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Physicians’ attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence

Abstract

Background

One of the most important and ethically challenging decisions made for children with life-limiting conditions is withholding/withdrawing life-sustaining treatments (LST). As important (co-)decision-makers in this process, physicians are expected to have deeply and broadly developed views. However, their attitudes and experiences in this area remain difficult to understand because of the diversity of the studies. Hence, the aim of this paper is to describe physicians’ attitudes and experiences about withholding/withdrawing LST in pediatrics and to identify the influencing factors.

Methods

We systematically searched Pubmed, Cinahl®, Embase®, Scopus®, and Web of Science™ in early 2021 and updated the search results in late 2021. Eligible articles were published in English, reported on investigations of physicians’ attitudes and experiences about withholding/withdrawing LST for children, and were quantitative.

Results

In 23 included articles, overall, physicians stated that withholding/withdrawing LST can be ethically legitimate for children with life-limiting conditions. Physicians tended to follow parents’ and parents-patient’s wishes about withholding/withdrawing or continuing LST when they specified treatment preferences. Although most physicians agreed to share decision-making with parents and/or children, they nonetheless reported experiencing both negative and positive feelings during the decision-making process. Moderating factors were identified, including barriers to and facilitators of withholding/withdrawing LST. In general, there was only a limited number of quantitative studies to support the hypothesis that some factors can influence physicians’ attitudes and experiences toward LST.

Conclusion

Overall, physicians agreed to withhold/withdraw LST in dying patients, followed parent-patients’ wishes, and involved them in decision-making. Barriers and facilitators relevant to the decision-making regarding withholding/withdrawing LST were identified. Future studies should explore children’s involvement in decision-making and consider barriers that hinder implementation of decisions about withholding/withdrawing LST.

Peer Review reports

Introduction

Children aged 1–18 years comprise over 30% of the global population [1]. Over the past few decades, survival rates of young children with severe diseases dramatically increased thanks to developments in modern medicine [2,3,4,5,6]. For instance, pneumonia deaths under five years decreased from 2.21 million in 1990 to almost 672,000 in 2019 [7]. In the United States, the 5-year survival rate for children diagnosed with non-Hodgkin's lymphoma increased from 43% in 1975 to 91% in 2012 [8], and the mortality rate for children with leukemia decreased by an average of 2.9% per year between 2001 and 2017 [9].

Despite the improvement in survival, children with life-limiting diseases are still suffering due to severe disease-related complications [10,11,12]. Continuing life-sustaining treatments (LST) beyond maximizing comfort for patients at the end of life (EOL) may no longer be in the child’s best interest, and it may generate moral distress in healthcare providers and parents [13, 14]. Hence, in some circumstances, withholding/withdrawing LST is ethically acceptable or advisable [15].

Withholding/Withdrawing LST is defined as not starting or discontinuing any therapy aimed at prolonging life, such as cardiopulmonary resuscitation, mechanical ventilation, medically administered nutrition and hydration, surgery, antibiotics, and dialysis [15,16,17]. Many pediatric deaths occur after healthcare professionals, parents, and the young patients agreed to withhold/withdraw LST [18,19,20]. However, deciding whether to withhold/withdraw LST in children with life-limiting conditions is ethically complex and sensitive [21,22,23,24,25,26,27,28,29]. For instance, who should make decisions for the incompetent child, and what if the parents and physicians disagree about the most appropriate option [30, 31]?

Physicians play an important role as (co-)decision-makers about withholding/withdrawing LST in pediatric patients [32, 33]. For example, a review of qualitative studies found that physicians normally are the ones to initiate withholding/withdrawing LST decisions [32]. Moreover, they are also responsible for protecting the best interest of the patient [32]. In this systematic review on physicians’ decision-making process about withholding/withdrawing LST in pediatric patients, we explored the role and experiences of the stakeholders involved in the decision-making process, the content and process of the decision-making, and the factors that can hinder or facilitate the decision-making [32]. Nevertheless, based on the qualitative literature, we could not comprehensively elucidate the real attitudes and experiences of physicians regarding withholding/withdrawing LST, nor the related influencing factors. Despite their important role in LST decision-making, physicians’ attitudes, experiences, and the influencing factors remain unclear. Gaining in-depth insight into physicians’ attitudes and experiences, and influencing factors, would greatly benefit both physicians and parents who face the challenges in understanding physicians’ decision-making about withholding/withdrawing LST. Thus, we conducted a systematic review of quantitative studies, as a complementary paper for the qualitative systematic review [32].

In this systematic review of quantitative evidence, we aimed to gain insight into physicians’ attitudes and experiences about withholding/withdrawing LST and the factors that influence their attitudes and experiences. We also analyze the evidence on the role of stakeholders and barriers and facilitators of the decision-making process, as perceived by physicians.

Methods

Design

We followed the Peer Review of Electronic Search Strategies (PRESS) guidelines [34] in performing our literature search for this systematic review of quantitative studies.

Search strategy

We searched five electronic databases: Pubmed, Cinahl®, Scopus®, Embase®, and Web of ScienceTM on March 17, 2021. Search strings consisted of six groups of search terms: (1) pediatrics; (2) target population (i.e., physicians); (3) end-of-life (EOL) care; (4) withholding/withdrawing; (5) LST; and (6) perspectives (e.g., perceptions, attitudes, experiences) (Supplemental File 1). The search results were merged, and duplicate hits were deleted before carrying out title, abstract, and full-text screening. We updated the initial search results with a complementary search on December 3 2021 limited to articles published in 2021. The search was complemented with snowballing and citation tracking to avoid missing relevant articles. Article selection followed the preferred reporting items for systematic reviews and meta-analyses (PRISMA) flow diagram (Fig. 1) [35].

Fig. 1
figure 1

PRISMA flowchart illustrating the process for identifying relevant articles in five electronic databases, and inclusion/exclusion reasons [35]

Inclusion and exclusion criteria

Guided by predefined inclusion and exclusion criteria (Table 1), two authors YZ and CG independently screened titles, abstracts, and full texts. Disagreements were settled by discussion until consensus was reached.

Table 1 Inclusion and exclusion criteria for selection of articles on physicians’ perspectives

Quality appraisal

Two authors YZ and CG independently evaluated the included studies using the quality appraisal tool developed by Hawker et al. [36]. The quality appraisal was indicative rather than evaluative; therefore, no studies were excluded based on their methodological quality.

Data extraction and synthesis

YZ extracted and synthesized data inspired by the first five phases of the Qualitative Analysis Guide of Leuven (QUAGOL) approach. Provisional results from these steps were regularly discussed with other two authors CG and AC [37, 38].

First, we repeatedly read the included articles to familiarize ourselves with the material. Second, we summarized the relevant information in a narrative format to identify the main themes for each article. Third, we created conceptual schemes for each article (see example in Supplemental File 2). Fourth, we merged individual schemes into a general scheme. Finally, we synthesized and reported these results following the structure of the general scheme.

Due to the diversity of the cases in the included articles, we classified them based on child’s chance of survival and severity of disability with the help of a pediatrician (Supplemental File 3). This allowed us to compare the cases and identify meaningful similarities and differences.

Results

Study characteristics

Our systematic search yielded 23 eligible articles published between 1999 and 2022 [16, 17, 39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59]; 15 of which published from 2010 to 2022 [17, 46,47,48,49,50,51,52,53,54,55,56,57,58,59]. These studies were conducted worldwide: United States (n = 9) [16, 17, 39, 41, 44,45,46, 48, 49]; Japan (n = 3) [40, 53, 54]; South Korea (n = 2) [57, 58]; Australia [43], Norway [47], Canada [50], Slovenia [52], Switzerland [55], and Saudi Arabia [56] (n = 1 each). Three studies were conducted in more than one country: One in several European countries [59], and two in multiple countries worldwide [42, 51].

