Total laryngectomy (TL) involves the removal of the entire larynx and redirection of the trachea to a neck stoma and is the last surgical treatment option for patients with laryngeal cancer [1,2]. Besides the loss of laryngeal speech, many patients who underwent TL face major pulmonary and other physical and psychosocial postoperative problems, which can negatively affect many health-related quality of life (HRQoL) aspects [3-9]. An important reason for these problems is the disconnection of the upper and lower airways whereby the warming, humidifying, and filtering of inhaled air, before it reaches the pulmonary tract, is no longer possible. Direct inhalation of (more) dry and cold air into the trachea causes pulmonary issues, such as thickening and crusting of the mucus, overproduction of mucosal secretions, and a reduction in the capacity of mucociliary clearance. This leads to an increased need to clear the airway from mucus by forced expectoration, increased involuntary coughing, and shortness of breath [3-5,10]. Moreover, owing to the loss of nasal filtering function and impaired mucociliary clearance, patients who underwent TL have an increased risk of chronic airway inflammation and infections [11-13]. The use of heat and moisture exchangers (HMEs) by patients who underwent TL reduces pulmonary problems. An HME helps by providing stoma occlusion and compensates for the temperature, humidification, and filtering deficit [14-23]. Multiple studies demonstrated the positive effects of HME use on pulmonary rehabilitation and respiratory health in patients, especially when adherence to HME use was high (ie, HME use day and night) [7,15,17,19,21,24-27]. High compliance to HME use has shown positive effects and resulted in decreases in coughing or forced expectorations in patients using HMEs day and night compared with less adherent users [17,28]. In addition, HMEs were found to be cost-effective because of fewer postoperative complications requiring treatments [13,29]. Despite the benefits of HMEs being clear in both clinical research and practice, a gap exists between the optimal physiological humidification level by the nasal function and the humidification capacity of the best HMEs [30]. It is challenging to bridge this gap, as an increase in the humidification capacity of HMEs is constricted by concurrent increases in breathing resistance and HME size. Patient compliance to HME use is also considered an issue, and a large variation in compliance (35%-70%) has been observed [17,28,31]. Many patients experience issues related to the situational use of HMEs, such as the breathing resistance being too high during physical activity, insufficient protection against airborne particles, and pulmonary problems at night [32]. Other reasons for noncompliance are mainly linked to issues related to peristomal adhesives (ie, skin irritation, poor attachment, and poor fit to the stoma shape) [7,28,33]. In this light, new HMEs have been developed focusing on improving HME performance (ie, providing the most optimal humidification possible while keeping the breathing resistance comfortable), situational usability, and HME attachments (improved security, skin-friendliness, and fit). Improvements in these areas will most likely positively influence patients’ HME compliance, pulmonary health, and, ultimately, quality of life (QoL) [32].

In this study, the potential effectiveness of 5 new HMEs (Provox Life) manufactured by Atos Medical AB (Hörby, Sweden) was evaluated. These new HMEs are also called the third-generation HMEs, as they follow the first-generation (Provox HME) and the second-generation (Provox XtraHMEs) HMEs with improved humidification properties compared with the first-generation HMEs. The new third-generation Provox Life HMEs include features that specialize them for situational use (ie, nighttime, home stay, moderate physical activity, high physical activity, and extra protection or filtration) and offer a range of attachments to suit individual patients’ needs. As limited empirical data are available on the use of the new HMEs, information on their expected effectiveness can be collected through expert opinion [34]. An evaluation of the effectiveness of the existing HMEs formed the basis for the assessment of the potential effectiveness of the new HMEs through expert opinion. The objective of this study was 3-fold; we aimed to (1) evaluate the effectiveness of the existing HMEs, (2) assess the potential effectiveness of the new HMEs among German clinical experts, and (3) elicit German expert judgments in a quantitative manner on the new HMEs’ expected effectiveness and impact on health care use.

