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The Lived Experience of ICU Clinicians During The.18
The Lived Experience of ICU Clinicians During The.18
The Lived Experience of ICU Clinicians During The.18
D
uring the first weeks of the coronavirus disease 2019 (COVID-19) pan-
demic, the healthcare system in France was rapidly overwhelmed by the
dramatic increase in cases (Fig. 1), prompting a complete readaptation
of hospital policies. Emergency departments’ operating procedures, drug pro-
curement, provision of critical care, decision-making, and patient and family-
centered care were profoundly reorganized in a matter of weeks (1). Intensive Copyright © 2021 by the Society of
care capacities were extended, new wards were built, additional staff was recruited Critical Care Medicine and Wolters
from other hospital units, personal protective equipment were made mandatory, Kluwer Health, Inc. All Rights Reserved.
patients were physically isolated, and visits for relatives were drastically limited. DOI: 10.1097/CCM.0000000000004939
TABLE 1.
ICUs and Study Participants’ Characteristics
ICU 01: “Located in a teaching hospital with a total capacity of 700 beds. The number of beds in the ICU was
increased from 12 to 30 during the first surge of the pandemic. A total of 128 critically ill COVID-19 patients
were admitted between March 1 and the May 31.”
Medical staff
01P01 Senior physician (31–40) Yes Yes
01P02 Registrar/assistant (31–40) Yes Yes
01P03 Resident (21–30) No No
01P04 Senior physician (41–50) Yes Yes
01P05 Senior physician (31–40) Yes Yes
Nursing staff
01N01 Nurse (21–30) Yes Yes
01N02 Nurse (31–40) Yes Yes
01NA03 Nurse assistant (41–50) Yes Yes
01NS04 Nurse supervisor (31–40) Yes Yes
01N05 Nurse (41–50) Yes Yes
ICU 02: “Located in a teaching hospital with a total capacity of 1,300 beds. The number of beds in the ICU was
increased from 24 to 36 during the first surge of the pandemic. A total of 95 critically ill COVID-19 patients
were admitted between the first of March and the 31st of May.”
Medical staff
02P01 Senior physician (41–50) Yes Yes
02P02 Registrar/assistant (31–40) Yes No
02P03 Resident (31–40) No No
02P04 Senior physician (41–50) Yes Yes
Nursing staff
02N01 Nurse (31–40) No No
02RT02 Respiratory therapist (21–30) Yes No
02NS03 Nurse supervisor (41–50) No No
02NA04 Nurse assistant (21–30) Yes No
02NS05 Nurse supervisor (51–60) No Yes
(Continued)
TABLE 1. (Continued).
ICUs and Study Participants’ Characteristics
ICU 03: “Located in a teaching hospital with a total capacity of 1,600 beds. The number of beds in the ICU was
increased from 24 to 32 during the first surge of the pandemic. A total of 110 critically ill COVID-19 patients
were admitted between March 1 and May 31.”
Medical staff
03P01 Senior physician (31–40) Yes Yes
03P02 Registrar/assistant (31–40) Yes Yes
03P03 Resident (21–30) No No
Nursing staff
03N02 Nurse (31–40) No No
03NA03 Nurse assistant (31–40) No No
03N04 Nurse (31–40) No No
03N05 Nurse (31–40) Yes Yes
03NS06 Nurse supervisor (41–50) Yes No
COVID-19 = coronavirus disease 2019.
Codes: P = physician, N = nurse, NA = nurse assistant, NS = nurse supervisor, RT = respiratory therapist.
and respiratory therapists), gender, level of seniority, distancing rules during the study period, interviews
and number of years of clinical experience in the ICU. were conducted over the phone.
Eligible participants (currently working in one of the The interview guide developed a priori by the inves-
ICUs and French speaking) were recruited by local tigators (N.K-.B., L.M., Z.C-.S. as well as three critical
investigators via e-mails, personal solicitations, and care physicians, one psychiatrist and one nurse with
participant referrals. Out of 28 eligible individuals 15 years of ICU experience) was structured around six
who were approached for participation in the study, 27 broad topics: 1) working conditions and professional
accepted, and one declined. The study was approved relationships, 2) difficulties in caring for severely ill
by the research ethics board Sud Méditerranée (2020- COVID-19 patients, 3) interactions with patients and
A00809-30; CNRIPH: 20.03.27.73019). All partici- families, 4) difficult decisions and end-of-life care, 5)
pants provided verbal informed consent, including repercussions on personal life, and 6) perspectives
permission to record the interview, and received no for the future (Supplemental Table 1, Supplemental
compensation. Digital Content 1, http://links.lww.com/CCM/G209).