All studies used questionnaires with closed-ended questions. Six studies complemented the closed-ended questions with open-ended questions or focus group discussions [17, 40, 45, 48, 50, 59]. Eight studies used scenarios or vignettes to guide attitudinal or experiential questions, which were classified based on the child’s chance of survival and/or severity of disability (cases are in Supplemental File 3) [39, 42, 45,46,47,48,49, 57].

Overall, we analyzed data from 5388 physicians that were reported in the included articles. Sample size ranged from 44 to 600 physicians. Except for four studies [16, 42, 56, 59], most studies reported response rates, which ranged from 9.9% to 85%. Ten studies reported physicians’ professional status [16, 39, 41, 43,44,45,46, 56, 58, 59]: 537 senior-level physicians (e.g., attending physicians) or physicians in specialty practice; 602 fellows or physicians in fellowship training; and 819 junior-level physicians (e.g., residents) or physicians in primary practice and general pediatrics training. Fourteen studies reported the gender [39, 43,44,45,46, 48, 49, 52, 53, 55,56,57,58,59]: 1850 males and 1574 females. Most of the included studies involved only physicians, except for four studies that also included other healthcare professionals [16, 17, 41, 42] (Table 2).

Table 2 Overview of included quantitative articles

Methodological quality

Table 3 summarizes the results of our quality appraisal analysis. The majority of included studies were rated as high quality, and only four were rated as moderate quality. Most studies had clear titles, abstracts, introductions, and aims; used appropriate methodologies; and reported understandable findings. However, some studies had low response rates, and the transferability or generalizability of study results were insufficient. Additionally, most studies superficially described ethical issues. For instance, they reported receiving ethical approval from their institutional review board and had obtained informed consent from participants, but few mentioned confidentiality issues or how they responsibly managed the collected data. Moreover, researchers failed to consider potential biases that could arise from the research relationship between researchers and participants.

Table 3 Quality appraisal of the included articles

Main findings

Following QUAGOL as a guide, we identified five themes capturing physicians’ attitudes and experiences regarding withholding/withdrawing LST in pediatrics practice. These themes are (1) general attitudes about withholding/withdrawing LST; (2) attitudes about withholding/withdrawing LST under request of parents and patients; (3) perceptions toward stakeholders’ involvement in the decision-making process; (4) past experiences with decision-making about withholding/withdrawing LST; and (5) physician-perceived facilitators and barriers relevant to the decision-making when it comes to withholding/withdrawing LST (Table 4).

Table 4 Themes of physicians’ attitudes and influencing factors identified in QUAGOL-Guided analysis and synthesis

General attitudes of physicians about withholding/withdrawing LST

General trends

Most physicians in three studies believed that withholding/withdrawing LST can be ethically legitimate when they consider cases involving children with life-limiting diseases at risk of therapeutic obstinacy [41, 51, 52]. In Burns et al., most physicians regarded withholding LST and withdrawing LST as ethically equivalent [41]. However, some physicians with fewer years of practice or those from low- and middle-income countries reported that withholding LST and withdrawing LST were ethically different [41, 51, 52].

Physicians’ attitudes toward withholding/withdrawing LST in pediatric patients varied based on patients’ survival chances (i.e., prognosis) and their medical conditions (e.g., severity of disability) (Supplemental File 2) [16, 40, 42, 49, 55]. Although for severely disabled patients, 51%-96% of physicians in Needle et al. agreed to withhold/withdraw LST, only 33% of them would actually recommend these options [49]. Physicians who preferred to withhold/withdraw LST were more likely to accept or to offer do-not-reintubate orders [49].

For severely disabled patients with little chance of survival, most physicians in Sakakihara et al. reported they would withhold/withdraw LST; for example, 41% would withhold cardiopulmonary resuscitation [40]. Similarly, in two studies, 83%-96% of physicians agreed to order comfort care and non-invasive ventilation when the child was in acute respiratory failure, intubated, and in critical conditions, or if a child’s condition had deteriorated within the previous 72 h [42, 55].

General arguments justifying physicians’ attitudes

Physicians referred to several ethical principles to justify their general attitudes toward withholding/withdrawing LST in children. Most physicians in three studies rated the child’s best interest as one of the most important principle guiding EOL decisions [16, 40, 52]. FutilityFootnote 1 of treatments and the child’s quality of lifeFootnote 2were considered in determining whether withholding/withdrawing treatments was in the child’s best interest [16, 40, 52].

Most physicians also deemed justice as an important principle for guiding their LST decision-making [16, 40, 41, 51, 52]. In Keenan et al., physicians who believed that resources were being used inappropriately preferred to limit all types of LST [16]. To the opposite, two studies found that many physicians advocated for continuing LST regardless of the high costs for the family or the hospital [40, 51]. This was especially the case for physicians in low- and middle-income countries [51]. Finally, in one study, respecting the child’s autonomy was also considered an important principle for EOL decisions [52].

Influencing factors

Some included articles assessed whether physician- and parents-related factors influence physicians’ attitudes toward withholding/withdrawing LST (Table 5).

Table 5 Statistical correlations between physicians’ attitudes in general and physician-related factors, case-related factors and parent-related factorsa

Physician-related factors accounted for the majority of influencing factors. However, most factors were tested and found statistically significant only in one study each. These factors are: physicians’ gender [49], age [49], personal preference [39], work place [49], specialty [39], country [55], and country’s economic status [51]. Three studies tested the influence of professional status [16, 39, 41]. Keenan et al. [16] and Burns et al. [41] found professional status insignificant, whereas Randolph et al. reported that attending physicians were more likely than physician fellows to withhold/withdraw LST for children with neurologic disabilities [39]. Finally, two studies found that physicians with more working experiences were more likely to withhold/withdraw LST [41, 55].

Regarding case-related factors, Randolph et al. found that physicians were more likely to withhold/withdraw in children with lower survival rate [39]. Keenan et al. found that physicians were more likely to withhold/withdraw LST in children with uncertain outcomes and severe disability [16]. Finally, only Randolph et al. tested family wishes and found physicians who considered family wishes more important were less likely to withhold/withdraw LST [39].

Physicians’ attitudes about withholding/withdrawing LST at the request of parents and/or patients

General trends

Physicians’ attitudes toward withholding/withdrawing LST differed in three situations: (1) parents alone or parents and the patient requested withholding/withdrawing LST; (2) parents alone requested continuing LST; and (3) parents and the patient had different opinions about whether to withhold/withdraw LST.

Parents alone or parents with patients requested withholding/withdrawing LST

In five studies, physicians reported they agreed to withhold/withdraw LST when parents requested it [39, 40, 45, 46, 57]. For severely disabled patients [39, 45], for patients with little chance of survival [39, 46, 57], for severely disabled patients with little chance of survival [39, 45, 57], and for patients with uncertain outcomes [45], most physicians would follow parents’ request to withhold/withdraw LST. By contrast, for patients with good chances of survival, 62%-80% of physicians would continue LST against the parents’ and patient’s request to decline continuing LST [46].

Parents requested continuing LST

Most physicians in four studies reported that they would not unilaterally withhold/withdraw LST against parents’ wishes and would continue to provide unrestricted care at the parents’ request until a consensus was reached [39, 41, 47, 48]. In one study, for patients with little chances of survival, most physicians would continue LST; this was especially the case for physicians who viewed parents’ wishes as extremely important [39]. For severely disabled patients with little chance of survival, 50%-80% of physicians in one study believed that parents or surrogates had the right to demand LST; thus, they would provide LST even though they believed it was not beneficial [47]. Furthermore, Devictor et al. reported that most of the physicians they surveyed would also continue LST; however, the physicians in Europe and South America indicated that they would start palliative care despite the disagreements with the parents [42]. Interestingly, 55% of physicians in the United States would implement a unilateral do-not-attempt-resuscitation (DNAR) order, whereas 54% would continue LST [48]. In contrast, for patients were severely disabled, 81% of physicians in a Japanese study would not provide non-medically indicated care or were not sure [40].

