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    Π•Π²Π°Π»ΡƒΠ°Ρ†ΠΈΡ˜Π° Π½Π° (1,3)--d-Π³Π»ΠΈΠΊΠ°Π½ СсСј Π²ΠΎ дијагноза Π½Π° ΠΈΠ½Π²Π°Π·ΠΈΠ²Π½ΠΈ ΠΈΠ½Ρ„Π΅ΠΊΡ†ΠΈΠΈ со Аspergillus

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    Invasive fungal infections caused by Aspergillus are a significant problem in immunocompromised and critically ill patients and associated with increased morbidity and mortality. Early diagnosis of invasive aspergillosis is still a big clinical and diagnostic challenge. Conventional methods are not sensitive enough, and therefore, there is a need for rapid, more sensitive methods for early diagnosis of invasive fungal infections with Aspergillus. The aim of this study was to evaluate the diagnostic performance, sensitivity and specificity of serological panfungal (1,3)-b-D-glucan marker compared to conventional method for diagnosis of invasive fungal infections with Aspergillus. Material and methods: Specimens of 125 patients divided into 4 groups (group I - immune deficiency, group II - prolonged ICU stay, group III - chronic aspergillosis, group IV - cystic fibrosis), classified according to clinical diagnosis and EORTC/MSG criteria, were analyzed at the Institute of Microbiology and Parasitology, with conventional and serological methods, during a period of two years. Results: A total of 71 isolates of Aspergillus were confirmed in this study. Four isolates were recovered from bloodculture of patients with primary immune deficiency. With BAL culture, Aspergillus was detected in the group of chronic aspergillosis (63.33%), followed by the groups of cystic fibrosis (56.67%), primary immune deficiency (51.43%), and the group with prolonged ICU stay (43.33%). Sensitivity and specificity of BAL culture were: 64.29% and 100%, 59.09% and 100%, 54.55% and 12.5%, 100% and 54.17%, in I, II, III and IV group, respectively. In 79.1% (53/67) from positive BAL cultures in all groups, A. fumigatus was confirmed, of which, 32.1% (17/53) in group III, followed by group I – 26.42% (14/53) and group IV – 26.42% (14/53), and 15.1% (8/53) in