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PLOS One logoLink to PLOS One
. 2022 Oct 20;17(10):e0275574. doi: 10.1371/journal.pone.0275574

A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: The global burden of disease study 1990–2019

Amirali Karimi 1,, Parnian Shobeiri 1,, Sina Azadnajafabad 1, Masoud Masinaei 1,2, Negar Rezaei 1,3, Ali Ghanbari 1, Nazila Rezaei 1, Mahtab Rouhifard 1, Sarvenaz Shahin 1, Mohammad-Mahdi Rashidi 1, Mohammad Keykhaei 1,4, Ameneh Kazemi 1, Erfan Amini 5, Bagher Larijani 3, Farshad Farzadfar 1,3,*
Editor: Deepak Dhamnetiya6
PMCID: PMC9584505  PMID: 36264881

Abstract

Introduction

Bladder cancer (BCa) is the second most common genitourinary cancer and among the leading causes of cancer-related deaths. We aimed to assess BCa quality of care (QOC) utilizing a novel multi-variable quality of care index (QCI).

Materials and methods

Data were retrieved from the Global Burden of Disease 1990–2019 database. QCI scores were calculated using four indices of prevalence-to-incidence ratio, Disability-Adjusted Life Years-to-prevalence ratio, mortality-to-incidence ratio, and Years of Life Lost-to-Years Lived with Disability ratio. We used principal component analysis to allocate 0–100 QCI scores based on region, age groups, year, and gender.

Results

Global burden of BCa is on the rise with 524,305 (95% UI 475,952–569,434) new BCa cases and 228,735 (95% UI 210743–243193) deaths in 2019, but age-standardized incidence and mortality rates did not increase. Global age-standardized QCI improved from 75.7% in 1990 to 80.9% in 2019. The European and African regions had the highest and lowest age-standardized QCI of 89.7% and 37.6%, respectively. Higher Socio-demographic index (SDI) quintiles had better QCI scores, ranging from 90.1% in high SDI to 30.2% in low SDI countries in 2019; however, 5-year QCI improvements from 2014 to 2019 were 0.0 for high and 4.7 for low SDI countries.

Conclusion

The global QCI increased in the last 30 years, but the gender disparities remained relatively unchanged despite substantial improvements in several regions. Higher SDI quintiles had superior QOC and less gender- and age-based inequalities compared to lower SDI countries. We encourage countries to implement the learned lessons and improve their QOC shortcomings.

Introduction

Bladder cancer (BCa) is the second most common genitourinary cancer and among the leading causes of cancer-related deaths worldwide [1]. BCa accounted for 5% of the total cancer costs in the European Union, with higher-income countries spending higher budgets on this cancer [2]. Besides the strangulating financial burden, BCa imposes a significant toll on the patients’ quality of life, either by the tumor behavior or the treatment-related adverse events [3]. Urothelial transitional cell carcinoma is the most common histologic type of BCa, followed by squamous cell carcinoma (SCC) and other less prevalent subtypes, all carrying poorer prognosis compared to the urothelial carcinoma [4,5].

Microscopic or gross hematuria is the most common presentation of BCa. At the time of diagnosis, 70% of the patients have non-muscle invasive disease; but during a 5-year period, 50–70% face tumor recurrence and 10–15% will turn into muscle-invasive disease. The other 30% are diagnosed on the muscle-invasive stage that carry an unfavorable prognosis despite aggressive treatments. In many cases, BCa and its recurrences will require a life-long surveillance. All these sophisticated processes require careful care and a considerable amount of budget, emphasizing the role of a well-designed system for its management.

Earlier studies reported an increased BCa incidence, mortality, and Disability-Adjusted Life Years (DALYs) [6,7]. A higher incidence of BCa requires more resource allocations by the healthcare systems [6]. Higher costs might consequently reduce the availability of health services for patients with BCa. Inequalities in allocating facilities and resources have decelerated the global success on fighting this disease [810]. Individuals and countries with lower socio-economic status may suffer more from the complications of BCa compared to higher socio-economic group [8]. Therefore, the Quality of care (QOC) measures should be calculated to analyze and address these inequalities [11]. QOC assures offering skilled and professional services to the patients to achieve the most desirable outcomes [12]. QOC assessment provides essential information on the function of the healthcare systems and visualizes their disparities to allocate quality care to individuals based on their gender, age, and ethnic status [11]. However, previous studies failed to evaluate QOC properly, especially for the BCa [12].

In this study, we aimed to propose the quality of care index (QCI) as a novel multi-variable indicator of QOC. We will compare the QCI scores of various world regions and discuss their age and gender disparities. Visualization of the scores will enable us to discuss the current controversies and hypothesize how to improve QOC. The application of QCI might help healthcare systems establish policies for more proficient and equal resource allocation.

Material and methods

2.1 Design and data resources

We gathered the data from the global burden of disease (GBD) 1990–2019 retrievable from IHME (Institute for Health Metrics and Evaluation) “GBD compare” tool [13]. GBD utilizes the 10th version of International Classification of Diseases (ICD-10) codes C67-C67.9, D09.0, D30.3, D41.4-D41.8, D49.4 for mapping BCa death and C67-C67.9, Z12.6-Z12.79, Z80.52, Z85.51 for mapping BCa new cases (details in S1 Table) [14,15]. The burden and the indices related to the QCI of BCa were then calculated. This study is conducted based on the GATHER (Guidelines for Accurate and Transparent Health Estimates Reporting) guidelines [16].

2.2 Quality of Care Index (QCI) and its validation

We developed this index to examine the healthcare systems’ ability to provide adequate care and access related to diseases. The process and rationale behind QCI development are discussed in the QCI protocol and earlier studies on this index [12,1720]. QCI constitutes four secondary indices discussed below, selected from six primary candidates. The elements of these indices include prevalence, incidence, DALYs, mortality, Years of Life Lost (YLLs), and Years Lived with Disability (YLDs).

PrevalencetoIncidenceratio(x)=Prevalence(x)Incidence(x) (1)
MortalitytoIncidenceratio(MIR)(x)=Mortality(x)Incidence(x) (2)
DALYstoPrevalenceratio(x)=DALYs(x)Prevalence(x) (3)
YLLstoYLDsratio(x)=YLLs(x)YLDs(x) (4)

X represents location (i.e.: countries, regions, or global scale), age group, sex, and year in the above equations.

As a multivariate analysis method, principal component analysis (PCA) is a mathematical approach that combines these abovementioned four secondary indices to create QCI. PCA uses entry datasets and extracts linear combination as orthogonal components [21]. Each of the four mentioned components represents a dimension, and the +200 location data (x) in all the studied 29 years are present in these dimensions. Then PCA uses a four-dimensional transformation of data points (or n-dimensional in other cases) and calculate an eigenvector that covers the highest span on its axis. The eigenvector that best describes the data points’ variance and variability, and hence has the highest discrimination capability, will be the first PCA component and considered as a composite characteristic. As mentioned, the first principal component encompasses the highest correlation with the entry variables and provides the best information. Herein, we named this first principal component as QCI and allocated a score of 0–100 to it [17]. Higher QCI scores illustrate a superior QOC for the countries and regions. Illustrations helped visualized the results and strengthened the understanding of QCI. The study by Mohammadi et al. describes the PCA method in more details [17,18].

