Paper
Is primary angioplasty an acceptable alternative to thrombolysis? Quantitative and qualitative study of patient and carer satisfaction
Fiona C. Sampson MSc,* Alicia O�Cathain PhD� and Steve Goodacre PhD� *Research Fellow, �Senior Research Fellow and �Professor of Emergency Medicine, ScHARR, University of Sheffield, Sheffield, UK
Correspondence
Fiona C. Sampson
ScHARR
University of Sheffield
Regent Street
Sheffield S1 4DA
UK
E-mail: [email protected]
Accepted for publication
7 October 2009
Keywords: angioplasty, myocardial
infarction, patient satisfaction
Abstract
Objective The National Infarct Angioplasty Project assessed the
feasibility of establishing a comprehensive primary angioplasty
service. We aimed to compare satisfaction at intervention hospitals
offering angioplasty-based care and control hospitals offering
thrombolysis-based care.
Design Mixed methods, with postal survey of patients and their
carers, supported by semi-structured interviews.
Setting and participants Survey of 682 patients and 486 carers, and
interviews with 33 patients and carers, in eight English hospitals.
Interventions Primary angioplasty or thrombolysis.
Main outcome measures Satisfaction with treatment.
Results Responses were received from 595 ⁄ 682 patients (87%) and 418 ⁄ 486 carers (86%). Satisfaction with overall care was high at both intervention and control sites (78% vs. 71% patients rated their
care as �excellent�, P = 0.074). Patient satisfaction was higher at intervention sites for some aspects of care such as speed of treatment
(80% vs. 67% �excellent�, P = 0.001). Convenience of visiting was rated lower at intervention sites by carers (12% vs. 1% �poor�, P = 0.001). During interviews, carers reported that they accepted
the added inconvenience of visiting primary angioplasty sites in the
context of this life-saving treatment. Patient satisfaction with
discharge and aftercare was lower in both treatment groups than
for other aspects of care.
Conclusions Reorganization of care to offer a primary angioplasty
service was acceptable to patients and their carers. Satisfaction levels
were high regardless of the type of care received, with the exception
of discharge and aftercare.
Primary angioplasty as an alternative to intra-
venous thrombolysis for patients with acute ST-
elevation myocardial infarction (STEMI) has
been shown to reduce mortality, re-infarction,
stroke and the need for coronary artery bypass
grafting. 1 Economic analyses suggest that if both
doi: 10.1111/j.1369-7625.2009.00589.x
350 � 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
treatments are routinely available, primary
angioplasty is likely to be cost-effective if it can
be delivered in a timely manner. 2 In the United
Kingdom (UK), primary angioplasty is not
currently the standard treatment for patients
with STEMI, although rates are increasing rap-
idly with over one in five STEMI patients
receiving reperfusion having primary angio-
plasty in England and Wales in 2007 ⁄ 8.3 Health policy makers in England have advocated
expediting the process of making primary
angioplasty the principal treatment for STEMI
patients. 4
In 2004, the British Cardiac Society and the
Department of Health established a working
group to consider the feasibility of implement-
ing a countrywide primary angioplasty service
for patients with STEMI in England. Ten hos-
pitals offering primary angioplasty took part in
the National Infarct Angioplasty Project
(NIAP) during 2005–6 and collected data on
call and treatment times, clinical measures and
outcomes for all patients admitted to their
hospitals during the year. The sites represented
a range of potential service models, including
single centres, centres taking referrals from local
hospitals and networks of centres working
together to serve local populations. 5 Due to the
specialist facilities and staffing required, the
routine provision of primary angioplasty
required significant reorganization of services,
with patients transferring from, or bypassing,
local emergency departments to go to a primary
angioplasty centre. There are concerns that
centralization of services will adversely affect
patient satisfaction, 6–8
and in this case that
carers would be inconvenienced by having to
travel greater distances to primary angioplasty
centres.
To date there has been little consideration of
the views of patients or their carers regarding the
development of primary angioplasty services.