Questions were open ended, and participants were
Data Collection encouraged to explore issues “they” considered rel-
evant. Interviews were conducted in French, audio-
This qualitative study sought to explore the ICU clini- recorded and transcribed verbatim by professional
cians’ experiences and practices during the COVID-19 transcribers. Interview data were anonymized during
surge, in the heat of the moment, in order to avoid transcription. Self-reported demographic data in-
recall bias and a posteriori reconstruction of their cluding sex, age, and employment history were also
experience. Interviews were conducted in French be- collected. Recruitment of new participants was inter-
tween April 16, 2020, and May 13, 2020, by researchers rupted when informational saturation was reached,
trained in qualitative methods (N.K-.B., L.M., Z.C-.S.). that is when no new relevant information emerged
Because of travel restrictions and stringent physical from the interviews (11).
TABLE 2.
Themes Derived From Qualitative Analysis
S. No. Themes
and the same clinical features. Physicians reported was occupied by patients presenting the exact same
being confused by the sudden deterioration of the clinical profile and physical features (Table 3, Q10).
patients (Table 3, Q8). Not being in control was an- Compared with the typical ICU patients, the clinical
other challenging experience for ICU clinicians. The trajectory of COVID-19 patients spanned over a much
absence of solid medical evidence was disconcerting, longer period (Table 3, Q11), and almost all patients
both at the individual level and at the level of the care were sedated and intubated for the entire duration of
team (Table 3, Q9). The high degree of clinical un- their stay in the ICU. Over time the repetitiveness be-
certainty during the first few weeks of the pandemic came tedious: “It’s not intellectually stimulating; we
led physicians to question themselves as well as their feel like we just aren’t able to move on” (01P01).
ability to treat these patients effectively. During the peak of hospital admissions, the rapid
During the interviews, nearly all participants transfer of the patient from the ICU to other wards
expressed a feeling of monotony. Every single ICU bed of the hospital was experienced as upsetting (Table 3,
TABLE 3.
Representative Quotes for Themes 1–3
S. No. Themes
TABLE 4.
Representative Quotes for Themes 4–6
S. No. Themes
4 Family members: working under new constraints and developing novel interactions.
Q17 “We’ve gone from being closed for the first 10 days to now, where families can come for end-of-life situ-
ations, and in other situations they can all come for at least one hour a day. (…) So, I think that was a
very good decision, to reintroduce some humanity” (01P01).
Q18 “I think it’s a shame, because I still feel like I’ve lost... because we’re busy all the time, there’re people every-
where, there’s noise all the time, so I have less time to say to myself ‘OK, I’m going to sit down with the family,
we’re going to do a little tour of the room, I’ll explain…’ (…). There’s a lack of something human” (01P02).
Q19 “Maybe it’s a little harder for families to express their feelings and ask questions over the phone. But we
try to say the same things we would say to their face. But it’s true that necessarily the relationship is not
the same, there’s no eye contact, no pausing, no seeing how the person reacts, no adapting ourselves
accordingly, there’s less of a relationship” (02P03).
Q20 “We set up a system where we were the ones who called the family at preset schedules and we had to
stick to them, because it was important to us, and we knew how they needed to hear from us as well”
(02P01).
Q21 “We create a bond that’s maybe a little stronger than usual, since we always have the one same person
on the phone each time” (02P02).
Q22 “For some patients we organize video calls, even if the patient is intubated. But at least the family can see
the room and see what’s going on, because just explaining with words (…) is very difficult” (02NA04).
5 End-of-life care: compensating for the absence of family members and rituals.
Q23 “For me personally, I found it very difficult to deal with the decisions to withdraw treatment in patients whose
families I had not been able to see and discuss the situation with. And that was hard because, for example,
when we extubated patients, the first terminal extubations, I didn’t feel like I could tell the family.” (01P01).
Q24 “My colleagues and I, we couldn’t bear to see people die alone. So, we held their hands until the end”
(01NA03).
