Journal of Clinical Gynecology and Obstetrics, ISSN 1927-1271 print, 1927-128X online, Open Access |
Article copyright, the authors; Journal compilation copyright, J Clin Gynecol Obstet and Elmer Press Inc |
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Original Article
Volume 9, Number 4, December 2020, pages 79-95
The Association Between Pelvic Organ Prolapse, Pelvic Pain and Pelvic Reconstructive Surgery Using Transvaginal Mesh: A Secondary Analysis of a Prospective Multicenter Observational Cohort Trial
Figure
Tables
Preoperative pain symptoms | Total population (n = 277) | Posterior/apical (n = 135) | Anterior/apical (n = 142) | POP-Q stage 2 (n = 122) | POP-Q stage 3 or 4 (n = 150) | |||||
---|---|---|---|---|---|---|---|---|---|---|
Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | |
The pairwise superscripts “a”, “b”, “c” and “d” on the relative frequencies of certain symptoms indicate significant differences between the posterior/apical and anterior/apical groups in terms of the prevalence rates of R2 (Fisher’s exact tests, P < 0.05). PFDI: pelvic floor disorder inventory; POP-Q: pelvic organ prolapse quantification system. | ||||||||||
PFDI 1 (pressure in the lower abdomen) | ||||||||||
Symptom-free | 131 | 47.30% | 56 | 41.50% | 75 | 52.80% | 55 | 45.10% | 73 | 48.70% |
Somewhat | 55 | 19.90% | 29 | 21.50% | 26 | 18.30% | 24 | 19.70% | 30 | 20.00% |
Moderate | 47 | 17.00% | 23 | 17.00% | 24 | 16.90% | 20 | 16.40% | 27 | 18.00% |
Quite a bit | 44 | 15.90% | 27 | 20.00% | 17 | 12.00% | 23 | 18.90% | 20 | 13.30% |
R2 (moderate or quite a bit) | 91 | 32.90% | 50 | 37.00%a | 41 | 28.90%a | 43 | 35.30% | 47 | 31.30% |
Observed cases | 277 | 100.0% | 135 | 100.0% | 142 | 100.0% | 122 | 100.0% | 150 | 100.0% |
PFDI 2 (pain in the lower abdomen or genital area) | ||||||||||
Symptom-free | 167 | 60.30% | 74 | 54.80% | 93 | 65.50% | 75 | 61.50% | 90 | 60.00% |
Somewhat | 47 | 17.00% | 23 | 17.00% | 24 | 16.90% | 18 | 14.80% | 28 | 18.70% |
Moderate | 37 | 13.40% | 25 | 18.50% | 12 | 8.50% | 16 | 13.10% | 19 | 12.70% |
Quite a bit | 26 | 9.40% | 13 | 9.60% | 13 | 9.20% | 13 | 10.70% | 13 | 8.70% |
R2 (moderate or quite a bit) | 63 | 22.80% | 38 | 28.10%b | 25 | 17.70%b | 29 | 23.80% | 32 | 21.40% |
Observed cases | 277 | 100.0% | 135 | 100.0% | 142 | 100.0% | 122 | 100.0% | 150 | 100.0% |
PFDI 3 (heaviness or dullness in the pelvic area) | ||||||||||
Symptom-free | 141 | 50.90% | 63 | 46.70% | 78 | 54.90% | 62 | 50.80% | 77 | 51.30% |
Somewhat | 61 | 22.00% | 26 | 19.30% | 35 | 24.60% | 27 | 22.10% | 33 | 22.00% |
Moderate | 39 | 14.10% | 24 | 17.80% | 15 | 10.60% | 13 | 10.70% | 25 | 16.70% |
Quite a bit | 36 | 13.00% | 22 | 16.30% | 14 | 9.90% | 20 | 16.40% | 15 | 10.00% |
R2 (moderate or quite a bit) | 75 | 27.10% | 46 | 34.10%c | 29 | 20.50%c | 33 | 27.10% | 40 | 26.70% |
Observed cases | 277 | 100.0% | 135 | 100.0% | 142 | 100.0% | 122 | 100.0% | 150 | 100.0% |
PFDI 6 (pelvic discomfort during standing or physical exertion) | ||||||||||
Symptom-free | 107 | 38.60% | 56 | 41.50% | 51 | 35.90% | 53 | 43.40% | 51 | 34.00% |
