Angélique Bourqui, Hugo Morin, Robin Huber, Chantal Csajka, Clara Podmore, Jean-Luc Wolfender, Emerson Queiroz Ferreira, Pierre-Yves Rodondi
Background: Andrographis paniculata products have gained in popularity for the management of respiratory infections since the COVID-19 pandemic. None of these products holds marketing authorisation and all are sold as herbal food supplements. Current herbal food supplement regulations generally do not impose quality assessments prior to commercialisation, such that the quality of herbal food supplements available to consumers is largely unknown.
Study aim: To assess the quality, purity and labelling accuracy of A. paniculata-containing products, focusing on andrographolide content (the pharmaceutically active component) and the presence of contaminants and residues.
Methods: Forty A. paniculata-containing products were purchased from 13 countries: 13 from pharmacies and 27 from online retailers readily accessible to consumers in Switzerland. Samples were analysed using ultra-high-performance liquid chromatography-ultraviolet (UHPLC-UV) and ultra-high-performance liquid chromatography-mass spectrometry (UHPLC-MS) based on the European Pharmacopoeia method. Contaminants and residues were assessed using inductively coupled plasma mass spectrometry and gas chromatography-mass spectrometry, respectively.
Results: All samples except one contained A. paniculata. The measured daily dose of andrographolide was compared to the labelled dose. Andrographolide content ranged from 29% to 174% of the labelled dose, with only 2 products accurately labelled, while 20 were underdosed and 1 overdosed. Two products contained quercetin, which interfered with UHPLC-UV analysis. Additionally, three online-purchased products contained toxic contaminants, including a heavy metal (mercury) or pesticides (strychnine, butralin).
Conclusion: This study reveals widespread mislabelling and underdosing in A. paniculata-containing food supplements marketed internationally, along with the presence of impurities that pose risks to consumers in products bought online. Regulatory authorities must implement stringent quality controls to ensure consumer safety and product transparency.
{"title":"Quality assessment of Andrographis paniculata products reveals significant labelling inaccuracies and contaminations.","authors":"Angélique Bourqui, Hugo Morin, Robin Huber, Chantal Csajka, Clara Podmore, Jean-Luc Wolfender, Emerson Queiroz Ferreira, Pierre-Yves Rodondi","doi":"10.57187/s.4728","DOIUrl":"https://doi.org/10.57187/s.4728","url":null,"abstract":"<p><strong>Background: </strong> Andrographis paniculata products have gained in popularity for the management of respiratory infections since the COVID-19 pandemic. None of these products holds marketing authorisation and all are sold as herbal food supplements. Current herbal food supplement regulations generally do not impose quality assessments prior to commercialisation, such that the quality of herbal food supplements available to consumers is largely unknown.</p><p><strong>Study aim: </strong>To assess the quality, purity and labelling accuracy of A. paniculata-containing products, focusing on andrographolide content (the pharmaceutically active component) and the presence of contaminants and residues.</p><p><strong>Methods: </strong>Forty A. paniculata-containing products were purchased from 13 countries: 13 from pharmacies and 27 from online retailers readily accessible to consumers in Switzerland. Samples were analysed using ultra-high-performance liquid chromatography-ultraviolet (UHPLC-UV) and ultra-high-performance liquid chromatography-mass spectrometry (UHPLC-MS) based on the European Pharmacopoeia method. Contaminants and residues were assessed using inductively coupled plasma mass spectrometry and gas chromatography-mass spectrometry, respectively.</p><p><strong>Results: </strong>All samples except one contained A. paniculata. The measured daily dose of andrographolide was compared to the labelled dose. Andrographolide content ranged from 29% to 174% of the labelled dose, with only 2 products accurately labelled, while 20 were underdosed and 1 overdosed. Two products contained quercetin, which interfered with UHPLC-UV analysis. Additionally, three online-purchased products contained toxic contaminants, including a heavy metal (mercury) or pesticides (strychnine, butralin).</p><p><strong>Conclusion: </strong>This study reveals widespread mislabelling and underdosing in A. paniculata-containing food supplements marketed internationally, along with the presence of impurities that pose risks to consumers in products bought online. Regulatory authorities must implement stringent quality controls to ensure consumer safety and product transparency.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4728"},"PeriodicalIF":1.9,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145763917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Although the medical literature is flooded with case descriptions, it is difficult to dismiss the significant impact that a clinical observation limited to one or two patients can have. Case reports can also play a critical role in other areas such as drug safety by serving as early warning signals for adverse drug reactions. Unlike the aggregated data and statistical abstractions of clinical trials or meta-analyses, case reports reflect the real-world context of medical practice, where decisions are made patient by patient. This alignment with everyday clinical experience makes case reports particularly relatable and valuable to practicing clinicians, offering insights that resonate far beyond the confines of population-based evidence. The "Swiss Medical Weekly" wishes to participate in the dissemination of high-quality case reports. A new section entitled "Clinical reasoning" will provide a dedicated platform for well-structured case reports while upholding the journal's high and very strict editorial standard and its Diamond Open Access model.