Q25 “There was one family, we made sure they could be in the room. It makes sense, (…) it’s a satisfaction
knowing the patient didn’t die alone, and that he was with his loved ones” (02NA04).
Q26 “The body is wrapped in a body bag, and we’re the last ones to see the body. (...) It’s been very difficult
for me (…) to realize that it’s over; it’s me and the patient, and then it’s over. I know that once the zip is
closed, once we get him to the morgue, no one will ever see him again, his family won’t see him. (…)
It’s the only thing that really deeply touched me” (03N02).
Q27 “There was an obligation to put the body in the coffin immediately, that is to close the coffin immediately,
within 24 hours, which prevented families from observing certain customs and religious rites—such as
the ritual of washing of the body in certain religions—and which also prevented the family from seeing
the deceased, since the coffin was closed” (01P02).
Q28 “I had the feeling that we were generating pathologic grief for dozens of people. It’s dreadful” (01P01).
Q29 “(…) For the family’s grieving process, it’s also very important for them to be able to see their loved-one
one last time (…). We feel reassured now, because we work with people, not just cases, so we mustn’t
forget that. It’s a critical situation and everything is reorganized, we’re completely confused, but there
are certain things that must not change, and that’s one of them” (03N02).
(Continued)
TABLE 4. (Continued).
Representative Quotes for Themes 4–6
S. No. Themes
6 The ICU clinician: full engagement in the face of the coronavirus disease crisis.
Q30 “What scares me the most is not necessarily being infected by the coronavirus, but it’s the risk of passing
it on to someone else, someone close to me. (...) I’m not scared for myself; I’m scared for my family and
friends” (03NA03).
Q31 “One night I woke up, I was sweating and I thought I had a fever, and in fact I was really stressed out,
that’s when I realized that I was actually really afraid of being infected and so I panicked, I had a hard
time breathing and I thought ‘well, that’s it’, I’ve got a severe form, I’m going to have to be intubated’”
(02RT02).
Q32 “The people we’re resuscitating are my parents. They are people in their 60s and 70s, who don’t neces-
sarily have a long medical history and who, overnight, find themselves in an extremely serious situation,
from which they might not recover. So, there is a lot of personal projection in these situations, which is
difficult” (01P01).
Q33 “My priority is that the patients who are being cared for in our beds leave the ICU alive, that’s the priority.
The priority is a public health priority; it’s clearly to save these people. Everything else is secondary. In
other words, if my children lose their [school] year, it’s secondary; it’s secondary to the lives of these
patients, and that’s how I explained it to them” (02NS05).
Q34 “I wonder if I shouldn’t do something else. At least for a while, because I need to see something different,
to do something different” (01P01).
Q35 “I’m starting to think about how long it’s going to last, and how we’re going to deal with it afterwards,
because this idea of a second peak is really scary” (01N01).
Q12). For some clinicians, the feeling of guilt added to disorientation (Table 4, Q18). Communicating solely
the frustration (Table 3, Q13). over the phone was sometimes experienced as unsat-
The working conditions (intensity, repetitiveness, isfactory as it did not convey nonverbal cues (Table 4,
personal protective equipment) and the total or par- Q19). Nevertheless, these interactions over the phone
tial restriction of family visits generated a sense of de- were important for clinicians, and specific policies
humanization. Participants highlighted the challenge were soon established (Table 4, Q20). In spite of initial
of providing care in a context of anonymity (Table 3, apprehension, these regular phone calls could be ful-
Q14). They also reported a decrease in empathy due to filling (Table 4, Q21). Other means of communication
the increased workload and monotony (Table 3, Q15). with family members, such as video calling, were also
At patient admission, due to restricted family visits, developed, but only marginally (Table 4, Q22).
clinicians felt they had to compensate for the absence
of a loved one at the bedside (Table 3, Q16). End-of-Life Care: Compensating for the
Absence of Family Members and Rituals
Family Members: Working Under New
The impossibility of meeting families face-to-face to
Constraints and Developing Novel Interactions
discuss the patients’ prognosis made end-of-life dis-
The initial ban on family visits was a negative experi- cussions more difficult than usual. The quality of com-
ence for all participating clinicians. In the three ICUs, munication was hindered, and some information was
rules were rapidly changed, and visits were allowed, al- omitted (Table 4, Q23).