An RLR, which provides knowledge synthesis in a timelier and resource-efficient manner, was conducted, as empirical data on the new HMEs are limited and expert opinion is essential to assess the potential efficacy of the new HMEs as soon as possible [35,36]. The search was conducted in PubMed. Articles were included if they were clinical studies, randomized controlled trials, reviews, or meta-analyses published between January 2010 and February 2021 in English, Dutch, or German. Articles needed to focus on identifying evidence on the clinical outcomes, health outcomes, and complications of HMEs in patients who underwent TL. Articles were excluded if they were concerning in vitro and ex vivo studies. The search was conducted in February 2021. The search string was as follows: ((laryngectomy AND ((HME OR “Heat and Moisture Exchanger” OR “Hygroscopic Condenser Humidifier”) OR (“Freehands HME”))) OR ((tracheostomy OR tracheotomy) AND (HME OR “Heat and Moisture Exchanger” OR “Hygroscopic Condenser Humidifier”)) OR ((laryngectomy OR tracheostomy OR tracheotomy) AND HMEF). The titles and abstracts were screened independently by 2 authors (AA and JCM). Full papers were retrieved if their titles and abstracts were considered relevant. As for the full-text screening, the selection was done by one author (AA) and checked by a second author (JCM). Disagreements were resolved by discussion, resulting in consensus. Data from each study were extracted using a standardized data abstraction form by one author (AA) and checked by another author (JCM). The extracted data included results on the effectiveness of HMEs in the outcome measures breathing resistance, cough, forced expectoration, tracheal dryness or irritation, mucus production or plugs, speech and voice quality, sleep quality, physiotherapy, pulmonary infection, pneumonia episode, QoL, and patient satisfaction.

Semistructured interviews with experts were conducted to validate the findings of the literature review and identify reasonable expectations regarding the potential of the new HMEs for use in patients who underwent TL. Experts were identified by Atos Medical GmbH (Troisdorf, Germany), as Germany is among the first countries to be introduced to the new HMEs. Experts were approached by the authors by mail. A total of 4 individual interviews were held with medical specialists or senior physicians in the ear-nose-throat field with a focus on oncology and head and neck surgeons at leading institutions in Germany. In this interview, the results of the RLR were discussed for validation, and it was discussed whether the new HMEs with better performance measured in the laboratory would lead to additional effects compared with the currently available HMEs. The following themes were included in the interview: breathing resistance, mucus production or plugs, tracheal dryness or irritation, cough and forced expectorations, sleep quality, speech and voice quality, physiotherapy, pulmonary infections (eg, tracheitis and tracheobronchitis), pneumonia episodes, psychological health, participation in society, QoL, patient satisfaction, and compliance (with HME use). An interview protocol (Multimedia Appendix 1) was prepared, including a brief introduction, an explanation of the research study, the process to be followed during the interview, the main questions, additional follow-up questions, and a final thank you statement. Experts were also introduced to information on the new HMEs (need for development of new HMEs, innovative adaptions made to the new HME devices, the different HMEs included in the new portfolio, and laboratory measurements concerning humidification and breathability of the new HMEs in comparison with their predecessors). The semistructured web-based interviews lasted 60 minutes on average. One independent author (AA) conducted all interviews in March and April 2021, and a second independent author (JCM) took notes during the interviews. Both authors are trained and experienced interviewers. The interviews were videorecorded and transcribed manually. Text segments were assigned a code if they were related to a specific theme, using an inductive, iterative process. The codes were based on the themes included in the interviews. The interviews were analyzed (AA and JCM) based on their themes to gain an insight into the additional effect of the new HMEs (content analysis).

