Facial pain – an interdisciplinary challenge

Im Praxis- und Klinikalltag wird der Zahnarzt regelmässig mit Patienten konfrontiert, die über Schmerzen im Gesicht klagen. Neben möglichen dentalen Ursachen können Erkrankungen aus anderen Fachgebieten, über die sich der Zahnarzt bewusst sein muss, verantwortlich für Gesichtsschmerzen sein. Eine genaue Schmerzanamnese ist daher ebenso wichtig wie eine gründliche klinische Untersuchung und die Einleitung gezielter diagnostischer Massnahmen, um dem Patienten schliesslich eine erfolgversprechende Therapie anbieten zu können. In diesem Artikel wird der Gesichtsschmerz aus der Perspektive der Fachbereiche Zahnmedizin, Neurologie und Neurochirurgie differenzialdiagnostisch erörtert, und es werden die unter- schiedlichen diagnostischen und therapeutischen Herangehensweisen erarbeitet. Ziel ist es, dem Patienten zeitraubende fehlgeleitete Therapien zu ersparen und ihn möglichst zeitnah einer effizienten, zielgerichteten Schmerztherapie zuzuführen, um die Entstehung einer Schmerzchronifizierung zu vermeiden.Acute pain has a warning function and is necessary to survive. Conversely, chronic or recurrent pain is a pathological entity itself and has tremendous impact on the quality of life of the patients . Facial pain is very common and can have various causes. The trigeminal nerve innervates the face, and tumours along its intracranial way as well as peripheral injury can lead to facial pain. Also, infections and systemic diseases, like multiple sclerosis, may cause pain in the face, so can vascular compressions of the trigeminal or glossopharyngeal nerve. Detailed pain history is crucial in order to rule out other than dental reasons for facial pain before invasive dental therapy is initiated. A multidisciplinary approach and additional imaging modalities might be necessary to find the optimal treatment for the patient

Brain of the sheep

<p>STL-Model of the sheep's brain derived from a T2 MRI dataset.</p

Evaluation and discussion of handmade face-masks and commercial diving-equipment as personal protection in pandemic scenarios.

ObjectivePandemic scenarios like the current Corona outbreak show the vulnerability of both globalized markets and just-in-time production processes for urgent medical equipment. Even usually cheap personal protection equipment becomes excessively expensive or is not deliverable at all. To avoid dangerous situations especially to medical professionals, but also to affected patients, 3D-printer and maker-communities have teamed up to develop and print shields, masks and adapters to help the medical personnel. In this study, we investigate three home-made respiratory masks for filter and protection efficacy and discuss the results and legal aspects.Materials and methodsA home-printed respiratory mask with a commercial filter, a scuba-diving mask with a commercial filter and a mask sewn from a vacuum cleaner bag were investigated with 99mTc-labeled NaCl-aerosol, and the respective filter-efficacy was measured under a scintigraphic camera.ResultsThe sewn mask from a vacuum cleaner bag had a filter efficacy of 69.76%, the 3D-printed mask of 39.27% and the scuba-diving mask of 85.07%.ConclusionHome-printed personal protection equipment can be a-yet less efficient-alternative against aerosol in case professional masks are not available, but legal aspects of their use and distribution have to be kept in mind in order to avoid compensation claims

Mastication after craniotomy: pilot assessment of postoperative oral health-related quality of life

Background!#!Neurosurgical approaches to the brain often require the mobilization of the temporal muscle. Many patients complain of postoperative pain, atrophy, reduced mouth opening, and masticatory problems. Although the pterional, frontolateral-extended-pterional, and temporal craniotomies are the most frequently used approaches in neurosurgery, a systematic assessment of the postoperative oral health-related quality of life has never been performed so far. This study evaluates the oral health-related quality of life of patients after pterional, frontolateral-extended-pterional, or temporal craniotomy using a validated and standardized dental questionnaire, compares the results with the normal values of the general population, and investigates whether this questionnaire is sensitive to changes caused by surgical manipulation of the temporal muscle.!##!Methods!#!The 'Oral Health Impact Profile' (OHIP14) is a validated questionnaire to assess the oral health-related quality of life. It asks the patients to assess their oral health situation within the past 7 days in 14 questions. Possible answers range from 0 (never) to 4 (very often). Sixty patients with benign intracranial processes operated through a lateral cranial approach were included. The questionnaire was answered before surgery (baseline) and 3 months and 15 months after surgery.!##!Results!#!Overall, postoperative OHIP scores increase significantly after 3 months and decrease after 15 months, but not to preoperative values. No factors can be identified which show a considerable relationship with the postoperative OHIP score.!##!Conclusions!#!Postoperative impairment of mouth opening and pain during mastication can be observed 3 to 15 months after surgery and sometimes cause feedback from patients and their dentists. However, in line with existing literature, these complaints decrease with time. The study shows that the OHIP questionnaire is sensitive to changes caused by surgical manipulation of the temporal muscle and can therefore be used to investigate the influence of surgical techniques on postoperative complaints. Postoperatively, patients show worse OHIP scores than the general population, demonstrating that neurosurgical cranial approaches negatively influence the patient's oral health-related wellbeing. Larger studies using the OHIP questionnaire should evaluate if postoperative physical therapy, speech therapy, or specialized rehabilitation devices can improve the masticatory impairment after craniotomy.!##!Trial registration!#!Clinical trial register: DRKS00011096

Effect of transcutaneous auricular vagal nerve stimulation on the fatigue syndrome in patients with gastrointestinal cancers — FATIVA: a randomized, placebo-controlled pilot study protocol