group II. Other species confirmed in BAL were A. flavus 16.42% (11/67) and A.terreus 4.48% (3/67). Sensitivity and specificity of the serological panfungal (1,3)-b-D-glucan (BDG) marker were: 64.71% and 85.71%, 50% and 87.5%, 36.36% and 50%, in groups I, II and III, respectively. No positive findings of the panfungal (1,3)-b-D-glucan (BDG) marker were found in the group with cystic fibrosis. Conclusion: The results obtained in this study have demonstrated that a positive (1,3)-b-D-glucan assay highlights the value of this test as a diagnostic adjunct in the serodiagnosis of invasive fungal infections with Aspergillus, and along with the results from conventional mycological investigation, helped in reaching a timely antifungal treatment with a favorable clinical outcome. Β Π˜Π½Π²Π°Π·ΠΈΠ²Π½ΠΈΡ‚Π΅ Ρ„ΡƒΠ½Π³Π°Π»Π½ΠΈ ΠΈΠ½Ρ„Π΅ΠΊΡ†ΠΈΠΈ со Aspergillus прСтставуваат сСриозСн ΠΏΡ€ΠΎΠ±Π»Π΅ΠΌ кај ΠΈΠΌΡƒΠ½ΠΎΠΊΠΎΠΌΠΏΡ€ΠΎΠΌΠΈΡ‚ΠΈΡ€Π°Π½ΠΈΡ‚Π΅ Π»ΠΈΡ†Π° ΠΈ ΠΊΡ€ΠΈΡ‚ΠΈΡ‡Π½ΠΎ Π±ΠΎΠ»Π½ΠΈΡ‚Π΅ Π»ΠΈΡ†Π°, ΠΈ сС асоцирани со Π·Π³ΠΎΠ»Π΅ΠΌΠ΅Π½ ΠΌΠΎΡ€Π±ΠΈΠ΄ΠΈΡ‚Π΅Ρ‚ ΠΈ ΠΌΠΎΡ€Ρ‚Π°Π»ΠΈΡ‚Π΅Ρ‚. Π Π°Π½Π° дијагноза Π½Π° ΠΈΠ½Π²Π°Π·ΠΈΠ²Π½Π°Ρ‚Π° аспСргилоза Π΅ сѐ ΡƒΡˆΡ‚Π΅ Π³ΠΎΠ»Π΅ΠΌ ΠΊΠ»ΠΈΠ½ΠΈΡ‡ΠΊΠΈ ΠΈ Π΄ΠΈΡ˜Π°Π³Π½ΠΎΡΡ‚ΠΈΡ‡ΠΊΠΈ ΠΏΡ€Π΅Π΄ΠΈΠ·Π²ΠΈΠΊ. ΠšΠΎΠ½Π²Π΅Π½Ρ†ΠΈΠΎΠ½Π°Π»Π½ΠΈΡ‚Π΅ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈ Π½Π΅ сС Π΄ΠΎΠ²ΠΎΠ»Π½ΠΎ сСнзитивни, ΠΈ Π·Π°Ρ€Π°Π΄ΠΈ Ρ‚ΠΎΠ°, сС Π½Π°ΠΌΠ΅Ρ‚Π½ΡƒΠ²Π° ΠΏΠΎΡ‚Ρ€Π΅Π±Π° Π·Π° Π±Ρ€Π·ΠΈ ΠΈ посСнзитивни ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈ Π·Π° Ρ€Π°Π½Π° дијагноза Π½Π° ΠΈΠ½Π²Π°Π·ΠΈΠ²Π½ΠΈ Ρ„ΡƒΠ½Π³Π°Π»Π½ΠΈ ΠΈΠ½Ρ„Π΅ΠΊΡ†ΠΈΠΈ со Aspergillus. Π¦Π΅Π»Ρ‚Π° Π½Π° ΠΎΠ²Π°Π° ΡΡ‚ΡƒΠ΄ΠΈΡ˜Π° бСшС Π΄Π° сС Π΅Π²Π°Π»ΡƒΠΈΡ€Π° Π΄ΠΈΡ˜Π°Π³Π½ΠΎΡΡ‚ΠΈΡ‡ΠΊΠΈΠΎΡ‚ пСрформанс, сСнзитивноста ΠΈ спСцифичноста Π½Π° ΡΠ΅Ρ€ΠΎΠ»ΠΎΡˆΠΊΠΈΠΎΡ‚ ΠΏΠ°Π½Ρ„ΡƒΠ½Π³Π°Π»Π΅Π½ ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ (1,3)-b-D-Π³Π»ΠΈΠΊΠ°Π½ спорСдСно со ΠΊΠΎΠ½Π²Π΅Π½Ρ†ΠΈΠΎΠ½Π°Π»Π½ΠΈΠΎΡ‚ ΠΌΠ΅Ρ‚ΠΎΠ΄ Π·Π° дијагноза Π½Π° ΠΈΠ½Π²Π°Π·ΠΈΠ²Π½ΠΈΡ‚Π΅ Ρ„ΡƒΠ½Π³Π°Π»Π½ΠΈ ΠΈΠ½Ρ„Π΅ΠΊΡ†ΠΈΠΈ со Aspergillus. ΠœΠ°Ρ‚Π΅Ρ€ΠΈΡ˜Π°Π» ΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈ: ΠŸΡ€ΠΈΠΌΠ΅Ρ€ΠΎΡ†ΠΈ ΠΎΠ΄ 125 ΠΏΠ°Ρ†ΠΈΠ΅Π½Ρ‚ΠΈ, ΠΏΠΎΠ΄Π΅Π»Π΅Π½ΠΈ Π²ΠΎ 4 Π³Ρ€ΡƒΠΏΠΈ (Π³Ρ€ΡƒΠΏΠ° I - ΠΈΠΌΡƒΠ½ Π΄Π΅Ρ„ΠΈΡ†ΠΈΡ‚, Π³Ρ€ΡƒΠΏΠ° II - ΠΏΡ€ΠΎΠ»ΠΎΠ½Π³ΠΈΡ€Π°Π½ ΠΏΡ€Π΅ΡΡ‚ΠΎΡ˜ Π²ΠΎ Π•Π˜Π›, Π³Ρ€ΡƒΠΏΠ° III - Ρ…Ρ€ΠΎΠ½ΠΈΡ‡Π½Π° аспСргилоза, Π³Ρ€ΡƒΠΏΠ° IV - цистична Ρ„ΠΈΠ±Ρ€ΠΎΠ·Π°), ΠΈ класифицирани спорСд ΠΊΠ»ΠΈΠ½ΠΈΡ‡ΠΊΠ°Ρ‚Π° дијагноза ΠΈ EORTC/MSG ΠΊΡ€ΠΈΡ‚Π΅Ρ€ΠΈΡƒΠΌΠΈΡ‚Π΅, Π±Π΅Π° Π°Π½Π°Π»ΠΈΠ·ΠΈΡ€Π°Π½ΠΈ Π½Π° Π˜Π½ΡΡ‚ΠΈΡ‚ΡƒΡ‚ΠΎΡ‚ Π·Π° ΠΌΠΈΠΊΡ€ΠΎΠ±ΠΈΠΎΠ»ΠΎΠ³ΠΈΡ˜Π° ΠΈ ΠΏΠ°Ρ€Π°Π·ΠΈΡ‚ΠΎΠ»ΠΎΠ³ΠΈΡ˜Π°, со ΠΊΠΎΠ½Π²Π΅Π½Ρ†ΠΈΠΎΠ½Π°Π»Π½ΠΈ ΠΈ ΡΠ΅Ρ€ΠΎΠ»ΠΎΡˆΠΊΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈ, Π²ΠΎ Ρ‚Π΅ΠΊ Π½Π° Π΄Π²Π΅-годишСн ΠΏΠ΅Ρ€ΠΈΠΎΠ΄. Π Π΅Π·ΡƒΠ»Ρ‚Π°Ρ‚ΠΈ: Π’ΠΊΡƒΠΏΠ½ΠΎ 71 ΠΈΠ·ΠΎΠ»Π°Ρ‚ Π½Π° Aspergillus Π±Π΅Π° ΠΏΠΎΡ‚Π²Ρ€Π΄Π΅Π½ΠΈ Π²ΠΎ ΠΎΠ²Π°Π° ΡΡ‚ΡƒΠ΄ΠΈΡ˜Π°. Π§Π΅Ρ‚ΠΈΡ€ΠΈ ΠΈΠ·ΠΎΠ»Π°Ρ‚ΠΈ Π±Π΅Π° Π΄ΠΎΠΊΠ°ΠΆΠ°Π½ΠΈ Π²ΠΎ Ρ…Π΅ΠΌΠΎΠΊΡƒΠ»Ρ‚ΡƒΡ€Π°, кај ΠΏΠ°Ρ†ΠΈΠ΅Π½Ρ‚ΠΈ со ΠΏΡ€ΠΈΠΌΠ°Ρ€Π΅Π½ ΠΈΠΌΡƒΠ½ Π΄Π΅Ρ„ΠΈΡ†ΠΈΡ‚. Π‘ΠΎ ΠΊΡƒΠ»Ρ‚ΡƒΡ€Π° Π½Π° БАЛ, Aspergillus Π½Π°Ρ˜Ρ‡Π΅ΡΡ‚ΠΎ бСшС Π΄Π΅Ρ‚Π΅ΠΊΡ‚ΠΈΡ€Π°Π½ Π²ΠΎ Π³Ρ€ΡƒΠΏΠ°Ρ‚Π° Π½Π° Ρ…Ρ€ΠΎΠ½ΠΈΡ‡Π½Π° аспСргилоза (63,33%), ΠΏΠΎ ΡˆΡ‚ΠΎ слСдуваа Π³Ρ€ΡƒΠΏΠΈΡ‚Π΅ со цистична Ρ„ΠΈΠ±Ρ€ΠΎΠ·Π° (56,67%), ΠΏΡ€ΠΈΠΌΠ°Ρ€Π΅Π½ ΠΈΠΌΡƒΠ½ Π΄Π΅Ρ„ΠΈΡ†ΠΈΡ‚ (51,43%), ΠΈ Π³Ρ€ΡƒΠΏΠ°Ρ‚Π° Π»ΠΈΡ†Π° со ΠΏΡ€ΠΎΠ»ΠΎΠ½Π³ΠΈΡ€Π°Π½ ΠΏΡ€Π΅ΡΡ‚ΠΎΡ˜ Π²ΠΎ Π΅Π΄ΠΈΠ½ΠΈΡ†ΠΈΡ‚Π΅ Π·Π° ΠΈΠ½Ρ‚Π΅Π½Π·ΠΈΠ²Π½ΠΎ Π»Π΅ΠΊΡƒΠ²Π°ΡšΠ΅ (43,33%). БСнзитивноста ΠΈ спСцифичноста Π½Π° ΠΊΡƒΠ»Ρ‚ΡƒΡ€ΠΈΡ‚Π΅ Π½Π° БАЛ Π±Π΅Π°: 64,29% ΠΈ 100%, 59,09% ΠΈ 100%, 54,55% ΠΈ 12,5%, 100% ΠΈ 54,17%, Π²ΠΎ I, II, III ΠΈ IV Π³Ρ€ΡƒΠΏΠ°, соодвСтно. Π’ΠΎ 79,1% (53/67) ΠΎΠ΄ ΠΏΠΎΠ·ΠΈΡ‚ΠΈΠ²Π½ΠΈΡ‚Π΅ ΠΊΡƒΠ»Ρ‚ΡƒΡ€ΠΈ Π½Π° БАЛ Π²ΠΎ ситС Π³Ρ€ΡƒΠΏΠΈ, бСшС Π΄ΠΎΠΊΠ°ΠΆΠ°Π½ A.fumigatus, ΠΎΠ΄ ΠΊΠΎΠΈ, 32,1% (17/53) ΠΎΠ΄ Π³Ρ€ΡƒΠΏΠ° III, ΠΏΠΎΡ‚ΠΎΠ° 26,42 % (14/53) ΠΎΠ΄ Π³Ρ€ΡƒΠΏΠ° I ΠΈ 26,42% (14/53) ΠΎΠ΄ Π³Ρ€ΡƒΠΏΠ° IV, ΠΊΠ°ΠΊΠΎ ΠΈ 15,1% (8/53) ΠΎΠ΄ Π³Ρ€ΡƒΠΏΠ° II. Π”Ρ€ΡƒΠ³ΠΈ спСциСси ΠΏΠΎΡ‚Π²Ρ€Π΄Π΅Π½ΠΈ Π²ΠΎ БАЛ Π±Π΅Π° A.flavus 16,42% (11/67) ΠΈ A.terreus 4,48% (3/67). БСнзитивноста ΠΈ спСцифичноста Π½Π° ΡΠ΅Ρ€ΠΎΠ»ΠΎΡˆΠΊΠΈΠΎΡ‚ ΠΏΠ°Π½Ρ„ΡƒΠ½Π³Π°Π»Π΅Π½ (1,3)-b-D-Π³Π»ΠΈΠΊΠ°Π½ (BDG) ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ Π±Π΅Π°: 64,71% ΠΈ 85,71%, 