The socio-demographic index (SDI) combines education, per capita income, and fertility rates to construct an overall development scale for the countries [22,23]. This index categorizes the countries into five quintiles based on their incomes; high, high-middle, middle, low-middle, and low-income countries [22]. We compared the SDI quintiles to further strengthen our results and discussion;

IHME previously developed Healthcare Access and Quality (HAQ) index [24]. We conducted a mixed effect model to validate QCI by assessing its correlation with the HAQ index. The model applied QCI as a dependent variable, and outpatient care utilization, inpatient care utilization, BCa prevalence, deaths, and attributed death to risk factors as independent variables with countries as the random effects. S2 Table demonstrates the details on the results of the conducted mixed effect model for QCI validation. QCI notably correlated with the HAQ index with Pearson’s correlation coefficient of 0.80.

2.3 Rationale for each QCI component

  1. Prevalence-to-incidence ratio: For a specific disease or condition, if the patients receive better QOC, the mortality rates will decrease and a larger portion of the patients will remain alive. Therefore, given a similar incidence, if the QOC is increased, the prevalence of the disease will be higher and prevalence-to-incidence ratio will increase.

  2. Mortality-to-incidence ratio (MIR): As mentioned above, given a similar incidence, a worse QOC will yield higher mortality rates and a higher mortality-to-incidence ratio.

  3. DALYs-to-prevalence ratio: Similar to MIR, if two regions have similar prevalence rates, the region with a lower QOC will have higher DALYs and consequently, a higher DALYs-to-prevalence ratio.

  4. YLLs-to-YLDs: In a case of worse disease management and QOC, patients decease earlier and their YLL increase. On the other hand, YLD will decrease as the patients have died earlier and will live less years with their disabilities. Therefore, lower QOC pertains to a higher YLLs-to-YLDs ratio.

2.4 Age and gender disparity

We presented our age groups as five-year intervals starting from 15 to 85+ years (15–19, 20–24, 2 …, 80–84, 85 plus). This strategy enabled us to pinpoint any accounts of age disparity for different locations. BCa has a negligible incidence below the age of 15 [13, 25]. We also utilized age-standardized values for the calculation of indices to increase the capabilities of more robust comparisons.

We also introduced the Gender Disparity Ratio (GDR) to analyze the gender-related availability of QOC.

GDR(x)=QCI(x)forfemalesQCI(x)formales

X represents a location, age group, and year in the above formula. GDR values nearing 1 implied equal QOC among males and females.

2.5 Statistical analysis

Age-standardized calculations were based on the GBD world population. We depicted a 95% uncertainty interval (UI) for primary indices. Results were considered significant if the groups did not show UI overlap. PCA method were used to calculate QCI as discussed above. All the statistical analyses and illustration were carried out using R statistical packages v4.0.4 (http://www.r-project.org/, RRID: SCR_001905).

Results

3.1 Incidence, mortality, and DALYs

Global

The number of BCa cases and mortality is on the rise globally. Worldwide, 524,305 (95% UI: 475,952–569,434) new BCa cases and 228,735 (210,743–243,193) deaths were recorded in 2019 compared to 234,754 (225,464–243,075) new cases and 121,500 (114,751–127,171) mortalities in 1990. However, age-standardized incidence rate per 100,000 did not increase in the same period. BCa incidence rate was 6.3 (6.0–6.5) in 1990, 6.5 (6.2–6.7) in 2005, and 6.5 (5.9–7.1) in 2019. There is a decreasing pattern of BCa death and DALYs rate worldwide from 1990 to 2019. BCa death rate is estimated at 3.5 (3.3–3.7), 3.2 (3–3.3), and 2.9 (2.7–3.1) in 1990, 2005, and 2019, respectively. The numbers were 66.6 (63.0–69.7), 60.4 (57.7–62.8), and 54.2 (50.4–58.0) for DALYs rate.

Male patients constituted most of the incident cases, deaths, and DALYs throughout these years. A similar concept was observed in 2019 for the male to female age-standardized rates (incidence: 11.3 vs. 2.7, deaths: 5.1 vs. 1.4, DALYs: 90.2 vs. 24.4) (Table 1).