Parents and patients have different opinions

When parents and patients have opposite opinions about withholding/withdrawing LST, physicians in two studies would continue LST to meet legal requirements [46, 58]. Talati et al. reported physicians’ attitudes under several conditions; these physicians were randomly chosen from the online directory of the American Academy of Pediatrics [46]. For patients with a good chance of survival, almost all physicians stated that they would continue LST under patients’ request even though their parents refuse treatments. When parents wanted to continue LST but patients refused it, 72%-96% physicians stated that they would continue LST. For patients with little chance of survival, 63%-85% agreed to continue LST if the patients wished to receive treatments.

However, in some cases, physicians’ attitudes varied depending on the patients’ age [46]. For instance, in the case of an 11-year-old patient who refused treatments, 80% of physicians stated that they would continue LST if the parents requested LST to continue. By contrast, in the case of a 16-year-old patient who refused treatments, 65% of physicians would withhold/withdraw LST if the parents requested LST to continue.

Arguments justifying physicians’ attitudes when faced with requests from parents and/or patients

We identified five ethical principles that played an important role in helping physicians justify their attitudes toward withholding/withdrawing LST when faced with requests from parents and/or patients: (1) best interest of parents, (2) parental autonomy, (3) best interest of the child, (4) minor’s autonomy, (5) and physician authority [46, 48, 55]. The best interest of parents, parental autonomy, and the best interest of the child were considered the most important principles in two studies [46, 55]. For instance, physicians practicing in Swiss hospitals tended to prioritize parental welfare [55]. However, some physicians believed that their authority and legal constraints justified their decision to reject family wishes [48, 55].

Influencing factors

Some studies tested whether physician-, case-, and parents-related factors influenced physicians’ attitudes toward withholding/withdrawing LST when physicians were faced with parents’ and/or patients’ requests (Table 6).

Table 6 Statistical correlations between physicians’ attitudes under request and physician-related factors, case-related factors and parents-related factorsa

Regarding physician-related factors, gender, religion, and professional specialty were tested in more than one study. Bahus and Føerde found that female physicians were more likely to withdraw LST for severely disabled children with little chance of survival, even though parents requested to continue LST [47]. To the opposite, Morparia et al., found gender statistically insignificant [48]. Morparia et al. found that more physicians identifying as Jewish (> 50%) would continue LST at the parents’ request for patients with disorders of consciousness than physicians identifying as Christian, Muslim, or Hindu [48]. Hoehn et al. reported that physicians who engaged in religious activities at least weekly were less likely to support DNAR, regardless of the parents’ or patients’ request [45].

Compared with pediatricians working in departments for disabled children, physicians working in critical care, emergency, or school health departments were more likely to support DNAR, regardless of parents’ or patients’ requests [45]. For pediatric patients with good chance of survival, internal medicine specialists and pediatricians were more willing to respect requests of parents and children to refuse treatments than pediatric hematologist/oncologists or adolescent-medicine specialists [46]. For patients who were severely disabled with little chance of survival, more pediatricians surveyed would continue LST at the request of parents compared to neurologists or surgeons [47].

Regarding case-related factors, Talati et al. reported that the patients’ prognosis and agreements made between the parents and their child were factors that significantly influenced physicians’ attitude toward withholding/withdrawing LST [46]. Further, physicians were more likely to respect the request of withholding/withdrawing LST from the parent–child dyad rather than from patients alone.

Physicians’ perceptions of stakeholders involved in the decision-making about withholding/withdrawing LST

The included articles also reported on how physicians perceive various stakeholders (i.e., physicians, parents, and patients) that are typically involved in withholding/withdrawing LST, their roles in the decision-making process, and influencing factors that moderated their perceptions (Table 7).

Table 7 Relationships between physicians’ perceptions of stakeholders involved in LST decision-making and certain physician-related factorsa

Perceptions of physicians’ involvement

Most physicians in six studies considered themselves to be the primary decision-maker in withholding/withdrawing LST [16, 39, 41, 46, 56, 58], the ones who most often initiated discussions about withholding/withdrawing LST [16, 41, 58], and the ones who should determine the specific medical procedure to maintain patients’ best interest [58]. In one study, physicians determined how much decisional authority patients and/or parents should have [46]. For instance, participating physicians from the American Academy of Pediatrics stated that they would give more authority to patients on issues with clear laws, rather than issues without clear laws [46]. In one study, although physicians considered themselves to be the primary decision-maker, 91% preferred to inform patients and parents about the DNAR status together with the entire medical team, instead of making decisions by themselves concerning DNAR status [56]. Similarly, in Randolph et al., when a patient is being treated by physicians from different specialties, most physicians stated that they would decide what intervention they would recommend to parents with the whole team [39].

Perceptions of parents’ involvement

Physicians tended to involve parents in the decision-making process about withholding/withdrawing LST [17, 42, 46, 47, 53, 54, 56, 57, 59]. For severely disabled patients with little chance of survival, physicians in two studies believed parents have the right to demand or refuse LST [47, 56]. Most physicians in three studies agreed to discuss withholding/withdrawing LST with the patients’ parents [17, 53, 54]. Nevertheless, Song et al. reported that, for patients with little chance of survival and for severely disabled patients with little chance of survival, 90% of pediatric neurologists and over 50% of pediatric intensivists rarely or never discussed advance care planning with parents [57]. For severely disabled patients with disorders of consciousness, physicians in two studies preferred to inform parents about DNAR [42, 56].

Physicians’ professional specialty and their country’s economic status influenced how they perceived parents’ involvement in the decision-making process about withholding/withdrawing LST (Table 7) [51, 53, 54]. Pediatric hematologists and internists in two studies were more likely to discuss withholding/withdrawing LST with parents than pediatric neurologists and pediatricians [53, 54]. Furthermore, in Sanchez Varela et al., compared with physicians working in middle- and high-income countries, those working in low-income countries were more likely to discuss the costs of treatments and healthcare with parents [51].

Perceptions of pediatric patients’ involvement

In general, physicians emphasized that it is necessary to involve patients in decision-making about withholding/withdrawing LST [17, 46, 53, 54, 56, 58, 59]. For example, in Talati et al., 58% of physicians believed that a 16-year-old patient could be a primary decision-maker [46].

However, in some studies conducted in East Asia, fewer physicians indicated that they would involve patients in the decision-making process [53, 54, 57, 58]. In two Japanese studies, only half of the physicians would discuss withholding/withdrawing LST with patients who had over one year or less than three months survival chance [53, 54]. For patients with little chance of survival or for severely disabled patients with little chance of survival, most of the physicians surveyed in two Korean studies would never discuss advance care planning with patients [57, 58].

Physicians’ professional specialty and their country’s economic status also influenced how they perceived patients’ involvement in the decision-making about withholding/withdrawing LST (Table 7) [51, 53, 54]. In one study, internists were significantly more likely to discuss withholding/withdrawing LST with patients than pediatricians, regardless of the patients’ expected survival chances [53]. In another study, pediatric neurologists were more likely to discuss this issue with patients than pediatric hematologists, especially for patients expected to survive less than three months [54]. However, for patients expected to survive for over one year, neurologists were more likely to discuss DNAR and the use of ventilators, while hematologists preferred to share treatment and care goals with these patients and their parents [54]. Moreover, Sanchez Varela et al. found that physicians in high-income countries were more likely than those in low- and middle-income countries to involve adolescent patients in their medical decision-making [51].