50% ΠΈ 87,5%, 36,36% ΠΈ 50%, Π²ΠΎ Π³Ρ€ΡƒΠΏΠΈΡ‚Π΅ I, II ΠΈ III, соодвСтно. НС Π±Π΅Π° Π΄Π΅Ρ‚Π΅ΠΊΡ‚ΠΈΡ€Π°Π½ΠΈ ΠΏΠΎΠ·ΠΈΡ‚ΠΈΠ²Π½ΠΈ Π½Π°ΠΎΠ΄ΠΈ ΠΎΠ΄ ΠΏΠ°Π½Ρ„ΡƒΠ½Π³Π°Π»Π½ΠΈΠΎΡ‚ (1,3)-b-D-Π³Π»ΠΈΠΊΠ°Π½ (BDG) ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ Π²ΠΎ Π³Ρ€ΡƒΠΏΠ°Ρ‚Π° со цистична Ρ„ΠΈΠ±Ρ€ΠΎΠ·Π°. Π—Π°ΠΊΠ»ΡƒΡ‡ΠΎΠΊ: Π Π΅Π·ΡƒΠ»Ρ‚Π°Ρ‚ΠΈΡ‚Π΅ ΠΎΠ΄ ΠΎΠ²Π°Π° ΡΡ‚ΡƒΠ΄ΠΈΡ˜Π° ΠΏΠΎΠΊΠ°ΠΆΠ°Π° Π΄Π΅ΠΊΠ° ΠΏΠΎΠ·ΠΈΡ‚ΠΈΠ²Π΅Π½ Π½Π°ΠΎΠ΄ Π½Π° (1,3)-b-D-Π³Π»ΠΈΠΊΠ°Π½ ја истакнува врСдноста Π½Π° овој тСст ΠΊΠ°ΠΊΠΎ Π΄ΠΈΡ˜Π°Π³Π½ΠΎΡΡ‚ΠΈΡ‡ΠΊΠΎ Π½Π°Π΄ΠΎΠΏΠΎΠ»Π½ΡƒΠ²Π°ΡšΠ΅ Π²ΠΎ ΡΠ΅Ρ€ΠΎΠ΄ΠΈΡ˜Π°Π³Π½ΠΎΠ·Π°Ρ‚Π° Π½Π° ΠΈΠ½Π²Π°Π·ΠΈΠ²Π½ΠΈΡ‚Π΅ Ρ„ΡƒΠ½Π³Π°Π»Π½ΠΈ ΠΈΠ½Ρ„Π΅ΠΊΡ†ΠΈΠΈ со Aspergillus, ΠΈ Π·Π°Π΅Π΄Π½ΠΎ со Ρ€Π΅Π·ΡƒΠ»Ρ‚Π°Ρ‚ΠΈΡ‚Π΅ ΠΎΠ΄ ΠΊΠΎΠ½Π²Π΅Π½Ρ†ΠΈΠΎΠ½Π°Π»Π½ΠΈΡ‚Π΅ миколошки ΠΈΡΠΏΠΈΡ‚ΡƒΠ²Π°ΡšΠ°, ΠΏΠΎΠΌΠ°Π³Π°Π°Ρ‚ Π²ΠΎ Π½Π°Π²Ρ€Π΅ΠΌΠ΅Π½Π° ΠΏΡ€ΠΈΠΌΠ΅Π½Π° Π½Π° Π°Π½Ρ‚ΠΈΡ„ΡƒΠ½Π³Π°Π»Π½Π° Ρ‚Π΅Ρ€Π°ΠΏΠΈΡ˜Π°, ΠΈ ΠΏΠΎΡΡ‚ΠΈΠ³Π½ΡƒΠ²Π°ΡšΠ΅ ΠΏΠΎΠ²ΠΎΠ»Π΅Π½ ΠΊΠ»ΠΈΠ½ΠΈΡ‡ΠΊΠΈ исход.

    Inequalities in the patterns of dermoscopy use and training across Europe : conclusions of the Eurodermoscopy pan-European survey

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    BACKGROUND: Dermoscopy is a widely used technique, recommended in clinical practice guidelines worldwide for the early diagnosis of skin cancers. Intra-European disparities are reported for early detection and prognosis of skin cancers, however, no information exists about regional variation in patterns of dermoscopy use across Europe.OBJECTIVE: To evaluate the regional differences in patterns of dermoscopy use and training among European dermatologists.MATERIALS & METHODS: An online survey of European-registered dermatologists regarding dermoscopy training, practice and attitudes was established. Answers from Eastern (EE) versus Western European (WE) countries were compared and their correlation with their respective countries' gross domestic product/capita (GDPc) and total and government health expenditure/capita (THEc and GHEc) was analysed.RESULTS: We received 4,049 responses from 14 WE countries and 3,431 from 18 EE countries. A higher proportion