Table 1. Bladder cancer numbers and age-standardized rates (per 100,000) of incidence, mortality, and Disability-Adjusted Life Years (DALYs) at Global and six WHO regions by sex.
1990 2005 2019
Incidence Deaths DALYs Incidence Deaths DALYs Incidence Deaths DALYs
Location Sex Number Rate Number Rate Rate Number Rate Number Rate Rate Number Rate Number Rate Rate
Global Both 234,754 (225,464–243,075) 6.3 (6–6.5) 121,500 (114,751–127,171) 3.5 (3.3–3.7) 66.6 (63–69.7) 350,187 (335,351–360,998) 6.5 (6.2–6.7) 163,613 (154,647–169,690) 3.2 (3–3.3) 60.4 (57.7–62.8) 524,305 (475,952–569,434) 6.5 (5.9–7.1) 228,735 (210,743–243,193) 2.9 (2.7–3.1) 54.2 (50.4–58)
Female 56,992 (53,455–60,307) 2.8 (2.6–2.9) 33,376 (30,658–35,843) 1.7 (1.5–1.8) 31.7 (29.2–34.3) 81,888 (75,817–85,654) 2.8 (2.6–2.9) 44,063 (40,138–46537) 1.5 (1.4–1.6) 27.9 (26.1–29.5) 116,438 (103,711–128,213) 2.7 (2.4–2.9) 59,527 (52,329–64,581) 1.4 (1.2–1.5) 24.4 (22.1–26.4)
Male 177,762 (170,773–184,132) 10.9 (10.4–11.3) 88,124 (83,470–91,864) 6.1 (5.8–6.4) 111.7 (105.6–116.6) 268,299 (259,060–276,156) 11.2 (10.7–11.6) 119,550 (114,047–123,576) 5.6 (5.3–5.8) 100.6 (96.1–104.3) 407,866 (371,297–443,750) 11.3 (10.2–12.3) 169,207 (156,921–180,655) 5.1 (4.7–5.4) 90.2 (83.6–96.6)
African Region Both 6,976 (5,713–8,399) 3.4 (2.8–4.1) 5,658 (4,603–6,871) 3 (2.5–3.7) 60.8 (49.4–73.9) 9,765 (8,318–11,652) 3.3 (2.8–4) 7,673 (6,460–9,298) 2.9 (2.4–3.5) 56.9 (47.9–69) 14,946 (12,758–17,128) 3.3 (2.9–3.8) 10,808 (9,325–12,274) 2.7 (2.3–3) 52.5 (45–60.1)
Female 2,263 (1,840–3,061) 2.1 (1.7–2.9) 1,852 (1,491–2,565) 1.9 (1.5–2.6) 38.8 (31.2–52.9) 3,115 (2,609–4,127) 2 (1.7–2.7) 2,508 (2,073–3,441) 1.8 (1.5–2.4) 35.2 (29.1–48.1) 4,549 (3,738–5,264) 1.9 (1.6–2.2) 3,492 (2,847–4,028) 1.6 (1.3–1.8) 31.3 (25.4–36.4)
Male 4,713 (3,735–5,907) 4.9 (3.9–6.2) 3,806 (2,990–4,841) 4.4 (3.5–5.6) 84.9 (66.8–107.7) 6,650 (5,549–8,223) 4.9 (4.1–6.1) 5,165 (4,213–6,497) 4.2 (3.5–5.4) 81.3 (66.5–101.9) 10,397 (8,585–12,101) 5.1 (4.2–5.8) 7,316 (6,104–8,461) 4 (3.4–4.6) 77.1 (64–89.3)
Eastern Mediterranean Region Both 11,345 (9,823–12,709) 6.4 (5.5–7.2) 7,534 (6,436–8,577) 4.7 (4–5.4) 100.5 (86.3–113.5) 20213 (18790–21758) 7.8 (7.2–8.3) 11,415 (10,517–12,360) 4.9 (4.5–5.4) 104.2 (96–112.3) 39,124 (32,304–48,252) 9.3 (7.8–11.3) 17,664 (14,880–21,407) 4.9 (4.1–5.8) 102.4 (86.2–124.2)
Female 2,044 (1,736–2,398) 2.4 (2–2.9) 1,498 (1,252–1,779) 1.9 (1.6–2.3) 42.2 (35.4–49.8) 3605 (3260–3950) 2.9 (2.6–3.2) 2395 (2124–2663) 2.1 (1.9–2.4) 45.3 (40.3–50.2) 6,521 (5,393–7,890) 3.3 (2.7–3.9) 3,718 (3,118–4,398) 2.1 (1.8–2.5) 44.1 (36.9–52.3)
Male 9,301 (8,004–10,518) 10 (8.5–11.4) 6,036 (5,084–6,928) 7.3 (6–8.4) 153.3 (130.2–174.9) 16,609 (15,255–18,085) 12.3 (11.2–13.4) 9,019 (8,210–9,901) 7.5 (6.9–8.3) 158.5 (144.4–173.4) 32,602 (26,680–40,762) 14.9 (12.3–18.3) 13,946 (11,641–17,149) 7.4 (6.2–9) 156.7 (129.9–192.9)
European Region Both 119,679 (115,725–122,720) 11 (10.7–11.3) 54,484 (52,146–56,043) 5.1 (4.8–5.2) 100.4 (96.8–103.9) 159,254 (152,653–163,326) 12.2 (11.7–12.5) 64,394 (60,680–66,292) 4.8 (4.6–5) 94.9 (91.1–97.7) 201,655 (178,323–225,564) 12.4 (10.9–13.8) 77,923 (70,920–83,278) 4.5 (4.1–4.8) 84.6 (78.7–90.5)
Female 25,303 (23,843–26,177) 3.8 (3.6–3.9) 13,529 (12,533–14,072) 2 (1.8–2.1) 36.2 (34.4–37.7) 33,187 (30,718–34,530) 4.3 (4–4.4) 15,933 (14,427–16,692) 1.9 (1.7–2) 34.5 (32.4–35.8) 41,735 (36,018–47,132) 4.4 (3.8–4.9) 19,063 (16,604–20,767) 1.8 (1.6–1.9) 31.6 (28.7–34)
Male 94,376 (91,642–96,715) 22.5 (21.8–23.1) 40,955 (39,464–42,038) 10.5 (10.1–10.9) 199.8 (192.9–206.4) 126,067 (122,150–129,023) 23.8 (22.9–24.4) 48,461 (46,374–49,714) 9.7 (9.1–10) 181 (174.3–186.3) 159,919 (141,017–179,441) 23.2 (20.5–26) 58,861 (54,088–62,723) 8.6 (7.9–9.1) 155.6 (144.5–166.5)
Region of the Americas Both 40,499 (38,894–41,579) 6.7 (6.4–6.9) 20,166 (19,037–20,819) 3.4 (3.2–3.5) 64 (61.5–65.9) 57,907 (55,188–59,484) 6.7 (6.4–6.8) 27,976 (26,085–29,041) 3.2 (3–3.3) 59.4 (56.8–61.2) 82,614 (73,277–92,728) 6.4 (5.7–7.2) 39,999 (36,462–42,491) 3.1 (2.8–3.2) 55.2 (51.6–58.4)
Female 12,091 (11,339–12,541) 3.5 (3.3–3.6) 6,163 (5,634–6,458) 1.8 (1.6–1.8) 32.8 (31–34.1) 17,565 (16,311–18,260) 3.6 (3.4–3.7) 8,842 (7,942–9,307) 1.7 (1.6–1.8) 31.9 (30–33.1) 24,161 (21,068–27,535) 3.4 (3–3.9) 11,869 (10,488–12,822) 1.6 (1.4–1.7) 29.1 (26.8–31)
Male 28,408 (27,501–29,100) 10.9 (10.5–11.1) 14,003 (13,422–14,397) 5.7 (5.4–5.9) 104.4 (100.8–107.4) 40,343 (38,841–41,315) 10.6 (10.2–10.8) 19,134 (18,102–19,748) 5.2 (4.9–5.4) 94 (90.2–96.8) 58,452 (50,821–66,984) 10.2 (8.9–11.6) 28,131 (25,912–29,772) 5 (4.6–5.3) 87.3 (81.9–92.2)
South-East Asia Region Both 11,102 (9,880–12,503) 1.8 (1.6–2.1) 8,424 (7,339–9,479) 1.6 (1.4–1.8) 30.9 (27–34.7) 18,521 (16,925–20,266) 1.9 (1.8–2.1) 13,130 (11,826–14,411) 1.6 (1.4–1.7) 29.3 (26.4–32.2) 34,474 (30,523–38,738) 2.1 (1.9–2.4) 22,524 (20,014–25,161) 1.5 (1.4–1.7) 29 (25.7–32.5)
Female 3,314 (2,648–4,264) 1.1 (0.9–1.4) 2,602 (2,068–3,313) 1 (0.8–1.2) 19.2 (15.3–24.5) 5,270 (4,514–6,171) 1.1 (0.9–1.3) 3,950 (3,405–4,682) 0.9 (0.8–1.1) 17.2 (14.8–20.4) 9,560 (8,185–10,975) 1.1 (1–1.3) 6,727 (5,630–7,774) 0.9 (0.7–1) 16.3 (13.6–18.8)
Male 7,788 (6,878–8,626) 2.6 (2.3–2.9) 5,822 (5,007–6,434) 2.3 (1.9–2.5) 42.8 (36.8–47.2) 13,250 (11,964–14,405) 2.9 (2.6–3.1) 9,180 (8,153–10,040) 2.3 (2–2.5) 42.4 (37.6–46.2) 24,914 (21,353–28,833) 3.3 (2.8–3.7) 15,797 (13,712–18,177) 2.3 (2–2.6) 42.9 (37.3–49.4)
Western Pacific Region Both 44,479 (40,907–48,003) 4.2 (3.9–4.5) 24,836 (22,490–27,092) 2.6 (2–2.8) 49.3 (44.7–53.9) 83,517 (77,781–89,117) 4.9 (4.6–5.2) 38,504 (35,770–41,394) 2.5 (2.3–2.7) 45.8 (42.7–49.4) 150,005 (131,044–170,665) 5.7 (5–6.4) 59,087 (51,799–66,594) 2.3 (2–2.6) 42.2 (37–47.7)
Female 11,788 (10,433–13,267) 2.1 (1.8–2.3) 7,613 (6,639–8,678) 1.4 (1.3–1.6) 27.5 (23.8–31.6) 18,882 (16,965–20,432) 2.1 (1.9–2.3) 10,284 (9,181–11,168) 1.2 (1.1–1.3) 21.4 (19.5–23.3) 29,555 (24,550–34,688) 2.1 (1.7–2.4) 14,466 (11,808–16,760) 1 (0.8–1.2) 17.4 (14.8–20.2)
Male 32,691 (29,728–35,909) 7.1 (6.5–7.7) 17,224 (15,265–19,088) 4.5 (4.1–4.9) 78 (69.2–86.2) 64,635 (59,984–69,792) 8.5 (7.8–9.1) 28,220 (26,072–30,676) 4.3 (4–4.7) 75.8 (70.1–82.1) 12,0450 (10,3293–14,0495) 10.1 (8.7–11.7) 44,621 (38,217–51,554) 4.3 (3.7–4.8) 72.5 (62.3–83.5)