Physicians’ past experiences in decision-making about withholding/withdrawing LST

The included articles described what physicians experienced as they participated in the decision-making process about withholding/withdrawing LST. This included their experiences during discussions with parents or patients, dealing with ethical issues, and dealing with DNAR. Factors that influenced their experiences were also described (Table 8).

Table 8 Statistical correlations between physicians’ past experiences with decision-making and physician-related factorsa

Experiences communicating with parents and/or patients

Many physicians were satisfied with the quality of the communication concerning withholding/withdrawing LST (Table 8) [17, 41, 43, 50]. In one article, 71% of physicians were confident in identifying the appropriate decision-makers for patients with life-limiting conditions [44]. In two articles, 40%-70% of physicians were confident in delivering bad news to patients and parents about the child’s likely death and believed they spent adequate time with patients and parents in this regard [50, 51]. Physicians working in middle- and high-income countries especially were confident that they communicated well [51]. In one study, 56% of physicians feeling comfortable in guiding family discussions had experience in writing medical orders for life-sustaining treatment [17]. In two studies, physicians were also confident in obtaining informed consent from adolescent patients without parental involvement [50], and respecting patients’ request to withhold information from their parents [44].

Some physicians felt unprepared to have EOL discussions with other stakeholders [43, 53, 54, 58]. In Forbes et al., senior-level physicians feared discussing withholding/withdrawing LST with parents, because they found informing parents that the child would likely not recover difficult [43]. Similarly, in Yoo et al., 86% of physicians experienced difficult feelings when discussing withholding/withdrawing LST with patients [58].

Experiences dealing with ethically sensitive decisions

In one study, physicians stated that decision-making about withholding/withdrawing LST was the most common and most challenging ethical issue in pediatric EOL care [59]. Other studies pointed toward the same result. In Kesselheim et al., only 30% and 19% of physicians, respectively, felt confident in making decisions about withdrawing assisted ventilation, or artificial nutrition and hydration [44]. In Boer et al., 30% of the physicians felt personally affected by the decision-making about withholding/withdrawing LST [59]. In Sanchez Varela et al., many physicians said it bothered their conscience to continue LST because they believed it should be withdrawn [51]. In one article, 58% of physicians were uncomfortable when parents and patients disagreed about withholding/withdrawing LST [50].

Several physician-related factors influenced their experiences dealing with ethical issues about withholding/withdrawing LST (Table 8) [51, 59]. First, physicians working in general pediatrics were significantly less likely to face ethical issues compared to physicians working in other specialties [59]. Second, compared with residents, physician-fellows faced more ethical issues, had more difficulties in dealing with these issues, and were more likely to be affected by them [59]. Third, physicians from southern European countries were significantly less likely to face ethical issues [59]. Last, physicians working in middle- and high-income countries were significantly more likely to disagree with the statements that withholding/withdrawing LST led to less time spent with patients and parents, or sometimes LST was discontinued too soon [51].

Experiences dealing with DNAR

In Aljethaily et al., most physicians were familiar with DNAR and relevant policy [56]. More senior-level physicians especially were familiar with DNAR compared to junior-level physicians (Table 8) [56]. In three articles, 47%-57% of physicians were confident and comfortable in assisting patients with DNAR and discussing it with patients and parents [44, 50, 56]. In one article, half of the physicians believed they were protected by law when carrying out DNAR orders [56]. In that study, more junior-level physicians believed they were legally protected compared to senior-level physicians [56].

Physician-perceived barriers and facilitators in decision-making about withholding/withdrawing LST

The included articles described various barriers and facilitators that physicians perceived were in place in decision-making about withholding/withdrawing LST. These barriers and facilitators changed, or moderated, attitudes in some ways.

Barriers

Physicians reported seven general barriers that hindered decision-making about withholding/withdrawing LST: (1) lack of palliative care support programs [57]; (2) lack of specific training about withholding/withdrawing LST for physicians [43, 53, 54]; (3) child’s uncertain prognosis and physicians’ unrealistic expectations about the therapeutic effect of LST [53, 54, 57, 58]; (4) physicians’ unfamiliarity with decisions about withholding/withdrawing LST made them unsure about when and how to discuss and implement withholding/withdrawing LST [43, 53, 54, 57, 58], and about their responsibilities in these discussions [43, 57]; (5) difficulty communicating within the healthcare team and conflicts between parents and patients [53, 54, 58]; (6) lack of time to implement withholding/withdrawing LST [53, 54, 57]; and (7) lack of relevant laws, policies, or guidelines to support decision-making [48, 53, 54].

Physicians also stated that there were four barriers related specifically to the parents and their child. In four articles, over half of the physicians considered communications with parents and patients as the most significant barrier they faced to overcome [43, 53, 54, 58]. Physicians worried that parents and patients could not fully comprehend the rationale behind withholding/withdrawing LST [53, 54]. Fifty-eight percent of physicians surveyed in Korea found that patients were unable to adequately discuss or express their opinions about withholding/withdrawing LST [58]. Some physicians were not sure how to help parents weigh the pros and cons of various treatment options [43]. Second, in five articles, 90% of physicians stated that disagreements with parents and patients hindered the decision-making process [43, 53, 54, 57, 58]. For example, physicians did not know how to deal with parents’ requests to continue LST for children in which treatment was not in their best interest [43]. Third, physicians agreed that upsetting parents and/or patients by, for example, taking away their hope or by losing their trust, could also serve as a barrier [43, 53, 54, 58]. Fourth, physicians were not sure which parent-related factors should influence the decision-making about withholding/withdrawing LST. These included, for example, the parents’ capacity to care for the child, economic status, and religious background [43].

Facilitators

Physicians also said there were six facilitators that affected their decision-making process about withholding/withdrawing LST. First, physicians in three studies said that the ethics committee was the most important resource for EOL decisions [39, 43, 48]. At least half of them would request an ethics consultation when parents demanded LST withdrawal for a severely disabled patient, or when parents demanded to continue LST for patients with little chance of survival [39]. Second, almost all physicians in three studies cited experiences related to them by senior-level colleagues or other clinicians, especially from the palliative care team, and web-based materials on palliative care as important facilitators [41, 43, 48]. Third, most physicians in two studies also cited supportive policies, guidelines, and specific documents that provided instructions on withholding/withdrawing LST as being important resources [40, 43]. Fourth, physicians in three studies considered specific education and training programs as being important facilitators (e.g., DNAR, interactive workshops and/or training programs about treatment-refusal management) [43, 56, 58]. Fifth, most physicians in three studies also cited communication skills as being common facilitators [43, 58, 59]. Thus, experiences related to non-confrontational discussions about withholding/withdrawing LST with parents made physicians feel confident in their abilities to handle these LST situations [43, 58, 59]. Sixth, most physicians in two studies considered advance directives as being helpful in making EOL decisions [17, 52]. For instance, these directives helped develop clear care goals for patients, increased the use of pediatric palliative care, clarified medical decision-making, and improved clinicians’ skills in discussing LST wishes with parents [17].

