Sanamed https://aseestant.ceon.rs/index.php/sanamed <p style="box-sizing: border-box; border: 0px; font-size: 16px; margin: 0px 0px 0.5em; outline: 0px; padding: 0px; vertical-align: baseline; color: #7a7a7a; font-family: Roboto, sans-serif;">SANAMED journal is international, peer-reviewed, multidisciplinary open-access medical journal, founded in 2006 and is published by the Association of medical doctors Sanamed, a nonprofit organization of physicians and scientists. The journal publishes: original articles, case reports, literature reviews, Systematic review, articles on history of medicine, articles for practitioners, book reviews, comments and letters to editor, and other medical information dedicated to the advancement of medical research, practice, and education, in the field of medicine and related fields.</p> <p style="box-sizing: border-box; border: 0px; font-size: 16px; margin: 0px 0px 0.5em; outline: 0px; padding: 0px; vertical-align: baseline; color: #7a7a7a; font-family: Roboto, sans-serif;">The journal is published both in electronic and print format, three times a year. Immediately after publication, all papers are available online for free, on the journal&rsquo;s website and other databases.</p> <p>The articles are printed in the English language with an abstract and title both in English and Serbian. Authors accept full responsibility for the accuracy of all content within the manuscript. Editor or Editorial Board of the Sanamed does not accept any responsibility for the statements in the articles.</p> <p>Submission of the manuscript implies that its publication has been approved by the responsible authorities at the institution where the work has been carried out. The publisher will not be held legally responsible should be any claims for compensation. Details of all funding sources for the work should be given.</p> en-US <p class="gmail_msg"><span class="lG">Journal </span><span class="lG">Sanamed </span>is published under an Open Access license. All its content is available free of charge. Users can read, download, copy, distribute, print, search the full text of articles, as well as establish HTML links to them, without having to seek the consent of the author or publisher.</p> <p class="gmail_msg">The right to use content without consent does not release the users from the obligation to give the credit to the <span class="lG">journal </span>and its content in a manner described under CC BY.</p> dzemail.detanac@gmail.com (Dzemail Smail Detanac) dzemail.detanac@gmail.com (Dzemail Detanac) Mon, 24 Oct 2022 11:16:11 +0200 OJS 3.1.2.0 http://blogs.law.harvard.edu/tech/rss 60 RISK FACTORS FOR POTENTIAL DRUG-DRUG INTERACTIONS OF ANALGESICS IN HOSPITALIZED UROLOGICAL PATIENTS https://aseestant.ceon.rs/index.php/sanamed/article/view/62550 <p class="Default" style="margin-top: 0in; text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; tab-stops: .5in 1.0in 1.5in 2.0in 2.5in 3.0in 3.5in 4.0in 4.5in 5.0in 5.5in 6.0in;"><strong><span style="font-family: 'Times Roman','serif';">Objective:</span></strong><span style="font-family: 'Times Roman','serif';"> To evaluate potential drug&ndash;drug interactions (pDDIs) involving analgesics in hospitalized urological patients and identify risk factors influencing their number.</span></p> <p class="Default" style="margin-top: 0in; text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; tab-stops: .5in 1.0in 1.5in 2.0in 2.5in 3.0in 3.5in 4.0in 4.5in 5.0in 5.5in 6.0in;"><strong><span style="font-family: 'Times Roman','serif';">Methods:</span></strong><span style="font-family: 'Times Roman','serif';"> This study involved a post hoc analysis based on data obtained from a retrospective observational cohort clinical study conducted at the Clinic of Urology, University Clinical Centre Kragujevac, Serbia. Of the original 220 patients, 191 who received analgesics were included. Daily pharmacotherapy data, along with demographic and clinical characteristics, were collected, while pDDIs were identified and classified using the Lexicomp Interaction Checker. Descriptive statistics were used to summarize the data. Multiple linear regression with backward elimination was used to identify independent predictors of the number of pDDIs.</span></p> <p class="Default" style="text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; tab-stops: .5in 1.0in 1.5in 2.0in 2.5in 3.0in 3.5in 4.0in 4.5in 5.0in 5.5in 6.0in; margin: 0in 0in 12.0pt 0in;"><strong><span style="font-family: 'Times Roman','serif';">Results:</span></strong><span style="font-family: 'Times Roman','serif';"> Analgesic-related pDDIs were detected in 175 patients (91.6%). Non-steroidal anti-inflammatory drugs (NSAIDs) were prescribed to 173 patients (90.6%), opioids to 53 (27.7%), and paracetamol to 54 (28.3%). The mean number of pDDIs per patient was 5.5 &plusmn; 5.5 (range 0&ndash;30). Category X interactions most frequently included NSAID combinations (diclofenac + ketorolac, ketorolac + metamizole), while category D interactions frequently involved enoxaparin + ketorolac and opioid&ndash;benzodiazepine pairs. Category C interactions were dominated by NSAID + potassium chloride and tramadol + ondansetron or atropine combinations. Multiple regression analysis identified diabetes, a higher number of prescribed drugs, and the use of NSAIDs or opioids as positive predictors of the number of pDDIs, whereas a cancer diagnosis was associated with a lower number.