Regional

The incidence, mortality, and DALYs of BCa are steadily increasing for all the six World Health Organization (WHO) regions among both genders. European region, Western Pacific region, and the region of the Americas were the main contributors to the incidence and mortality of BCa. European region had 201,655 (178,323–225,564) new cases and 77,923 (70,920–83,278) mortalities in 2019. These numbers were 150,005 (131,044–170,665) and 59,087 (51,799–66,594) for Western Pacific region, and 82,614 (73,277–92,728) and 39,999 (36,462–42,491) for the region of the Americas in the same year. The African region shared the least estimates with 14,946 (12,758–17,128) new cases and 10,808 (9,325–12,274) mortalities. In 2019, European region 12.4 (10.9–13.8), Eastern Mediterranean region 9.3 (7.8–11.3), and the region of the Americas 6.4 (5.7–7.2) had the highest age-standardized incidence rate per 100,000, while South-East Asia region had the lowest incidence rate of 2.1 (1.9–2.4).

3.2 QCI

Global age-standardized QCI improved from 68.4% and 75.7% in 1990 and 2005, to 79.8% and 80.9% in 2014 and 2019. Higher SDI quintiles had better QCI scores, ranging from 90.1% in high SDI countries to 30.2% in low SDI countries; however, lower SDI countries showed better 5-year improvements in QCI. The net QCI change was 0.0 for high, 1.1 for high-middle, 4.7 for middle, 5.3 for low-middle, and 4.7 for low SDI countries from 2014 to 2019 (Table 2).

Table 2. Age-standardized QCI values (%) and GDR of the selected locations in 1990, 2005, 2014, and 2019.

1990 2005 2014 2019
Location Both Female Male GDR Both Female Male GDR Both Female Male GDR Both Female Male GDR
Global 68.4 63.3 69.6 0.91 75.7 70.7 77.1 0.92 79.8 74.9 81.2 0.92 80.9 76.0 82.4 0.92
Socio-demographic index (SDI) quintiles
High SDI 81.6 78.9 81.8 0.96 88.1 85.8 88.6 0.97 90.1 88.6 90.5 0.98 90.1 88.9 90.6 0.98
High-middle SDI 70.8 65.9 71.3 0.92 79.2 75.2 79.7 0.94 84.9 81.6 85.2 0.96 86.0 82.8 86.4 0.96
Middle SDI 44.4 34.8 47.2 0.74 61.1 51.8 63.8 0.81 71.7 61.3 74.7 0.82 76.4 66.1 79.4 0.83
Low-middle SDI 24.7 21.1 26.7 0.79 34.5 30.2 36.8 0.82 44.7 39.4 47.2 0.83 50.0 43.9 52.8 0.83
Low SDI 12.7 9.9 14.5 0.68 17.2 16.5 17.8 0.93 25.5 23.1 27.0 0.86 30.2 27.4 31.9 0.86
WHO regions
African Region 21.3 17.7 23.2 0.76 26.4 21.7 28.8 0.75 32.8 26.8 35.8 0.75 37.6 31.0 40.9 0.76
Eastern Mediterranean Region 43.9 32.6 47.5 0.69 58.1 43.6 62.4 0.70 66.3 51.4 70.7 0.73 71.5 56.8 75.8 0.75
European Region 78.3 74.3 78.7 0.94 85.2 82.0 85.8 0.96 89.3 87.0 89.8 0.97 89.7 87.5 90.3 0.97
Region of the Americas 74.0 75.7 73.3 1.03 77.4 78.1 77.4 1.01 78.0 79.5 77.7 1.02 78.4 80.1 78.2 1.02
South-East Asia Region 27.7 21.9 30.6 0.72 38.6 32.0 41.7 0.77 46.6 40.6 49.1 0.83 50.7 44.6 53.5 0.83
Western Pacific Region 62.0 53.3 63.9 0.83 75.6 69.6 75.5 0.92 83.0 77.1 83.6 0.92 85.3 79.8 85.9 0.93
Top 5 countries in 2019 with highest age-standardized QCI values
Italy 91.1 89.5 91.4 0.98 98.3 97.3 98.4 0.99 100 100 100 1 99.4 99.6 99.6 1
Australia 87.8 85.3 88.4 0.96 91.3 88.1 92.6 0.95 93.8 91.8 95.0 0.97 98.1 97.7 98.4 0.99
Iceland 89.8 87.2 91.2 0.96 95.8 94.2 96.9 0.97 97.7 95.5 98.7 0.97 97.5 96.0 98.4 0.98
Japan 89.1 84.0 90.4 0.93 94.4 90.1 95.1 0.95 96.6 92.7 97.6 0.95 97.2 93.9 98.1 0.96
Spain 86.5 79.9 87.1 0.92 94.7 88.7 95.3 0.93 97.2 93.5 97.7 0.96 97.2 93.1 97.9 0.95
Bottom 5 countries in 2019 with lowest age-standardized QCI values
Chad 11.6 8.3 13.9 0.60 11.8 8.5 13.9 0.61 17.0 13.5 19.2 0.70 20.5 16.8 23.0 0.73
Guinea 9.0 5.8 11.3 0.51 14.0 11.2 15.7 0.71 15.5 13.1 17.0 0.77 19.7 16.8 21.6 0.78
South Sudan 10.2 8.0 11.6 0.69 12.2 10.9 13.7 0.80 13.1 12.3 14.5 0.85 15.6 14.5 17.2 0.84
Somalia 5.7 3.5 7.5 0.47 6.5 3.8 8.4 0.45 9.5 6.6 11.4 0.58 11.0 8.0 13.0 0.62
Central African Republic 3.1 4.1 3.1 1.32 2.7 2.7 2.8 0.96 5.4 4.8 5.4 0.89 6.8 6.3 6.8 0.93

Year 2014 was added to the previously mentioned years (1990, 2005, and 2019) to find the 5-year differences in the values (2014 to 2019).

In 2019, the top 3 regions were the European region (age-standardized QCI = 89.7%), the Western Pacific region (85.3%), and the region of the Americas (78.4%). The lowest were the African region (37.6%), the South-East Asia region (50.7%), and the Eastern Mediterranean region (71.5%). Italy (99.4%), Australia (98.1%), Iceland (97.5%), Japan (97.2%), and Spain (97.2%) ranked as the top 5; while Central African Republic (6.8%), Somalia (11.0%), South Sudan (14.5%), Guinea (16.8%), and Chad (16.8%) were the bottom 5 countries (Table 2, Fig 1A).

Fig 1.

Fig 1

A) Age-standardized map of Quality of Care Index (QCI) scores for both genders in 2019 B) Gender Disparity Ratio (GDR) scores in 2019 (Contains information from OpenStreetMap and OpenStreetMap Foundation, which is made available under the Open Database License).

Fig 2 depicts the scatter plot of age-standardized QCI for different countries based on the six WHO world regions. The trend was similar throughout the years, with African region remaining the lowest and European regions owning the highest age-standardized QCI scores during the study period. Eastern Mediterranean region improved more rapidly towards higher SDI and QCI scores compared to the other WHO regions. Similarly, North Africa and Middle East region had the best progress among the seven GBD super-regions (S1 Fig). Both figures demonstrate an almost-linear relationship between the countries’ SDI and the observed QCI score, illustrating the indisputable correlation between the two variables. These two figures were depicted for every ten year to demonstrate the changes for each decade.

Fig 2. Scatter plot of age-standardized QCI (%) for the countries by the 6 WHO regions.

Fig 2

Note that the following locations were not initially part of the WHO regions; however, we assigned them to the regions of their locations based on the GBD secretariat opinion. Bermuda, Greenland, and Puerto Rico were assigned to the region of the Americas; Guam, Northern Mariana islands, Taiwan, and Tokelau to the Western Pacific region; and Palestine to the Eastern Mediterranean region.

3.3 Gender disparity

Males received better care worldwide compared to females, as the age-standardized GDR stood at 0.92 in 2019. Fig 1B illustrates the geographical distribution of gender disparity. This number remained constant throughout 1990–2019, as the Global GDR was 0.91 in 1990 and 0.92 in 2005, 2014. The disparity inversely correlated with the level of SDI. High (GDR = 0.98) and high-middle SDI (GDR = 0.96) quintiles approached 1, while the numbers were 0.83 for middle and low-middle and 0.86 for low SDI groups. No change in the GDR was observed in the last five years for different SDIs, with a minor increase of 0.01 in the GDR of the middle SDI group. However, GDR for the low SDI improved significantly since 1990 with the net change of 0.18, followed by middle SDI quintile that increased 0.09 in the GDR value. The numbers for low-middle, high-middle, and high SDI groups increased 0.04, 0.04, and 0.02, respectively.

The region of the Americas was the only region with a GDR above 1 (1.02). European region and Western Pacific region followed it with GDR values of 0.97 and 0.93. Eastern Mediterranean region (0.75), the African region (0.75), and the South-East Asia region (0.83) had higher rates of gender disparity. While the South-East Asia region (GDR change: 0.11), Western Pacific region (GDR change: 0.10), and Eastern Mediterranean region (GDR change: 0.06) ameliorated their GDR by more than 0.05 since 1990, the African region showed no progress (GDR change: 0.00) (Table 2).

GDR also changed with age groups. GDR was above 1 for all the SDI quintiles before the age of 25 and above 95; however, all these regions showed numbers below 1 in the age groups in between.

3.4 Age disparity

Age disparities exist between the age groups in our analysis, evident in Figs 3 and 4. The QCI score is readily increasing in both genders and overall and in all the SDI quintiles since 1990. The global trend resembles more the high and high-middle SDI countries. In 2019, QCI scores of high SDI, high-middle SDI, and overall SDI were above 75 for all the three presented age groups (15–49, 50–75, and 75+) and did not differ much. However, older patients had more remarkably lower SDI in the middle, low-middle, and low SDI countries. In these lower SDI quintiles, 15–49 years had the best QCI scores and 75 plus had the worst numbers.

Fig 3. QCI (%) for age-groups of 15–49, 50–74, and 75+ at Global and Socio-demographic index (SDI) quintiles for both genders 1990–2019.

Fig 3

Fig 4. Age trend of QCI (%) in 5-year categories at Global and Socio-demographic index (SDI) quintiles in 2019.

Fig 4

Fig 4 presents the data for 2019 and the age of the patients are divided into 5-year categories. The overall results showed similar points to Fig 3. In most of the SDI quintiles, QCI scores decline from 15–19 to 20–24, then rise from 20–24 to 30–34, and finally decrease in the 35–39 to 85+ age groups. The 35–85+ years graphs slope differently based on the SDI of the countries. High and high-middle SDI countries experience an approximate plateau for the 35–85+ age group, with a modest decrease in the later parts. On the other hand, middle, low-middle, and low SDI countries demonstrate a steep decline in QCI of 35–85+ years old BCa patients, with an increase in QCI for 35–39 years old patients in low-middle and low SDI countries. Overall, 15–19 years old patients in global (74.0% for 15–19 and 75.7% for 85+), high (84.7% for 15–19 and 80.8% for 85+), and high-middle SDI groups (82.2% for 15–19 and 79.8% for 85+) scored similar to the older patients in 2019. Contrarily, QCI in older BCa patients of the middle (78.5% for 15–19 and 48.6% for 85+), low-middle (61.2% for 15–19 and 28.0% for 85+), and low SDI countries (48.4% for 15–19 and 13.6% for 85+) was substantially lower compared to 15–19 years old group. Middle SDI countries scored better than the global average below 50–54, while they continued to distance from the global QCI after 50 years old.

Discussion

This presented analysis of GBD 2019 shows the increasing incidence, mortality, and DALYs of BCa. Despite this, the age-standardized rates (per 100,000) of these parameters remained stable worldwide and for most of the regions, while the global age-standardized deaths and DALYs rates significantly decreased. Meantime, age-standardized global QCI is steadily increasing, starting from 68.4% in 1990 and reaching 80.9% in 2019. European region had the highest and African region had the lowest QCI scores throughout the years (2019: 89.7% vs. 37.6%). Gender and age disparities existed throughout the years globally and were more pronounced in the lower SDI quintiles. Global GDR was 0.92 in 2019 and did not improve significantly since 1990 (GDR = 0.91). In 2019, high and low SDI countries had GDRs of 0.98 and 0.85, respectively. Furthermore, patients older than 75 years had gravely lower QCI scores in the middle-to-low SDI quintiles, compared to the youngest BCa patients.

The findings in this study comes concordant to previous GBD analysis regarding the increasing incidence and mortality of BCa, as the world population ages. They found a slight decrease in global age-standardized incidence (1990–2019 change: -5.99%), and a more pronounced reduction in deaths and DALYs (-17.88% and -21.82%, respectively) [6]. While we did not observe a lower incidence rate, our findings confirm the aforementioned decreased age-standardized deaths and DALYs rates. Previous studies utilizing GLOBACAN data from 1990s to 2012 also produce similar results [26,27]. They found stagnant or decreasing incidence rates for men, while incidence in women were on the rise. The death rates, however, were on a decline in most of the countries.

The regional pattern of QCI resembles the findings in the previous studies. In the thyroid, hematologic, neurologic, and breast malignancies, the African region had the lowest QCI scores while the European and Western Pacific regions had the highest scores [12,18,19,28]. The highest and lowest rated countries also had similar patterns, with the highest scoring countries being consistently from higher SDI countries, and the worst QCI scores relating to lower SDI countries.

Gender disparity patterns for BCa was also similar to that of thyroid, hematologic, and neurologic malignancies. In the studies, In the lower SDI quintiles, the GDR values demonstrate lower values, while the higher SDI countries had higher values approaching 1 (equal for both genders) [12,18,19]. Nevertheless, the age disparity patterns are more specific to each cancer. In the aforementioned cancers, the higher SDI quintiles had lower age-based inequalities; however, the target age groups for age disparities differed. Older patients in lower SDI countries had poorer QCI scores compared to younger patients in thyroid cancer [12], similar to our findings on BCa. On the other hand, children were the main targets of inequalities for neurologic malignancies in lower SDI countries [18].