Discussion

Our results describing physicians’ attitudes about withholding/withdrawing LST in pediatrics rest on an extensive QUAGOL-based analysis of 23 quantitative studies. These articles focused on different aspects of physicians’ attitudes and experiences as important (co-)decision-makers for medical care. The themes that emerged from our analysis were (1) general attitudes toward withholding/withdrawing LST; (2) attitudes about withholding/withdrawing LST when requested by parents and patients; (3) perceptions of stakeholders’ involvement in the decision-making process; (4) past experiences with decision-making about withholding/withdrawing LST; and (5) physician-perceived barriers and facilitators relevant to the decision-making when it comes to withholding/withdrawing LST. Prior to our analysis only limited information was available about what drives physicians’ decision-making in these ethically challenging situations. Although our analysis revealed that most physicians in the included studies agreed to share decision-making with parents and/or their children (i.e., patients), they reported experiencing both negative and positive feelings about the process. We found only limited evidence to support the hypothesis that some factors can influence physicians’ attitudes about withholding/withdrawing LST in pediatric patients.

Decision-making based on patients’ chance of survival and severity of disability

We found that physicians’ attitudes were influenced by patients’ chance of survival and severity of disability. Generally, most physicians agreed to withhold/withdraw LST for patients with life-limiting conditions, if the parents or parents and the patient did not specify their treatment preferences [16, 40,41,42, 49, 51, 52, 55]. However, for patients with little chance, both with and without severe disability, most physicians would follow the parents’ and patients’ wishes to withhold/withdraw LST [39, 40, 45, 46, 57], or to continue LST [39, 41, 42, 47, 48]. Additionally, physicians would continue LST when parents and patients disagree on treatments, regardless of patients’ chance of survival [46, 58].

Our results are consistent with results from some qualitative studies. These studies reported that physicians’ attitudes toward withholding/withdrawing LST are influenced by children’s medical condition and prognosis, especially their chance of survival and disability [60,61,62,63,64,65,66,67,68]. In Zaal-Schuller et al., physicians said acute deterioration of children’s medical condition is the most common reason to initiate withholding/withdrawing LST discussions [63]. In two studies, physicians suggested that decisions about withholding/withdrawing LST should be based on children’s condition and prognosis [64, 65]. In this scenario, physicians would withhold/withdraw LST for patients with irreversible conditions or degenerative conditions (i.e., severe neurological impairment) [60, 62].

While physicians’ attitudes can be influenced by children’s medical condition and prognosis in straightforward cases, some cases are more complicated and are difficult to classify, adding uncertainties to physicians’ attitudes [16, 45]. Additionally, there are many differences in the cases included in the studies, which also create significant challenges in comparing physicians’ attitudes [16, 45]. Further, some studies describe children’s “quality of life” and “futility” of the treatments without defining these value-laden terms [16, 40, 52], which made comparing physicians’ attitudes difficult. In these cases, physicians’ attitudes varied greatly.

The Royal College of Pediatrics and Child Health in the UK suggested making individualized decisions about withholding/withdrawing LST based on the patients’ medical condition and disability [25]. In response to physicians’ concerns when they were unsure about the possible outcomes of their decisions, the Canadian Pediatric Society suggested focusing on minimizing harms to children whose outcomes were uncertain [69]. In acute cases, it is recommended providing LST first and to make decisions after collecting adequate medical information, seeking guidance from more experienced clinicians, and assessing the evolution of the patient’s clinical status [25].

Involvement of pediatric patients in the decision-making

In our analysis, most physicians in five studies agreed with the necessity to involve pediatric patients in the decision-making toward withholding/withdrawing their LST; this was especially the case for physicians working in western countries [17, 46, 56, 59]. Physicians maintained the best interest of the patients and respected their autonomy, adolescents in particular [46]. However, physicians also faced challenges in weighting the importance of the best interest and autonomy of patients and their parents, especially when these principles clashed [70].

Compared to their western counterparts, fewer Japanese [53, 54] and Korean [57, 58] physicians working in some East Asian countries said, in practice, they would involve the patients in the decision-making. Moreover, many of these physicians seldom or never discussed withholding/withdrawing LST with patients [53, 54, 57, 58]. These results were consistent with our previous review of qualitative studies, which found that physicians struggled to involve patients in the decision-making and mostly only involved adolescents [32]. Importantly, many child deaths involved young babies/infants or acute events that resulted in inability to communicate with the children, which prevents their involvement. This might explain why only few eligible studies discussed children involvement.

Our results were confirmed by two other Japanese studies on physician–patient communication in pediatric cancer care [71, 72]. In Otani et al., physicians struggled to deliver bad news to patients and regarded it as a heavy burden [72]. Similarly, in Parsons et al., 35% of physicians rarely or never informed patients about their medical diagnosis [71]. While informing patients of their diagnosis, most physicians endorsed the availability of communication training to physicians and professional psychosocial services for children [71]. This suggests that physicians have not reached a consensus on how to involve patients in the decision-making [32].

The American Academy of Pediatrics and the Canadian Pediatric Society recommended that physicians should involve patients in the decision-making process to respect their autonomy [15, 69]. In many Asian countries, however, family wishes, rather than the patient’s autonomy, were considered central to the decision-making [73]. Rosenberg et al., therefore, suggested respecting cultural differences and said that physicians should remain open to the perspectives of healthcare professionals and family in whether to involve patients in the decision-making [73].

Weak evidence to support factors influencing physicians’ attitudes

We analyzed factors that influenced physicians’ attitudes toward withholding/withdrawing LST from three angles: (1) how they influenced their decision-making in general and under request of parents and patients [16, 39, 41, 45,46,47,48,49, 51, 52, 55]; (2) how they influenced physicians’ perceptions about stakeholders involved in the decision-making [51, 53, 54]; and (3) how they influenced physicians’ experiences with stakeholders’ involvement [51, 56, 59]. These included physician-related factors, parent-related ones, and patient-related ones. Our results were consistent with two quantitative studies [74, 75], which reported that physician-, parent-, and patient-related factors influenced EOL discussions with patients. For instance, female physicians, younger physicians, physicians with clearly expressed religious beliefs, and physicians with more clinical experience were more likely to discuss withholding/withdrawing LST with patients [74, 75].

Guidelines from the UK, US, and Canada also acknowledge that physicians’ religious and cultural beliefs; parents’ religious and cultural beliefs; patients’ medical condition and prognosis, age, and their decision-making capacity might influence physicians’ decisions [15, 25, 69]. This acknowledgment indicates that these physician-, parent-, and patient-related factors would influence physicians’ attitudes and experiences toward withholding/withdrawing LST. However, most studies examined just a few influencing factors, with few studies assessing many factors. Our analysis failed to find strong evidence supporting the hypothesis that these factors influence decision-making. This suggests that future quantitative research may need to continue to seek more robust evidence to support the hypothesis that these factors influence physicians’ attitudes about withholding/withdrawing LST.

Barriers and facilitators

Our results identified some physician-perceived facilitators of and barriers to decision-making. The two main barriers reported in our study—i.e., lack of specific training on withholding/withdrawing LST and conflicts between physicians and parents—are consistent with those reported in Zhong’s et al. analysis of qualitative evidence [32]. The facilitators reported in the present review differ from those reported in Zhong et al. [32] but are complementary. In the present review, we identified six physician-related and context-related facilitators. These include the ethics committee, experiences of physicians’ senior-level colleagues or other clinicians, supportive policies and guidelines, advance directives, and specific education and training programs (especially those focusing on communication skills). Zhong et al. [32], on the other hand, identified four parent-related and patient-related facilitators, including routine LST discussions with parents, practical and psychosocial support for parents, parents’ experiences with and understanding of children’s previous treatments, and children’s clinical appearance.

Strengths and limitations

The main strength of this review is the rigorous and systematic methodology used. We systematically searched five databases, and systematically extracted and synthesized the data from eligible studies. Two authors independently screened the studies according to a-priori-stated inclusion/exclusion criteria, and then performed a quality appraisal of the 23 included studies. Being inspired by the QUAGOL guide, three authors reflected critically and conceptually on the data. Second, the included studies were conducted in countries from four continents: North America, Europe, Oceania, and Asia. This ensured that a variety of cultures and contexts were represented in our results. Third, although we did not restrict our literature search to one period, most included studies were published after 2000, with 15 published between 2010 and 2022, ensuring that the evidence was contemporary. Fourth, we reported and analyzed data from a large sample size of 5388 physicians, ensuring the accuracy of the results.