SEE is a process that allows experts to express their judgment in a statistical and quantitative form. SEE was used to estimate the effectiveness of the new HMEs in health care use. The process consisted of the following steps: selection of experts, characterization of effect measures (ie, effects and use), defining of the scope and format of the elicitation, design of the elicitation protocol, preparation of the elicitation session, elicitation of expert judgments, and data analysis [34]. First, based on the RLR and expert interviews, information on the effect variables of HMEs that are currently being used was collected, which was included in the survey. A survey was set up according to the bins and chips method (IWAB and HJMV). In this method, experts were asked to indicate the lower and upper limits of their estimation of a specific effect variable (eg, difficulties with breathing) [37]. Experts assigned weights (0-100) to the effect variable to indicate the weight of their effect estimate in different intervals (0-10, 11-20, 21-30, etc). The stronger the expert believed that a specific effect lies in a given interval, the greater the weight for that interval was. This provides an estimated effect distribution (a mean effect and spread). For every expert judgment on each effect variable, a mean was calculated. Subsequently, the sample mean was calculated, which indicated the estimation of all expert judgments combined. For the analysis, we multiplied the weight by the average of the intervals. Thereafter, the sum of these outcomes was divided by the total weights assigned by the experts. In this manner, a weighted average per expert was established. The sum of all weighted averages of experts was averaged, and the corresponding SDs were calculated, resulting in our final indicator of experts’ beliefs. For some effect variables, the experts were asked to indicate the lower and upper limits of their estimation in absolute numbers. For these effect variables, the last category would not be a set interval (eg, 60-70), but it ended with a category “equal or more than X (i.e., ≥X).” In cases where an expert could be pointing at an amount higher than X, the assigned weight was multiplied by X + 1 interval. An example of a question with fictional answers is provided in Multimedia Appendix 2. The participants were sent the electronic survey contained in Multimedia Appendix 3 (Atos Medical, unpublished data, 2021, [12,16,28,29,31,38-44]) via a web link (SurveyMonkey, Momentive Inc). German experts were identified by Atos Medical GmbH and approached by an independent author (IWAB) via mail, including the 4 experts interviewed in the previous step of this study. Before participating in the web-based survey, the experts were required to read a white paper on the new HMEs and their developmental background and watch a video presentation about the new HMEs’ product portfolio to provide information on the properties of the new HMEs. If the experts did not read the white paper and watch the video presentation and were, therefore, assumed to have no basic knowledge of the new HMEs, they could not take part in the survey. The survey started with 6 general questions regarding current profession, years of experience in caring for patients with laryngeal cancer, years of experience in caring for patients who underwent TL, years of experience in prescribing and/or monitoring the use of HMEs, years of experience as a scientific researcher in the field of laryngeal cancer, and whether they had prescribed the new HMEs. The experts were also asked whether they had read the white paper on the new HMEs and watched the video on the new HMEs. The survey contained 16 other questions about the following effect variables: breathing, shortness of breath, tracheal climate (n=2), mucus production or plugging (n=2), coughing, forced expectorations, sleep quality, speech quality, psychological aspects, physiotherapy, tracheobronchitis or pneumonia episodes, social contacts, QoL, and patient satisfaction. At the end of the questionnaire, the participants could provide general comments or remarks. The participants were given 1 week to complete the questionnaire. After 1 week, a reminder email was sent to complete the questionnaire within a week. The analysis was conducted by 1 author (IWAB) and checked by 2 other authors (AA and HJMV).

As this study did not involve patients or study participants, an ethical research approval was not needed according to Article 1b of the Dutch Medical Research in Human Subjects Act [45]. Notwithstanding, all the participants provided their consent, and all the data were processed anonymously. The participants could withdraw from the study at any time without any consequences. The participants were financially compensated for their input in the SEE questionnaire.

A total of 62 publications were identified in PubMed. After screening the titles and abstracts of these studies, the full text of 38 (61%) of them were assessed. Of these 38 studies, 10 (16%) were included in the analysis. In total, 3 (30%) randomized controlled trials [28,29,40], 3 (30%) time-series studies in which patients acted as their own controls [31,41,42], 1 (10%) retrospective comparative cohort study [43], 1 (10%) retrospective clinical and survey study [12], 1 (10%) multigroup design study (study design was not reported by the authors themselves) [16], and 1 (10%) case-control study [44] were included. The new generation of HMEs were compared with a control (no HME use) [12,16,28,39-41], an external humidifier [29,43,44], or a previous generation HME [31]. The studies were performed in 7 different countries, namely the United States [16,43], Canada [44], France [29,40], Italy [41,42], Spain [31], the Netherlands [12], and Poland [28]. The studies included a total of 550 patients, with a minimum of 30 patients [41,42] and a maximum of 89 patients [12].

