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Gender Differences in Clinical Outcomes After

Percutaneous Coronary Intervention—Analysis of


15,106 Patients from the Cardiac Registry of Pakistan
Database
Ghazal Peerwani, MSca, Saud Munib Khan, MBBSb, Mustafa Dilawar Khan, MBBSb,
Faiza Bashir, MBBSb, Sana Sheikh, MSca, David J. Ramsey, PhDc,d, Saba Aijaz, MBBS, FCPSa,e,
Zainab Samad, MD, MSf, Rehan Malik, MBAa, Bashir Hanif, MDe, and Salim S. Virani, MD, PhDc,d,*

There is a scarcity of data on gender differences in outcomes during and after percutane-
ous coronary intervention (PCI) in the South Asian population. We assessed the gender
differences in in-hospital mortality and complications in patients who underwent PCI. We
conducted a cross-sectional study of 15,106 patients from the CROP (Cardiac Registry of
Pakistan) CathPCI database. Logistic regression was used to determine factors associated
with in-hospital mortality (primary outcome), access site hematoma, and bleeding compli-
cations. Approximately 19.6% were women. Women were older (mean age = 57.3 vs 54.4
years) and had a higher prevalence of diabetes (49.3% vs 32.6%), hypertension (72.8% vs
56.4%), peripheral arterial disease (1.5% vs 1%), and cerebrovascular accident (1.2% vs
0.8%) than men (p <0.05).Unadjusted in-hospital mortality was higher in women than in
men (odds ratio [OR]: 1.6, 95% confidence interval [CI] 1.1 to 2.2); however, after adjust-
ing for age, hypertension, diabetes, history of cerebrovascular accident, and ST-elevation
myocardial infarction at presentation in the multiple logistic regression model, in-hospital
mortality was comparable between men and women (adjusted OR [AOR] 1.2, 95% CI 0.8
to 1.7). The results remained consistent after propensity score matching of 5,904 patients
(2,952 in each group, OR 1.3, 95% CI 0.9 to 2.0 for in-hospital mortality). Bleeding compli-
cations (1.2% vs 0.4%, AOR 2.6, 95% CI 1.4 to 4.5) and access site hematoma (2% vs
0.6%, AOR 2.8, 95% CI 1.8 to 4.5) were higher in women than in men. In conclusion, the
incidence of in-hospital mortality was higher for women versus men, but adjusted risks
were similar, likely driven by a greater co-morbidity burden among women. Published
by Elsevier Inc. (Am J Cardiol 2023;188:61−67)

Worldwide, 1/3 of all deaths in women are attributed differences in hormones might also play a role in this
to cardiovascular diseases.1 Women with cardiovascular disparity.7 Finally, barriers in healthcare access because of
disease have a worse prognosis and higher mortality social or cultural norms, out-of-pocket health expenditures,
than men.2,3 This gender disparity also extends to and delayed treatment in women because of more atypical
patients with acute coronary syndrome who have under- presentation can also attribute to worse post-PCI outcomes
gone percutaneous coronary intervention (PCI). Findings in women, especially in low- and middle-income coun-
from US National CathPCI registry suggest higher unad- tries.7 There is a scarcity of large-scale studies highlight-
justed in-hospital mortality (1.7% vs 1.1%) and post- ing the gender differences in presentation and post-PCI
PCI complications (8.3% vs 5.4%) in women than in outcomes in the South Asian (SA) population. Delayed
men.4 Factors explaining this disparity in post-PCI out- presentation and limited healthcare access in this region of
comes between men and women include older age and the world can be exaggerated in women compared with
higher baseline risk in women.4−6 In addition, the men because of sociocultural barriers. To study this possi-
inherent biologic differences, including differences in ble gender disparity, we aimed to determine the gender
gene expressions that affect cardiovascular functions or differences in in-hospital mortality and complications in
patients who underwent PCI and captured in the CROP
a
Departments of Clinical Research Cardiology; bMedical College, (Cardiac Registry of Pakistan). We also explored factors
Ziauddin University, Karachi, Pakistan; cMichael E. DeBakey Veterans associated with in-hospital mortality and other post-PCI
Affairs Medical Center, Houston, Texas; dDepartment of Medicine, Baylor complications.
College of Medicine, Houston, Texas; eClinical Cardiology, Tabba Heart
Institute, Karachi, Pakistan; and fDepartment of Medicine, Aga Khan Uni-
versity, Karachi, Pakistan. Manuscript received July 8, 2022; revised manu- Methods
script received and accepted November 10, 2022.
Funding: none. The data on 15,106 patients were extracted from the
See page 66 for disclosure information. CROP CathPCI database, which includes 25 facilities from
*Corresponding author: Tel: 713-440-4410; fax: 713-748-7359. the 3 provinces of Pakistan, including Sindh, Khyber
E-mail address: virani@bcm.edu (S.S. Virani). Pakhtunkhwa, and Punjab. The database started in 2016 at