</span></p> <p class="Default" style="text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; tab-stops: .5in 1.0in 1.5in 2.0in 2.5in 3.0in 3.5in 4.0in 4.5in 5.0in 5.5in 6.0in; margin: 0in 0in 12.0pt 0in;"><strong><span style="font-family: 'Times Roman','serif';">Conclusion:</span></strong><span style="font-family: 'Times Roman','serif';"> Analgesic-related pDDIs affect the majority of hospitalized urological patients. Avoiding high-risk combinations, close monitoring, and multidisciplinary medication review in patients with risk factors may help reduce preventable harm.</span></p> Ivan Milovanović, Ana Pejčić, Zoran Kovačević, Katarina Janićijević Copyright (c) 2026 Sanamed https://creativecommons.org/licenses/by/4.0 https://aseestant.ceon.rs/index.php/sanamed/article/view/62550 Mon, 26 Jan 2026 11:22:13 +0100 HÜRTHLE-CELL CARCINOMA OF THE THYROID: CLINICOPATHOLOGIC FEATURES AND SURGICAL OUTCOMES AT A SINGLE INSTITUTION https://aseestant.ceon.rs/index.php/sanamed/article/view/62873 <p class="Default" style="margin-top: 0in; text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none;"><strong><span style="font-family: 'Times Roman','serif';">Background: </span></strong><span style="font-family: 'Times Roman','serif';">H&uuml;rthle cell carcinoma (HCC) is a rare differentiated thyroid malignancy with variable biological behavior. This study evaluates clinicopathologic features, treatment patterns, and long-term outcomes in patients managed at a single tertiary institution.</span></p> <p class="Default" style="margin-top: 0in; text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none;"><strong><span style="font-family: 'Times Roman','serif';">Methods:</span></strong><span style="font-family: 'Times Roman','serif';"> We retrospectively reviewed medical records of patients with histologically confirmed HCC between January 2005 and December 2020. Demographics, tumor characteristics, surgical treatment, adjuvant radioactive iodine (RAI) therapy, recurrence, and survival were analyzed. Outcomes were compared with reported retrospective series and discussed in the context of current ATA guidelines.</span></p> <p class="Default" style="margin-top: 0in; text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none;"><strong><span style="font-family: 'Times Roman','serif';">Results:</span></strong><span style="font-family: 'Times Roman','serif';"> Forty-eight patients were identified (mean age, 58.7 </span><span dir="RTL" lang="AR-SA" style="font-family: 'Arial Unicode MS','sans-serif'; mso-ascii-font-family: 'Times Roman'; mso-hansi-font-family: 'Times Roman';">&plusmn; </span><span style="font-family: 'Times Roman','serif';">11.4 years; female-to-male ratio, 2.2:1). Mean tumor size was 38.5 </span><span dir="RTL" lang="AR-SA" style="font-family: 'Arial Unicode MS','sans-serif'; mso-ascii-font-family: 'Times Roman'; mso-hansi-font-family: 'Times Roman';">&plusmn; </span><span style="font-family: 'Times Roman','serif';">14.2 mm. Minimally invasive disease was present in 29 patients (60.4%), and widely invasive disease in 19 (39.6%). Total thyroidectomy was performed in 36 patients (75%), and lobectomy in 12 (25%). RAI therapy was administered to 30 patients (62.5%), predominantly in widely invasive cases. Median follow-up was 104 months (range, 24&ndash;192 months). Recurrence occurred in 8 patients (16.7%), with a median time to relapse of 78 months. Five- and ten-year overall survival (OS) rates were 91.3% and 81.5%, respectively. Disease-specific survival (DSS) was 95.6% at 5 years and 90.2% at 10 years. Ten-year disease-free survival (DFS) was 82.1%.</span></p> <p class="Default" style="margin-top: 0in; text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none;"><strong><span lang="FR" style="font-family: 'Times Roman','serif'; mso-ansi-language: FR;">Conclusions: </span></strong><span style="font-family: 'Times Roman','serif';">Our results support existing evidence that minimally invasive HCC carries an excellent prognosis, while widely invasive tumors have a higher risk of recurrence. Long-term follow-up is essential, given the potential for late recurrence. These findings are consistent with current ATA guidelines recommending risk-tailored treatment and surveillance strategies.</span></p> Muhammad Memon Copyright (c) 2026 Sanamed https://creativecommons.org/licenses/by/4.0 https://aseestant.ceon.rs/index.php/sanamed/article/view/62873 Mon, 16 Feb 2026 14:38:24 +0100 ASSOCIATION OF THE TP53 PIN3 16-BP DUPLICATION POLYMORPHISM WITH ORAL SQUAMOUS CELL CARCINOMA RISK AND PROGNOSIS https://aseestant.ceon.rs/index.php/sanamed/article/view/63271 <p class="Default" style="text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; margin: 0in 0in 12.0pt 0in;"><strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">Background/Aim:</span></strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;"> Oral squamous cell carcinoma (OSCC) is associated with multiple risk factors, including genetic variations such as the TP53 PIN3 16-bp duplication polymorphism. This study aimed to assess the association between this polymorphism and susceptibility to OSCC in the Montenegrin population and to evaluate its influence on OSCC prognosis and progression.