Somewhat | 57 | 20.60% | 23 | 17.00% | 34 | 23.90% | 21 | 17.20% | 36 | 24.00% |
Moderate | 58 | 20.90% | 29 | 21.50% | 29 | 20.40% | 23 | 18.90% | 34 | 22.70% |
Quite a bit | 55 | 19.90% | 27 | 20.00% | 28 | 19.70% | 25 | 20.50% | 29 | 19.30% |
R2 (moderate or quite a bit) | 113 | 40.80% | 56 | 41.50% | 57 | 40.10% | 48 | 39.40% | 63 | 42.00% |
Observed cases | 277 | 100.0% | 135 | 100.0% | 142 | 100.0% | 122 | 100.0% | 150 | 100.0% |
PFDI 7 (pain in lower back most days) | ||||||||||
Symptom-free | 126 | 45.50% | 54 | 40.00% | 72 | 50.70% | 56 | 45.90% | 68 | 45.30% |
Somewhat | 46 | 16.60% | 23 | 17.00% | 23 | 16.20% | 20 | 16.40% | 24 | 16.00% |
Moderate | 42 | 15.20% | 24 | 17.80% | 18 | 12.70% | 15 | 12.30% | 26 | 17.30% |
Quite a bit | 63 | 22.70% | 34 | 25.20% | 29 | 20.40% | 31 | 25.40% | 32 | 21.30% |
R2 (moderate or quite a bit) | 105 | 37.90% | 58 | 43.00%d | 47 | 33.10%d | 46 | 37.70% | 58 | 38.60% |
Observed cases | 277 | 100.0% | 135 | 100.0% | 142 | 100.0% | 122 | 100.0% | 150 | 100.0% |
PFDI 46 (abdominal or lower back pain when straining for any reason) | ||||||||||
Symptom-free | 167 | 60.30% | 71 | 52.60% | 96 | 67.60% | 68 | 55.70% | 95 | 63.30% |
Somewhat | 42 | 15.20% | 27 | 20.00% | 15 | 10.60% | 25 | 20.50% | 17 | 11.30% |
Moderate | 36 | 13.00% | 21 | 15.60% | 15 | 10.60% | 17 | 13.90% | 18 | 12.00% |
Quite a bit | 32 | 11.60% | 16 | 11.90% | 16 | 11.30% | 12 | 9.80% | 20 | 13.30% |
R2 (moderate or quite a bit) | 68 | 24.60% | 37 | 27.50% | 31 | 21.90% | 29 | 23.70% | 38 | 25.30% |
Observed cases | 277 | 100.0% | 135 | 100.0% | 142 | 100.0% | 122 | 100.0% | 150 | 100.0% |
Location of pain symptoms | Prevalences of the irrelevant and relevant pain complaints in the front, visceral, back and all areas into different samples in the baseline | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total sample (n = 277) | Posterior/apical (n = 135) | Anterior/apical (n = 142) | X2-tests for testing posterior/apical vs. anterior/apical (P-values) | POP-Q stage 2 (n = 122) | POP-Q stage 3 or 4 (n = 150) | X2-tests for testing stage 2 vs. stage 3 or 4 (P-values) | ||||||
Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | |||
When considering all complaints, more than 61.30% of the female patients revealed at least one relevant pain symptom, irrespective of the affiliation sample. The area with the least frequent RPCs was the anterior area. For each considered sample, Cochran’s Q-tests followed by the McNemar tests were applied for testing differences between the three areas: anterior area (F), visceral (V) and posterior (B), in terms of the prevalence rates of RPCs, whereas differences in the prevalence rates of PRC between the “paP” and “aaP” groups as well as between the “S2P” and “S34P” groups were tested about significance for each considered area (sympotom domain) with X2-test. “+” indicates significant (marginally significant) area or group differences at a Bonferroni corrected level of significance (nominal level of significance α = 0.05). POP-Q: pelvic organ prolapse quantification system; PFDI: pelvic floor disorder inventory; IPC: irrelevant pain complaint; RPC: relevant pain complaint. | ||||||||||||