However, this study also has some limitations. First, attitudes and experiences as reported in this review study might be different from physicians’ real behaviors. Second, results of the studies were difficult to compare due to diversity and complexity of cases. We mitigated this issue by classifying cases (Supplemental File 3) to make comparisons more feasible. Third, we found weak evidence to support the factors influencing physicians’ attitudes. Besides, the included studies were published in a span of more than 20 years. Many contextual factors, i.e., law, might have been changed, adding difficulties to compare physicians’ attitudes. Fourth, almost all included studies were carried out in high-income countries; this might have introduced bias. Fifth, we included only studies published in English, since this was the only common language among the four authors. Sixth, some studies had low response rates. We reported these results with a judicious use of language, especially for the information relevant to generalizability of findings. Seventh, some studies used unclear value-laden-terms, e.g., children’s “quality of life”, “futility” of the treatments without defining them. We reported these results cautiously as well.

Conclusions

We found that physicians preferred to withhold/withdraw LST in patients with life-limiting conditions, in general, and tended to follow parents’ and patients’ wishes if they specified treatment preferences. This means that for especially challenging decisions about a child’s life-limiting condition, physicians may want to specifically ask what the parents’ and patients’ treatment preferences are in order to get clear guidance in their decision-making and to ensure that the parents and patients clearly understand what treatments are available. Most physicians agreed to involve parents and patients in the decision-making, but they experienced both positive and negative feelings in the decision-making process. Since some barriers and facilitators relevant to EOL decision-making may be present, physicians may want to reflect on such factors well before being faced with EOL decisions in a time-pressured environment. Such reflections may bring a rapprochement among all stakeholders when physicians make one decision over another.

Availability of data and materials

All data generated or analyzed during this study are included in this published article and its supplementary information files.

Notes

  1. Futility: Definition given by the study. Futility was understood as both identified qualitative futility, i.e. the treatment will not result in sufficiently good quality of life and physiologic futility, i.e. the treatment is not effective in curing the disease or managing the symptoms [16].

  2. Quality of life: Definition given by the study. The quality of life was understood as living independently [40].

Abbreviations

LST:

Life-sustaining treatments

EOL:

End-of-life

QUAGOL:

Qualitative Analysis Guide of Leuven

DNAR:

Do-not-attempt-resuscitation

References

  1. United Nations International Children's Emergency Fund. The State of the World's Children 2021. Interactive dashboard and statistical tables. 2021. https://data.unicef.org/resources/sowc-2021-dashboard-and-tables/. Accessed 3 Oct 2022.

  2. Adamson PC. Improving the outcome for children with cancer: development of targeted new agents. CA Cancer J Clin. 2015;65(3):212–20.

    PubMed  PubMed Central  Google Scholar 

  3. World Health Organization. Levels and Trends in Child Mortality: Report 2021. 2021. https://www.who.int/publications/m/item/levels-and-trends-in-child-mortality-report-2021. Accessed 3 Oct 2022.

  4. World Health Organization. Maternal, newborn, child and adolescent health and ageing. https://platform.who.int/data/maternal-newborn-child-adolescent-ageing/child-data. Accessed 3 Oct 2022.

  5. National Cancer Institute. Cancer in children and adolescents. 2021. https://www.cancer.gov/types/childhood-cancers/child-adolescent-cancers-fact-sheet#what-is-the-prognosis-for-children-and-adolescents-with-cancer-nbsp. Accessed 3 Oct 2022.

  6. National Cancer Institute. Childhood cancer data initiative. https://nccrexplorer.ccdi.cancer.gov/application.html?site=1&data_type=1&graph_type=2&compareBy=sex&chk_sex_3=3&chk_sex_2=2&race=1&age_range=1&advopt_precision=1&advopt_show_ci=on&advopt_display=2. Accessed 3 Oct 2022.

  7. Roser M, Ritchie H, Dadonaite B. Child and Infant Mortality. 2013. Updated 2019. https://ourworldindata.org/child-mortality. Accessed 3 Oct 2022.

  8. Jemal A, Ward EM, Johnson CJ, Cronin KA, Ma J, Blythe R, et al. Annual report to the nation on the status of cancer, 1975–2014, featuring survival. J Natl Cancer Inst. 2017;109(9):djx030.

    PubMed  PubMed Central  Google Scholar 

  9. Islami F, Ward EM, Sung H, Cronin KA, Tangka FKL, Sherman RL, et al. Annual report to the nation on the status of cancer, part 1: national cancer statistics. J Natl Cancer Inst. 2021;113(12):1648–69.

    PubMed  PubMed Central  Google Scholar 

  10. Lauby C, Boelle PY, Taam RA, Bessaci K, Brouard J, Dalphin ML, et al. Health-related quality of life in infants and children with interstitial lung disease. Pediatr Pulmonol. 2019;54(6):828–36.

    PubMed  Google Scholar 

  11. Grygiel A, Ikolo F, Stephen R, Bleasdille D, Robbins-Furman P, Nelson B, et al. Sickle cell disease in Grenada: quality of life and barriers to care. Mol Genet Genomic Med. 2021;9(1):e1567.

    PubMed  Google Scholar 

  12. Osunkwo I, Andemariam B, Minniti CP, Inusa BPD, Rassi FE, Francis-Gibson B, et al. Impact of sickle cell disease on patients’ daily lives, symptoms reported, and disease management strategies: results from the international Sickle Cell World Assessment Survey (SWAY). Am J Hematol. 2021;96(4):404–17.

    PubMed  PubMed Central  Google Scholar 

  13. McDougall R, Notini L, Phillips J. Conflicts between parents and health professionals about a child’s medical treatment: using clinical ethics records to find gaps in the bioethics literature. J Bioeth Inq. 2015;12(3):429–36.

    PubMed  Google Scholar 

  14. Prentice T, Janvier A, Gillam L, Davis PG. Moral distress within neonatal and paediatric intensive care units: a systematic review. Arch Dis Child. 2016;101(8):701–8.

    PubMed  Google Scholar 

  15. Weise KL, Okun AL, Carter BS, Christian CW. Committee on bioethics; section on hospice and palliative medicine; committee on child abuse and neglect. Guidance on forgoing life-sustaining medical treatment. Pediatrics. 2017;140(3):e20171905.

    PubMed  Google Scholar 

  16. Keenan HT, Diekema DS, O’Rourke PP, Cummings P, Woodrum DE. Attitudes toward limitation of support in a pediatric intensive care unit. Crit Care Med. 2000;28(5):1590–4.

    PubMed  CAS  Google Scholar 

  17. Boss RD, Hutton N, Griffin PL, Wieczorek BH, Donohue PK. Novel legislation for pediatric advance directives: surveys and focus groups capture parent and clinician perspectives. Palliat Med. 2015;29(4):346–53.

    PubMed  Google Scholar 

  18. Lantos JD. Does pediatrics need its own bioethics? Perspect Biol Med. 2010;53(4):613–24.

    PubMed  Google Scholar 

  19. Zawistowski CA, DeVita MA. A descriptive study of children dying in the pediatric intensive care unit after withdrawal of life-sustaining treatment. Pediatr Crit Care Med. 2004;5(3):216–23.

    PubMed  Google Scholar 

  20. Keele L, Meert KL, Berg RA, Dalton H, Newth CJL, Harrison R, et al. Limiting and withdrawing life support in the PICU: for whom are these options discussed? Pediatr Crit Care Med. 2016;17(2):110–20.