In Table 1, the effects reported by these studies are shown. Breathing was equal or less strenuous for HME users when compared with the control group [41]. A statistically nonsignificant effect with regard to breathing effort was achieved in 1 (10%) study [40]. Patients also reported a statistically significant decrease in shortness of breath [28,42]. However, 1 (10%) study reported a higher shortness of breath [16]. No difference was experienced in breathing resistance compared with a previous generation HME device [31]. Moreover, improvements in the tracheal climate were observed, as patients experienced significantly less tracheal dryness or irritation when using an HME [41,42] or when using an HME with improved humidification capacities [31]. Studies also reported statistically significantly lower mucus production and a lower rate of mucus plugging in patients who used an HME [42-44]. A statistically nonsignificant improvement was observed in mucus production compared with a control [41] or when using an HME with better humidification capacities [31]. Statistically significant effects of HME use also included a significant decrease in coughing (episodes) [28,29,40,42] and daily forced expectorations [28,29,42]; 2 (20%) studies reported a statistically nonsignificant difference in the number of coughs or forced expectorations when compared with a previous generation HME [31] or a control [41]. Moreover, HME use has been linked to statistically significant improvements in sleep, as patients experience fewer sleep disturbances [29,42]. However, 4 (40%) studies reported no statistically significant difference in sleep quality [16,28,31,44]. A statistically significant improvement in speech quality was observed in HME-compliant patients [42]. A statistically nonsignificant improvement in voice quality was found in patients using HME [16,28,31,40]. One (10%) of the studies reported a statistically significant difference in psychological stress [42], whereas in the other studies, patients reported no differences in psychosocial aspects [16,28,31]. HME use also significantly reduced the number of days requiring physiotherapy after surgery [44]. The number of tracheobronchitis or pneumonia episodes per patient per year in non-HME users was statistically significantly higher than that in HME users [12]. When using a hands-free device, patients have statistically significantly more frequent social contacts [16]. One (10%) of the studies reported a statistically nonsignificant improvement in social contacts [42]. The QoL of patients who underwent laryngectomy statistically significantly increased in 1 (10%) study [42] but not in the other study that examined this [40]. A statistically significant increase in patient satisfaction was observed in 1 (10%) study [29], and a statistically nonsignificant difference was observed in 2 (20%) studies [41,42].

All 4 experts stated that they would expect the use of the new HMEs to lead to improved outcomes compared with the use of the current HMEs. Because the optimized breathing resistance adapted to different situations while also maintaining high humidification levels by the HMEs of the new portfolio, it is likely that patients will tend to use the HME more often. One of the experts stated that “a better product that has significant benefits for the patient would lead to a higher compliance (participant 1).” All 4 experts were convinced that improved humidification, breathability, and situational usability together with improved HME attachments will lead to an optimized breathing experience with limited shortness of breath. One of the experts interviewed said that “if you change some problems in current available HMEs like humidity and breathing resistance, probably the compliance will increase (participant 2).” All the experts pointed out that with a better performance on the humidification and breathing resistance ratio, the tracheal climate would improve, as this leads to higher humidification and improved temperature. Experts indicated that they expect that when using the new HME, patients will experience less irritation when inhaling cold or dry air or small particles. A better HME with increased humidification levels will also reduce excess mucus and mucus plugs, (involuntary) coughing, and forced expectorations. Consequently, the sleep quality will get improved. The new HMEs would prevent patients from having dry and hard sticky mucus, which often needs to be removed mechanically with a forceps. Moreover, complications such as a reduced diameter of the trachea due to mucus obstruction affecting the trachea’s functionality were expected to occur less frequently. By preventing these complications, patients are expected to experience breathing problems less often. There was a consensus among experts that because of the larger positive effects of the new HMEs compared with current HMEs and higher adherence to HME use, the rates of inflammation and infection (eg, tracheitis, tracheobronchitis, and pneumonia episodes) will decrease, resulting in reduced care consumption by the patient (eg, fewer hospital readmissions) and, thus, reduced health care costs. One of the experts mentioned that the “length of hospital stay, if even it happened, will be less, because people get better and hospital readmission will probably even decrease (participant 1)”. An overall improvement in pulmonary health because of the use of the new HMEs will lead to an increase in the HRQoL and satisfaction of the patient. In turn, this will lead to an improved psychological health in the patient. Patients who can cope well with coughing and other symptoms feel confident to participate in social activities. Improvements in all these domains will contribute to a higher participation of the patient in society, and for patients of working age, these increase the chances of returning to work. This would entail patients having more social contact. Even though one of the experts mentioned that “voice quality is one of the most important things for patients with laryngectomy, (participant 3)” overall, the experts did not expect to see any effects of using the new HMEs on speech, voice quality, or the requirement of physiotherapy.

In Figure 1, the statements in the upper boxes (orange part) are based on laboratory measurements, patient-reported outcomes, and user evaluations of the new-generation HMEs, which result in the box in the blue part. The boxes in the pink layer contain the effects of using HMEs, which the experts believe will further improve when using the new-generation HMEs, resulting in the outcomes given in the boxes in the green part. The causal relationships among the effects in the pink section were not explicitly discussed with the experts; however, they indicated that the effects were all related to each other.