0002-9149/Published by Elsevier Inc. www.ajconline.org


https://doi.org/10.1016/j.amjcard.2022.11.020
62 The American Journal of Cardiology (www.ajconline.org)

the Tabba Heart Institute, and with the collaborative efforts patients (2,952 in each group). Once the 2 groups were well
of the Pakistan Society of Interventional Cardiology and matched, we evaluated whether the primary outcome (in-
Health Research Advisory Board, it is expanding. Standard- hospital mortality) was significantly different between the 2
ized data collection is ensured at each facility and gathered groups.
every 3 weeks in the CROP registry. Data quality is main- Ethical approval was obtained from the Tabba Heart
tained by real-time data checks built into the online data Institute Institutionalized Review Board: THI/IRB/SQ/10-
collection system. 11-2021/091.
Patients aged >18 years with coronary artery disease
(CAD) who underwent coronary intervention at CROP
Results
operating facilities during 2016 to 2019 were included in
this study. Our results included 15,106 patients from the CROP
Our outcomes of interest of this study included in-hospi- CathPCI database. Of these, 12,150 were men (80.4%) and
tal mortality (primary outcome), hematoma, and any bleed- 2,956 were women (19.6%). Baseline characteristics by
ing complications after PCI. Hematoma was defined as gender are described in Table 1. Women were significantly
≥5 cm of blood collection at the percutaneous entry site older than men (mean age = 57.3 vs 54.4 years). Traditional
within 72 hours of PCI.8,9 Likewise, bleeding complication risk factors, including hypertension (72.8% vs 56.4%), dia-
was defined as a decrease in hemoglobin ≥4 g/100 ml or betes (49.3% vs 32.6%), history of CVA (1.2% vs 0.8%),
blood transfusion or intervention to stop or reverse bleeding and peripheral arterial disease (1.5% vs 1.0%) were more
within 72 hours of the procedure.8 Data were also extracted prevalent in women than in men (p <0.05). In contrast,
on patients’ demographic characteristics, history of co-mor- tobacco use (36.9% vs 6.9%), history of MI (27.1% vs
bidities, procedural characteristics and signs, and symptoms 20.8%), previous PCI (8.9% vs 6.7%), and family history of
at presentation and were used as explanatory variables. premature CAD (16.2% vs 14.5%) were more frequent in
We report baseline characteristics for all variables in the men than in women (p <0.05 for all). No significant differ-
form of frequency (percentage) for categorical variables ences were noted between men and women in terms of the
and mean § SD for quantitative variables. Chi-square/ history of heart failure, dyslipidemia, previous coronary
Fischer’s exact tests and independent sample Student’s t artery bypass grafting or valve surgery, dialysis, atrial fibril-
test were used to assess the difference between categorical lation/flutter, and chronic lung disease (p >0.05 for all).
and quantitative variables between men and women. After Coronary angiography findings showed that women
evaluating raw frequencies, we performed multivariable were more likely to have more nonobstructive or single-
logistic regression to determine whether the female gender vessel disease, whereas men were more likely to have 2- or
was independently associated with in-hospital mortality 3-vessel disease; however, the difference was not signifi-
(primary outcome), hematoma, and bleeding complications. cant (p >0.05). PCI indications did not significantly differ
For each of the regression analyses, a prespecified set of between men and women (p >0.05).
baseline variables including age, hypertension, diabetes Table 2 describes periprocedural and postprocedural out-
mellitus, use of tobacco, history of cerebrovascular accident comes among men and women. Significantly higher unad-
(CVA), previous myocardial infarction (MI), and ST-eleva- justed in-hospital mortality was noted in women (1.7%)
tion MI (STEMI) were added into the model. These varia- than in men (1.1%) (p <0.05). The need for coronary artery
bles were selected based on significance on univariate bypass grafting after PCI and dialysis were significantly
analysis and their clinical significance. We also performed more in men than in women (p <0.05). Hemodynamic
sensitivity analyses in patients with premature CAD (those instability during or after PCI was more common in women
aged <50 years). There were sufficient numbers of out- (8.4%) than in men (6.2%). Similarly, overall bleeding
comes in the overall model to adjust for baseline factors; complications (1.2% vs 0.4%), access site hematoma (2%
however, in the premature group, the model was statisti- vs 0.6%), and the need for transfusion (1% vs 0.5%) were
cally less robust because of the lower numbers of outcomes. also more frequent in women. The need for intra-aortic bal-
Crude and adjusted odds ratios (ORs), along with 95% con- loon pump, coronary perforation, cardiac arrest, arrhyth-
fidence intervals (CIs) were reported for the covariates in mias, cardiogenic shock, periprocedural MI, stroke, stent
each multivariable regression model. thrombosis, gastrointestinal, genitourinary, and retroperito-
To account for the baseline differences between men and neal bleeding did not significantly differ between women
women, we also performed propensity score matching as and men (p >0.05) (Table 2, Figure 1).
part of the sensitivity analyses. The following covariates Although unadjusted in-hospital mortality was higher in
were matched between men and women: age, tobacco use, women than men (1.6, 1.1 to 2.2), this association became
previous heart failure, family history of premature CAD, nonsignificant after the adjustment. In the multivariable-
dyslipidemia, hypertension, diabetes mellitus, peripheral adjusted models (Table 3), in-hospital mortality was com-
arterial disease, previous CVA, previous MI, previous PCI, parable between men and women (OR: 1.2, 95% CI: 0.8 to
previous coronary artery bypass grafting, previous valve 1.7) after adjusting for age, presence of diabetes mellitus,
surgery, currently on dialysis, coronary angiography find- presence of hypertension, history of CVA, and STEMI at
ings, left main artery disease, right CAD, left anterior presentation (Table 3).
descending artery disease, left circumflex artery disease, After propensity score matching, the baseline variables
disease in ramus intermedius, and PCI indication. The 2 were well balanced between the groups (Supplementary
groups of men and women were matched 1:1 using a caliper Table 1). We successfully matched 5,904 patients (2,952 in
of 0.02, resulting in the successful matching of 5,904 each group of men and women). The odds of in-hospital
Coronary Artery Disease/Gender Differences in Outcomes After PCI 63