{"title":"Is it still useful to publish case reports?","authors":"Gérard Waeber, Stefano Bassetti, Stefan Weiler","doi":"10.57187/s.5203","DOIUrl":"https://doi.org/10.57187/s.5203","url":null,"abstract":"<p><p>Although the medical literature is flooded with case descriptions, it is difficult to dismiss the significant impact that a clinical observation limited to one or two patients can have. Case reports can also play a critical role in other areas such as drug safety by serving as early warning signals for adverse drug reactions. Unlike the aggregated data and statistical abstractions of clinical trials or meta-analyses, case reports reflect the real-world context of medical practice, where decisions are made patient by patient. This alignment with everyday clinical experience makes case reports particularly relatable and valuable to practicing clinicians, offering insights that resonate far beyond the confines of population-based evidence. The \"Swiss Medical Weekly\" wishes to participate in the dissemination of high-quality case reports. A new section entitled \"Clinical reasoning\" will provide a dedicated platform for well-structured case reports while upholding the journal's high and very strict editorial standard and its Diamond Open Access model.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"5203"},"PeriodicalIF":1.9,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145715795","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
NTHL1-associated tumour syndrome, formerly known as NTHL1-associated polyposis, is a rare autosomal recessive tumour predisposition in which biallelic carriers of pathogenic NTHL1 variants develop multiple, predominantly adenomatous, polyps and have an increased risk of colorectal cancer and extracolonic tumour manifestations. The Nth like DNA glycosylase 1 (NTHL1) gene encodes for an enzyme involved in the base excision repair pathway which plays an important role in the maintenance of genomic integrity in the cell. Upon identification of our first Swiss biallelic NTHL1 carrier, we performed a literature survey on mono- and biallelic NTHL1 carriers, followed by genotype-phenotype correlations in order to delineate the clinical manifestations and review current screening recommendations. A comprehensive literature search was conducted to identify all individuals with NTHL1 variants reported since the initial discovery in 2015 to 2022, followed by a genotype-phenotype analysis on a total of 216 individuals, 59 being biallelic and 157 monoallelic NTHL1 carriers. 81.4% of biallelic NTHL1 carriers presented with colon polyps, the majority (69%) exhibiting between 5 and 99 polyps. Interestingly, though not statistically significant, 19% (6/31; p = 0.0766) of carriers homozygous for the recurrent p.Gln90Ter variant displayed a classical (>100 polyps) polyposis phenotype compared to none of the compound heterozygous patients (n = 20); additionally, compound heterozygotes were diagnosed with breast cancer twice as often as homozygous women (75% vs 38.9%, p = 0.0717). Among biallelic carriers, colorectal carcinomas were reported in 50.8% (n = 30; median age at diagnosis: 49 years) and extracolonic malignancies in 55.9% (n = 33), with breast (53.3%), skin (27.1%), endometrial (16.7%) and bladder cancer (8.5%) being the most frequent. Among monoallelic NTHL1 carriers, 15.3% (n = 24) presented with colon polyps and 17.8% (n = 28; median age at diagnosis: 55 years) with colon carcinomas. Timely surveillance measures are essential for early colorectal and breast cancer detection, treatment and prognosis. Prospectively gathered data are needed to further establish and refine clinical guidelines for individuals with NTHL1-associated tumour syndrome.
{"title":"Genotype-phenotype correlations in <i>NTHL1</i>-associated tumour syndrome: case report and literature review.","authors":"Agata Bukowska, Henrik Horváth, Karl Heinimann","doi":"10.57187/s.4554","DOIUrl":"10.57187/s.4554","url":null,"abstract":"<p><p>NTHL1-associated tumour syndrome, formerly known as NTHL1-associated polyposis, is a rare autosomal recessive tumour predisposition in which biallelic carriers of pathogenic NTHL1 variants develop multiple, predominantly adenomatous, polyps and have an increased risk of colorectal cancer and extracolonic tumour manifestations. The Nth like DNA glycosylase 1 (NTHL1) gene encodes for an enzyme involved in the base excision repair pathway which plays an important role in the maintenance of genomic integrity in the cell. Upon identification of our first Swiss biallelic NTHL1 carrier, we performed a literature survey on mono- and biallelic NTHL1 carriers, followed by genotype-phenotype correlations in order to delineate the clinical manifestations and review current screening recommendations. A comprehensive literature search was conducted to identify all individuals with NTHL1 variants reported since the initial discovery in 2015 to 2022, followed by a genotype-phenotype analysis on a total of 216 individuals, 59 being biallelic and 157 monoallelic NTHL1 carriers. 81.4% of biallelic NTHL1 carriers presented with colon polyps, the majority (69%) exhibiting between 5 and 99 polyps. Interestingly, though not statistically significant, 19% (6/31; p = 0.0766) of carriers homozygous for the recurrent p.Gln90Ter variant displayed a classical (>100 polyps) polyposis phenotype compared to none of the compound heterozygous patients (n = 20); additionally, compound heterozygotes were diagnosed with breast cancer twice as often as homozygous women (75% vs 38.9%, p = 0.0717). Among biallelic carriers, colorectal carcinomas were reported in 50.8% (n = 30; median age at diagnosis: 49 years) and extracolonic malignancies in 55.9% (n = 33), with breast (53.3%), skin (27.1%), endometrial (16.7%) and bladder cancer (8.5%) being the most frequent. Among monoallelic NTHL1 carriers, 15.3% (n = 24) presented with colon polyps and 17.8% (n = 28; median age at diagnosis: 55 years) with colon carcinomas. Timely surveillance measures are essential for early colorectal and breast cancer detection, treatment and prognosis. Prospectively gathered data are needed to further establish and refine clinical guidelines for individuals with NTHL1-associated tumour syndrome.