</span></p> <p class="Default" style="text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; margin: 0in 0in 12.0pt 0in;"><strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">Materials and Methods:</span></strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;"> Genomic DNA extracted from 60 patients with OSCC and 71 cancer-free controls was analyzed using the polymerase chain reaction</span><span lang="DE" style="font-family: 'Times Roman','serif';">&ndash;</span><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">restriction fragment length polymorphism (PCR-RFLP) technique to identify TP53 PIN3 genotypes and allele frequencies. Clinical and pathological data, along with three-year follow-up outcomes, were also analyzed.</span></p> <p class="Default" style="text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; margin: 0in 0in 12.0pt 0in;"><strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">Results:</span></strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;"> During the follow-up period, 12 patients (20%) experienced local recurrence of disease and 6 patients (10%) developed regional metastases, with no distant metastases detected. No significant associations were observed between the PIN3 16-bp duplication polymorphism and patient age, tumor site, grade, disease recurrence, or metastasis (p &gt; 0.05). A significant association between TP53 genotypes and advanced stage of disease was found (p = 0.006). There were no significant differences in disease-free survival among genotypes: A1A1 (28.26 </span><span dir="RTL" lang="AR-SA" style="font-family: 'Arial Unicode MS','sans-serif'; mso-ascii-font-family: 'Times Roman'; mso-hansi-font-family: 'Times Roman';">&plusmn; </span><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">1.70 months), A1A2 (35.00 </span><span dir="RTL" lang="AR-SA" style="font-family: 'Arial Unicode MS','sans-serif'; mso-ascii-font-family: 'Times Roman'; mso-hansi-font-family: 'Times Roman';">&plusmn; </span><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">0.94 months), and A2A2 (30.00 </span><span dir="RTL" lang="AR-SA" style="font-family: 'Arial Unicode MS','sans-serif'; mso-ascii-font-family: 'Times Roman'; mso-hansi-font-family: 'Times Roman';">&plusmn; </span><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">5.20 months) (p = 0.38). Additionally, no significant differences in allele or genotype frequencies between patients and controls were observed (p &gt; 0.05).</span></p> <p class="Default" style="text-align: justify; text-justify: inter-ideograph; line-height: normal; mso-hyphenate: none; margin: 0in 0in 12.0pt 0in;"><strong><span lang="IT" style="font-family: 'Times Roman','serif'; mso-ansi-language: IT;">Conclusion.</span></strong><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;"> The TP53 PIN3 16-bp duplication polymorphism cannot be considered a risk factor for OSCC development in the Montenegrin population. Furthermore, this polymorphism does not modulate susceptibility to OSCC progression.</span></p> Marija Antunović Copyright (c) 2026 Sanamed https://creativecommons.org/licenses/by/4.0 https://aseestant.ceon.rs/index.php/sanamed/article/view/63271 Fri, 20 Feb 2026 17:10:11 +0100 POST-LAPAROSCOPIC SHOULDER PAIN: A NARRATIVE REVIEW OF A FREQUENT POSTOPERATIVE SEQUELA https://aseestant.ceon.rs/index.php/sanamed/article/view/63427 <p class="MsoNormal" style="text-align: justify; line-height: normal;"><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">While the adoption of laparoscopic surgery has enhanced patient safety, comfort, and satisfaction, a considerable number of patients experience post-laparoscopic shoulder pain (PLSP), which can slow recovery. The English-language literature was reviewed after searching major academic databases and engines, including PubMed, Google Scholar, ResearchGate, and Web of Science, to summarize the current understanding of the etiopathogenesis, associated risk factors, and management strategies for post-laparoscopic shoulder pain. The precise etiology remains undefined, and several theories have been proposed to explain PLSP. The most widely accepted theory suggests that PLSP is a form of referred pain caused by diaphragmatic irritation due to stretching from pneumoperitoneum or the presence of residual gases and fluids. Currently, there are no universally accepted protocols for either the prevention or treatment of PLSP; consequently, a wide range of modalities are applied based on the surgeon</span><span dir="RTL" lang="AR-SA" style="font-family: 'Arial Unicode MS','sans-serif'; mso-ascii-font-family: 'Times Roman'; mso-hansi-font-family: 'Times Roman';">&rsquo;</span><span style="font-family: 'Times Roman','serif'; mso-ansi-language: EN-US;">s expertise and preference. There is a clear need to improve awareness of this condition to enable the standardization of management options, thereby optimizing patient outcomes.</span></p> Sajad Ahmad Salati, Saleh AlSuwaydani Copyright (c) 2026 Sanamed https://creativecommons.org/licenses/by/4.0 https://aseestant.ceon.rs/index.php/sanamed/article/view/63427 Fri, 20 Feb 2026 17:09:09 +0100