Anterior area (PFDI 1 and PFDI 2) | ||||||||||||
IPCs (IPC: PFDI 1 = R1 and PFDI 2 = R1) | 172 | 62.10% | 79 | 58.50% | 93 | 65.50% | X2(1) = 1.43 | 74 | 60.70% | 95 | 63.30% | X2(1) = 0.20 |
RPCs (RPC: PFDI 1 = R2 or PFDI 2 = R2) | 105 | 37.90% | 56 | 41.50% | 49 | 34.50% | P = 0.231 | 48 | 39.30% | 55 | 36.70% | P = 0.650 |
Total cases | 277 | 100.00% | 135 | 100.00% | 142 | 100.00% | 122 | 100.00% | 150 | 100.00% | ||
Visceral area (PFDI 3 and PFDI 6) | ||||||||||||
IPCs (IPC: PFDI 3 = R1 and PFDI 6 = R1) | 148 | 53.40% | 67 | 49.60% | 81 | 57.00% | X2(1) = 1.52 | 69 | 56.60% | 76 | 50.70% | X2(1) = 0.93 |
RPCs (RPC: PFDI 3 = R2 or PFDI 6 = R2) | 129 | 46.60% | 68 | 50.40% | 61 | 43.00% | P = 0.216 | 53 | 43.40% | 74 | 49.30% | P = 0.332 |
Total cases | 277 | 100.00% | 135 | 100.00% | 142 | 100.00% | 122 | 100,00% | 150 | 100.00% | ||
Posterior area (PFDI 7 and PFDI 46) | ||||||||||||
IPCs (IPC: PFDI 7 = R1 and PFDI 46 = R1) | 155 | 56.00% | 68 | 50.40% | 87 | 61.30% | X2(1) = 3.33 | 67 | 54.90% | 85 | 56.70% | X2(1) = 0.08 |
RPCs (RPC: PFDI 7 = R2 or PFDI 46 = R2) | 122 | 44.00% | 67 | 49.60% | 55 | 38.70% | P = 0.067 | 55 | 45.10% | 65 | 43.30% | P = 0.772 |
Total cases | 277 | 100.00% | 135 | 100.00% | 142 | 100.00% | 122 | 100.00% | 150 | 100.00% | ||
Testing global and simple differences in the occurrence of relevant complaints between regions (Cochran’s Q- and McNemar tests) | Q(DF = 2) = 6.92 | Q(DF = 2) = 3.97 | Q(DF = 2) = 3.32 | Q(DF = 2) = 1.25 | Q(DF = 2) = 7.97 | |||||||
P = 0.0314+ | P = 0.137 | P = 0.189 | P = 0.533 | P = 0.0186+ | ||||||||
F/V | F/V | |||||||||||
All areas | ||||||||||||
IPCs (PFDI: 1, 2, 3, 6, 7 and 46, all PFDIs = R1) | 90 | 32.50% | 35 | 25.90% | 55 | 39.70% | X2(1) = 5.52 | 37 | 21.30% | 51 | 34.00% | X2(1) = 1.41 |
RPCs (at least one of the PFDIs = R2) | 187 | 67.50% | 100 | 74.10% | 87 | 61.30% | P = 0.018+ | 85 | 69.70% | 99 | 66.00% | P = 0.519 |
Total cases | 277 | 100.00% | 135 | 100.00% | 142 | 100.00% | 122 | 100.00% | 150 | 100.00% |
Pre- and postoperative pain symptoms (total population, n = 277) | Baseline (phase 0) | 6 months after surgery (phase 1) | 12 months after surgery (phase 2) | 24 months after surgery (phase 3) | Cochran’s Q-tests for tesing global effects (P-values) | McNemar tests for testing simple effects (phase pairs with significant differences) | ||||
---|---|---|---|---|---|---|---|---|---|---|
Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | |||
Frequencies at each postoperative stage refer to the number of patients who were observed in this stage. The global time effects on the prevalence rates of R2 and of the “symptom-free” outcome were tested for significance with Cochran’s Q-tests. Whenever significant global effects were revealed, McNemar tests were subsequently performed to test the simple effects, i.e., for identifying the phase pairs with significant differences in the investigated prevalence rates. “*” (number pairs) indicates significant global effects on (phase pairs with significant differences in) the investigated prevalence rates at a Bonferroni corrected level of significance α* (where α* < α (= 0.05)). POP: pelvic organ prolapse; PFDI: pelvic floor disorder inventory. | ||||||||||