A total of 24 German experts were invited to participate in a web-based survey. Of those invited, 21 (88%) experts agreed to participate, of whom 19 (90%) completed the survey. These participants were head and neck surgeons (n=11, 58%), otolaryngologists (n=3, 16%), and speech therapists (n=5, 26%). A total of 15 (79%) experts had heard about the new HMEs before but had never prescribed them, whereas 4 (21%) experts had prescribed the new HMEs at least once. Experts had an average of 18.00 (SD 7.86) years of experience with providing care to patients with laryngeal cancer, 17.32 (SD 8.09) years with providing care to patients who underwent TL, 13.05 (SD 5.85) years with prescribing and/or monitoring the use of HMEs, and 7.95 (SD 9.06) years as a scientific researcher in the field of laryngeal cancer.

The average expert judgments are listed in Table 2 (refer to Multimedia Appendix 4 for the average scores per interval).

Experts believed that, on average, 51% (SD 24%) of patients will experience a decrease in tracheal dryness or irritation when comparing the use of the new HMEs to a previous generation HME after 12 weeks of use. An average decrease of 33% (SD 32%) was expected in patients experiencing mucus plug events when using the new HMEs compared with patients using second-generation HMEs in the postoperative period. It was expected that after 12 weeks of using the new HMEs, 53% (SD 22%) of patients will have decreased mucus production compared with no HME use. On average, 25% (SD 23%) of patients were expected to have better speech quality after 12 weeks of using the new HMEs compared with using the second-generation HMEs. An average decrease of 0.74 days (SD 0.70) in the number of days requiring chest physiotherapy was expected in patients using the new HMEs, compared with those using second-generation HMEs, after 12 weeks, and these patients were also expected to experience an average decrease of 34% (SD 32%) in pulmonary infections on a yearly basis. After 12 weeks of HME use, an average increase of 13% (SD 18%) in the number of social contacts and 33% (SD 30%) in overall QoL were expected in patients using the new HMEs compared with those using the second-generation HMEs. The use of the new HMEs was expected to result in 44% (SD 30%) of patients being more satisfied with their HME when compared with patients using the second-generation HMEs after 12 weeks. Experts expected an average of 53% (SD 28%) of patients breathing better after 12 weeks of using the new HMEs, and, on average, 48% (SD 25%) of patients were expected to experience a decrease in shortness of breath after 12 weeks of using the new HMEs. Experts believed that, on average, 59% (SD 19%) of patients will experience a decrease in tracheal dryness or irritation after 12 weeks of using the new HMEs. The average number of daily coughs after 12 weeks of using the new HMEs was expected to be 2.95 (SD 1.61) per patient, and the number of daily forced expectorations per patient after 12 weeks of new HME use was expected to be 2.46 (SD 1.42). Experts indicated that 48% (SD 22%) of patients will experience sleeping problems after 12 weeks of using the new HMEs. On average, 24% (SD 20%) of the patients were expected to experience psychosocial problems after 12 weeks of using the new HMEs.

The rapid review identified the benefits of the current HMEs regarding breathing effort, tracheal dryness and irritation, mucus production and plugging, inflammation and infection rates, sleep quality, QoL, and patient satisfaction, which were confirmed for the new HMEs by the experts during the interviews and SEE. There were some discrepancies regarding cough, forced expectorations, and psychosocial aspects: in the interviews, the experts mentioned that the new HMEs will improve these aspects, but this was not observed in SEE. In addition, the interviewed experts did not expect to see an effect of using the new HMEs on speech quality and the requirement of physiotherapy, but the SEE showed a positive effect for these variables. According to the interviewed experts, the new HME portfolio will presumably lead to higher adherence to HME use by patients and fewer health complaints and complications because of the improved HME properties, resulting in lower health care use (eg, reduced hospital readmissions).