Table 1
Comparison of baseline characteristics between men and women
Characteristics Women Men p Value
n (%) n (%)
2956 (19.6%) 12150 (80.4%)
Age* 57.3 § 10.56 54.4§10.7 <0.001
Tobacco use 205 (6.9%) 4478 (36.9%) <0.001
Prior heart failure 95 (3.2%) 291 (2.4%) NS
Family history of premature CAD 427 (14.5%) 1967 (16.2%) <0.001
Dyslipidemia 600 (20.3%) 2524 (20.8%) NS
Hypertension 2151 (72.8%) 6856 (56.4%) <0.001
Diabetes mellitus 1456 (49.3%) 3962 (32.6%) <0.001
Peripheral arterial disease 43 (1.5%) 123 (1%) 0.04
Prior cerebrovascular accident 34 (1.2%) 92 (0.8%) 0.04
Prior MI 615 (20.8%) 3291 (27.1%) <0.001
Prior PCI 197 (6.7%) 1079 (8.9%) <0.001
Prior CABG 52 (1.8%) 278 (2.3%) NS
Prior valve surgery 16 (0.5%) 48 (0.4%)
Currently on dialysis 17 (0.6%) 81 (0.7%) NS
Coronary angiography
None 52 (1.8%) 170 (1.4%) NS
Single vessel 1458 (49.3%) 5775 (47.5%)
2 vessels 927 (31.3%) 2230 (18.4%)
3 vessels 519 (17.6%) 3975 (32.7%)
Left main artery disease 50 (1.7%) 249 (2.1%) NS
Right coronary artery disease 1343 (45.4%) 5515 (45.4%) NS
Left anterior descending artery disease 1504 (50.9%) 6239 (51.4%) NS
Left circumflex artery disease 1102 (37.3%) 4706 (38.7%) NS
Disease in ramus intermedius 33 (1.1%) 329 (2.7%) <0.001
PCI indication
Immediate STEMI 410 (14%) 1893 (15.7%) NS
STEMI unstable >12 hours 45 (1.5%) 231 (1.9%)
STEMI stable >12 hours 536 (18.3%) 2091 (17.3%)
STEMI stable after thrombolytic 68 (2.3%) 317 (2.6%)
After failed thrombolytic 18 (0.6%) 95 (0.8%)
NSTEMI/unstable angina 1426 (48.7%) 5767 (47.7%)
Staged PCI 106 (3.6%) 362 (3.0%)
Other 321 (11.0%) 1332 (11.0%)
CABG = coronary artery bypass graft; CAD = coronary artery disease; MI = myocardial infarction; NS = nonsignificant; NSTEMI = non-ST elevation myo-
cardial infarction; PCI = percutaneous coronary intervention; STEMI = ST elevation myocardial infarction.
* Mean § standard deviation.