PFDI 1 (pressure in the lower abdomen) | ||||||||||
Symptom-free | 131 | 47.30% | 213 | 82.90% | 213 | 85.90% | 163 | 88.10% | P < 0.00001* | 0/1, 0/2, 0/3 |
Somewhat | 55 | 19.90% | 23 | 8.90% | 18 | 7.30% | 12 | 6.50% | ||
Moderate | 47 | 17.00% | 14 | 5.40% | 9 | 3.60% | 8 | 4.30% | ||
Quite a bit | 44 | 15.90% | 7 | 2.70% | 8 | 3.20% | 2 | 1.10% | ||
R2 (moderate or quite a bit) | 91 | 32.90% | 21 | 8.10% | 17 | 6.80% | 10 | 5.40% | P < 0.00001* | 0/1, 0/2, 0/3 |
Observed cases | 277 | 100.00% | 257 | 100.00% | 248 | 100.00% | 185 | 100.00% | ||
PFDI 2 (pain in the lower abdomen or genital area) | ||||||||||
Symptom-free | 167 | 60.30% | 217 | 84.40% | 218 | 87.90% | 171 | 92.40% | P < 0.00001* | 0/1, 0/2, 0/3 |
Somewhat | 47 | 17.00% | 18 | 7.00% | 16 | 6.50% | 9 | 4.90% | ||
Moderate | 37 | 13.40% | 15 | 5.80% | 8 | 3.20% | 3 | 1.60% | ||
Quite a bit | 26 | 9.40% | 7 | 2.70% | 6 | 2.40% | 2 | 1.10% | ||
R2 (moderate or quite a bit) | 63 | 22.80% | 22 | 8.50% | 14 | 5.60% | 5 | 2.70% | P < 0.00001* | 0/1, 0/2, 0/3 |
Observed cases | 277 | 100.00% | 257 | 100.00% | 248 | 100.00% | 185 | 100.00% | ||
PFDI 3 (heaviness or dullness in the pelvic area) | ||||||||||
Symptom-free | 141 | 50.90% | 226 | 87.90% | 223 | 89.90% | 170 | 91.90% | P < 0.00001* | 0/1, 0/2, 0/3 |
Somewhat | 61 | 22.00% | 22 | 8.60% | 13 | 5.20% | 10 | 5.40% | ||
Moderate | 39 | 14.10% | 5 | 1.90% | 6 | 2.40% | 3 | 1.60% | ||
Quite a bit | 36 | 13.00% | 4 | 1.60% | 6 | 2.40% | 2 | 1.10% | ||
R2 (moderate or quite a bit) | 75 | 27.10% | 9 | 3.50% | 12 | 4.80% | 5 | 2.70% | P < 0.00001* | 0/1, 0/2, 0/3 |
Observed cases | 277 | 100.00% | 257 | 100.00% | 248 | 100.00% | 185 | 100.00% | ||
PFDI 6 (pelvic discomfort during standing or pshysically exerting) | ||||||||||
Symptom-free | 107 | 38.60% | 218 | 84.80% | 224 | 90.30% | 169 | 91.40% | P < 0.00001* | 0/1, 0/2, 0/3 |
Somewhat | 57 | 20.60% | 19 | 7.40% | 9 | 3.60% | 7 | 3.80% | ||
Moderate | 58 | 20.90% | 13 | 5.10% | 12 | 4.80% | 7 | 3.80% | ||
Quite a bit | 55 | 19.90% | 7 | 2.70% | 3 | 1.20% | 2 | 1.10% | ||
R2 (moderate or quite a bit) | 113 | 40.80% | 20 | 7.80% | 15 | 6.00% | 9 | 4.90% | P < 0.00001* | 0/1, 0/2, 0/3 |
Observed cases | 277 | 100.00% | 257 | 100.00% | 248 | 100.00% | 185 | 100.00% | ||
PFDI 7 (pain in lower back most days) | ||||||||||
Symptom-free | 126 | 45.50% | 182 | 70.80% | 178 | 71.80% | 139 | 75.10% | P < 0.00001* | 0/1, 0/2, 0/3 |
Somewhat | 46 | 16.60% | 25 | 9.70% | 22 | 8.90% | 13 | 7.00% | ||
Moderate | 42 | 15.20% | 25 | 9.70% | 19 | 7.70% | 17 | 9.20% | ||
Quite a bit | 63 | 22.70% | 25 | 9.70% | 29 | 11.70% | 16 | 8.60% | ||
R2 (moderate or quite a bit) | 105 | 37.90% | 50 | 19.40% | 48 | 19.40% | 33 | 17.80% | P < 0.00001* | 0/1, 0/2, 0/3 |
Observed cases | 277 | 100.00% | 257 | 100.00% | 248 | 100.00% | 185 | 100.00% | ||
PFDI 46 (abdominal or lower back pain when straining for any reason) | ||||||||||
Symptom-free | 167 | 60.30% | 210 | 81.70% | 205 | 82.70% | 156 | 84.30% | P < 0.00001* | 0/1, 0/2, 0/3 |