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4554"},"PeriodicalIF":1.9,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145763361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Walter Knirsch, Alexandra De Silvestro, Celine Steger, Verena Rathke, Roland Weber, Michael Von Rhein, Juliane Schneider, Damian Hutter, Bettina Reich, Ulrike Held, Annette Hackenberg, Ruth Tuura O'Gorman, Raimund Kottke, Andras Jakab
<p><strong>Study aims: </strong>Our objective was to establish a multicentre foetal-to-neonatal magnetic resonance (MR) neuroimaging programme for neonates undergoing surgery for complex congenital heart disease (CHD). We assessed structural and volumetric MRI findings at different timepoints in various types of CHD and evaluated neurodevelopmental outcomes at one year of age. Additionally, we analysed the feasibility, challenges and limitations of implementing this MR neuroimaging programme.</p><p><strong>Methods: </strong>In this prospective, multicentre observational study, we examined brain development and growth in infants with complex CHD requiring neonatal cardiac surgery. Brain MRI was performed at multiple timepoints: at the 32nd week of gestation, after birth (both before and after stage I surgery), and before stage II surgery in single-ventricle CHD. We analysed and compared cardiac diagnoses, treatment approaches, structural and volumetric brain MRI findings and neurodevelopmental outcomes at one year of age (assessed using the Bayley III scale) with those of healthy controls.</p><p><strong>Results: </strong>Between April 2020 and September 2023, 81 patients and 15 healthy controls underwent at least one MRI. Cardiac diagnoses were biventricular CHD (66.7%), single-ventricle CHD (25.9%) and borderline left ventricle CHD (7.4%). New structural cerebral lesions were found before stage I or after stage I including white matter injury in 3.8% and 8.7%, respectively, ischaemic cerebral lesions in 11.5 and 11.6%, intraventricular haemorrhages in 7.7% and 7.2%, and subdural haemorrhages in 33.6% and 26.1%. Total brain volume at 32.6 (interquartile range [IQR]: 31.3-33.3) gestational weeks was 228.9 ml (213.1-241.2) in biventricular CHD, 194.4 ml (165.3-223.6) in single-ventricle CHD and 196.4 ml (186.4-235.2) in normal healthy controls. After birth, at 6 days (3-16) of life total brain volume was 337.1 ml (310.3-350.2) in biventricular CHD, 331.6 ml (305.9-350.7) in single-ventricle CHD and 406.8 ml (389.9-438.7) in normal healthy controls. After stage I, at 26.5 days (18.3-40.8) total brain volume was 367.7 ml (341.8-385.5) in biventricular CHD, 353.6 ml (338.2-375.7) in single-ventricle CHD and 514.1 ml (482.9-554.6) at 116 days (94.5-118.5) in patients with single-ventricle CHD. At 12.1 months of age, neurodevelopmental performance determined by the Bayley III scale (mean ± SD [standard deviation]) was lower for patients with single-ventricle CHD (cognitive composite score [CCS]: 92.9 ± 13.1; language composite score [LCS]: 88.5 ± 12.0; motor composite score [MCS]: 85.6 ± 14.5) than in patients with biventricular CHD (CCS: 101.2 ± 11.1; LCS: 95.7 ± 13.1; MCS: 87.6 ± 18.0) or in healthy controls (CCS: 113.3 ± 5.6; LCS: 102.3 ± 7.9; MCS: 100.7 ± 8.2). Feasibility for performing cerebral MRI was limited due to maternal/patient safety reasons and further logistical infrastructural reasons.</p><p><strong>Conclusions: </strong>Structural cerebr
{"title":"Serial cerebral magnetic resonance imaging before and after birth in patients with complex congenital heart disease - a prospective, multicentre observational study.","authors":"Walter Knirsch, Alexandra De Silvestro, Celine Steger, Verena Rathke, Roland Weber, Michael Von Rhein, Juliane Schneider, Damian Hutter, Bettina Reich, Ulrike Held, Annette Hackenberg, Ruth Tuura O'Gorman, Raimund Kottke, Andras Jakab","doi":"10.57187/s.4466","DOIUrl":"https://doi.org/10.57187/s.4466","url":null,"abstract":"<p><strong>Study aims: </strong>Our objective was to establish a multicentre foetal-to-neonatal magnetic resonance (MR) neuroimaging programme for neonates undergoing surgery for complex congenital heart disease (CHD). We assessed structural and volumetric MRI findings at different timepoints in various types of CHD and evaluated neurodevelopmental outcomes at one year of age. Additionally, we analysed the feasibility, challenges and limitations of implementing this MR neuroimaging programme.</p><p><strong>Methods: </strong>In this prospective, multicentre observational study, we examined brain development and growth in infants with complex CHD requiring neonatal cardiac surgery. Brain MRI was performed at multiple timepoints: at the 32nd week of gestation, after birth (both before and after stage I surgery), and before stage II surgery in single-ventricle CHD. We analysed and compared cardiac diagnoses, treatment approaches, structural and volumetric brain MRI findings and neurodevelopmental outcomes at one year of age (assessed using the Bayley III scale) with those of healthy controls.