As mentioned earlier, the global burden of BCa is rapidly increasing as the world population ages. Despite the declining rates of tobacco smoking- as the most recognized BCa risk factor- in both genders since 1990 in almost all countries [29], the BCa incidence rate has still remained stagnant. Meanwhile, high and high-middle SDI countries reduced the age-specific incidence rates by controlling the risk factors, while the rates increased in the middle and low-middle countries [6]. The stable global BCa incidence rate- despite the declining smoking rates- might partly relate to the lack of overlap between the regions with the highest BCa prevalence and those with the highest share of smoking. More than 50% of the BCa cases exist in the top 20% human development index (HDI) countries, while only 5% are diagnosed in the low HDI countries [30]. The education and socio-economic status inversely correlate with BCa incidence [31,32]. Moreover, the effect of smoking on the BCa burden is more emphasized in high SDI countries [7]. Meanwhile, nearly 80% of the current smokers live in the low and low-middle income countries [33]. Furthermore, men share the most cases of BCa with a three-fold incidence compared to women [30], while the middle SDI countries had the highest prevalence of smoking among men [29]. Altogether, countries with higher BCa prevalence are not the ones with greater smoking rates, and this factor can diminish the effect of smoking cessation. On the other hand, efforts failed to successfully assess the changes in the impact of environmental and occupational risk factors of BCa during the past years, such as polycyclic aromatic hydrocarbons, aromatic amines, chlorinated hydrocarbons, and arsenic [3437]. The progress in the early detection and treatment of the BCa might rationalize the decrease in the observed deaths and DALYs.

The differences in QCI values between SDI quintiles markedly escalate when going down from high to low SDI countries, with the highest gap between the middle and low-middle SDI groups. This increase in gaps demonstrates the growing healthcare access inequalities for BCa based on the countries’ level of development. A previous global analysis also confirms that the most developed countries are witnessing the highest decreases in BCa death rates, raising the alarm sign for further inequalities in healthcare access in the future [26].

About 85% of the BCa cases are diagnosed following an episode of painless gross hematuria, and the others present with painless microscopic hematuria [3,38]. Subsequently, the patients will require cystoscopy and other work-ups for diagnosis, followed by costly treatments and regular life-long follow-ups [6]. All these steps impose strangling financial burdens, meaning too much for low-income countries [18,39]. Nevertheless, the numbers in our study might overestimate the QOC deficiencies in African and low SDI countries; as we know, SCC is more common in African countries due to the higher prevalence of Schistosomiasis [40]. As mortality is an important variable in QCI, the poorer prognosis of SCC might drop the QCI numbers in the African countries [5], compared to the other parts of the world where urothelial transitional cell carcinomas are the vast majority of cases.

QCI changes in the last five years are more prominent in lower SDI quintiles, while no 5-year improvement in the QCI score was observed in the high SDI group. This might reflect that the scientific discoveries in the last five years could not increase BCa’s QOC and survival, evident by the stagnant QCI in high SDI countries that have quick access to new treatment modalities and innovations. On the other hand, lower SDI quintiles are pushing themselves towards better availability of healthcare access. Furthermore, economic and social developments are changing the epidemiologic pattern of BCa in the African region, from SCC with poorer prognosis to transitional cell carcinoma [41,42]. In recent years, immunotherapeutic agents are capturing the scene and raising hopes for an increased QOC and survival [43]. However, their high cost should raise the alarm of a possible surge in the QOC disparities between the higher and lower SDI quintiles [7].

Some countries with the highest QOC held multi-disciplinary conferences to provide national guidelines and resolve the discrepancies regarding the BCa in their countries [44,45]. An earlier study also found that countries with high QCI scores in thyroid cancer developed national consensus guidelines and constructed cancer registries [12]. These national efforts can strengthen the QOC in the countries and identify and solve the issues specific to each country.

The global age-standardized QCI score comes above the value for the middle SDI countries and runs close to the values for high and high-middle SDI countries, explained by the high prevalence of BCa in developed countries [3032]. The gap between the global QCI values and middle SDI’s QCI gets more pronounced when comparing the patients older than 65. The increased gap for the older patients can be rationalized by the higher life expectancies of the high and high-middle SDI countries compared to the other quintiles [46,47]. Therefore, the patients’ composition, and eventually QCI scores, draw closer to the patients from the higher SDI countries and away from the middle and lower SDI groups in the older ages.

Men are more frequently diagnosed with BCa than women; however, the difference is estimated to narrow down as the percentage of women smoking cigarettes increases [34]. Women suffer from higher mortality to incidence ratio compared to men [48]. This finding comes accordant to our GDR calculations of 0.92 in 2019; however, GDR comes above one below 25 and above 95 years of age. Worse outcomes in women were linked to higher BCa stages and grades with more prevalent multifocal tumors and undesirable histological findings at the time of diagnosis [30,49,50]. Studies also introduced Gender discrimination as a possible contributor to this observation in earlier studies [30,49]. We hypothesize that the gender disparity contributes more to the higher rates of adverse events in women. The GDR approaches 1 in high and high-middle SDI countries with more-widely available healthcare access for both genders, while the number drops to 0.86 and below for other SDI quintiles. The outcomes are superior in higher SDI countries regardless of gender, whereas poorer outcomes are present for women in the lower SDI groups.

Overall, BCa remains a huge healthcare issue with an increasing burden worldwide with little survival improvements in recent years [51]. Urologic malignancies- among them BCa- were among the worst cancers in patient satisfaction [52]. Healthcare policymakers should implement due programs to combat the associated adverse events. Screening the asymptomatic individuals has no proven benefits in the studies and should not be recommended routinely [53], especially for the low-income countries where budget allocations have to be directed towards the most cost-beneficial actions. Therefore, addressing the risk factors remains an important step to decrease the burden of BCa. Reducing tobacco smoking is the most-effective intervention to prevent BCa [54], and healthcare systems should focus the most on this behavior. Secondly, countries at higher risk should reduce the environmental and occupation exposure, and maximize the protection of the people largely exposed to the pollutants [3437]. Thirdly, endemic regions should implement specific measures to diminish schistosomiasis rates, such as improving sanity and changing behavioral patterns [41].

This study comes with some limitations. First, we could not estimate ethnic and racial inequalities due to the lack of GBD data. Second, IHME-GBD databases might have imprecise or deficient registries for some of the countries. Third, the GBD database did not dichotomize BCa into muscle-invasive and non-muscle-invasive subtypes, while analyzing the data on muscle-invasive BCa comes with great benefits, as it is responsible for a large proportion of BCa-related deaths and DALYs. To our knowledge, this study provides the first comprehensive estimates of BCa QOC using QCI as a validated parameter. Despite all the mentioned limitations, QCI calculations extracted numerous invaluable information requiring specific attention by the international community. Countries can learn from the potentials generated by this score to re-organize their healthcare systems and provide quality care to BCa patients.