Somewhat | 42 | 15.20% | 16 | 6.20% | 13 | 5.20% | 10 | 5.40% | ||
Moderate | 36 | 13.00% | 15 | 5.80% | 18 | 7.30% | 10 | 5.40% | ||
Quite a bit | 32 | 11.60% | 16 | 6.20% | 12 | 4.80% | 9 | 4.90% | ||
R2 (moderate or quite a bit) | 68 | 24.60% | 31 | 12.00% | 30 | 12.10% | 19 | 10.30% | P < 0.00001* | 0/1, 0/2, 0/3 |
Observed cases | 277 | 100.00% | 257 | 100.00% | 248 | 100.00% | 185 | 100.00% |
Location of pain symptoms | Baseline (phase 0) | 6 m after surgery (phase 1) | 12 m after surgery (phase 2) | 24 m after surgery (phase 3) | Cochran’s Q-tests for testing global effects (Q-values and corresponding P-values) | McNemar tests for testing simple effects (phase pairs with signigicant differences) | ||||
---|---|---|---|---|---|---|---|---|---|---|
Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | |||
Additionally, the cure rates, ORs and 95% CIs of the ORs, when comparing the postoperative prevalence rates of RPCs with those at baseline, were entered. OR is the chance of symptom occurrence in an experimental condition (say A) divided by the chance of symptom occurrence in another experimental condition (say B). An OR equal to 1 means identical chances for symptom occurrence in both experimental conditions. Cochran’s Q-tests followed by McNemar tests were applied for testing global and simple effects of the surgery on the occurrence of RPCs in each complaint area. The same tests were also performed to test global and local complaint-area differences in the occurrence of RPC at baseline as well as at each postoperative phase (6, 12 and 24 months after surgery). “*” (“+”) indicates significant global surgery or region effects at a Bonferroni corrected level of significance (at the nominal level of significance α = 0.05). Number (capital letter) pairs characterize significant differences between corresponding phase or complaint-area pairs. Note that the analysis of single effects with the McNemar tests was only performed when the prior applied Cochran’s tests supply significant global effects. RPC: relevant pain complaint; OR: odds ratio; CI: confidence interval; PFDI: pelvic floor disorder inventory. | ||||||||||
Front area (PFDI 1 and PFDI 2) | ||||||||||
Observed cases | 277 | 257 | 248 | 185 | Q(DF = 3) = 136.56 | |||||
RPCs | 105 | 37.90% | 30 | 11.70% | 23 | 9.30% | 11 | 5.90% | P < 0.00001* | 0/1, 0/2, 0/3 |
Cure rates of the RPC | 69.13% | 75.46% | 84.43% | |||||||
OR of the RPC | 0.216 | 0.167 | 0.104 | |||||||
95% CI of OR | 0.14 - 0.34 | 0.10 - 0.27 | 0.05 - 0.20 | |||||||
Visceral area (PFDI 3 and PFDI 6) | ||||||||||
Observed cases | 277 | 257 | 248 | 185 | Q(DF = 3) = 193.41 | |||||
RPCs | 129 | 46.60% | 22 | 8.60% | 18 | 7.30% | 11 | 5.90% | P < 0.00001* | 0/1, 0/2, 0/3 |
Cure rates of the RPC | 81.55% | 84.33% | 87.34% | |||||||
OR of the RPC | 0.107 | 0.090 | 0.073 | |||||||
95% CI of OR | 0.07 - 0.17 | 0.05 - 0.15 | 0.04 - 0.13 | |||||||
Posterior area (PFDI 7 and PFDI 46) | ||||||||||
Observed cases | 277 | 257 | 248 | 185 | Q(DF = 3) = 37.44 | |||||