    PubMed  PubMed Central  Google Scholar 

  21. Diekema DS, Botkin JR, Committee on Bioethics. Clinical report–Forgoing medically provided nutrition and hydration in children. Pediatrics. 2009;124(2):813–22.

    PubMed  Google Scholar 

  22. Section on Hospice and Palliative Medicine and Committee on Hospital Care. Pediatric palliative care and hospice care commitments, guidelines, and recommendations. Pediatrics. 2013;132(5):966–72.

    Google Scholar 

  23. Clark JD, Dudzinski DM. The culture of dysthanasia: attempting CPR in terminally ill children. Pediatrics. 2013;131(3):572–80.

    PubMed  Google Scholar 

  24. Mercurio MR, Murray PD, Gross I. Unilateral pediatric “do not attempt resuscitation” orders: the pros, the cons, and a proposed approach. Pediatrics. 2014;133(Suppl 1):S37–43.

    PubMed  Google Scholar 

  25. Larcher V, Craig F, Bhogal K, Wilkinson D, Brierley J. Royal college of paediatrics and child health. Making decisions to limit treatment in life-limiting and life-threatening conditions in children: a framework for practice. Arch Dis Child. 2015;100 Suppl 2:s3–23.

    PubMed  Google Scholar 

  26. Carter BS. Should we always honour parental requests? Acta Paediatr. 2018;107(6):916–8.

    PubMed  Google Scholar 

  27. Kirsch RE, Balit CR, Carnevale FA, Latour JM, Larcher V. Ethical, cultural, social, and individual considerations prior to transition to limitation or withdrawal of life-sustaining therapies. Pediatr Crit Care Med. 2018;19(8S Suppl 2):S10–8.

    PubMed  Google Scholar 

  28. Sisk BA, Canavera K, Sharma A, Baker JN, Johnson LM. Ethical issues in the care of adolescent and young adult oncology patients. Pediatr Blood Cancer. 2019;66(5):e27608.

    PubMed  Google Scholar 

  29. Bolcato M, Russo M, Feola A, Pietra BD, Tettamanti C, Bonsignore A, et al. The motion of the Italian national bioethics committee on aggressive treatment towards children with limited life expectancy. Healthcare (Basel). 2020;8(4):448.

    PubMed  Google Scholar 

  30. Gillam L, Sullivan J. Ethics at the end of life: who should make decisions about treatment limitation for young children with life-threatening or life-limiting conditions? J Paediatr Child Health. 2011;47(9):594–8.

    PubMed  Google Scholar 

  31. Akdeniz M, Yardımcı B, Kavukcu E. Ethical considerations at the end-of-life care. SAGE Open Med. 2021;9:20503121211000920.

    PubMed  PubMed Central  Google Scholar 

  32. Zhong Y, Cavolo A, Labarque V, Gastmans C. Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence. BMC Palliat Care. 2022;21(1):113.

    PubMed  PubMed Central  Google Scholar 

  33. Rhodes R, Holzman IR. Is the best interest standard good for pediatrics? Pediatrics. 2014;134 Suppl 2(Suppl 2):S121–9.

    PubMed  Google Scholar 

  34. Sampson M, McGowan J, Cogo E, Grimshaw J, Moher D, Lefebvre C. An evidence-based practice guideline for the peer review of electronic search strategies. J Clin Epidemiol. 2009;62(9):944–52.

    PubMed  Google Scholar 

  35. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gøtzsche PC, Loannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ. 2009;339:b2700.

    PubMed  PubMed Central  Google Scholar 

  36. Hawker S, Payne S, Kerr C, Hardey M, Powell J. Appraising the evidence: reviewing disparate data systematically. Qual Health Res. 2002;12(9):1284–99.

    PubMed  Google Scholar 

  37. de DierckxCasterlé B, De Vliegher K, Gastmans C, Mertens E. Complex qualitative data analysis: lessons learned from the experiences with the qualitative analysis guide of Leuven. Qual Health Res. 2021;31(6):1083–93.

    Google Scholar 

  38. de DierckxCasterlé B, Gastmans C, Bryon E, Denier Y. QUAGOL: a guide for qualitative data analysis. Int J Nurs Stud. 2012;49(3):360–71.

    Google Scholar 

  39. Randolph AG, Zollo MB, Egger MJ, Guyatt GH, Nelson RM, Stidham GL. Variability in physician opinion on limiting pediatric life support. Pediatrics. 1999;103(4):e46.

    PubMed  CAS  Google Scholar 

  40. Sakakihara Y. Ethical attitudes of Japanese physicians regarding life-sustaining treatment for children with severe neurological disabilities. Brain Dev. 2000;22(2):113–7.

    PubMed  CAS  Google Scholar 

  41. Burns JP, Mitchell C, Griffith JL, Truog RD. End-of-life care in the pediatric intensive care unit: attitudes and practices of pediatric critical care physicians and nurses. Crit Care Med. 2001;29(3):658–64.

    PubMed  CAS  Google Scholar 

  42. Devictor DJ, Tissieres P, Gillis J, Truog R. WFPICCS Task Force on Ethics. Intercontinental differences in end-of-life attitudes in the pediatric intensive care unit: results of a worldwide survey. Pediatr Crit Care Med. 2008;9(6):560–6.

    PubMed  Google Scholar 

  43. Forbes T, Goeman E, Stark Z, Hynson J, Forrester M. Discussing withdrawing and withholding of life-sustaining medical treatment in a tertiary paediatric hospital: a survey of clinician attitudes and practices. J Paediatr Child Health. 2008;44(7–8):392–8.

    PubMed  Google Scholar 

  44. Kesselheim JC, Johnson J, Joffe S. Pediatricians’ reports of their education in ethics. Arch Pediatr Adolesc Med. 2008;162(4):368–73.

    PubMed  Google Scholar 

  45. Hoehn KS, Acharya K, Joseph JW, Ross LF. Pediatricians’ attitudes toward resuscitation in children with chronic illnesses. Pediatr Crit Care Med. 2009;10(3):369–74.

    PubMed  Google Scholar 

  46. Talati ED, Lang CW, Ross LF. Reactions of pediatricians to refusals of medical treatment for minors. J Adolesc Health. 2010;47(2):126–32.

    PubMed  Google Scholar 

  47. Bahus MK, Føerde R. Parents as decision-makers–do the attitudes of Norwegian doctors conform to law? Eur J Health Law. 2011;18(5):531–47.

    PubMed  Google Scholar 

  48. Morparia K, Dickerman M, Hoehn KS. Futility: unilateral decision making is not the default for pediatric intensivists. Pediatr Crit Care Med. 2012;13(5):e311–5.

    PubMed  Google Scholar 

  49. Needle JS, Mularski RA, Nguyen T, Fromme EK. Influence of personal preferences for life-sustaining treatment on medical decision making among pediatric intensivists. Crit Care Med. 2012;40(8):2464–9.

    PubMed  Google Scholar 

  50. Rapoport A, Obwanga C, Sirianni G, Librach SL, Husain A. Not just little adults: palliative care physician attitudes toward pediatric patients. J Palliat Med. 2013;16(6):675–9.

    PubMed  Google Scholar 

  51. Sanchez Varela AM, Johnson LM, Kane JR, Kasow KA, Quintana Y, Coan A, et al. Ethical decision making about end-of-life care issues by pediatric oncologists in economically diverse settings. J Pediatr Hematol Oncol. 2015;37(4):257–63.

    PubMed  Google Scholar 

  52. Grosek S, Orazem M, Kanic M, Vidmar G, Groselj U. Attitudes of Slovene paediatricians to end-of-life care. J Paediatr Child Health. 2016;52(3):278–83.