mortality in the propensity matched sample remained non- p >0.05). Post-PCI complications, including perforation,
significant between men and women (OR 1.3, 95% C: 0.9 hemodynamic instability, hematoma at the access site, and
to 2.0). bleeding complications, were comparable between men and
Age and women gender were independently associated women aged <50 years (p >0.05) (Figure 1).
with post-PCI bleeding complications and hematoma at the History of CVA (13.7, 1.5 to 127.6) and STEMI (9.9, 3.8
access site (Table 3). to 25.6) at presentation were independently associated with
in-hospital mortality in patients aged <50 years (Table 5).
Female gender was not significantly associated with in-hos-
Premature CAD (<50 years)
pital mortality (1.8, 0.5 to 5.9) or bleeding complications
Traditional risk factors, such as hypertension (66.1% vs (2.0, 0.3 to 11.2) in the multivariable-adjusted models;
49.2%), diabetes (43.3% vs 26.4%), and previous heart fail- however, it was associated with access site hematoma
ure (3.7% vs 2.3%), were more common in young women because women were 6.8 times (1.7 to 27.2) more likely to
than in young men (p <0.001). In contrast, tobacco use and develop hematoma at the access site than men.
previous MI were more prevalent in men than in women (p
<0.001). Significant differences were seen in PCI indication
Discussion
between men and women; STEMI (immediate, unstable,
stable) was common in men, whereas non-STEMI was In the present study, we found a higher in-hospital mor-
common in women (p <0.001). No significant differences tality in women than in men. This increase in mortality
were seen between men in women regarding other baseline could be explained by baseline differences between men
characteristics (Table 4). and women. In the risk-adjusted analysis, women were
There was no significant difference in immediate in-hos- twice as likely to have post-PCI bleeding complications and
pital mortality between men and women (0.6% vs 0.6%, thrice as likely to have hematoma at the access site.
64 The American Journal of Cardiology (www.ajconline.org)

Table 2
Comparison of periprocedural and postprocedural mortality and complications between women and men
Characteristics Women Men p Value
n (%) n (%)
2956 (19.6%) 12150 (80.4%)
In-hospital mortality 50 (1.7%) 132 (1.1%) <0.001
Need for intra-aortic balloon pump 6 (0.7%) 20 (0.6%) NS
Coronary dissection during PCI 59 (2.1%) 212 (1.8%) NS
Coronary perforation during PCI 7 (0.2%) 28 (0.2%) NS
Abrupt coronary artery closure 13 (0.5%) 40 (0.3%) NS
No reflow during PCI 88 (3.1%) 306 (2.6%) NS
Hemodynamic instability during or after PCI 65 (8.4%) 174 (6.2%) 0.03
Arrhythmias during or after PCI 34 (1.4%) 119 (4.2%) NS
Cardiac arrest during or after PCI 20 (2.6%) 61 (2.2%) NS
Need for CABG 6 (0.2%) 66 (0.5%) 0.02
Cardiogenic shock during or after PCI 37 (2.9%) 112 (2.3%) NS
Stent thrombosis 5 (0.3%) 16 (0.2%) NS
Periprocedural myocardial infarction 5 (0.3%) 26 (0.5%) NS
Need for dialysis after PCI 1 (0.1%) 23 (0.5%) 0.04*
Stroke after PCI 3 (0.1%) 3 (0.02%) NS*
Cardiac Tamponade 1 (0.1%) 5 (0.1%) NS*
Bleeding within 72 hours of the PCI 23 (1.2%) 34 (0.4%) <0.001
Need for blood transfusion after PCI 21 (1%) 38 (0.5%) <0.001
Access site hematoma after PCI (within 72 hours) 40 (2%) 50 (0.6%) <0.001
NS = nonsignificant p >0.05; PCI = percutaneous coronary intervention.
* Fischer’s exact test.