</p><p><strong>Results: </strong>Between April 2020 and September 2023, 81 patients and 15 healthy controls underwent at least one MRI. Cardiac diagnoses were biventricular CHD (66.7%), single-ventricle CHD (25.9%) and borderline left ventricle CHD (7.4%). New structural cerebral lesions were found before stage I or after stage I including white matter injury in 3.8% and 8.7%, respectively, ischaemic cerebral lesions in 11.5 and 11.6%, intraventricular haemorrhages in 7.7% and 7.2%, and subdural haemorrhages in 33.6% and 26.1%. Total brain volume at 32.6 (interquartile range [IQR]: 31.3-33.3) gestational weeks was 228.9 ml (213.1-241.2) in biventricular CHD, 194.4 ml (165.3-223.6) in single-ventricle CHD and 196.4 ml (186.4-235.2) in normal healthy controls. After birth, at 6 days (3-16) of life total brain volume was 337.1 ml (310.3-350.2) in biventricular CHD, 331.6 ml (305.9-350.7) in single-ventricle CHD and 406.8 ml (389.9-438.7) in normal healthy controls. After stage I, at 26.5 days (18.3-40.8) total brain volume was 367.7 ml (341.8-385.5) in biventricular CHD, 353.6 ml (338.2-375.7) in single-ventricle CHD and 514.1 ml (482.9-554.6) at 116 days (94.5-118.5) in patients with single-ventricle CHD. At 12.1 months of age, neurodevelopmental performance determined by the Bayley III scale (mean ± SD [standard deviation]) was lower for patients with single-ventricle CHD (cognitive composite score [CCS]: 92.9 ± 13.1; language composite score [LCS]: 88.5 ± 12.0; motor composite score [MCS]: 85.6 ± 14.5) than in patients with biventricular CHD (CCS: 101.2 ± 11.1; LCS: 95.7 ± 13.1; MCS: 87.6 ± 18.0) or in healthy controls (CCS: 113.3 ± 5.6; LCS: 102.3 ± 7.9; MCS: 100.7 ± 8.2). Feasibility for performing cerebral MRI was limited due to maternal/patient safety reasons and further logistical infrastructural reasons.</p><p><strong>Conclusions: </strong>Structural cerebr","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4466"},"PeriodicalIF":1.9,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145763844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Can lifesaving be punishable? Performing resuscitation in an emergency places individuals under great pressure. Empirical studies indicate that potential helpers often hesitate to intervene for fear of legal consequences. However, this concern is unfounded. The article examines four scenarios: death despite resuscitation, harmful or unwanted resuscitation, and omission of aid. The conclusion is unequivocal: in case of doubt, initiating resuscitation ("in dubio pro REA") is legally safe. Only in cases where it is clearly established that resuscitation is not desired does the exception apply, meaning that no assistance should be rendered ("no means no"). This article analyses criminal liability risks in resuscitation based on Swiss law. Nevertheless, the findings are broadly transferable to other jurisdictions, as the relevant offences are universally codified.
拯救生命会受到惩罚吗?在紧急情况下进行复苏会使人承受很大的压力。实证研究表明,由于担心法律后果,潜在的帮助者往往不愿干预。然而,这种担心是没有根据的。本文考察了四种情况:尽管复苏死亡,有害或不必要的复苏,和遗漏援助。结论是明确的:在怀疑的情况下,启动复苏(“in dubio pro REA”)在法律上是安全的。只有在明确确定不需要复苏的情况下,才适用例外情况,即不应提供任何帮助(“不意味着不”)。本文以瑞士法律为依据,对复苏中的刑事责任风险进行了分析。然而,调查结果可广泛地转移到其他司法管辖区,因为有关罪行是普遍编纂的。
{"title":"In dubio pro REA: criminal liability risks in resuscitation.","authors":"Marc Thommen","doi":"10.57187/s.5033","DOIUrl":"https://doi.org/10.57187/s.5033","url":null,"abstract":"<p><p>Can lifesaving be punishable? Performing resuscitation in an emergency places individuals under great pressure. Empirical studies indicate that potential helpers often hesitate to intervene for fear of legal consequences. However, this concern is unfounded. The article examines four scenarios: death despite resuscitation, harmful or unwanted resuscitation, and omission of aid. The conclusion is unequivocal: in case of doubt, initiating resuscitation (\"in dubio pro REA\") is legally safe. Only in cases where it is clearly established that resuscitation is not desired does the exception apply, meaning that no assistance should be rendered (\"no means no\"). This article analyses criminal liability risks in resuscitation based on Swiss law. Nevertheless, the findings are broadly transferable to other jurisdictions, as the relevant offences are universally codified.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"5033"},"PeriodicalIF":1.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145715851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Martin Kiebler, Ana Paula Simões-Wüst, Nicole Ochsenbein-Kölble
<p><strong>Study aims: </strong>Premature birth is the leading cause of neonatal morbidity and mortality. Tocolytics aim to temporarily inhibit preterm contractions, allowing time for lung maturation induction, which reduces neonatal complications. Guidelines recommend limiting tocolysis to 48 hours and avoiding its use beyond 34 weeks of gestation. However, international surveys indicate that clinical practice often deviates from guidelines, revealing a gap between evidence-based recommendations and real-world practice. We aimed to evaluate current practices in the use of tocolysis and antenatal corticosteroid treatment in Switzerland and their alignment with international and national guidelines for preterm birth management.</p><p><strong>Methods: </strong>This national cross-sectional survey (15 February to 30 May 2024) used an anonymous online questionnaire distributed to 94 chief physicians of obstetric departments and 481 private-practice gynaecologists via e-mail, as well as through newsletters and social media channels of the Swiss Society of Gynaecology and Obstetrics in German, French and Italian. Chief physicians were contacted through the Chief Physicians' Conference e-mail list and asked to share the survey with their medical teams. Private-practice gynaecologists were reached via practice e-mail addresses obtained through the authors' personal networks and a clinic internal directory, as no centralised registry exists. Eligible participants were those actively involved in obstetrics or pregnancy care. The primary outcomes were duration and timing of tocolysis. Data is shown for the overall cohort and stratified by physician group (hospital, private-practice and attending physicians). The estimated response rate among specialists was 13% overall, with higher participation by hospital physicians (25%) and lower participation by private-practice physicians (8%).