beit with some restrictions (Table 4, Q17). All participating clinicians—without exception—
However, fewer and shorter interactions with family expressed distress with the loneliness of dying dur-
members were mentioned as a source of frustration and ing the initial surge: “It’s not death itself, it’s seeing the
patient die alone, without any family; that’s what’s diffi- the future (Table 4, Q34). During interviews, the clini-
cult” (01P02). Clinicians were uncomfortable with this cians’ principal fear remained the threat of a second
situation and felt they should not leave the patients wave of the epidemic (Table 4, Q35).
alone (Table 4, Q24). When possible, the presence of
family members brought meaning to the end of life DISCUSSION
(Table 4, Q25). When family members could not be
present, clinicians (and more specifically, nurses) felt This qualitative study carried out in the midst of the
a strong responsibility because they were not only the COVID-19 pandemic shows that although the expe-
last ones to see the patient alive but also the last ones to rience of ICU clinicians changed rapidly over a short
see the deceased’s body (Table 4, Q26). Clinicians were period of time it remained intense, both professionally
aware that the absence of rituals could be harmful, and and emotionally. During the first tumultuous days of
yet, they could not change the rules (Table 4, Q27). the surge, clinicians working in the ICU lost all sense
Clinicians were concerned that these particu- of normality. ICU culture was disrupted, and the cli-
larly difficult circumstances would increase the risk nicians’ sense of belonging and their professional
of complicated grief among relatives (Table 4, Q28). identity were shaken. Many clinicians spontaneously
However, once rules regarding family visits were soft- described symptoms of acute stress: they felt like in a
ened, clinicians felt more at ease with end-of-life care daze, they were more alert to danger, and they experi-
(Table 4, Q29). enced troubled sleep and bad dreams (14). As in the
study by Sun et al (7), these negative emotions were
more pronounced in the first week of the pandemic,
The ICU Clinician: Full Engagement in the Face
of the COVID-19 Crisis suggesting that frontline clinicians may benefit from
early psychologic support.
The fear of being contaminated and of contaminat- The initial surge was complex not only because of the
ing their loved ones was strong among ICU clinicians repeated changes in clinical protocols or because of the
(Table 4, Q30). However, they were very attentive to exponential number of patients with severe COVID-19
their own symptoms and reported being overwhelmed pneumonia but also because of the unparalleled de-
with anxiety (Table 4, Q31). Several participants gree of uncertainty surrounding the disease trajectory.
described this anxiety as being extremely burdensome. The lack of control and the absence of proven effec-
Identification with patients was often mentioned tive treatment were unsettling for ICU clinicians (15).
during the interviews. The patients who were admitted Physicians’ experience first oscillated between feelings
to the ICU sometimes reminded them of themselves, of stimulation and powerlessness and over time turned
but more often, they reminded them of their loved to a feeling of monotony, fueled by the homogeneity of
ones (Table 4, Q32). patients’ clinical profile and symptoms. Monotonous
Caring for ICU patients during the first few days work has been shown to have a negative impact on
and weeks of the pandemic was described as an intense wellbeing with a decrease of job satisfaction and an
physical and emotional experience. Indeed, clinicians increase of psychologic distress (16). However, the re-
felt physically and emotionally exhausted, and many petitiveness mentioned by the participants was partly
stated they suffered from insomnia or nightmares. “I counterbalanced by the unexpected evolution of some
couldn’t cut myself off from the situation” (01N02), patients, characterized by a rapid deterioration at times
“I feel nervous night and day” (02RT02). While in where hope of recovery was high, adding a supplemen-
the ICU, their physical experience was described tary feeling of ineffectiveness that was sometimes ex-
as extreme: “It’s an exhausting, suffocating experi- perienced as depressing (7, 17).
ence” (01P04). In spite of all the difficulties, clinicians Contrary to what they anticipated and to what was
described themselves as being fully engaged in their reported in publications (18), in the participating
work (Table 4, Q33). For most participants, this ex- ICUs, patient triage did not seem to be an issue dur-
perience confirmed their strong attachment to inten- ing the first peak of the pandemic. More difficult was
sive care medicine. However, for others, the intensity the inability to fully adhere to the standard practice of
of the event called into question their motivation for patient and family-centered care (19). The absence or
rare presence of family members was one of the most safeguarding positive relationships among colleagues
difficult experiences for clinicians. They felt deprived was a priority as they can bring support during times
of one of their important roles, that is, care and sup- of upheaval and protection from loss of meaning.