The unadjusted in-hospital mortality during or after PCI Data from 8,771 patients who underwent PCI in the registry
was significantly higher in women than in men; however, of Blue Cross Blue Shield of Michigan Cardiovascular
after adjusting for age, diabetes, hypertension, peripheral Consortium showed higher unadjusted in-hospital mortality
arterial disease, history of CVA, and STEMI at presenta- (OR 1.8, 95% CI 1.5 to 2.2) in women, but after adjusting
tion, the in-hospital mortality became comparable. The for risk factors, no difference was seen between both gender
findings of our study extend to the results of other studies. in early mortality.10 Studies from United States and

Figure 1. Comparison of clinical outcomes between men and women with CAD and premature CAD. CABG = coronary artery bypass grafting.
Coronary Artery Disease/Gender Differences in Outcomes After PCI 65

Table 3
Factors associated with in-hospital mortality, bleeding complications, and hematoma at access site after multivariable logistic regression analyses
Characteristics In-hospital mortality Bleeding complications Hematoma at access site
AOR (95% CI) (within 72 hours of PCI) AOR (95% CI)
AOR(95% CI)
Women 1.2 (0.8−1.7) 2.6 (1.4−4.5)* 2.8 (1.8−4.5)*
Age 1.04 (1.03−1.05)* 1.04 (1.01−1.07)* 1.04 (1.02−1.06)*
Hypertension 1.5 (1.1−2.1)* 1.1 (0.6−2.1) 0.8 (0.5−1.3)
Tobacco use 0.9 (0.6−1.4) 1.1 (0.6−2.1) 0.8 (0.4−1.4)
Diabetes mellitus 1.6 (1.2−2.2)* 1.04 (0.6−1.8) 0.9 (0.6−1.4)
Prior CVA 3.5 (1.6−7.6)* 3.2 (0.7−2.4) 1.05 (0.1−7.6)
Prior MI 0.8 (0.5−1.2) 1.3 (0.7−2.4) 1.1 (0.6−1.7)
STEMI at presentation 5.3 (3.8−7.4)* 1.28 (0.7−2.4) 0.7 (0.4−1.2)
AOR = adjusted odds ratio; CI = confidence interval; CVA = cerebrovascular accident; MI = myocardial infarction; STEMI = ST elevation myocardial
infarction.
* Significant (p <0.05).

Germany replicated similar results.4,11,12 Gender-related a higher burden of modifiable risk factors. In addition, after
differences in unadjusted in-hospital mortality during or propensity score matching, the difference in-hospital mor-
after PCI, as hypothesized by various studies, can be due to tality between men and women remained nonsignificant.
the older age of women at presentation and increased bur- In the SA context, there might be other sociocultural fac-
den of modifiable risk factors, including diabetes and tors that can influence the difference in mortality between
hypertension.13,14 This was also observed in our study men and women. Possible factors include delayed treat-
because women were significantly older than men and had ment, limited access to healthcare, and health-seeking

Table 4
Comparison of baseline characteristics of men and women with premature coronary artery disease (<50 years) (n = 4481)
Characteristics Women Men p Value
n (%) n (%)
631 (14.1%) 3850 (85.9%)
Age* 42.7 § 5.1 42.3 § 5.3 NS
Tobacco use 61 (9.7%) 1731 (45.0%) <0.001
Prior heart failure 23 (3.7%) 89 (2.3%) 0.04
Family history of premature CAD 117 (18.5%) 842 (21.9%) NS
Dyslipidemia 106 (16.8%) 730 (19.0%) NS
Hypertension 417 (66.1%) 1894 (49.2%) <0.001
Diabetes mellitus 273 (43.3%) 1015 (26.4%) <0.001
Peripheral arterial disease 9 (1.4%) 32 (0.8%) NS
Prior cerebrovascular accident 2 (0.3%) 16 (0.4%) NSy
Prior MI 155 (24.6%) 1212 (31.5%) <0.001
Prior PCI 27 (4.3%) 231 (6%) NS
Prior CABG 7 (1.1%) 28 (0.7%) NS
Prior valve surgery 2 (0.3%) 12 (0.3%) NSy
Currently on dialysis 1 (0.2%) 19 (0.5%) NSy
Coronary angiography
None 6 (1.0%) 39 (1.0%) NS
Single vessel 358 (56.7%) 2125 (55.2%)
2 vessels 179 (28.3%) 1105 (28.7%)
3 vessels 88 (14.0%) 581 (15.1%)
Left main artery disease 12 (1.9%) 37 (1.0%) 0.04
Right coronary artery disease 237 (37.6%) 1578 (40.0%) NS
Left anterior descending artery disease 329 (52.1%) 1917 (50.0%) NS
Left circumflex artery 207 (32.8%) 1269 (33.0%) NS
Disease in ramus intermedius 7 (1.1%) 96 (2.5%) 0.03
PCI indication
Immediate STEMI 64 (10.2%) 630 (16.4%) <0.001
STEMI unstable >12 hours 9 (1.4%) 63 (1.6%)
STEMI stable >12 hours 97 (14.5%) 427 (11.1%)
STEMI stable after thrombolytic 16 (2.6%) 124 (3.2%)
After failed thrombolytic 6 (1%) 27 (0.7%)
NSTEMI/unstable angina 357 (56.9%) 2112 (55.0%)
Staged PCI 17 (2.7%) 110 (3.0%)
Other 57 (10.7%) 346 (9.0%)
CABG = coronary artery bypass graft; CAD = coronary artery disease; MI = myocardial infarction; NS = nonsignificant p >0.05; NSTEMI = non-ST-eleva-
tion myocardial infarction; PCI = percutaneous coronary intervention; STEMI = ST-elevation myocardial infarction.
* Mean § standard deviation.
y
Fischer’s exact test.
66 The American Journal of Cardiology (www.ajconline.org)