</p><p><strong>Results: </strong>A total of 319 obstetricians participated in the survey (201 hospital, 68 private-practice and 50 attending physicians). Maintenance tocolysis was still practiced by 54% of survey participants. While 80% of the respondents adhered to international/national guidelines by limiting tocolysis to 34 weeks of gestation, 20% reported administering tocolytics beyond this point. Tocolysis was primarily used in cases of preterm labour; in contrast, its use in premature preterm rupture of membranes without contractions was limited, with most physicians administering it only during antenatal corticosteroid treatment administration. Furthermore, similarities were observed among physician groups in prioritising indications and contraindications for tocolysis, but variations existed in the use of tocolytics in special situations (e.g. high-risk pregnancies or cervical cerclage).</p><p><strong>Conclusion: </strong>Most participating Swiss obstetricians adhere to existing guidelines for preterm birth management, but discrepancies remain - particularly regarding t
{"title":"Insights into tocolytic use and preterm birth management: a Swiss cross-sectional survey.","authors":"Martin Kiebler, Ana Paula Simões-Wüst, Nicole Ochsenbein-Kölble","doi":"10.57187/s.4453","DOIUrl":"https://doi.org/10.57187/s.4453","url":null,"abstract":"<p><strong>Study aims: </strong>Premature birth is the leading cause of neonatal morbidity and mortality. Tocolytics aim to temporarily inhibit preterm contractions, allowing time for lung maturation induction, which reduces neonatal complications. Guidelines recommend limiting tocolysis to 48 hours and avoiding its use beyond 34 weeks of gestation. However, international surveys indicate that clinical practice often deviates from guidelines, revealing a gap between evidence-based recommendations and real-world practice. We aimed to evaluate current practices in the use of tocolysis and antenatal corticosteroid treatment in Switzerland and their alignment with international and national guidelines for preterm birth management.</p><p><strong>Methods: </strong>This national cross-sectional survey (15 February to 30 May 2024) used an anonymous online questionnaire distributed to 94 chief physicians of obstetric departments and 481 private-practice gynaecologists via e-mail, as well as through newsletters and social media channels of the Swiss Society of Gynaecology and Obstetrics in German, French and Italian. Chief physicians were contacted through the Chief Physicians' Conference e-mail list and asked to share the survey with their medical teams. Private-practice gynaecologists were reached via practice e-mail addresses obtained through the authors' personal networks and a clinic internal directory, as no centralised registry exists. Eligible participants were those actively involved in obstetrics or pregnancy care. The primary outcomes were duration and timing of tocolysis. Data is shown for the overall cohort and stratified by physician group (hospital, private-practice and attending physicians). The estimated response rate among specialists was 13% overall, with higher participation by hospital physicians (25%) and lower participation by private-practice physicians (8%).</p><p><strong>Results: </strong>A total of 319 obstetricians participated in the survey (201 hospital, 68 private-practice and 50 attending physicians). Maintenance tocolysis was still practiced by 54% of survey participants. While 80% of the respondents adhered to international/national guidelines by limiting tocolysis to 34 weeks of gestation, 20% reported administering tocolytics beyond this point. Tocolysis was primarily used in cases of preterm labour; in contrast, its use in premature preterm rupture of membranes without contractions was limited, with most physicians administering it only during antenatal corticosteroid treatment administration. Furthermore, similarities were observed among physician groups in prioritising indications and contraindications for tocolysis, but variations existed in the use of tocolytics in special situations (e.g. high-risk pregnancies or cervical cerclage).</p><p><strong>Conclusion: </strong>Most participating Swiss obstetricians adhere to existing guidelines for preterm birth management, but discrepancies remain - particularly regarding t","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4453"},"PeriodicalIF":1.9,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145715822","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nora Haag, Mathilde Le Vu, Adrian V Jaeggi, David Baud, David Desseauve, Martin Haeusler, Kaspar Staub, Katarina L Matthes
Introduction: Human childbirth remains a complex and risky process for both mothers and infants, even with modern advancements in medical care. This study investigated the prevalence of obstetric interventions, namely caesarean sections, episiotomies, and forceps deliveries, along with the role of maternal-foetal body size mismatch in influencing delivery outcomes.
Methods: Utilising two datasets from similar archival sources in two Swiss cities (Basel and Lausanne) from the 1920s, we explored the relevance of a mismatch between the body size of the mother and the foetus as a risk factor for obstetrical interventions and the duration of the expulsion phase during delivery.