RPCs | 122 | 44.00% | 62 | 24.10% | 56 | 22.60% | 39 | 24.10% | P < 0.00001* | 0/1, 0/2, 0/3 |
Cure rates of the RPC | 45.23% | 48.64% | 45.23% | |||||||
OR of the RPC | 0.403 | 0.370 | 0.339 | |||||||
95% CI of OR | 0.28 - 0.57 | 0.26 - 0.53 | 0.23 - 0.51 | |||||||
Testing global and simple differences in the occurence of relevant complaints between areas (Cochran's Q- and McNemar tests) | Q(DF = 2) = 6.92 P = 0.0314+ F/V | Q(DF = 2) = 37.33 P < 0.00001* F/B, V/B | Q(DF = 2) = 44.10 P < 0.00001* F/B, V/B | Q(DF = 2) = 36.46 P < 0.00001* F/B, V/B | ||||||
All areas (PFDI 1, 2, 3, 6, 7 and 46) | ||||||||||
Observed cases | 277 | 257 | 248 | 185 | Q(DF = 3) = 122.20 | |||||
RPCs | 187 | 67.50% | 80 | 31.10% | 67 | 27.00% | 46 | 24.90% | P < 0.00001* | 0/1, 0/2, 0/3 |
Cure rates of the RPC | 53.93% | 59.98% | 63.11% | |||||||
OR of the RPC | 0.218 | 0.178 | 0.159 | |||||||
95% CI of OR | 0.16 - 0.30 | 0.13 - 0.25 | 0.11 - 0.23 |
Regional dependent pain (posterior/apical (n = 135) versus anterior/apical (n = 142)) | Comparisons of postoperative RPCs in the front, visceral, back and all areas between patients with posterior/apical and anterior/apical POP-Q defect | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Baseline (phase 0) | 6 m after surgery (phase 1) | 12 m after surgery (phase 2) | 24 m after surgery (phase 3) | Cochran’s Q-tests for testing global effects | McNemar tests for testing simple effects | |||||
Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | |||
“*” (“+”) indicates significant global surgery or group effects on the prevalence of RPC at a Bonferroni corrected level of significance (at the nominal level of significance α = 0.05). Number pairs characterize significant differences between the corresponding phases. The prevalence rates of RPCs were significantly reduced after surgery in both groups and that for each complaint area (anterior, visceral, posterior and all areas (Cochran’s Q-tests, followed by McNemar tests, P < α*, where α* a Bonferroni corrected α (α* < α = 0.05)). Comparisons of the RPC frequencies between “paP” and “aaP” patients into each phase (baseline and 6, 12, 24 months after surgery) and in each complaint area showed that “aaP” patients had significantly more pain reduction than “paP” patients 6 and 24 months after surgery and that in any complaint area (X2-tests, P-values significant at the nominal α (= 0.05) or at a Bonferroni corrected level of significance α*, where α* < α). RPC: relevant pain complaint; POP-Q: pelvic organ prolapse quantification system; PFDI: pelvic floor disorder inventory. | ||||||||||
Front area (PFDI 1 and PFDI 2) (RPC: “PFDI 1 = R2 or PFDI 2 = R2”) | ||||||||||
RPC in the posterior/apical sample | 56 | 41.50% | 15 | 11.80% | 16 | 13.00% | 10 | 9.10% | Q(DF = 3) = 67.37 | 0/1, 0/2, 0/3 |
Total cases | 135 | 127 | 123 | 110 | P < 0.00001* | |||||
RPC in the anterior/apical sample | 49 | 34.50% | 15 | 11.50% | 7 | 5.60% | 1 | 1.30% | Q(DF = 3) = 72.73 | 0/1, 0/2, 0/3 |
Total cases | 142 | 130 | 125 | 75 | P < 0.00001* | |||||
X2-tests for testing posterior/apical vs. anterior/apical | X2(1) = 1.43 P = 0.231 | X2(1) = 0.004 P = 0.945 | X2(1) = 4.04 P = 0.044+ | X2(1) = 4.79 P = 0.028+ | ||||||