Table 5
Factors associated with in-hospital mortality, bleeding complications, and hematoma at access site in patients with premature CAD (<50 years of age) after
multivariable logistic regression analyses.
Characteristics In-hospital mortality Bleeding complications Hematoma at
AOR (95% CI) (within 72 hours of PCI) access site
AOR(95% CI) AOR (95% CI)
Female 1.8 (0.5−5.9) 2.0 (0.3−11.2) 6.8 (1.7−27.2)*
Age 1.0 (0.9−1.1) 1.1 (0.9−1.3) 1.04 (0.9−1.1)
Hypertension 1.1 (0.4−2.6) 2.8 (0.5−14.5) 0.3 (0.07-1.1)
Tobacco use 2.1 (0.9−5.1) 1.1 (0.2−5.0) 2.6 (0.7−10.0)
Diabetes mellitus 0.8 (0.3−2.2) 0.6 (0.1−3.1) 0.5 (0.1−2.6)
Prior CVA 13.7 (1.4−127.5)* - -
Prior MI 1.3 (0.4−3.3) 2.6 (0.6−11.1) 1.7 (0.5−5.7)
STEMI at presentation 9.9 (3.8−25.6)* 1.3 (0.2−6.9) 0.3 (0.03−2.5)
AOR = adjusted odds ratio; CI = confidence interval; CVA = cerebrovascular accident; MI = myocardial infarction; STEMI = ST-elevation myocardial
infarction.
* Significant (p <0.05).

barriers. Gender inequities are deeply rooted and extensive was seen in the risk-adjusted analysis but data are scarce to
gaps exist in education and healthcare, and nutrition.15,16 compare this finding from our study. Because most of the
The gender disparity that occurs in the healthcare system PCI procedures in Pakistan are performed using a femoral
also stems from healthcare-seeking behaviors.17 Unless approach, strategies geared toward a higher uptake of PCI
there is a severe life-threatening situation, women generally using a radial approach could narrow this gender gap in
are not taken to healthcare facilities, resulting in delayed bleeding outcomes.
treatment and increased risk of worst outcomes.17 The fam- Given the observational nature of our analyses, our study
ily usually governs decisions regarding women in SA set- has limitations. The unavailability of some important varia-
tings; hence, in most households, women don’t have the bles, including symptom onset-to-presentation time, door-
autonomy to go to the hospital and seek medical help for to-balloon time, and use of anticoagulants precluded further
themselves, leading to the loss of valuable hours in which assessment of determinants of mortality and bleeding com-
lives can be saved.18 However, further studies are needed to plications in our study. Variability in data reporting by par-
explore the relevance and the relative contribution of vari- ticipating centers across Pakistan, and underestimating or
ous sociocultural factors in determining differences overestimating co-morbidities because of inadequate
between men and women. screening protocols or data capture cannot be ruled out.
In the younger age subsample, previous studies reported The strength of our analyses includes the inclusion of
higher unadjusted and adjusted in-hospital mortality in data from 3 provinces of Pakistan. The findings can be gen-
women than in men (aged ≤55 years),4,6 but our study find- eralizable to other developing countries of South Asia
ings suggest comparable in-hospital mortality in men and because these provide insight into the gender differences in
women aged <50 years, supporting the premise that age PCI outcomes in resource-limited settings. The large sam-
indeed is a major determinant of in-hospital mortality in ple size from the CROP CathPCI Registry is another
both genders. strength of this study.
We found an increased risk of post-PCI complications,
predominantly bleeding and access site hematoma in
women compared with men in both univariate and multivar- Conclusion
iable analyses. This finding is aligned with previous studies
Higher in-hospital mortality was seen in women; how-
that suggested a higher rate of bleeding complications in
ever, the mortality was comparable between men and
women than men across all ages.19,20 The differences in the
women after adjusting for baseline risk factors and co-mor-
use of anticoagulants or antiplatelets, platelet biology,
bidities. Crude and adjusted post-PCI complications, pre-
congestive heart failure, and hypotension might explain this
dominantly bleeding, and access site hematoma were more
disparity;4,21 however, these factors were not explored in
frequent in women than men. There was no significant dif-
our study. Various studies have suggested a 3- to 10-fold
ference in early mortality and complications between men
increase in early mortality because of post-PCI bleeding,
and women in the younger age group except for access site
which might also explain the higher unadjusted mortality in
hematoma. The findings of the study will help guide
women in our study.21,22 The difference in bleeding compli-
patients and clinicians to make appropriate decisions and
cation was not found in the younger subsample in both risk
develop quality improvement initiatives to improve clinical
the unadjusted and adjusted analyses. These findings con-
outcomes.
trast with previous studies because several single- and mul-
ticenter studies suggested increased peri- and post-PCI
vascular and bleeding complications in women compared
Disclosures
with men in the younger age group.4,23,24 The difference
between young men and women in access site hematoma The authors have no conflicts of interest to declare.
Coronary Artery Disease/Gender Differences in Outcomes After PCI 67