Results: Over 91% of births (1290/1407 in Basel and 1062/1145 in Lausanne) featured the foetal head in a normal position (either the right or left occiput anterior position). Episiotomies were performed in 8-17% of cases (233/1407 in Basel and 98/1145 in Lausanne) and forceps deliveries in 1-5% (17/1407 in Basel and 54/1145 in Lausanne). Caesarean sections were rare (<1%, 19/1407 in Basel and 6/1145 in Lausanne). Key findings indicated that larger foetal head diameters and narrower pelvic measurements were linked to prolonged expulsion phases and an increased likelihood of intervention. Abnormal head positions and first-time births were also associated with obstetrical interventions. Additionally, rickets was documented in 2% of mothers (23/1145) in Lausanne, correlating with increased forceps use and caesarean section rates.
Conclusion: This research provides insights into obstetric practices and maternal health conditions over a century ago, emphasising the significant impact of maternal-foetal body size mismatches on childbirth complications in a historical context.
{"title":"Association between a mismatch of maternal/neonatal body size and obstetrical interventions in Switzerland in the 1920s: a cross-sectional study.","authors":"Nora Haag, Mathilde Le Vu, Adrian V Jaeggi, David Baud, David Desseauve, Martin Haeusler, Kaspar Staub, Katarina L Matthes","doi":"10.57187/s.4546","DOIUrl":"https://doi.org/10.57187/s.4546","url":null,"abstract":"<p><strong>Introduction: </strong>Human childbirth remains a complex and risky process for both mothers and infants, even with modern advancements in medical care. This study investigated the prevalence of obstetric interventions, namely caesarean sections, episiotomies, and forceps deliveries, along with the role of maternal-foetal body size mismatch in influencing delivery outcomes.</p><p><strong>Methods: </strong>Utilising two datasets from similar archival sources in two Swiss cities (Basel and Lausanne) from the 1920s, we explored the relevance of a mismatch between the body size of the mother and the foetus as a risk factor for obstetrical interventions and the duration of the expulsion phase during delivery.</p><p><strong>Results: </strong>Over 91% of births (1290/1407 in Basel and 1062/1145 in Lausanne) featured the foetal head in a normal position (either the right or left occiput anterior position). Episiotomies were performed in 8-17% of cases (233/1407 in Basel and 98/1145 in Lausanne) and forceps deliveries in 1-5% (17/1407 in Basel and 54/1145 in Lausanne). Caesarean sections were rare (<1%, 19/1407 in Basel and 6/1145 in Lausanne). Key findings indicated that larger foetal head diameters and narrower pelvic measurements were linked to prolonged expulsion phases and an increased likelihood of intervention. Abnormal head positions and first-time births were also associated with obstetrical interventions. Additionally, rickets was documented in 2% of mothers (23/1145) in Lausanne, correlating with increased forceps use and caesarean section rates.</p><p><strong>Conclusion: </strong>This research provides insights into obstetric practices and maternal health conditions over a century ago, emphasising the significant impact of maternal-foetal body size mismatches on childbirth complications in a historical context.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4546"},"PeriodicalIF":1.9,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145715837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jonathan A Sobel, Marie-Céline Zanella, Rebecca Grant, Camille B Valera, Maria Suveges, Laura Urbini, Khaled Mostaguir, Sara Botero, Ursina Roder, Davide Bosetti, Rami Sommerstein, Ulrich Heininger, Petra Zimmermann, Peter W Schreiber, Domenica Flury, Anita Niederer-Loher, Philipp Jent, Alexia Cusini, Didier Pittet, Stephan Harbarth, Anne Iten, Olivia Keiser
Background: In 2018, a hospital-based surveillance system for influenza (CH-SUR) was established in six tertiary care hospitals in Switzerland. From March 2020 onwards, this surveillance system was expanded to include more institutions, as well as COVID-19.
Aim: To quantitatively evaluate the timeliness and completeness of CH-SUR data and to qualitatively assess stakeholder perceptions of the importance, reliability and adaptability of the surveillance system.
Methods: All patients admitted to one of the participating centres for more than 24 hours and who had a laboratory-confirmed influenza virus or SARS-CoV-2 infection were included in CH-SUR. For all cases, we evaluated the timeliness and completeness of reporting to CH-SUR. A qualitative survey among CH-SUR stakeholders assessed perceived importance, understanding, reliability and adaptability of CH-SUR.
Results: Up to 20 centres participated in CH-SUR. Between December 2018 and October 2023, 7375 cases of influenza were reported and between March 2020 and October 2023, 49,235 cases of COVID-19 were reported to CH-SUR. During the COVID-19 pandemic, time to data entry and completeness improved over time; the median delay of data entry in CH-SUR was 5 days (interquartile range [IQR]: 2-23) for COVID-19 and 4 days (IQR: 2-15) for influenza during the period 2018-2023. The completeness of variables was high (99.4%), with the exception of COVID-19 or annual influenza vaccination status (respectively, 15% and 72% "Unknown" responses). Stakeholders perceived the system as important, relevant, understandable and adaptable.
Conclusion: CH-SUR provided critical epidemiological and clinical information on hospitalised influenza and COVID-19 cases across Switzerland during the pandemic. Our evaluation highlighted the importance and relevance of this system among CH-SUR stakeholders, as well as its importance for preparedness and response to future infectious disease outbreaks.