port of the family as well as quality communication, Investing in these relationships was a coping strategy,
suggesting that the ban and/or restricted visiting poli- suggesting that developing peer support and team re-
cies should be reevaluated, for the benefit both of the silience is a priority. Systematic approaches designed
family and the clinicians. Telephone communication to integrate teamwork into practice have shown to be
seemed only partially satisfactory, as it precluded non- effective (29). As described in other studies and differ-
verbal communication and, thus, made it very difficult ent contexts, in a time of crisis team solidarity is often
to take the families’ needs and emotions into account reinforced (7, 30). Throughout the interviews, clini-
(20, 21). cians expressed a feeling of pride and satisfaction in
Due to substantial restrictions to family visits, cli- having been part of this mission and appreciated the
nicians also felt that they had to compensate for the social recognition that accompanied it.
absence of relatives at two crucial time points: first, at Our study presents several limitations. First, it was
admission and before sedation to reassure the patient conducted in three ICUs located in large teaching hos-
and second, near the end of life, when important deci- pitals in the center of Paris. These ICUs share a number
sions arise. Caring for these dying patients was fraught of common features that make them a homogeneous
with challenges and generated a strong feeling of re- setting for qualitative research, but they are most likely
sponsibility. During the initial phase of the COVID- not representative of all ICUs in the country. Likewise,
19 pandemic, clinicians found themselves facing these although our purposive sampling strategy was
situations alone, which are not only loaded with med- designed to maximize the diversity of ICU clinicians
ical issues but also represent an anthropologically sa- who participated in the study, it does not guarantee the
cred sequence (22): without families, clinicians were generalizability of our findings to all ICU clinicians.
left with little nonmedical input to feed the deci- Participation in qualitative interviews was voluntary,
sion-making process; they often had sole responsibility creating a possible selection bias: clinicians with dif-
for the patient at the end of life and after death had ficulties in (or reluctance to) expressing themselves or
occurred. They were concerned that the context may their experiences during the epidemic may have been
generate complicated grief in family members (23, 24). omitted. It should also be noted that our study is solely
Previous research has shown that epidemics bring dis- focused on healthcare professionals working in the set-
ruption to social norms, rituals, and mourning prac- ting of ICUs, when many other hospital settings and
tices (25), suggesting the need to provide a supportive medical specialties were involved in caring for severely
framework for families in end-of-life situations, in- ill COVID-19 patients. Finally, face-to-face interviews
cluding open visiting and the possibility of performing were not possible due to strict social distancing meas-
rituals that allow a sense of continuity. ures, and we had to resort to conducting interviews by
Working in an ICU is complex and physically, cog- telephone, which may have negatively impacted the
nitively, and emotionally demanding (26). During the richness of the empirical data that we collected (31).
first few days and weeks of the pandemic, this became
overwhelming. The high workload, coupled with an
CONCLUSIONS
especially heavy emotional burden, did not, how-
ever, affect the physicians’ and nurses’ level of profes- This qualitative study provides in-depth understanding
sional engagement. Previous research has found that of the experience of ICU clinicians during the very first
work engagement is often positively associated with weeks of the COVID-19 pandemic. Lessons learnt from
personal wellbeing and performance at work (27). this study offer important insight to better anticipate
Recognizing this engagement may help decrease stress policies and measures in future pandemics. First, con-
and risk of burnout (28). Our study also shows that cern about family members was strong and reveals that
working within an atmosphere of good professional family-centered care is a core aspect of ICU clinicians’
relationships reinforced a sense of safety for clinicians. identity. Policies restricting family visits urgently need
In spite of all the changes and the occasional tensions, to be reevaluated as the pandemic continues. Second,
this reevaluation is particularly important in end-of-life 3. Azoulay E, Cariou A, Bruneel F, et al: Symptoms of anxiety,
situations during which open visiting is fundamental depression, and peritraumatic dissociation in critical care cli-
nicians managing patients with COVID-19. A cross-sectional
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study. Am J Respir Crit Care Med 2020; 202:1388–1398
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4. Kleinpell R, Ferraro DM, Maves RC, et al: Coronavirus disease
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