Existing research focuses largely upon experi-
ences of angioplasty as an elective procedure. 9
As part of an independent evaluation of the
NIAP pilot sites, we undertook a study of
patients� and carers� views of care provided at NIAP sites compared with views of patients and
carers at hospitals providing mainly thrombol-
ysis-based care.
Methods
Design and setting
The study was part of a wider evaluation which
included studies of the workforce and economic
implications of NIAP. The patient and carer
satisfaction component of this wider study was a
cross-sectional comparison of care provided in
four hospitals offering mainly primary angio-
plasty (intervention sites) and four hospitals
offering mainly thrombolysis-based care (control
sites) in England. A mixed methods design was
used 10
drawing on the strengths of quantitative
research to measure differences in patient and
carer satisfaction between hospitals offering
mainly primary angioplasty and those offering
mainly thrombolysis, and the strengths of qual-
itative research to understand the important
components of satisfaction and elaborate on the
findings from the quantitative research. 11
The
study was undertaken in three phases: qualita-
tive interviews with patients and carers to
understand the key aspects of their experience
and to develop a questionnaire for use in the
survey; a survey of patients and carers in both
intervention and control hospitals; and further
qualitative interviews with patients to examine
issues raised in earlier phases of the study.
Recruitment
For the �phase 1� interviews, nurses approached patients with STEMI who were admitted to
hospital at two of the intervention sites. Con-
sent was gained for a researcher to approach
both the patient and their carer for interview.
We used purposive sampling to select intervie-
wees experiencing the range of referral routes
within NIAP sites (i.e. via the emergency
department, direct to catheter lab, hospital
bypass). Based on these interviews we developed
a questionnaire for patients and a questionnaire
for carers. For the �phase 2� survey, nurses recorded the admission of all patients with
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
351
STEMI at the four intervention and four con-
trol sites. To comply with ethics committee
requirements, nurses asked patients to consent
to being sent a questionnaire and to provide
details of a carer where possible. Patients who
were critically ill, unable to consent due to
cognitive impairment, or unable to understand
English were excluded. A questionnaire, and up
to two reminders, were then sent to patients and
carers at around 1 week after admission.
Recruitment took place between February and
November 2007. For the �phase 3� interviews, we followed up an issue which arose from phase 1
by selecting survey respondents who felt that
they had been �fixed� by their treatment or not,12
and also followed up an issue which arose from
phase 2 by selecting survey respondents who
reported their discharge and aftercare as
unsatisfactory.
Interview schedules and questionnaire
The phase 1 interviews followed a critical inci-
dent technique to identify key aspects of care. 13
Interviewees were asked to describe the positive
and negative aspects of their experience from
onset of symptoms to discharge home. The
development of the phase 2 questionnaire was
informed by the research brief and findings from
the phase 1 interviews. The patient questionnaire
consisted of 27 satisfaction items using a five
point scale �excellent� �very good� �good� �fair� �poor� and the extra option of �not sure� because some patients may have been unaware of events
for parts of their care. Items addressed com-
munication with staff, speed and efficiency of
care, management of pain and comfort, conve-
nience of family visiting the hospital, discharge,
post-discharge care, the different places of care,
and care overall. Other questions addressed
demographical information, experience of
transfer between hospitals and permission for an
interview at a later time. There were four open-
ended questions about good and poor aspects of
care. The carer questionnaire was similar, with a
focus on convenience of visiting the patient.
Phase 3 interviews focused on care after dis-
charge from hospital.
Analysis
Survey data was analysed using SPSS version
12.0 and STATA version 8. We dichotomized
satisfaction items into �excellent� vs. �very good to poor�, because patients who tick �excellent� tend to find no fault with a service.