{"title":"Overview and evaluation of a nationwide hospital-based surveillance system for influenza and COVID-19 in Switzerland (CH-SUR): 2018-2023.","authors":"Jonathan A Sobel, Marie-Céline Zanella, Rebecca Grant, Camille B Valera, Maria Suveges, Laura Urbini, Khaled Mostaguir, Sara Botero, Ursina Roder, Davide Bosetti, Rami Sommerstein, Ulrich Heininger, Petra Zimmermann, Peter W Schreiber, Domenica Flury, Anita Niederer-Loher, Philipp Jent, Alexia Cusini, Didier Pittet, Stephan Harbarth, Anne Iten, Olivia Keiser","doi":"10.57187/s.4213","DOIUrl":"https://doi.org/10.57187/s.4213","url":null,"abstract":"<p><strong>Background: </strong>In 2018, a hospital-based surveillance system for influenza (CH-SUR) was established in six tertiary care hospitals in Switzerland. From March 2020 onwards, this surveillance system was expanded to include more institutions, as well as COVID-19.</p><p><strong>Aim: </strong>To quantitatively evaluate the timeliness and completeness of CH-SUR data and to qualitatively assess stakeholder perceptions of the importance, reliability and adaptability of the surveillance system.</p><p><strong>Methods: </strong>All patients admitted to one of the participating centres for more than 24 hours and who had a laboratory-confirmed influenza virus or SARS-CoV-2 infection were included in CH-SUR. For all cases, we evaluated the timeliness and completeness of reporting to CH-SUR. A qualitative survey among CH-SUR stakeholders assessed perceived importance, understanding, reliability and adaptability of CH-SUR.</p><p><strong>Results: </strong>Up to 20 centres participated in CH-SUR. Between December 2018 and October 2023, 7375 cases of influenza were reported and between March 2020 and October 2023, 49,235 cases of COVID-19 were reported to CH-SUR. During the COVID-19 pandemic, time to data entry and completeness improved over time; the median delay of data entry in CH-SUR was 5 days (interquartile range [IQR]: 2-23) for COVID-19 and 4 days (IQR: 2-15) for influenza during the period 2018-2023. The completeness of variables was high (99.4%), with the exception of COVID-19 or annual influenza vaccination status (respectively, 15% and 72% \"Unknown\" responses). Stakeholders perceived the system as important, relevant, understandable and adaptable.</p><p><strong>Conclusion: </strong>CH-SUR provided critical epidemiological and clinical information on hospitalised influenza and COVID-19 cases across Switzerland during the pandemic. Our evaluation highlighted the importance and relevance of this system among CH-SUR stakeholders, as well as its importance for preparedness and response to future infectious disease outbreaks.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4213"},"PeriodicalIF":1.9,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145715883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: The primary objective was to measure the impact of passive exposure to an educational video about Chlamydia trachomatis infection shown in a gynaecology department waiting room on young women's knowledge on the subject. The secondary objective was to explore the participants' interest in improving their knowledge of Chlamydia trachomatis and their opinions on receiving this information during a consultation in the emergency room.
Methods: A prospective, interventional, controlled, non-randomised study. Participants were recruited between January and June 2022. 120 women aged 15-35 years were included. The intervention consisted of passive exposure to a 2-minute cartoon presenting basic foundational points of Chlamydia trachomatis displayed in the waiting room. The control group was not exposed to the video. After the intervention, an in-person knowledge interview was performed with each participant.
Main outcome measures: The main outcome measures were the knowledge scores obtained in the interviews with the exposed and control groups.
Results: Both groups were similar regarding sociodemographic variables. The average knowledge scores from the interview were similar in the two groups. Video exposure was not associated with diminution of lower scores. Participants' baseline knowledge was higher than expected on the basis of a literature review.
Conclusion: The passive learning intervention described in this study did not improve the participants' knowledge about Chlamydia trachomatis. During the one-to-one interview, participants were keen to receive information about Chlamydia trachomatis but the quantitative results show that the short video in the waiting room had no impact on their knowledge. Future studies should focus on pre-assessed, randomised, one-to-one or small-group active interventions.