Conclusion

This study introduces the first calculations of QCI and the related age and gender disparities for BCa. The global QCI steadily increased in the last 30 years, but the gender disparities remained relatively unchanged despite substantial improvements in several regions. High and high-middle SDI countries had superior QOC and less gender- and age-based inequalities compared to lower SDI countries. Middle-to-low SDI quintiles have lower QCI scores compared to higher quintiles; specifically, older patients in the lower quintiles receive less quality care and should be emphasized more in the healthcare programs. We recommend the proficient healthcare systems publish more information on their strategies to support BCa patients. We encourage follow-up studies to evaluate the countries’ progress and offer precious findings for healthcare policy makers.

Supporting information

S1 Fig. Scatter plot of age-standardized QCI (%) for the countries by the 7 GBD super-regions.

(PDF)

S1 Table. ICD-10 codes of bladder cancer mapped for GBD 2019.

(PDF)

S2 Table. The coefficients of the mixed-effect regression model.

(DOCX)

Acknowledgments

We profoundly thank all staff and colleagues in Non-Communicable Diseases Research Center (NCDRC) and Endocrinology and Metabolism Research Institute (EMRI) at Tehran University of Medical Sciences, helping conducting such valuable studies.

Abbreviations

BCa

Bladder cancer

DALY

Disability-Adjusted Life Years

GATHER

Guidelines for Accurate and Transparent Health Estimates Reporting

GBD

Global burden of disease

GDR

Gender Disparity Ratio

HAQ

Healthcare Access and Quality

HDI

Human development index

ICD-10

International Classification of Diseases-10

IHME

Institute for Health Metrics and Evaluation

PCA

Principal component analysis

QOC

Quality of care

SCC

Squamous cell carcinoma

SDI

Socio-demographic index

WHO

World Health Organization

YLD

Years Lived with Disability

YLL

Years of Life Lost

Data Availability

Data Availability Statement: The study protocol and data used in this work are available both from [https://www.protocols.io/view/quality-of-care-index-qci-bprjmm4n] and the Global Burden of Disease Results Tool [https://ghdx.healthdata.org/gbd-results-tool]. The authors confirm they had no special access or privileges to the data that other researchers would not have.

Funding Statement

The author(s) received no specific funding for this work.

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Decision Letter 0

Deepak Dhamnetiya

7 Jun 2022

PONE-D-22-07813A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: the global burden of disease study 1990-2019PLOS ONE

Dear Prof. Farshad Farzadfar,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

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Deepak Dhamnetiya, MD

Academic Editor

PLOS ONE

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Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

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Reviewer #1: Yes

Reviewer #2: No

**********

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Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Comment: Thanks to the authors for their hard work on this study “A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: the global burden of disease study 1990-2019”. Overall, the article is well-written and has a relevant emphasis. These recommendations and comments, however, may help to enhance this study enough to get it published.

Comment-1: The article has no page number and no line number making it difficult to reference texts for revision.

Comment-2: After reading the introduction, I think it would have been beneficial to have a little more information there.

Comment-3: Please elaborate more about PCA method.

Comment-4: Try to make the discussion more focused on key variable.

Reviewer #2: Congratulations for your effort to represent about such data of regionally and globally concerned. Analysis is worked well and you can discuss comprehensively according to you findings. In addition to these, the following comments are recommended.

1.Firstly, authors should prepare the manuscript according to the PLOS ONE guidelines that include to add number line by line. It is useful for reviewers to give comments to authors. So may I highlight my comments as subtitles or page number in spite of line number.

2. Author cited the Table 1 and Table 2 in the text for the findings but they were not found as neither main table nor supplementary table. The Table 1 you attached as supplementary information is for ICD-10Code.

3.For material and methods, mixed effect model for QCI validation is good to show as the supplementary table or figure.

4. In results section 3.1, findings on national level should be included to reflect the Title of manuscript.

Moreover, all indices of PCA are necessary to be described because the author showed incidence, mortality and DALYs and left over about prevalence, YLLs and YLDs.

5. For section 3.1, corresponding table or figures will make clear presentation about the findings.

6. For section 3.2 QCI, the reason of analysis for only 1990, 2005,2014 and 2019 should be mentioned (refers to the first line of the first paragraph)

7.For Age disparity, age interval are not equally described where they are (a) 3.4, first paragraph, third line , 50-75 and (b) 3.4, second paragraph, second line, 30-43

8. Age group should be included in text for high and high middle SDI countries in place of writing as "above mentioned age group and in the later part" for easy understanding of the readers. (3.4, second paragraph, third to fifth line)

9. The purpose of supplementary figure 1 should be mentioned and what its difference from figure 1 is wanted to know.

10. The year specification as 1990, 2000, 2010 and 2019 for these above figures should be explained for better presentation.

**********

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Reviewer #1: No

Reviewer #2: No

**********

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PLoS One. 2022 Oct 20;17(10):e0275574. doi: 10.1371/journal.pone.0275574.r002

Author response to Decision Letter 0


10 Sep 2022

A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: the global burden of disease study 1990-2019

Editor's Comments to Author:

Dear Prof. Farshad Farzadfar,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by June 16, 2022. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Deepak Dhamnetiya, MD

Academic Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. We note that Figure 1 in your submission contain [map/satellite] images which may be copyrighted. All PLOS content is published under the Creative Commons Attribution License (CC BY 4.0), which means that the manuscript, images, and Supporting Information files will be freely available online, and any third party is permitted to access, download, copy, distribute, and use these materials in any way, even commercially, with proper attribution. For these reasons, we cannot publish previously copyrighted maps or satellite images created using proprietary data, such as Google software (Google Maps, Street View, and Earth). For more information, see our copyright guidelines: http://journals.plos.org/plosone/s/licenses-and-copyright.

We require you to either (1) present written permission from the copyright holder to publish these figures specifically under the CC BY 4.0 license, or (2) remove the figures from your submission:

1. You may seek permission from the original copyright holder of Figure 1 to publish the content specifically under the CC BY 4.0 license.

We recommend that you contact the original copyright holder with the Content Permission Form (http://journals.plos.org/plosone/s/file?id=7c09/content-permission-form.pdf) and the following text:

“I request permission for the open-access journal PLOS ONE to publish XXX under the Creative Commons Attribution License (CCAL) CC BY 4.0 (http://creativecommons.org/licenses/by/4.0/). Please be aware that this license allows unrestricted use and distribution, even commercially, by third parties. Please reply and provide explicit written permission to publish XXX under a CC BY license and complete the attached form.”

Please upload the completed Content Permission Form or other proof of granted permissions as an "Other" file with your submission.

In the figure caption of the copyrighted figure, please include the following text: “Reprinted from [ref] under a CC BY license, with permission from [name of publisher], original copyright [original copyright year].”

2. If you are unable to obtain permission from the original copyright holder to publish these figures under the CC BY 4.0 license or if the copyright holder’s requirements are incompatible with the CC BY 4.0 license, please either i) remove the figure or ii) supply a replacement figure that complies with the CC BY 4.0 license. Please check copyright information on all replacement figures and update the figure caption with source information. If applicable, please specify in the figure caption text when a figure is similar but not identical to the original image and is therefore for illustrative purposes only.

The following resources for replacing copyrighted map figures may be helpful:

USGS National Map Viewer (public domain): http://viewer.nationalmap.gov/viewer/

The Gateway to Astronaut Photography of Earth (public domain): http://eol.jsc.nasa.gov/sseop/clickmap/

Maps at the CIA (public domain): https://www.cia.gov/library/publications/the-world-factbook/index.html and https://www.cia.gov/library/publications/cia-maps-publications/index.html

NASA Earth Observatory (public domain): http://earthobservatory.nasa.gov/

Landsat: http://landsat.visibleearth.nasa.gov/

USGS EROS (Earth Resources Observatory and Science (EROS) Center) (public domain): http://eros.usgs.gov/#

Natural Earth (public domain): http://www.naturalearthdata.com/

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Answer: Thanks for your suggestions. We revised the article according to the journal style. Furthermore, we added the license statement for Figure 1.