of WE respondents reported dermoscopy use (98% vs. 77%, p<0.001) and training during residency (43% vs. 32%) or anytime (96.5% vs. 87.6%) (p<0.001) compared to EE respondents. The main obstacles in dermoscopy use were poor access to dermoscopy equipment in EE and a lack of confidence in one's skills in WE. GDPc, THEc and GHEc correlated with rate of dermoscopy use and dermoscopy training during residency (Spearman rho: 0.5-0.7, p<0.05), and inversely with availability of dermoscopy equipment.CONCLUSION: The rates and patterns of dermoscopy use vary significantly between Western and Eastern Europe, on a background of economic inequality. Regionally adapted interventions to increase access to dermoscopy equipment and training might enhance the use of this technique towards improving the early detection of skin cancers

    Dermatologist-like explainable AI enhances trust and confidence in diagnosing melanoma

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    Abstract Artificial intelligence (AI) systems have been shown to help dermatologists diagnose melanoma more accurately, however they lack transparency, hindering user acceptance. Explainable AI (XAI) methods can help to increase transparency, yet often lack precise, domain-specific explanations. Moreover, the impact of XAI methods on dermatologists’ decisions has not yet been evaluated. Building upon previous research, we introduce an XAI system that provides precise and domain-specific explanations alongside its differential diagnoses of melanomas and nevi. Through a three-phase study, we assess its impact on dermatologists’ diagnostic accuracy, diagnostic confidence, and trust in the XAI-support. Our results show strong alignment between XAI and dermatologist explanations. We also show that dermatologists’ confidence in their diagnoses, and their trust in the support system significantly increase with XAI compared to conventional AI. This study highlights dermatologists’ willingness to adopt such XAI systems, promoting future use in the clinic
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