14 We
undertook multilevel logistic regression
accounting for clustering by site using the
XTLOGIT function in STATA. We adjusted for
age and sex to determine whether the proportion
of patients reporting �excellent� differed in intervention and control sites. It was important
to adjust for age because older people tend to
report higher levels of satisfaction. 15
Because of
the large number of statistical tests undertaken,
the significance level was taken as P < 0.01
rather than the usual P < 0.05. Free text com-
ments at the end of the questionnaire were read
by one of the authors (FS) and key themes were
identified. 16
These indicated the strength of
feeling that respondents had about certain
aspects of their care and elucidated answers
within the structured part of the questionnaire.
The interviews were transcribed verbatim. We
used the first stages of �framework analysis�17 by reading transcripts to identify themes and cod-
ing all transcripts systematically according to the
thematic framework. The way in which different
aspects of having primary angioplasty contrib-
uted to a sense of �feeling fixed� has been pub- lished elsewhere.
12 Here, we report only the
aspects of the qualitative findings which elabo-
rate on the quantitative survey results.
Presentation of results
Three types of results are presented below. First,
the survey data is used to identify differences
between intervention and control sites. Second,
the proportion of survey respondents reporting
�excellent� care is compared for the range of sat- isfaction items to identify poorly perceived
aspects of care. Finally, findings from the inter-
views, and free text comments from the survey,
are used to elaborate on issues raised in the survey
data. We have combined these results within a set
of themes addressing key aspects of care.
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
352
Results
Sample characteristics
Survey
For the survey, 1165 STEMI patients were iden-
tified across all eight sites, of whom 144 did not
meet inclusion criteria (see Fig. 1). Of the 1021
eligible patients, 682 (67%) were recruited into
the study. There was no difference in recruitment
rates between intervention and control sites: 66%
(432 ⁄ 659) vs. 69% (250 ⁄ 362), P = 0.255. Rea- sons for non-recruitment included patient refusal,
patients being missed, or patients being dis-
charged or transferred before nurses could
approach them for consent. Patients who were
recruited were younger than non-recruited
patients (mean age 62 vs. 67, P = 0.001) and a
higher proportion of males was recruited than
females (60% vs. 51%, P = 0.006).
The response rate to the survey was 87%
(595 ⁄ 682) for patients and 86% (418 ⁄ 486) for carers. Questionnaires were completed on aver-
age 4 weeks after admission. There was no
difference in response rates between intervention
and control sites for patients (86% vs. 89%,
P = 0.244). The response rate was similar for
male and female patients (87% vs. 89%,
P = 0.588) but respondents were older than
non-respondents (mean age 62 vs. 59,
P = 0.033). Any statistically significant differ-
ences between patient respondents in interven-
tion and control sites were related to the
standard treatment offered within those sites
(Table 1). That is, patients in intervention sites
were more likely to have primary angioplasty
and be transferred between hospitals.
Interviews
Prior to the survey, we undertook interviews
with ten patients and six carers from interven-
tion sites on average 2 weeks post-admission.
After the survey, we interviewed a further 11
patients at intervention sites and six patients at
control sites who had responded to the survey.
Overall satisfaction
Satisfaction levels with different aspects of care
are displayed in descending order for patients
(Table 2) and carers (Table 3). Overall satisfac-
tion with care was high in both intervention and
control sites, for patients and carers. Although it
appeared that overall satisfaction was higher at
intervention than control sites for both patients
(78% vs. 71% �excellent�) and carers (63% vs. 55% �excellent�), these were not statistically sig- nificantly different (P = 0.074 and P = 0.116
respectively). This was reflected in the open
comments on the questionnaires and in the
qualitative interviews. Both patients and carers
praised the care, with almost one in ten patients
adding additional comments to the question-
naire about how excellent their treatment had
been. During interviews, patients referred to
their treatment as �exceptional� or �first class� and expressed gratitude for the service they had
received.
Recruitment of patients for the patient questionnaire
Critically ill = 57 Cognitive impairment = 13
Unable to understand English = 27
Discharged/transferred = 102 Missed = 18
Refused = 22 No reason given/other = 85
Identified n = 756
Eligible n = 659
Intervention Control
Identified n = 409
Eligible n = 362
Critically ill = 33 Cognitive impairment = 11
Unable to understand English = 3
Discharged/transferred = 25 Missed = 62 Refused = 0
No reason given/other = 25
Recruited n = 432
Responded n = 372
Did not return questionnaire = 60 Recruited n = 250
Responded n = 223
Did not return questionnaire = 27
Figure 1 Flow diagram of patients recruited for the patient questionnaire.