The finding that HME use reduces coughing and forced expectorations in patients who underwent laryngectomy is comparable with the findings from previous studies [7,17], and the finding that patients who use an HME experience better sleep has also been reported before [13]. In line with our study, 2 studies reported improvements in coughing, the mean daily frequency of sputum production, forced expectoration, shortness of breath, sleep problems, and perceived voice quality [15,24]. In comparison with an earlier study [42], the SEE demonstrated that fewer patients (than reported) are expected to experience a decrease in tracheal dryness or irritation when using the new HMEs compared with when using the second-generation HMEs. However, when we directly asked the experts if they expected an increase or decrease in patients experiencing tracheal dryness or irritation with the new HMEs compared with the second-generation HMEs, they reported a decrease on average. In addition, compared with patients using the second-generation HMEs, the experts expected a reduction in patients experiencing mucus plug events in the postoperative period. In comparison, another study reported that approximately one-tenth of the patients using a second-generation HME developed mucus plugs during the postoperative period [43]. After 12 weeks of using the new HMEs, approximately half of the patients were expected to experience decreased mucus production compared with no HME use. This is more than what was reported for the first-generation HMEs [31] and less than what was reported for the second-generation HMEs [41]. Besides, on average, the breathing results expected with the use of the new HMEs were less improved than those reported with the use of the first-generation HMEs [40]. Experts expected that more patients will experience a decrease in shortness of breath with the use of the new HMEs compared with results obtained from the use of the first- and second-generation HMEs [31]. The experts also expected that the average number of daily coughs after 12 weeks of using the new HMEs will be slightly higher than that reported after using the second-generation HMEs [42]. The same applies to the average number of daily forced expectorations per patient [42]. The percentage of patients experiencing sleeping problems after 12 weeks of using the new HMEs is expected to be notably lower than that after using the first-generation HMEs [28]. The number of patients who are expected to experience psychosocial problems after using the new HMEs is similar to number of patients reported to experience psychosocial problems after using the first- and second-generation HMEs [31].

To the best of our knowledge, this study is the first to investigate the expected effects of the new HMEs. A strength of this study is the use of a mixed methods approach, which helped to gain a deeper understanding of the effectiveness of HMEs than would be possible with the use of either approach alone. A second strength is the overall consensus among clinicians from leading German institutions on the benefits of the new HMEs compared with the current HMEs. Moreover, by using the literature and expert beliefs at an early stage in the life cycle of the new generation of HMEs, information can be generated to support decision-making [46].

A limitation to consider is the number of experts interviewed. Even though the sample size was small, consensus on the views on the new generation of HMEs was observed when interviewing the experts independently from each other. A second limitation is that most experts who completed the SEE survey did not yet have experience with prescribing the new HMEs. Hence, the current effect estimations are likely to be an underestimation of the true effect, as experts most likely filled in the survey conservatively. This point is addressed by our results; it is noticeable that the experts responded more conservatively when there was no comparison in the question than when a comparison was included. The categories tracheal dryness or irritation, mucus plug events, mucus production, speech quality, physiotherapy, pulmonary infections, social contacts, QoL, and patient satisfaction did contain a comparison, all showing results in favor of the new HMEs. The questions regarding the categories of breathing, shortness of breath, daily coughs, daily forced expectorations, sleeping problems, and psychosocial problems did not contain a comparator, and the results mostly showed a less favorable expected effect for the new HMEs, except for sleeping and psychosocial problems. Because the standard of care of all the experts was second-generation Provox HMEs, it might be possible that the experts subconsciously used these HMEs as comparators in their mind when answering the questions without comparators. In addition, some questions in the SEE survey contained categories in which experts could choose X or greater than X (ie, ≥X). When the experts entered weights in this category, we did not know exactly how much the expert meant by X or greater than X. We interpreted this by giving this category the value X plus 1 interval so that it would have a greater impact on the calculated mean. This could be an underestimation of the value given by the experts. As this category was barely used by the experts, it should not be regarded as a major limitation of the study.

It is recommended that the SEE survey be conducted once more after the experts have gained experience with the new HMEs, as the current effect estimations might be underestimated. To generate primary data on the actual use of the new HMEs by patients, it is recommended that a clinical study be set up to evaluate the effectiveness of the new HMEs. Both the perspectives of patients and health care providers need to be included in future studies on HMEs to gain a complete picture of the value of the new HMEs. Next, as in the current reimbursement landscape, a new medical device needs to be not only effective in improving patient outcomes but also cost-effective, and conducting an economic analysis is recommended.

According to German experts, the use of the new HMEs with improved humidification levels by patients who underwent laryngectomy is expected to have additional (clinical) effectiveness on pulmonary health and QoL aspects compared with the currently available HMEs.