{"title":"Primary prevention of Chlamydia trachomatis infection in young women: impact of an informational video in a Swiss gynaecology emergency department.","authors":"Solene Perret, Guillaume Favre, Karine Lepigeon, Patrice Mathevet, Martine Jacot-Guillarmod","doi":"10.57187/s.4329","DOIUrl":"https://doi.org/10.57187/s.4329","url":null,"abstract":"<p><strong>Objectives: </strong>The primary objective was to measure the impact of passive exposure to an educational video about Chlamydia trachomatis infection shown in a gynaecology department waiting room on young women's knowledge on the subject. The secondary objective was to explore the participants' interest in improving their knowledge of Chlamydia trachomatis and their opinions on receiving this information during a consultation in the emergency room.</p><p><strong>Methods: </strong>A prospective, interventional, controlled, non-randomised study. Participants were recruited between January and June 2022. 120 women aged 15-35 years were included. The intervention consisted of passive exposure to a 2-minute cartoon presenting basic foundational points of Chlamydia trachomatis displayed in the waiting room. The control group was not exposed to the video. After the intervention, an in-person knowledge interview was performed with each participant.</p><p><strong>Main outcome measures: </strong>The main outcome measures were the knowledge scores obtained in the interviews with the exposed and control groups.</p><p><strong>Results: </strong>Both groups were similar regarding sociodemographic variables. The average knowledge scores from the interview were similar in the two groups. Video exposure was not associated with diminution of lower scores. Participants' baseline knowledge was higher than expected on the basis of a literature review.</p><p><strong>Conclusion: </strong>The passive learning intervention described in this study did not improve the participants' knowledge about Chlamydia trachomatis. During the one-to-one interview, participants were keen to receive information about Chlamydia trachomatis but the quantitative results show that the short video in the waiting room had no impact on their knowledge. Future studies should focus on pre-assessed, randomised, one-to-one or small-group active interventions.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4329"},"PeriodicalIF":1.9,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145715825","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marcel Aebi, Jana Dreyer, Christoph Siedler, Karoline Niedenzu, Évi Forgó Baer, Carmelo Campanello, Andreas Wepfer, Francesco Castelli, Thierry Urwyler
Background: Psychosocial maturity is one of the key factors for understanding the course of criminal offences in juveniles and young adults. Until recently, forensic-psychiatric assessments to diagnose a severe disorder of personality development remained mostly unguided because validated instruments were not available. A new tool, the Young Adult Personality Development (YAPD) instrument, was introduced in 2021 and consists of three dimensions related to psychosocial maturity: YAPD environmental, YAPD pathology and YAPD developmental tasks failure. The current study tested the reliability (internal consistency, interrater reliability) and concurrent validity of these dimensions.
Methods: We analysed files of a consecutive sample of young adults in the Canton of Zurich (2007 to 2020, n = 234, mean age: 21.33 years, SD: 1.74 years), who were either assigned to specialised institutional treatment for young adults (Swiss Penal Code [SPC] Article 61) or outpatient treatment (SPC Article 63). Intraclass correlation coefficient (ICC) agreements were used to analyse interrater reliability of YAPD dimensions across three independent raters. In the absence of a gold standard, we analysed concurrent validity by measuring the associations of the YAPD dimensions with expert opinion and sample status (judicial decisions on measures) using multiple logistic regressions.
Results: Expert-rated personality development disorder was found to be highly prevalent in both samples. The YAPD dimensions showed adequate-to-good interrater reliability (ICC: 0.74-0.92). In logistic regression models, YAPD developmental tasks failure was related to diagnoses of severe development disorder and juridical decision on a measure for young adults according to SPC Art. 61. YAPD environmental was related to the diagnosis of a severe development disorder. YAPD pathology was found to be unrelated to the diagnosis of severe personality development disorder.
Conclusions: Our findings support the YAPD developmental tasks failure dimension and to a lesser degree the YAPD environmental dimension as valid dimensions to diagnose severe personality development disorder. Structured assessment instruments such as the YAPD may further improve diagnostic decision-making in forensic psychiatry and psychology.
{"title":"Assessing psychosocial maturity to diagnose severe personality development disorders in young adult males adjudicated of serious criminal offences: a psychometric validation study of a new instrument.","authors":"Marcel Aebi, Jana Dreyer, Christoph Siedler, Karoline Niedenzu, Évi Forgó Baer, Carmelo Campanello, Andreas Wepfer, Francesco Castelli, Thierry Urwyler","doi":"10.57187/s.3793","DOIUrl":"https://doi.org/10.57187/s.3793","url":null,"abstract":"<p><strong>Background: </strong>Psychosocial maturity is one of the key factors for understanding the course of criminal offences in juveniles and young adults. Until recently, forensic-psychiatric assessments to diagnose a severe disorder of personality development remained mostly unguided because validated instruments were not available. A new tool, the Young Adult Personality Development (YAPD) instrument, was introduced in 2021 and consists of three dimensions related to psychosocial maturity: YAPD environmental, YAPD pathology and YAPD developmental tasks failure. The current study tested the reliability (internal consistency, interrater reliability) and concurrent validity of these dimensions.</p><p><strong>Methods: </strong>We analysed files of a consecutive sample of young adults in the Canton of Zurich (2007 to 2020, n = 234, mean age: 21.33 years, SD: 1.74 years), who were either assigned to specialised institutional treatment for young adults (Swiss Penal Code [SPC] Article 61) or outpatient treatment (SPC Article 63). Intraclass correlation coefficient (ICC) agreements were used to analyse interrater reliability of YAPD dimensions across three independent raters. In the absence of a gold standard, we analysed concurrent validity by measuring the associations of the YAPD dimensions with expert opinion and sample status (judicial decisions on measures) using multiple logistic regressions.</p><p><strong>Results: </strong>Expert-rated personality development disorder was found to be highly prevalent in both samples. The YAPD dimensions showed adequate-to-good interrater reliability (ICC: 0.74-0.92). In logistic regression models, YAPD developmental tasks failure was related to diagnoses of severe development disorder and juridical decision on a measure for young adults according to SPC Art. 61. YAPD environmental was related to the diagnosis of a severe development disorder. YAPD pathology was found to be unrelated to the diagnosis of severe personality development disorder.</p><p><strong>Conclusions: </strong>Our findings support the YAPD developmental tasks failure dimension and to a lesser degree the YAPD environmental dimension as valid dimensions to diagnose severe personality development disorder. Structured assessment instruments such as the YAPD may further improve diagnostic decision-making in forensic psychiatry and psychology.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"3793"},"PeriodicalIF":1.9,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145522916","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}