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
353
The way I was treated by the staff from the cleaner
to the doctors was excellent and if private care is
better then I would like to see it (patient 15, survey)
Speed and efficiency
Patients were very satisfied with the time they
waited for treatment, and the efficiency with
which they were treated, with significantly
higher satisfaction levels at intervention than
control sites for both aspects of care [see items
(a) and (d), Table 2]. Again, these high levels of
satisfaction were reflected in the open comments
on the questionnaire and in the qualitative
interviews. During the interviews at intervention
sites, patients and carers expressed amazement
at the short time period between contacting the
emergency services to the completion of treat-
ment. They perceived an efficiency and
�smoothness� in the care provided, and were impressed at the teamwork involved, often
describing how the team were awaiting their
arrival.
This for me was the NHS working at its very best.
From the 999 call to coming out of surgery took
3.5 h (patient 307, survey)
Table 1 Characteristics of respondents to patient and carer surveys
Intervention
% (n ⁄ N) Control
% (n ⁄ N) All
% (n ⁄ N) P
Patients
Male 76% (282 ⁄ 372) 74% (165 ⁄ 223) 75% (447 ⁄ 595) 0.633* Mean age (range, SD) 63.1 (25–92, 12.04) 61.34 (25–92, 12.02) 62.4 (25–92, 12.05) 0.098
�
Primary angioplasty received 92% (341 ⁄ 372) 5% (12 ⁄ 223) 59% (353 ⁄ 595) <0.001* Admission �in hours� 39% (116 ⁄ 297) 38% (78 ⁄ 203) 39% (194 ⁄ 500) 0.886* Transfer to second hospital 28% (101 ⁄ 366) 6% (13 ⁄ 215) 20% (114 ⁄ 581) <0.001*
Carers
Male 22% (59 ⁄ 263) 19% (28 ⁄ 147) 21% (87 ⁄ 410) 0.421* Mean age (range, SD) 55 (16–85, 14.06) 57 (22–90, 13.2) 56 (16–90, 13.8) 0.106
�
Living with patient 82% (216 ⁄ 262) 86% (127 ⁄ 148) 84% (343 ⁄ 410) 0.376*
*Chi-square. �Student t-test.
Table 2 Patient satisfaction with hospital treatment for a heart attack (% rating each aspect of care as �excellent�)
Intervention
% (n ⁄ N) Control
% (n ⁄ N) Adjusted odds
ratio (95% CI)* P-value
(a) Efficiency with which you were treated 83% (305 ⁄ 369) 74% (162 ⁄ 219) 1.72 (1.14, 2.59) 0.009 (b) Professional skill and ability of doctors and nurses 81% (297 ⁄ 368) 73% (161 ⁄ 221) 1.50 (1.10, 2.24) 0.052 (c) Overall experience of being treated for a heart attack 78% (287 ⁄ 367) 71% (155 ⁄ 218) 1.42 (097, 2.09) 0.074 (d) Time waited before having treatment 80% (292 ⁄ 364) 67% (148 ⁄ 219) 2.17 (1.45, 3.22) 0.001 (e) Confidence in doctors and nurses treating you 75% (278 ⁄ 369) 69% (151 ⁄ 219) 1.32 (0.86, 2.03) 0.549 (f) Confidence in the treatment received 71% (263 ⁄ 370) 61% (134 ⁄ 218) 1.52 (1.06, 2.17) 0.022 (g) Explanations given about what was wrong with you 56% (206 ⁄ 365) 50% (109 ⁄ 220) 1.18 (0.68, 2.03) 0.549 (h) Ease and convenience for friends and family to visit 54% (196 ⁄ 363) 51% (111 ⁄ 219) 1.12 (0.80, 1.58) 0.502 (i) Explanations given of risks & benefits of treatment 47% (170 ⁄ 361) 44% (96 ⁄ 216) 1.07 (0.70, 1.62) 0.750 (j) Time spent waiting to be discharged from hospital 38% (115 ⁄ 306) 46% (84 ⁄ 182) 0.77 (0.51, 1.55) 0.205 (k) Involvement in decisions about treatment 37% (133 ⁄ 357) 32% 70 ⁄ 216) 1.23 (0.75, 2.01) 0.409 (l) Information about medication & potential side-effects 34% (104 ⁄ 308) 38% (69 ⁄ 183) 0.81 (0.54, 1.23) 0.322 (m) Support and follow-up provided once left hospital 36% (108 ⁄ 300) 32% (56 ⁄ 175) 1.04 (0.62, 1.75) 0.873 (n) Information given about how to manage condition
in future
25% (78 ⁄ 311) 30% (55 ⁄ 182) 0.68 (0.47, 0.99) 0.049
*Adjusted for patient age and sex.