    PubMed  Google Scholar 

  53. Yotani N, Kizawa Y, Shintaku H. Differences between pediatricians and internists in advance care planning for adolescents with cancer. J Pediatr. 2017;182:356–62.

    PubMed  Google Scholar 

  54. Yotani N, Kizawa Y, Shintaku H. Advance care planning for adolescent patients with life-threatening neurological conditions: a survey of Japanese paediatric neurologists. BMJ Paediatr Open. 2017;1(1):e000102.

    PubMed  PubMed Central  Google Scholar 

  55. Wosinski B, Newman CJ. Physicians’ attitudes when faced with life-threatening events in children with severe neurological disabilities. Dev Neurorehabil. 2019;22(1):61–6.

    PubMed  Google Scholar 

  56. Aljethaily A, Al-Mutairi T, Al-Harbi K, Al-Khonezan S, Aljethaily A, Al-Homaidhi HS. Pediatricians’ perceptions toward do not resuscitate: a survey in Saudi Arabia and literature review. Adv Med Educ Pract. 2020;11:1–8.

    PubMed  PubMed Central  Google Scholar 

  57. Song IG, Kang SH, Kim MS, Kim CH, Moon YJ, Lee J. Differences in perspectives of pediatricians on advance care planning: a cross-sectional survey. BMC Palliat Care. 2020;19(1):145.

    PubMed  PubMed Central  Google Scholar 

  58. Yoo SH, Choi W, Kim Y, Kim MS, Park HY, Keam B, et al. Difficulties doctors experience during life-sustaining treatment discussion after enactment of the life-sustaining treatment decisions act: a cross-sectional study. Cancer Res Treat. 2021;53(2):584–92.

    PubMed  Google Scholar 

  59. Boer MCD, Zanin A, Latour JM, Brierley J. Paediatric residents and fellows ethics (PERFEct) survey: perceptions of European trainees regarding ethical dilemmas. Eur J Pediatr. 2022;181(2):561–70 Epub 2021 Aug 24.

    PubMed  Google Scholar 

  60. Carnevale FA, Farrell C, Cremer R, Canoui P, Séguret S, Gaudreault J, et al. Struggling to do what is right for the child: pediatric life-support decisions among physicians and nurses in France and Quebec. J Child Health Care. 2012;16(2):109–23.

    PubMed  Google Scholar 

  61. de Vos MA, Bos AP, Plötz FB, van Heerde M, de Graaff BM, Tates K, et al. Talking with parents about end-of-life decisions for their children. Pediatrics. 2015;135(2):e465–76.

    PubMed  Google Scholar 

  62. Lotz JD, Jox RJ, Meurer C, Borasio GD, Führer M. Medical indication regarding life-sustaining treatment for children: focus groups with clinicians. Palliat Med. 2016;30(10):960–70.

    PubMed  PubMed Central  Google Scholar 

  63. Zaal-Schuller IH, Willems DL, Ewals FVPM, van Goudoever JB, de Vos MA. How parents and physicians experience end-of-life decision-making for children with profound intellectual and multiple disabilities. Res Dev Disabil. 2016;59:283–93.

    PubMed  CAS  Google Scholar 

  64. Birchley G, Gooberman-Hill R, Deans Z, Fraser J, Huxtable R. “Best interests” in paediatric intensive care: an empirical ethics study. Arch Dis Child. 2017;102(10):930–5.

    PubMed  Google Scholar 

  65. Cicero-Oneto CE, Valdez-Martinez E, Bedolla M. Decision-making on therapeutic futility in Mexican adolescents with cancer: a qualitative study. BMC Med Ethics. 2017;18(1):74.

    PubMed  PubMed Central  Google Scholar 

  66. Richards CA, Starks H, O’Connor MR, Bourget E, Hays RM, Doorenbos AZ. Physicians perceptions of shared decision-making in neonatal and pediatric critical care. Am J Hosp Palliat Care. 2018;35(4):669–76.

    PubMed  Google Scholar 

  67. Jongaramraung J, Chanprasit C, Mesukko J, Niyomkar S, Reungrongrat S. End-of-life decisions for children in a Thai pediatric intensive care unit: a qualitative descriptive study. Pac Rim Int J Nurs Res. 2020;24(3):321–34.

    Google Scholar 

  68. Zaal-Schuller IH, Geurtzen R, Willems DL, de Vos MA, Hogeveen M. What hinders and helps in the end-of-life decision-making process for children: parents’ and physicians’ views. Acta Paediatr. 2022;111(4):873–87.

    PubMed  PubMed Central  Google Scholar 

  69. Coughlin KW. Medical decision-making in paediatrics: Infancy to adolescence. Paediatr Child Health. 2018;23(2):138–46.

    PubMed  PubMed Central  Google Scholar 

  70. Cavolo A, de Casterlé BD, Naulaers G, Gastmans C. Neonatologists’ decision-making for resuscitation and non-resuscitation of extremely preterm infants: ethical principles, challenges, and strategies-a qualitative study. BMC Med Ethics. 2021;22(1):129.

    PubMed  PubMed Central  Google Scholar 

  71. Parsons SK, Saiki-Craighill S, Mayer DK, Sullivan AM, Jeruss S, Terrin N, et al. Telling children and adolescents about their cancer diagnosis: cross-cultural comparisons between pediatric oncologists in the US and Japan. Psychooncology. 2007;16(1):60–8.

    PubMed  Google Scholar 

  72. Otani H, Morita T, Esaki T, Ariyama H, Tsukasa K, Oshima A, et al. Burden on oncologists when communicating the discontinuation of anticancer treatment. Jpn J Clin Oncol. 2011;41(8):999–1006.

    PubMed  PubMed Central  Google Scholar 

  73. Rosenberg AR, Starks H, Unguru Y, Feudtner C, Diekema D. Truth telling in the setting of cultural differences and incurable pediatric illness: a review. JAMA Pediatr. 2017;171(11):1113–9.

    PubMed  PubMed Central  Google Scholar 

  74. Kim MS, Lee J, Sim JA, et al. Discordance between physician and the general public perceptions of prognostic disclosure to children with serious illness: a Korean nationwide study. J Korean Med Sci. 2018;33(49):e327.

    PubMed  PubMed Central  Google Scholar 

  75. Yoshida S, Ogawa C, Shimizu K, et al. Japanese physicians’ attitudes toward end-of-life discussion with pediatric patients with cancer. Support Care Cancer. 2018;26(11):3861–71.

    PubMed  Google Scholar 

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Acknowledgements

Not applicable.

Funding

This work was supported by the China Scholarship Council, China [grant number 202008440377] to YZ; the Research Foundation-Flanders (FWO; Dutch: Fonds voor Wetenschappelijk Onderzoek-Vlaanderen), Belgium (grant number 1144319N) to AC.

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Contributions

YZ contributed to the study design, data processing, methodological quality assessment, manuscript drafting and revision. AC contributed to data processing, manuscript reviewing and revision. VL contributed to manuscript reviewing and study supervision. CG contributed to the study design, data processing, methodological quality assessment, and manuscript reviewing and supervision.

Corresponding author

Correspondence to Yajing Zhong.

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Overview of Bibliographic Databases Searched, Search Strings Used, and Search Results of Articles Identified [32].

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Example conceptual scheme our synthesis and analysis.

Additional file 3.

Classification of the cases in the included articles according to the child’s severity of disability and/or chance of survival.

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Zhong, Y., Cavolo, A., Labarque, V. et al. Physicians’ attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence. BMC Palliat Care 22, 145 (2023). https://doi.org/10.1186/s12904-023-01260-y

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