The relevance of reducing Veress needle overshooting.

Safe insertion of the Veress needle during laparoscopy relies on the surgeons' technical skills in order to stop needle insertion just in time to prevent overshooting in the underlying organs. To reduce this risk, a wide variety of Veress needle systems were developed with safety mechanisms that limit the insertion speed, insertion depth or decouple the driving force generated by the surgeon's hand on the needle. The aim of this study is to evaluate current surgeons' perceptions related to the use of Veress needles and to investigate the relevance of preventing overshooting of Veress needles among members of the European Association of Endoscopic Surgery (EAES). An online survey was distributed by the EAES Executive Office to all active members. The survey consisted of demographic data and 14 questions regarding the use of the Veress needle, the training conducted prior to usage, and the need for any improvement. A total of 365 members residing in 58 different countries responded the survey. Of the responding surgeons, 36% prefer the open method for patients with normal body mass index (BMI), and 22% for patients with high BMI. Of the surgeons using Veress needle, 68% indicated that the reduction of overshoot is beneficial in normal BMI patients, whereas 78% indicated that this is beneficial in high BMI patients. On average, the members using the Veress needle had used it for 1448 (SD 3031) times and felt comfortable on using it after 22,9 (SD 78,9) times. The average years of experience was 17,6 (SD 11,1) and the surgeons think that a maximum overshoot of 9.4 (SD 5.5) mm is acceptable before they can safely use the Veress needle. This survey indicates that despite the risks, Veress needles are still being used by the majority of the laparoscopic surgeons who responded. In addition, the surgeons responded that they were interested in using a Veress needle with an extra safety mechanism if it limits the risk of overshooting into the underlying structures.

Is there an adequate alternative to commercially manufactured face masks? A comparison of various materials and forms.

BACKGROUND: There is a worldwide shortage of medical-grade face masks. Donning masks can play an important role in curbing the spread of SARS-CoV-2. AIM: To conclude whether there is an effective mask for the population to wear in public that could easily be made during a medical face mask shortage using readily available materials. METHODS: We determined the effectiveness of readily available materials and models for making a face mask. The outcomes were compared with N95/FFP2/KN95 masks that entered the Netherlands in April-May 2020. Masks were tested to determine whether they filtered a minimum of 35% of 0.3-µm particles, are hydrophobic, seal on the face, are breathable, and can be washed. FINDINGS: Fourteen of the 25 (combinations of) materials filtered at least 35% of 0.3-µm particles. Four of the materials proved hydrophobic, all commercially manufactured filters. Two models sealed the face. Twenty-two of the 25 materials were breathable at <0.7 mbar. None of the hydrophobic materials stayed intact after washing. CONCLUSIONS: It would be possible to reduce the reproduction rate of SARS-CoV-2 from 2.4 to below one if 39% of the population would wear a mask made from ePM1 85% commercially manufactured filter fabric and in a duckbill form. This mask performs better than 80% of the imported N95/FFP2/KN95 masks and provides a better fit than a surgical mask. Two layers of quilt fabric with a household paper towel as filter is also a viable choice for protecting the user and the environment.

[Results of the ABC ' buddy project' whereby students were paid to befriend worryingly inactive youngsters with a psychotic disorder]. / Betaalde vriendendienst bij zorgwekkend inactieve jongeren met een psychotische stoornis; een vergelijkend onderzoek naar het ABC-buddyproject.

BACKGROUND: Psychology students ('buddies’) could earn € 25,- by visiting a patient, on one afternoon or evening per week, in order to provide friendship and engage the patient in a joint activity. An additional sum of € 20,- was made available to finance the joint activity. AIM: To find out whether this activity and social participation of patients who had a buddy increased more than in patients without a buddy. METHOD: In a quasi-experimental study 28 young, worryingly inactive patients who had a buddy were matched individually with patients without a buddy. Measurements were taken prior to the buddy contacts and after a period of 18 months. General functioning was used as a secondary outcome measure, in addition to the measure of activities and social participation. RESULTS: No patients in either group showed any improvement in activity, participation level and general functioning. CONCLUSION: Recruiting and paying buddies to befriend and stimulate worryingly inactive youngsters with a psychotic disorder did not increase the youngsters' activity, their social participation or their general functioning.