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1.
J Child Adolesc Psychiatr Nurs ; 36(2): 114-123, 2023 05.
Article in English | MEDLINE | ID: mdl-36380398

ABSTRACT

BACKGROUND: Attention deficit hyperactivity disorder is a common psychiatric disorder with a worldwide prevalence of about five percent among children and adolescents. This disorder affects most aspects of their lives e.g., academic performance and social relations, and their overall quality of life is reduced compared to healthy peers. The majority of children with ADHD are treated with medication that potentially has an insufficient effect and/or frequently occurring side effects. OBJECTIVES: To enable nurses and other health care professionals to guide children with ADHD and their families in their choices of treatment, based on the best available literature on the association between nonpharmacological interventions and quality of life. DATA SOURCES: A literature search was performed in the databases CENTRAL, Embase, PubMed, CINAHL, and PsycINFO. Seven randomized controlled trials were included in this systematic review. They examined the use of polyunsaturated fatty acids, physical activity, psychoeducation, cognitive therapy, cognitive training, hippotherapy, and behavioral therapy. CONCLUSIONS: The study of behavioral therapy in the form of a sleep intervention detected an improvement in quality of life which was statistically significant compared to the control group. IMPLICATIONS FOR PRACTICE: Children with ADHD and a sleep disorder may gain improvement in their quality of life from a sleep intervention.


Subject(s)
Attention Deficit Disorder with Hyperactivity , Cognitive Behavioral Therapy , Adolescent , Child , Humans , Attention Deficit Disorder with Hyperactivity/drug therapy , Quality of Life
2.
Trials ; 23(1): 579, 2022 Jul 19.
Article in English | MEDLINE | ID: mdl-35854390

ABSTRACT

BACKGROUND: Inferior scapular notching is a complication unique to reverse shoulder arthroplasty. The most efficient technique to avoid inferior scapular notching has been reported to be lateralization of the glenoid offset. This study aims to compare radiological and functional outcomes of the DELTA Xtend® Reverse Shoulder System Lateralized Glenosphere Line Extension (intervention group) with the Standard DELTA Xtend® Reverse Shoulder System (control group). We hypothesize that the lateralization improves the patient outcome by decreasing the risk of inferior scapular notching without increasing the risk of migration and loosening of glenoid component. METHODS: In this randomized controlled trial, all Danish citizens with rotator cuff arthropathy or degeneration of the glenohumeral joint with severe posterior wear and allocated for a reverse total shoulder arthroplasty at the department of orthopaedic surgery at Herlev and Gentofte Hospital, Copenhagen University Hospital, will be considered for participation. The exclusion criteria are as follows: below 50 years of age, cognitive or linguistic impairment, insufficient glenoid bone stock, previous fracture in the upper extremity and autoimmune-mediated inflammatory arthritis. There will be included a total of 122 patients of which 56 will participate in the radiostereometric analysis. This number of patients allows 20% to drop out. The co-primary outcomes are the pattern and magnitude of the migration of the glenoid component assessed by radiostereometric analysis and the Western Ontario Osteoarthritis of the Shoulder index. The secondary outcomes are inferior scapular notching, patient-reported and functional outcomes (Oxford shoulder score, Constant-Murley score and pain), side effects and complications, changes in bone mineral density and economy. The included patients will be examined before the surgery, within 1 week and 3, 6, 12 and 24 months after. DISCUSSION: No previous studies have compared the conventional reverse shoulder arthroplasty with the lateralized reverse shoulder arthroplasty in a randomized controlled trial regarding migration and functional outcome. Furthermore, radiostereometric analysis has not been used to evaluate the migration of reverse shoulder arthroplasty in a randomized controlled trial. This study intends to determine which treatment has the most optimal outcome for the benefit of future patients with an indication for reverse shoulder arthroplasty. TRIAL REGISTRATION: The study has been notified to Pactius and has approval number P-2021-231. Furthermore, the study will be registered on Clinicaltrials.gov before starting the inclusion.


Subject(s)
Joint Diseases , Shoulder Joint , Shoulder Prosthesis , Humans , Joint Diseases/surgery , Randomized Controlled Trials as Topic , Range of Motion, Articular , Shoulder Joint/surgery , Shoulder Prosthesis/adverse effects , Treatment Outcome
4.
Ugeskr Laeger ; 183(31)2021 Aug 02.
Article in Danish | MEDLINE | ID: mdl-34378522

ABSTRACT

Sjögren's syndrome (SS) is a common autoimmune disease with a prevalence of 1%. SS affects primarily women between the age of 30 and 50 years. The classic manifestations are sicca symptoms, musculoskeletal pain and fatigue but the disease can affect all organs. SS is associated with the antibody anti-SSA antibodies. The patients have a 15-20 times higher risk of lymphoma and an increased risk of spontaneous abortion and AV-block in life-born children. In this review, we share the diagnostic process and risk stratification and outline the treatments available from private practice.