Acknowledgments 11. Heer T, Hochadel M, Schmidt K, Mehilli J, Zahn R, Kuck KH, Hamm
C, B€ohm M, Ertl G, Hoffmeister HM, Sack S, Senges J, Massberg S,
The authors would like to acknowledge PharmEvo Pri- Gitt AK, Zeymer U. Sex differences in percutaneous coronary inter-
vention-insights from the coronary angiography and PCI registry of
vate Limited for their logistic support in the CROP (Cardiac the German society of cardiology. J Am Heart Assoc 2017;6:e004972.
Registry of Pakistan) registry. 12. Singh M, Rihal CS, Gersh BJ, Roger VL, Bell MR, Lennon RJ, Ler-
man A, Holmes DR. Mortality differences between men and women
after percutaneous coronary interventions: a 25-year, single-center
Supplementary materials experience. J Am Coll Cardiol 2008;51:2313–2320.
13. Berger JS, Elliott L, Gallup D, Roe M, Granger CB, Armstrong PW,
Supplementary material associated with this article can Simes RJ, White HD, Van de Werf F, Topol EJ, Hochman JS, Newby
be found in the online version at https://doi.org/10.1016/j. LK, Harrington RA, Califf RM, Becker RC, Douglas PS. Sex differen-
amjcard.2022.11.020. ces in mortality following acute coronary syndromes. JAMA
2009;302:874–882.
14. Milcent C, Dormont B, Durand-Zaleski I, Steg PG. Gender differences
in hospital mortality and use of percutaneous coronary intervention in
1. Siemens Healthineers. Women and cardiovascular disease a woman’s acute myocardial infarction: microsimulation analysis of the 1999
heart - unique features of cardiovascular disease in women. Available Nationwide French Hospitals Database. Circulation 2007;115:833–
at: https://www.siemens-healthineers.com/en-in/clinical-specialities/ 839.
womens-health-information/laboratory-diagnostics/women-and-heart- 15. World Bank. Pakistan - country gender assessment: bridging the gen-
disease. Accessed on 5th July, 2022. der gap - opportunities and challenges. Available at: https://ideas.
2. Di Giosia P, Passacquale G, Petrarca M, Giorgini P, Marra AM, Ferro repec.org/p/wbk/wboper/8453.html. Accessed on 5th July, 202.
A. Gender differences in cardiovascular prophylaxis: focus on anti- 16. United Nations Children’s Fund. Multiple indicator cluster survey
platelet treatment. Pharmacol Res 2017;119:36–47. (MICS) 2015. Available at: https://www.unicef.org/kazakhstan/en/
3. Gao Z, Chen Z, Sun A, Deng X. Gender differences in cardiovascular reports/multiple-indicator-cluster-survey-mics-2015. Accessed on 5th
disease. Med Novel Technol Devices 2019;4:100025. July, 2022.
4. Lichtman JH, Wang Y, Jones SB, Leifheit-Limson EC, Shaw LJ, Vac- 17. Rizvi N, S Khan K, Shaikh BT. Gender: shaping personality, lives and
carino V, Rumsfeld JS, Krumholz HM, Curtis JP. Age and sex differ- health of women in Pakistan. BMC Womens Health 2014;14:53.
ences in inhospital complication rates and mortality after percutaneous 18. Qureshi N, Shaikh BT. Women’s empowerment and health: the role of
coronary intervention procedures: evidence from the NCDRÒ . Am institutions of power in Pakistan. East Mediterr Health J
Heart J 2014;167:376–383. 2007;13:1459–1465.
5. Poon S, Goodman SG, Yan RT, Bugiardini R, Bierman AS, Eagle KA, 19. Numasawa Y, Kohsaka S, Miyata H, Noma S, Suzuki M, Ishikawa S,
Johnston N, Huynh T, Grondin FR, Schenck-Gustafsson K, Yan AT. Nakamura I, Nishi Y, Ohki T, Negishi K, Takahashi T, Fukuda K.
