diarrhea/drug therapy , Diarrhea/etiology , Diarrhea/parasitology , Dientamoeba/isolation & purification , Dientamoebiasis/complications , Dientamoebiasis/parasitology , Feces/parasitology , Humans , Real-Time Polymerase Chain Reaction , Treatment Outcome
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