Visceral area (PFDI 3 and PFDI 6) (RPC: “PFDI 3 = R2 or PFDI 6 = R2” | ||||||||||
RPC in the posterior/apical sample | 68 | 50.40% | 14 | 11.00% | 14 | 11.40% | 10 | 9.10% | Q(DF = 3) = 136.56 | 0/1, 0/2, 0/3 |
Total cases | 135 | 127 | 123 | 110 | P < 0.00001* | |||||
RPC in the anterior/apical sample | 61 | 43.00% | 8 | 6.20% | 4 | 3.20% | 1 | 1.30% | Q(DF = 3) = 93.23 | 0/1, 0/2, 0/3 |
Total cases | 142 | 130 | 125 | 75 | P < 0.00001* | |||||
X2-tests for testing posterior/apical vs. anterior/apical | X2(1) = 1.52 P = 0.256 | X2(1) = 1.94 P = 0.162 | X2(1) = 6.16 P = 0.013+ | X2(1) = 4.79 P = 0.028+ | ||||||
Posterior area (PFDI 7 and PFDI 46) (RPC: “PFDI 7 = R2 or PFDI 46 = R2”) | ||||||||||
RPC in the posterior/apical sample | 67 | 49.60% | 37 | 29.10% | 39 | 31.70% | 29 | 26.40% | Q(DF = 3) = 19.21 | 0/1, 0/2, 0/3 |
Total cases | 135 | 127 | 123 | 110 | P = 0.0002* | |||||
RPC in the anterior/apical sample | 55 | 38.70% | 25 | 19.20% | 17 | 13.60% | 10 | 13.30% | Q(DF = 3) = 21.98 | 0/1, 0/2, 0/3 |
Total cases | 142 | 130 | 125 | 75 | P = 0.0001* | |||||
X2-tests for testing posterior/apical vs. anterior/apical | X2(1) = 3.33 P = 0.067 | X2(1) = 3.44 P = 0.063 | X2(1) = 11.62 P < 0.0001* | X2(1) = 4.55 P = 0.032+ | ||||||
All areas (PFDI: 1, 2, 3, 6, 7 and 46) (RPC: “at least one of the PFDIs = R2” | ||||||||||
RPC in the posterior/apical sample | 100 | 74.10% | 45 | 35.40% | 48 | 39.00% | 35 | 31.80% | Q(DF = 3) = 65.15 | 0/1, 0/2, 0/3 |
Total cases | 135 | 127 | 123 | 110 | P < 0.00001* | |||||
RPC in the anterior/apical sample | 87 | 61.30% | 35 | 26.90% | 19 | 15.20% | 11 | 14.70% | Q(DF = 3) = 61.42 | 0/1, 0/2, 0/3 |
Total cases | 142 | 130 | 125 | 75 | P < 0.00001* | |||||
X2-tests for testing posterior/apical vs. anterior/apical | X2(1) = 5.52 P = 0.018+ | X2(1) = 2.17 P = 0.140 | X2(1) = 17.84 P < 0.0001* | X2(1) = 7.02 P = 0.008* |
Regional dependent pain (POP-Q stage 2 (n = 122) versus POP-Q stage 3 or 4 (n = 150)) | Comparisons of postoperative RPCs in the front, visceral, back and all areasbetween patients with POP-Q stage 2 and POP-Q stage 3 or 4 | |||||||||
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Baseline (phase 0) | 6 m after surgery (phase 1) | 12 m after surgery (phase 2) | 24 m after surgery (phase 3) | Cochran’s Q-tests for testing global effects | McNemar tests for testing simple effects | |||||
Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | Absolute frequency | Relative frequency | |||
“*” (“+”) indicates significant global surgery or group effects on the prevalence of RPC at a Bonferroni corrected level of significance (at the nominal level of significance α = 0.05). Number pairs characterize significant (or marginal significant differences whenever provided with the superscript “+”) differences between the corresponding phases. The prevalence rates of RPCs were significantly reduced after surgery in both groups and that for each complaint area (anterior, visceral, posterior and all complaints) (Cochran’s Q-tests, followed by McNemar tests, P < α*, where