Bridging the gender gap: insights from a contemporary analysis of Gender differences in in-hospital clinical outcomes after percutaneous
sex-related differences in the treatment and outcomes of patients with coronary interventions: an insight from a Japanese multicenter regis-
acute coronary syndromes. Am Heart J 2012;163:66–73. try. PLoS ONE 2015;10:e0116496.
6. Radovanovic D, Erne P, Urban P, Bertel O, Rickli H, Gaspoz JM. 20. Wanha W, Kawecki D, Roleder T, Pluta A, Marcinkiewicz K, Mora-
AMIS Plus Investigators. Gender differences in management and out- wiec B, Kret M, Pawlowski T, Smolka G, Ochala A, Wojakowski W.
comes in patients with acute coronary syndromes: results on 20 290 Gender differences and bleeding complications after PCI on first and
patients from the AMIS Plus Registry. Heart 2007;93:1369–1375. second generation DES. Scand Cardiovasc J 2017;51:53–60.
7. Lee CY, Liu KT, Lu HT, Mohd Ali R, Fong AYY, Wan Ahmad WA. 21. Manoukian SV, Feit F, Mehran R, Voeltz MD, Ebrahimi R,
Sex and gender differences in presentation, treatment and outcomes in Hamon M, Dangas GD, Lincoff AM, White HD, Moses JW, King
acute coronary syndrome, a 10 year study from a multi-ethnic Asian SB, Ohman EM, Stone GW. Impact of major bleeding on 30-day
population: the Malaysian national cardiovascular disease database— mortality and clinical outcomes in patients with acute coronary
acute coronary syndrome (NCVD-ACS) registry. PLoS One 2021;16: syndromes: an analysis from the ACUITY Trial. J Am Coll Car-
e0246474. diol 2007;49:1362–1368.
8. Shroff AR, Fernandez C, Vidovich MI, Rao SV, Cowley M, Bertrand 22. Fuchs S, Kornowski R, Teplitsky I, Brosh D, Lev E, Vaknin-Assa H,
OF, Patel TM, Pancholy SB. Contemporary transradial access practi- Ben-Dor I, Iakobishvili Z, Rechavia E, Battler A, Assali A. Major
ces: results of the second international survey. Catheter Cardiovasc bleeding complicating contemporary primary percutaneous coronary
Interv 2019;93:1276–1287. interventions—incidence, predictors, and prognostic implications.
9. Andersen K, Bregendahl M, Kaestel H, Skriver M, Ravkilde J. Hae- Cardiovasc Revasc Med 2009;10:88–93.
matoma after coronary angiography and percutaneous coronary inter- 23. Argulian E, Patel AD, Abramson JL, Kulkarni A, Champney K,
vention via the femoral artery frequency and risk factors. Eur J Palmer S, Weintraub W, Wenger NK, Vaccarino V. Gender differen-
Cardiovasc Nurs 2005;4:123–127. ces in short-term cardiovascular outcomes after percutaneous coronary
10. Jackson EA, Moscucci M, Smith DE, Share D, Dixon S, Greenbaum interventions. Am J Cardiol 2006;98:48–53.
A, Grossman PM, Gurm HS. The association of sex with outcomes 24. Khawaja FJ, Rihal CS, Lennon RJ, Holmes DR, Prasad A. Temporal
among patients undergoing primary percutaneous coronary interven- trends (over 30 years), clinical characteristics, outcomes, and gender
tion for ST elevation myocardial infarction in the contemporary era: in patients ≤ 50 years of age having percutaneous coronary interven-
insights from the Blue Cross Blue Shield of Michigan Cardiovascular tion. Am J Cardiol 2011;107:668–674.
Consortium (BMC2). Am Heart J 2011;161:106–112. e1.

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