Patient-expressed perceptions of wait-time causes and wait-related satisfaction

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PERCEPTIONS OF WAIT-TIME CAUSES

105

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Copyright © 2015 Multimed Inc. Following publication in 

Current Oncology

, the full text of each article is available immediately and archived in PubMed Central (PMC).

ORIGINAL ARTICLE

Patient-expressed perceptions 

of wait-time causes and 

wait-related satisfaction

M. Mathews 

p

h

d

,* D. Ryan 

ma

,*  

and D. Bulman 

p

h

d

Ü

underlying reasons for wait-related satisfaction or 

dissatisfaction. Although our findings shed light 

on patient experiences with the health system and 

identify where interventions could help to inform the 

expectations of patients and the public with respect 

to wait time, more research is needed to understand 

wait-related satisfaction among cancer patients.

KEY WORDS

Wait times, patient satisfaction, breast cancer, pros

tate cancer, colorectal cancer, lung cancer

1.

BACKGROUND

ìPatient satisfactionî refers to personal evaluations 

by patients about whether their lived health care ex

periences measure up to their expectations

1

. Patient 

satisfaction is generally accepted as a dimension of 

quality of care

2

 and patient-centred care

3

. A num

ber of studies have examined patient satisfaction in 

cancer care and have highlighted communication 

between the physician (and other members of the 

team) and the patient

3,4

. Nonetheless, wait times for 

care are frequently cited as a cause of patient dis

satisfaction with the health care system

5

.

Studies examining wait times for cancer care and 

wait-related satisfaction have a number of limitations. 

First, some studies examine the length of time spent 

in a waiting room preceding a single visit; few stud

ies have looked at waits as patients progress from 

symptoms, to testing, and to diagnosis and treatment. 

Second, some researchers have described wait times 

for the various intervals from symptoms to treat

ment, but we found only one Canadian study that 

considered patient satisfaction with those waits. In 

a study of colorectal cancer patients in Nova Scotia, 

researchers found only a modest correlation between 

length of wait and wait-related satisfaction

6

.

Does patient satisfaction vary based on the cause 

of the wait? Wait times along the pathway from 

symptoms to treatment are commonly described in 

ABSTRACT

Background

This study set out to identify patterns in the causes of 

waits and wait-related satisfaction.

Methods

We conducted qualitative interviews with urban, 

semi-urban, and rural patients (

n

= 60) to explore 

their perceptions of the waits they experienced in the 

detection and treatment of their breast, prostate, lung, 

or colorectal cancer. We asked participants to de

scribe their experiences from the onset of symptoms 

to the start of treatment at the cancer clinic and their 

satisfaction with waits at various intervals. Interview 

transcripts were coded using a thematic approach.

Results

Patients identified five groups of wait-time causes:

ï

Patient-related (beliefs, preferences, and non-cancer 

health issues)

ï

Treatment-related (natural consequences of treatment)

ï

System-related (the organization or functioning 

of groups, workforce, institution, or infrastructure 

in the health care system)

ï

Physician-related (a single physician responsible 

for a specific element in the patientís care)

ï

Other causes (disruptions to normal operations 

of a city or community as a whole)

With the limited exception of physician-related 

absences, the nature of the cause was not linked to 

overall satisfaction or dissatisfaction with waits.

Conclusions

Causes in themselves do not explain wait-related 

satisfaction. Further work is needed to explore the 

Curr Oncol

, Vol. 22, pp. 105-112; doi: http://dx.doi.org/10.3747/co.22.2243

MATHEWS 

et al. 

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Copyright © 2015 Multimed Inc. Following publication in 

Current Oncology

, the full text of each article is available immediately and archived in PubMed Central (PMC).

the literature as resulting from patient and provider 

delay. ìPatient delayî refers to the interval from the 

onset of symptoms to the first medical consultation, 

usually with the patientís regular physician

7ñ9

. ìPro

vider delayî refers to the period after the first visit to 

a health care provider (in Canada, usually the general 

practitioner or family physician)

6,10,11

. The terminol

ogy suggests that waits during those periods result 

from the provider or the patient. For example, a lengthy 

wait to see a physician about symptoms is attributed to 

the patient, and delays occurring after the initial visit 

are attributed to physician- or health systemñrelated 

issues. Although some studies have described patient 

and provider delays, we were unable to find studies that 

examined the relationship between patient satisfaction 

and wait time causes. The purpose of the present study 

was therefore to identify patterns in causes of waits 

and wait-related satisfaction.