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
354
The speed ⁄ efficiency of (transfer hospital) sending me to the (intervention hospital) who, in turn,
dealt with me with such speed that I was in the
door, up the lift and straight into theatre – bril-
liant! (patient 242, survey)
Convenience of care
Carers in general had lower levels of satisfac-
tion with convenience of visiting than for other
aspects of care [see items (h) and (i), Table 3].
There was no difference between intervention
and control sites in proportions rating conve-
nience of visiting as �excellent� for either patients [see item (h), Table 2] or carers [item
(h), Table 3]. However, the distribution of
satisfaction for this variable for carers was
different than for other variables, with a large
proportion of carers rating convenience of
hospital for visiting as fair or poor. A higher
proportion of carers rated convenience of vis-
iting the hospital as �poor� at intervention than control sites (12% (30 ⁄ 257) vs. 1% (2 ⁄ 143) �poor�, P = 0.001). During the qualitative interviews with carers from intervention sites,
concerns were raised about the prohibitive cost
of parking facilities and worries about travel-
ling long distances, especially at night. How-
ever, carers also reported that they were
willing to accept this inconvenience in the
context of the life-saving nature of primary
angioplasty.
I think it�s a good thing he was brought there you know, I think if he had gone to his local hospital
then he mightn�t, you know, I wouldn�t rate his chances to be honest (carer 5, phase 1 interview)
Discharge and aftercare
Satisfaction levels with hospital discharge pro-
cedures and aftercare were notably lower than
for other aspects of care for both intervention
and control sites [see items (j), (l), (m) and (n),
Table 2]. Patient satisfaction with information
about how to manage the condition in future
was lower in intervention than control sites
although this was not statistically significant at
the 0.01 level (P = 0.049). This was explored
further in �phase 3� qualitative interviews where patients explained how they spent a long time
waiting for hospital discharge, often involving
several hours waiting for drugs from the phar-
macy. They also felt there was a lack of consis-
tency regarding follow-up care and advice.