Abstract Background Cancer-related fatigue (CRF) is defined as a “distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportional to recent activity and interferes with usual functioning.” CRF is frequently observed in cancer patients even before the initiation of tumor therapy. Its cause is not clear, but in addition to primary effects of therapy, a tumor-induced elevated level of inflammatory cytokines may play a role. Transcutaneous auricular vagal nerve stimulation (taVNS) is a noninvasive way to activate central nervous pathways and modulate pain perception and the immune system. It has positive effects on autoimmune conditions and can also improve fatigue associated with Sjogren’s syndrome. It is the main purpose of this feasibility study to investigate the feasibility of daily taVNS against CRF. Therefore, the stimulation protocol of the newly introduced smartphone app of the manufacturer is evaluated. Additionally, the effect taVNS on CRF and quality of life (QoL) shall be evaluated. Methods Thirty adult patients with gastrointestinal tumors during or after treatment, relevant CRF (Hornheide questionnaire) and life expectancy > 1 year, are enrolled. Patients are randomized to treatment or sham arm and be informed that they will either feel the stimulation or not. Treatment group will receive left-sided tragus above-threshold stimulation with 25 Hz, 250 µs pulse width, and 28-s/32-s on/off paradigm for 4 h throughout the day for 4 weeks. Sham group will receive no stimulation via a nonfunctional electrode. A daily stimulation protocol with time and average intensity is automatically created by a smartphone app connected to the stimulator via Bluetooth®. Multidimensional Fatigue Inventory-20, Short-Form 36 and Beck Depression Inventory questionnaires will be filled out before and after 4 weeks of stimulation. Discussion Primarily, the patients’ daily stimulation time and intensity will be evaluated through the electronic protocol after 4 weeks. Secondarily, the effect of taVNS on cancer-related fatigue and QoL will be measured through the questionnaires. As taVNS seems to modulate inflammatory cytokines, this noninvasive method may — if accepted by the patients — be a promising adjunct in the treatment of cancer-related fatigue. Trial registration The study was approved by local ethics committee (21–7395) and registered at the DRKS database (DRKS00027481)

Haemodynamic Responses to Selective Vagal Nerve Stimulation under Enalapril Medication in Rats.

Selective vagal nerve stimulation (sVNS) has been demonstrated to lower blood pressure (BP) in rats without causing major side effects. This method might be adapted for the treatment of therapy-resistant hypertension in patients. Converting enzyme inhibitors (CEIs) are among the first drugs that are administered for arterial hypertension and prominently reduce BP primarily by interacting with the renin-angiotensin system of the kidneys. Beyond the reduction of BP, CEI have a positive effect on the survival rate after myocardial infarction; they reduce the rates of stroke and improve the neurohormonal status in heart-failure patients. If sVNS might be introduced as a therapy against resistant hypertension, patients will at least partially stay on their CEI medication. It is therefore the aim of this study to investigate the influence of the CEI enalapril on the haemodynamic and respiratory effects of sVNS. In 10 male Wistar rats, a polyimide-based multichannel-cuff-electrode was placed around the vagal nerve bundle to selectively stimulate the aortic depressor nerve fibres. Stimulation parameters were adapted to the thresholds of the individual animals and included repetition frequencies between 30 and 50 Hz, amplitudes of 0.5 to 1.5 mA and pulse widths between 0.4 ms and 1.0 ms. BP responses were detected with a microtip transducer in the left carotid artery, and electrocardiography was recorded with subcutaneous electrodes. After intravenous administration of enalapril (2 mg/kg bodyweight), the animals' mean arterial blood pressures (MAPs) decreased significantly, while the heart rates (HRs) were not significantly influenced. The effects of sVNS on BP and HR were attenuated by enalapril but were still present. We conclude that sVNS can lower the MAP during enalapril treatment without relevant side effects

Sonographic-Assisted Catheter-Positioning in Intracerebral Hemorrhage

Introduction: Intracerebral structures and pathologies such as intracerebral hemorrhages (ICH) can be displayed sufficiently by transcranial sonography (TCS). In some patients with ICH clot evacuation via surgery or catheter drainage to reduce secondary parenchymal injuries may be necessary. We hypothesized that bedside-placement of drainage-catheters, which is a minimal invasive evacuation-technique complicated by a higher rate of catheter misplacement can be optimized via TCS.Methods: Eleven consecutive ICH-patients diagnosed via computertomography (CT) were included in this prospective observational pilot study. All patients were examined via TCS, firstly in order to illustrate the hematoma, secondly to optimize catheter placement. Catheter placement was primarily validated via CT.Results: The TCS-depiction of ICH-extension was optimal in 10 patients; one patient showed a partially insufficient transtemporal bone window. Catheter positioning could be traced and adapted correctly via TCS-examination in all patients. Follow-up CT-scans confirmed TCS-description of catheter-positioning in all patients without any complications. Reduction of symptoms and ICH-volumes confirmed effectiveness of treatment.Conclusions: The illustration of ICH and the drainage-placement is possible via TCS in a cost- and time-efficient way

Acute effects of the administration of enalapril on BP and MAP.

<p>The upper plot illustrates the BP reduction induced by the administration of enalapril. After a rapid decline in the first 10 seconds after application, the development of an equilibrium state required more than 100 seconds. Because the PA oscillation obscured the observation of the BP, the lower plot illustrates the calculated MAP values. The remaining oscillation visible in the lower plot was due to respiration. The red line in the upper plot and the upper red line in the lower plot mark the average MAP of 106 mmHg prior to administration of enalapril. The red line in the lower plot indicates the steady state of the MAP (at 58 mmHg). The black vertical arrow indicates the moment of enalapril application.</p