Using qualitative interviews, we asked patients 

from Newfoundland and Labrador to describe their 

experiences from the onset of symptoms to the start 

of treatment at the cancer clinic. As in other provinces 

in Canada, Newfoundland and Labrador has invested 

resources in improving wait times for cancer care

12

By examining the care-seeking process, we adopt a 

patient-centred approach and aim to better understand 

the patientís experience of cancer and interactions with 

the health care system. The study contributes to the 

understanding of public perceptions of wait times and 

efforts to improve timely access to cancer care.

2.

METHODS

Memorial Universityís Human Investigations Com

mittee approved the study. We conducted semis

tructured qualitative interviews with breast, lung, 

colorectal, and prostate cancer patients who, in an 

earlier survey, had expressed satisfaction or dis

satisfaction with their wait times while seeking care 

for their cancer.

Eligible study participants were residents of New

foundland and Labrador who were 19 years of age or 

older and who had been diagnosed between January 

2009 and August 2011. We excluded participants with 

previous or multiple cancer diagnoses because their 

wait-time experiences might differ from those of 

patients who are diagnosed with one type of cancer 

for the first time. For the initial survey, we recruited 

cancer patients from regional cancer clinics across the 

province and mailed invitations to individuals identi

fied through the provincial cancer registry. The survey 

gathered information about dates in the care-seeking 

process, satisfaction with interval-specific wait times 

(for example, from symptoms to first visit with a health 

care provider, from first visit to diagnosis, and so on), 

and clinical and personal characteristics. A fuller 

description of the survey procedures are provided 

elsewhere

13

. At the end of the survey, respondents were 

invited to take part in the qualitative interview, and 

willing respondents were later contacted to complete 

consent forms and schedule interviews.

Patients were selected for an interview based 

on their responses to survey questions about com

munity of residence and satisfaction with various 

waits. From among the survey respondents, we 

identified urban (population =100,000), semi-urban 

(population 10,001ñ99,999), and rural (population 

=10,000) residents who were satisfied or dissatisfied 

with their overall wait time from onset of symptoms 

to care at the cancer clinic. Because patients were 

overwhelmingly satisfied with the overall wait time, 

we then amended our recruitment to patients who had 

expressed dissatisfaction with any wait interval. For 

each cancer type and community size, we recruited 

a minimum of 3 patients who were satisfied or dis

satisfied with their wait time experiences. The final 

number of interviews was determined when satura

tion of ideas and concepts was reached

14

.

The interviews were conducted in person or by 

telephone and ranged in length from 8 minutes to 

82 minutes. We asked participants about their wait 

times and causes of waits from onset of symptoms 

to receiving treatment for their cancer, their level of 

satisfaction with those wait times, any barriers to 

receiving care in their community, factors that might 

make cancer care accessible in their area, and what 

could have been done to improve their wait times or 

the quality of care that they received. Each interview 

was tape-recorded and later transcribed verbatim.

Using a thematic approach, three members of the 

research team each independently read 4 transcripts 

to identify key themes and concepts. We then devel

oped a template to code the remaining transcripts. 

To ensure consistency in coding, we defined and 

described each code. Each transcript was then read 

and coded by two members of the team (one research 

assistant read and coded all transcripts). Throughout 

this process, data from previous interviews were con

tinuously compared to identify concepts, categories, 

clusters, and themes

14,15

. Disagreements in coding 

were resolved by consensus. Where disagreements 

arose, members of the research team re-examined 

the descriptions of individual themes to determine 

the source of disagreement. Those discussions led, as 

needed, to clarification of code and theme definitions, 

the creation of new themes, or the integration of new 

ideas within a theme. The NVivo

9 qualitative data 

analysis software (version

9, 2010: QSR International, 

Doncaster, Australia) was then used to re-code all 

transcripts using the final coding template.

In the present article, we focus on the causes 

of disruptions in timely care. Numbers are used to 

identify individual participants.

3.

RESULTS

Of 128 invited patients, 60 (46.9%) participated in an 

interview. Table

i

 shows participant characteristics 

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