Patients discussed how they found it difficult to
absorb information about the drugs they were
taking and future management of their condi-
tion during the hospital stay immediately fol-
lowing their heart attack. Some reported
anxiety, when they suffered side-effects from
their medication because they did not know
what was �normal� and what might be a warning sign of something more serious, particularly if
they felt that they had not received adequate
Table 3 Carer satisfaction with hospital treatment for a heart attack (% rating each aspect of care as �excellent�)
Intervention
% (n ⁄ N) Control
% (n ⁄ N) Adjusted odds
ratios (95% CI)* P-value
(a) Professional skill and ability of doctors & nurses 75% (198 ⁄ 265) 66% (98 ⁄ 149) 1.31 (0.63, 2.71) 0.468 (b) Confidence in doctors & nurses treating patient 68% (181 ⁄ 265) 65% (97 ⁄ 149) 0.99 (0.49, 2.23) 0.985 (c) Overall impression of treatment & care in hospital 63% (167 ⁄ 263) 55% (81 ⁄ 147) 1.50 (0.90, 2.49) 0.116 (d) Reassurance and support offered 60% (158 ⁄ 265) 55% (82 ⁄ 144) 1.20 (0.70, 2.06) 0.503 (e) Confidence in the treatment received 59% (157 ⁄ 265) 53% (79 ⁄ 147) 1.10 (0.55, 2.22) 0.783 (f) Information you were given about what was
happening to patient
49% (130 ⁄ 263) 43% (64 ⁄ 149) 1.23 (0.71, 2.14) 0.462
(g) Opportunity to ask doctors and nurses questions 51% (135 ⁄ 266) 37% (55 ⁄ 149) 1.79 (1.06, 3.01) 0.028 (h) Convenience of hospital for you to visit patient 28% (72 ⁄ 261) 34% (50 ⁄ 145) 0.72 (0.46, 1.12) 0.149 (i) Visiting times 30% (77 ⁄ 258) 31% (46 ⁄ 148) 0.93 (0.54, 1.60) 0.799 (j) Facilities available to visitors 28% (71 ⁄ 254) 19% (28 ⁄ 144) 1.61 (0.93, 2.78) 0.089
*Adjusted for carer age and sex.
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
355
follow-up. When people had received aftercare
they were happy with it, but some patients
reported not receiving aftercare, or receiving it
too late after discharge.
I felt I could have done with more [support]. There
were lots of small things that worried me, the
things that didn�t seem enough to ask my GP about really (patient 123, interview)
For the intervention sites, problems with
aftercare may have been exacerbated by speedier
discharge or transfer back to a feeder hospital
before medication and rehabilitation procedures
had been fully explained.
There was not enough time to inform me about
medication etc. as the ambulance was waiting to
take me back to (transfer hospital) (patient 321,
survey)
Discussion
Patients and carers found care at primary
angioplasty hospitals as acceptable as throm-
bolysis-based care. There were a few differences
between the two types of care, and differences
mainly favoured primary angioplasty hospitals.
A key exception was carer satisfaction with the
convenience of travelling to visit the patient.
This is a potential problem when services are
centralized and indeed appeared to be a problem
for primary angioplasty. However, qualitative
interviews with carers identified that carers were
willing to accommodate this inconvenience in
the context of the life-saving treatment of the
patient.
Another potential concern was about infor-
mation offered to patients about how to manage
the problem in the future. Shorter lengths of stay
associated with primary angioplasty may affect
the ability of staff to inform patients about after
care due to the shorter length of stay associated
with primary angioplasty. 18
As well as identify-
ing differences between patients and carers
receiving two types of care, the survey also
showed that patients and carers at both inter-
vention and control sites were highly satisfied
with many aspects of emergency treatment for
STEMI, with the exception of hospital discharge
and aftercare.
A recent Department of Health policy review
cites patient experience as the most important
lever for service improvement in the NHS and
there is a strong drive towards using outputs
from patient and public involvement activity in
influencing service planning and develop-
ment. 19,20
However, relatively little research has
been undertaken to date on patient views of
primary angioplasty which could influence ser-
vice delivery. Patient satisfaction with elective
angioplasty in the United States has been found
to be high, although the experience of elective
angioplasty is likely to be different from that of
primary angioplasty. 9 Recent studies of patient
views of primary angioplasty in the UK both
found that patients undergoing primary angio-
plasty were very positive about their experiences
and also support our concerns about the infor-
mation needs of these patients for their after-
care. 21–23
Radcliffe et al. found that experiences
of aftercare were varied and some patients still
had unanswered questions when interviewed,
being particularly disappointed with their fol-
low-up in primary care. 23
Astin et al. reported
some misconceptions around the perception of
what had happened and the seriousness of the
condition and advocate further patient educa-
tion post-discharge. 22
It is important to consider the information
needs of primary angioplasty patients because
patient satisfaction with medical treatment and
information are associated with improved
physical and mental health related quality of life
in patients with angina pectoris. 24
In particular,
advice on how to improve health is associated
with improved physical health, 24
demonstrating
the importance of adequate information and
access to cardiac rehabilitation services.