Subject(s)
Sjogren's Syndrome , Adult , Child , Fatigue , Female , Humans , Middle Aged , Prevalence , Sjogren's Syndrome/complications , Sjogren's Syndrome/diagnosis , Sjogren's Syndrome/drug therapy
5.
Pediatr Transplant ; 25(5): e13946, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33314484

ABSTRACT

We aimed to assess short- and long-term mortality, including factors associated with mortality, for children referred to a pediatric intensive care unit (ICU) at Rigshospitalet, Denmark, following haematopoietic cell transplantation (HCT). Data regarding admission to ICU and mortality following HCT for children below 16 years of age between 2000 and 2017 were retrospectively analyzed. We identified 55 ICU admissions in 39 patients following 46 HCTs. The overall in-ICU, in-hospital, 3-month, and 1-year mortality rates were 33.3%, 43.6%, 46.2%, and 51.3%, respectively. Patients admitted from 2000 to 2010 had a 3-month mortality of 63.2% and 1-year mortality of 68.4%, compared to 30% and 35% (P = .040 and P = .039) for patients admitted from 2011 to 2017. The main reason for ICU admission was respiratory failure (78.2%). Mechanical ventilation (MV) was associated with a higher long-term mortality (P = .044), and use of inotropes or vasopressors was associated with increased mortality at all times (all P > .006). Extracorporeal life support, renal replacement therapy, longer ICU stay, and longer time with MV were not associated with increased mortality. Over the past two decades, mortality was significantly reduced in pediatric HCT patients admitted to the ICU. The cause is probably multifactorial and warrants further studies. Our findings support admissions of critically ill pediatric HCT patients to intensive care with encouraging outcomes of even long-term admissions.


Subject(s)
Critical Care/trends , Hematopoietic Stem Cell Transplantation/adverse effects , Hematopoietic Stem Cell Transplantation/mortality , Intensive Care Units, Pediatric/trends , Adolescent , Child , Child, Preschool , Denmark , Female , Follow-Up Studies , Humans , Infant , Infant, Newborn , Infections/etiology , Infections/mortality , Infections/therapy , Male , Patient Admission , Respiratory Insufficiency/etiology , Respiratory Insufficiency/mortality , Respiratory Insufficiency/therapy , Retrospective Studies , Survival Analysis , Treatment Outcome
6.
BMJ Case Rep ; 13(12)2020 Dec 21.
Article in English | MEDLINE | ID: mdl-33370941

ABSTRACT

A 9-year-old girl was admitted to the paediatric intensive care unit with acute respiratory failure due to influenza. Nine months earlier, she presented with unexplained lymphoedema of the lower extremities and monocytopenia. She had a history of occasional finger warts and onychomycoses. During hospitalisation, the patient was diagnosed with Emberger syndrome caused by GATA2 deficiency. The admission was complicated by thromboses in the right hand, leading to amputation of multiple fingers. From then on, the patient has been in good recovery, the function of her right hand was improving and an allogeneic haematopoietic cell transplantation has now been successfully performed.


Subject(s)
Fingers/pathology , GATA2 Deficiency/complications , GATA2 Transcription Factor/deficiency , Influenza A virus/immunology , Respiratory Distress Syndrome/immunology , Amputation, Surgical , Anti-Bacterial Agents/therapeutic use , Antiviral Agents/therapeutic use , Child , Codon, Nonsense , DNA Mutational Analysis , Drug Therapy, Combination , Female , Fingers/surgery , GATA2 Deficiency/diagnosis , GATA2 Deficiency/genetics , GATA2 Deficiency/immunology , GATA2 Transcription Factor/genetics , Gangrene/immunology , Gangrene/surgery , Glucocorticoids/therapeutic use , Hematopoietic Stem Cell Transplantation , Humans , Influenza A virus/isolation & purification , Influenza, Human/complications , Influenza, Human/immunology , Influenza, Human/therapy , Influenza, Human/virology , Lung/diagnostic imaging , Lung/immunology , Respiration, Artificial , Respiratory Distress Syndrome/diagnosis , Respiratory Distress Syndrome/therapy , Severity of Illness Index , Tomography, X-Ray Computed
7.
Acta Paediatr ; 100(5): 784-6, 2011 May.
Article in English | MEDLINE | ID: mdl-21158911

ABSTRACT

AIM: To present current and new knowledge on congenital self-healing reticulohistiocytosis, a benign variant of cutaneous Langerhans cell histiocytosis presenting with skin lesions in the neonatal period. METHODS: We describe and photo document two cases of this rare disease and review the literature. RESULTS: Only few newborns have acute access to a neonatal dermatologist, and we demonstrate how the spontaneous cutaneous involution may happen even prior to the first dermatological assessment. As no sole criterion can reliably distinguish the self-healing form from disseminated disease, multidisciplinary assessment and follow-up are essential. CONCLUSION: Our data document how easily the diagnosis congenital self-healing reticulocytosis may be missed and emphasize the importance and value of instant clinical photographing at the neonatal unit and the use of teledermatology whenever congenital self-healing reticulohistiocytosis is suspected.


Subject(s)
Histiocytosis, Langerhans-Cell/congenital , Diagnosis, Differential , Histiocytosis, Langerhans-Cell/diagnosis , Humans , Infant, Newborn , Male , Skin Diseases/etiology
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