α* a Bonferroni corrected α (α* < α = 0.05)). Comparisons of the RPC frequencies between “S2P” and “S34P” patients into each phase (baseline and 6, 12, 24 months after surgery) and in each complaint area showed that “S34P” patients had significantly more pain reduction than “S2P” patients 6 and 24 months after surgery in the anterior, posterior and the whole area (X2-tests, P-values significant at the nominal α (= 0.05) or at a Bonferroni corrected level of significance α*, where α* < α). POP-Q: pelvic organ prolapse quantification system; RPC: relevant pain complaint; PFDI: pelvic floor disorder inventory. | ||||||||||
Front area (PFDI 1 and PFDI 2) (RPC: “PFDI 1 = R2 or PFDI 2 = R2”) | ||||||||||
RPC in the “POP-Q stage 2” sample | 48 | 39.30% | 13 | 11.60% | 16 | 14.30% | 9 | 9.90% | Q(DF = 3) = 49.25 | 0/1, 0/2, 0/3 |
Total cases | 122 | 112 | 112 | 91 | P < 0.00001* | |||||
RPC in the “POP-Q stage 3/4” sample | 55 | 36.70% | 17 | 12.10% | 6 | 4.60% | 2 | 2.20% | Q(DF = 3) = 86.28 | 0/1, 0/2, 0/3 |
Total cases | 150 | 140 | 131 | 89 | P < 0.00001* | |||||
X2-tests for testing POP-Q stage 2 vs. POP-Q stage 3 or 4 | X2(1) = 0.20 P = 0.650 | X2(1) = 0.02 P = 0.896 | X2(1) = 6.90 P = 0.008* | X2(1) = 4.58 P = 0.032+ | ||||||
Visceral area (PFDI 3 and PFDI 6) (RPC: “PFDI 3 = R2 or PFDI 6 = R2”) | ||||||||||
RPC in the “POP-Q stage 2” sample | 53 | 43.40% | 13 | 11.60% | 12 | 10.70% | 8 | 8.80% | Q(DF = 3) = 65.26 | 0/1, 0/2, 0/3 |
Total cases | 122 | 112 | 112 | 91 | P < 0.00001* | |||||
RPC in the “POP-Q stage 3/4” sample | 74 | 49.30% | 9 | 6.40% | 6 | 4.60% | 3 | 3.40% | Q(DF = 3) = 124.70 | 0/1, 0/2, 0/3 |
Total cases | 150 | 140 | 131 | 89 | P < 0.00001* | |||||
X2-tests for testing POP-Q stage 2 vs. POP-Q stage 3 or 4 | X2(1) = 0.93 P = 0.332 | X2(1) = 2.09 P = 0.146 | X2(1) = 3.31 P = 0.068 | X2(1) = 2.30 P = 0.129 | ||||||
Posterior area (PFDI 7 and PFDI 46) (RPC: “PFDI 7 = R2 or PFDI 46 = R2”) | ||||||||||
RPC in the “POP-Q stage 2” sample | 55 | 43.40% | 32 | 28.60% | 36 | 32.10% | 27 | 29.70% | Q(DF = 3) = 11.24 | 0/1, 0/2+, 0/3+ |
Total cases | 122 | 112 | 112 | 91 | P = 0.0105+ | |||||
RPC in the “POP-Q stage 3/4” sample | 74 | 49.30% | 30 | 21.40% | 20 | 15.30% | 12 | 13.50% | Q(DF = 3) = 25.96 | 0/1, 0/2, 0/3 |
Total cases | 150 | 140 | 131 | 89 | P < 0.00001* | |||||
X2-tests for testing POP-Q stage 2 vs. POP-Q stage 3 or 4 | X2(1) = 0.08 P = 0.772 | X2(1) = 1.71 P = 0.190 | X2(1) = 9.69 P = 0.002* | X2(1) = 6.94 P = 0.008* | ||||||
All areas (PFDI: 1, 2, 3, 6, 7 and 46) (RPC: “at least one of the PFDIs = R2”) | ||||||||||
RPC in the “POP-Q stage 2” sample | 55 | 45.10% | 39 | 34.80% | 44 | 39.30% | 32 | 35.20% | Q(DF = 3) = 39.64 | 0/1, 0/2, 0/3 |
Total cases | 122 | 112 | 112 | 91 | P < 0.00001* | |||||
RPC in the “POP-Q stage 3/4” sample | 65 | 43.30% | 41 | 29.30% | 22 | 16.80% | 14 | 15.70% | Q(DF = 3) = 81.38 | 0/1, 0/2, 0/3 |
Total cases | 150 | 140 | 131 | 89 | P < 0.00001* | |||||
X2-tests for testing POP-Q stage 2 vs. POP-Q stage 3 or 4 | X2(1) = 1.41 P = 0.559 | X2(1) = 0.87 P = 0.348 | X2(1) = 15.43 P < 0.0001* | X2(1) = 8.93 P = 0.002* |