We have revised the manuscript according to the journal instructions and thoughtful suggestions of the reviewers and all the issues were addressed in response to the reviewers.

*********************************

Reviewer(s)' Comments to Author:

Reviewer: 1

Comments to the Author

Thanks to the authors for their hard work on this study “A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: the global burden of disease study 1990-2019”. Overall, the article is well-written and has a relevant emphasis. These recommendations and comments, however, may help to enhance this study enough to get it published.

Q1: The article has no page number and no line number making it difficult to reference texts for revision.

A1: Many thanks for the kind comments. We added the page and line numbers, and also edited the manuscript thoroughly to fit with the journal format accordingly.

*********************************

Q2: After reading the introduction, I think it would have been beneficial to have a little more information there.

A2: Many thanks. We added a complete paragraph to the introduction accordingly.

*********************************

Q3: Please elaborate more about PCA method.

A3: Many thanks. We added several more sentences to the methods describing this method and highlighted them accordingly.

*********************************

Q4: Try to make the discussion more focused on key variable.

A4: Many thanks for the instructive comment. We went through several important studies related to our manuscript and added their data to our study to strengthen our discussion accordingly.

Reviewer: 2

Congratulations for your effort to represent about such data of regionally and globally concerned. Analysis is worked well and you can discuss comprehensively according to your findings. In addition to these, the following comments are recommended.

Q1: Firstly, authors should prepare the manuscript according to the PLOS ONE guidelines that include to add number line by line. It is useful for reviewers to give comments to authors. So may I highlight my comments as subtitles or page number in spite of line number.

A1: Many thanks for your kind words. We added the page and line numbers and completely revised the manuscript according the Plos one guidelines.

*********************************

Q2: Author cited the Table 1 and Table 2 in the text for the findings but they were not found as neither main table nor supplementary table. The Table 1 you attached as supplementary information is for ICD-10Code.

A2: Many thanks. The tables were submitted as separate files, but we added them to the text in the revisions according the journal style, and can be visible now. Supplementary table 1 is about ICD-10 codes, but table 1 and table 2 present important data regarding our study.

*********************************

Q3: For material and methods, mixed effect model for QCI validation is good to show as the supplementary table or figure.

A3: Many thanks. We added the requested table as supplementary table 2 (S2 Table) accordingly.

*********************************

Q4: In results section 3.1, findings on national level should be included to reflect the Title of manuscript.

Moreover, all indices of PCA are necessary to be described because the author showed incidence, mortality and DALYs and left over about prevalence, YLLs and YLDs.

A4: Many thanks.

The main aim of this study is QCI that combines all those mentioned variables using PCA. Section 3.1 starts as an introduction to the results section that makes the readers familiar with the epidemiologic situation of BCa, the main novelty of the study is related to the QCI that contains more extensive results, including those of national level. Therefore, we tried not to make this section over-extended, and only tried to focus on the main indices of mortality, incidence, and DALY.

*********************************

Q5: For section 3.1, corresponding table or figures will make clear presentation about the findings.

A5: Many thanks. Table 1 is added to the text that extensively presents the findings accordingly.

*********************************

Q6: For section 3.2 QCI, the reason of analysis for only 1990, 2005,2014 and 2019 should be mentioned (refers to the first line of the first paragraph)

A6: Many thanks. The main years in the study were 1990 and 2019, and we also added the year between these values. We added the year 2014 to the analysis to find the 5-year differences. We added the reasoning to the Table 2 footnote (corresponding to section 3.2) accordingly.

*********************************

Q7: For Age disparity, age interval are not equally described where they are (a) 3.4, first paragraph, third line , 50-75 and (b) 3.4, second paragraph, second line, 30-43

A7: Many thanks for the precise comment. The 30-43 number was wrong, the right number was 30-34 and was corrected accordingly.

The first paragraph describes 3 overall age groups (Figure 3) (according to the age groups of GBD data), while the second paragraph describes ages by 5-year intervals (Figure 4).

*********************************

Q8: Age group should be included in text for high and high middle SDI countries in place of writing as "above mentioned age group and in the later part" for easy understanding of the readers. (3.4, second paragraph, third to fifth line)

A8: Many thanks. Revised accordingly.

*********************************

Q9: The purpose of supplementary figure 1 should be mentioned and what its difference from figure 1 is wanted to know.

A9: Many thanks. Supplementary figure 1 demonstrates all the countries in a manner that their region of origin is available. Furthermore, Supplementary Figure 1 also illustrates the situation in various years. Therefore, as we added to the text (highlighted accordingly), this figure facilitates the interpretation of the regions’ progress during the years. On the other hand, Figure 1 shows the situation of the QCI scores and GDR (gender disparity ratio) in specific countries using a word map.

The most similar figure to Supplementary figure 1 is figure 2 that we believe is what the respected reviewer meant. The difference is that figure 2 is related to 6 “WHO” regions, Supplementary figure 1 is related to “GBD” super-regions. We clarified this matter and highlighted accordingly.

*********************************

Q10: The year specification as 1990, 2000, 2010 and 2019 for these above figures should be explained for better presentation.

A10: Many thanks. Added to the text and highlighted accordingly.

Attachment

Submitted filename: Response_2022.08.24.docx

Decision Letter 1

Deepak Dhamnetiya

21 Sep 2022

A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: the global burden of disease study 1990-2019

PONE-D-22-07813R1

Dear Dr. Farshad Farzadfar,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

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Kind regards,

Deepak Dhamnetiya, MD

Academic Editor

PLOS ONE

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

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Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

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2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: No

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Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

Reviewer #2: Thank you so much for your detailed reply for my previous comments and congratulations for your great efforts. Your manuscript is acceptable for publication but I am still interested to the data for some QCI constitutes; Prevalence, YLLs and YLDs. If you are feasible, may I suggest to add these data as supporting information for your perfect publication.

**********

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Reviewer #1: No

Reviewer #2: Yes: Dr. May Soe Aung, Associate Professor, University of Medicine (1), Yangon, Myanmar

**********

Acceptance letter

Deepak Dhamnetiya

10 Oct 2022

PONE-D-22-07813R1

A global, regional, and national survey on burden and Quality of Care Index (QCI) of bladder cancer: the global burden of disease study 1990-2019

Dear Dr. Farzadfar:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Deepak Dhamnetiya

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Fig. Scatter plot of age-standardized QCI (%) for the countries by the 7 GBD super-regions.

    (PDF)

    S1 Table. ICD-10 codes of bladder cancer mapped for GBD 2019.

    (PDF)

    S2 Table. The coefficients of the mixed-effect regression model.

    (DOCX)

    Attachment

    Submitted filename: Response_2022.08.24.docx

    Data Availability Statement

    Data Availability Statement: The study protocol and data used in this work are available both from [https://www.protocols.io/view/quality-of-care-index-qci-bprjmm4n] and the Global Burden of Disease Results Tool [https://ghdx.healthdata.org/gbd-results-tool]. The authors confirm they had no special access or privileges to the data that other researchers would not have.


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