Strengths and limitations
Recent UK Department of Health policy advo-
cates finding new ways to measure patient
experience. 25
The use of both qualitative and
quantitative methods allowed us to achieve a
more comprehensive understanding of patient
and carer views than one method alone. The
qualitative component allowed us to explore
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
356
issues that were salient to participants, whilst the
survey allowed us to identify differences between
intervention and control sites. A recent editorial
highlights the dangers of reporting �superficial assessments of service users� opinions�, as overall positive experiences can mask important con-
cerns with aspects of service provision. 26
In our
phase one interviews, we indeed found that
patients were initially reluctant to criticize the
service due to their generally excellent experience
and gratitude at receiving life-saving treatment,
although some negative aspects were very briefly
mentioned. We then undertook a survey using a
specific, wide ranging list of items and indeed
identified some aspects of care that patients and
carers were unhappy with, whilst being generally
very satisfied with care. The second set of
interviews then allowed us to probe further into
these negative aspects.
Whilst our study supported that of other
studies looking at the patient experience of
primary angioplasty, we were able to attribute
some of the findings to the new service itself,
rather than solely the experience of having being
treated for a heart attack as we included patients
from a �control� group who had received mainly thrombolysis. The survey was based on a large
sample of patients from four intervention and
four control sites with a high response rate
(87%), suggesting little effect of any non-
response bias. However, although recruitment
rates for the survey were reasonable (67%),
nearly two-fifths of patients who were not
recruited were missed because they were trans-
ferred or discharged early. We may therefore
have underrepresented the views of transfer
patients who were repatriated back to their
original hospital within the intervention group.
Also, a large number of comparisons have been
tested statistically and at least one may have
occurred by chance. Further, this was an
observational study, and sites were not ran-
domized to be intervention or control. Therefore
differences found between sites may be related to
characteristics of the sites other than the main
type of care offered. Finally, intervention sites
were self-selected and therefore keen to provide
an innovative service. It is possible that patients
at sites offering primary angioplasty in the future
may have a less positive experience than those at
these �early implementer� sites.
Implications for practice
Hospitals can offer primary angioplasty without
being concerned about adversely affecting
patient or carer satisfaction. However, they will
need to ease the added burden of travel for
carers by informing them of travel reimburse-
ment schemes and the availability of overnight
accommodation. Additionally, the information
needs of primary angioplasty patients need to be
taken more seriously. In fact the last stages of
care need attention regardless of the type of
treatment offered in a hospital, particularly
given the drive to reduce length of stay and
expedite discharge for patients post-STEMI.
The discharge and aftercare of STEMI patients
requires considerable attention to increase
satisfaction levels to those with earlier parts of
care.
Conclusions
Reorganization of care to offer a primary
angioplasty service was acceptable to patients
and their carers with the exception of conve-
nience of visiting the hospital for carers, and
information needs of patients about how to
manage their condition in the future. Satisfac-
tion levels were high regardless of the type of
care received, with the exception of discharge
and aftercare.
Acknowledgements
We would like to thank all of the patients and
their carers who took part in interviews and
completed questionnaires as well as the hospital
staff who helped to recruit them. We would also
like to thank Kathryn Paulucy for clerical
assistance.
Conflicts of interest
No conflicts of interest have been declared.
Patient and carer satisfaction with primary angioplasty, F C Sampson, A O�Cathain and S Goodacre
� 2010 The Authors. Health Expectations � 2010 Blackwell Publishing Ltd Health Expectations, 13, pp.350–358
357
Source of funding
This article presents independent research com-
missioned by the UK National Institute for
Health Research Service Delivery and Organi-
zation Programme. The views expressed in this
publication are those of the authors and not
necessarily those of the NHS, the NIHR or the
Department of Health.
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