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This article was downloaded by: [Swedish Consortia Trial]On: 9 September 2008Access details: Access Details: [subscription number 777347451]Publisher Informa HealthcareInforma Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House,37-41 Mortimer Street, London W1T 3JH, UK
Acta Obstetricia et Gynecologica ScandinavicaPublication details, including instructions for authors and subscription information:http://www.informaworld.com/smpp/title~content=t716100748
Regression of pelvic girdle pain after delivery: follow-up of a randomised singleblind controlled trial with different treatment modalitiesH. Elden a; H. Hagberg a; M. Fagevik Olsen b; L. Ladfors a; H. C. Ostgaard c
a Perinatal Center, Department of Obstetrics and Gynecology, Sahlgrenska University Hospital, GöteborgUniversity, Sweden b Department of Occupational Therapy and Physical Therapy, Sahlgrenska UniversityHospital, Göteborg University, Sweden c Department of Orthopedics, Sahlgrenska Academy, SahlgrenskaUniversity Hospital, Göteborg University, Sweden
First Published on: 10 December 2007
To cite this Article Elden, H., Hagberg, H., Olsen, M. Fagevik, Ladfors, L. and Ostgaard, H. C.(2007)'Regression of pelvic girdle painafter delivery: follow-up of a randomised single blind controlled trial with different treatment modalities',Acta Obstetricia etGynecologica Scandinavica,87:2,201 — 208
To link to this Article: DOI: 10.1080/00016340701823959
URL: http://dx.doi.org/10.1080/00016340701823959
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ORIGINAL ARTICLE
Regression of pelvic girdle pain after delivery: follow-up of arandomised single blind controlled trial with different treatmentmodalities
H. ELDEN1, H. HAGBERG1, M. FAGEVIK OLSEN2, L. LADFORS1 & H.C. OSTGAARD3
1Perinatal Center, Department of Obstetrics and Gynecology, 2Department of Occupational Therapy and Physical Therapy,
and 3Department of Orthopedics, Sahlgrenska Academy, Sahlgrenska University Hospital, Goteborg University, Sweden
AbstractObjective. An earlier publication showed that acupuncture and stabilising exercises as an adjunct to standard treatment waseffective for pelvic girdle pain during pregnancy, but the post-pregnancy effects of these treatment modalities are unknown.The aim of this follow-up study was to describe regression of pelvic girdle pain after delivery in these women. Design. Arandomised, single blind, controlled trial. Setting. East Hospital and 27 maternity care centres in Goteborg, Sweden.Population. Some 386 pregnant women with pelvic girdle pain. Methods. Participants were randomly assigned to standardtreatment plus acupuncture (n�125), standard treatment plus specific stabilising exercises (n�131) or to standardtreatment alone (n�130). Main outcome measures. Primary outcome measures: pain intensity (Visual Analogue Scale).Secondary outcome measure: assessment of the severity of pelvic girdle pain by an independent examiner 12 weeks afterdelivery. Results. Approximately three-quarters of all the women were free of pain 3 weeks after delivery. There were nodifferences in recovery between the 3 treatment groups. According to the detailed physical examination, pelvic girdle painhad resolved in 99% of the women 12 weeks after delivery. Conclusions. This study shows that irrespective of treatmentmodality, regression of pelvic girdle pain occurs in the great majority of women within 12 weeks after delivery.
Key words: Pelvic girdle pain, pregnancy, acupuncture, stabilising exercises, randomised controlled trial
Abbreviations: P4-test: posterior pelvic pain provocation test
Introduction
Pelvic girdle pain is a common complaint for women
during pregnancy causing considerable disability and
distress (1,2). Risk factors are a history of previous
low back pain, trauma, higher level of stress, and low
job satisfaction (3). In some women, it can be the
beginning of a chronic condition (4,5).
Pelvic girdle pain can be divided into subgroups
depending on the number of affected joints in the
pelvic girdle. Women with pelvic girdle syndrome,
i.e. bilateral sacroiliac pain plus symphysiolysial
pain, have been found to have the worst prognosis,
and those with isolated symphysiolysial pain, the
best prognosis (6). Postpartum follow-up studies
have shown that 10�75% of the women had persist-
ing pain 1�3 months after delivery (7,8).
The reason for the discrepancy between the results
from different studies could be that different criteria
for pelvic girdle pain have been used, and that
women with lumbar pain have also been included
(1,5,7�12).
However, in 2004, a new definition based on
existing systematic reviews and a national guideline
was published (13), which states that the diagnosis
can only be reached after exclusion of lumbar causes,
and that it should be based on both reports from the
women and a physical standardised examination
including specific clinical tests which reproduce
pain in the pelvic girdle. Standard treatment for
Correspondence: Helen Elden, Perinatal Center, Department of Obstetrics and Gynecology, Institute for Clinical Sciences, Sahlgrenska University Hospital/
East, University of Goteborg, SE-416 85 Sweden. E-mail: [email protected]
Acta Obstetricia et Gynecologica. 2008; 87: 201�208
(Received 12 March 2007; accepted 21 November 2007)
ISSN 0001-6349 print/ISSN 1600-0412 online # 2008 Taylor & Francis
DOI: 10.1080/00016340701823959
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pelvic girdle pain usually consists of a pelvic belt,
home training programme exercises, and patient
education, although the efficacy of these interven-
tions remains questionable (14).
Currently there are indications that acupuncture
(15�19) and stabilising exercises (19) are efficient
during pregnancy. To our knowledge, no study
has presented findings of the post-pregnancy effects
of acupuncture and stabilising exercises for pelvic
girdle pain. In the present study, we present 12-week
follow-up results of women who were randomised to
standard treatment, (12) standard treatment plus
acupuncture or standard treatment plus specific
stabilising exercises (19).
Material and methods
This study was carried out at East Hospital, Sahl-
grenska Academy and at 27 maternity care centres in
the hospitals reference area in Goteborg, Sweden,
from 2000 to 2002. The trial was approved by the
local ethics committee and the women gave their
informed consent before entering the study. The
study comprised 1 week baseline registration of pain,
treatment for 6 weeks, follow-up within 1 week after
end of treatment, and follow-up 12 weeks after
delivery. Inclusion criteria were healthy women at
12�31 completed gestational weeks, well integrated
in the Swedish language with singleton fetuses and
defined pelvic girdle pain, according to the criteria of
Ostgaard (Table I) (20). Patients with other pain
conditions, systemic disorders, or contraindications
to treatment were excluded. The pregnancy-related
part of this study has been reported previously (19).
Interventions
Patients were given standard treatment, standard
treatment plus acupuncture or standard treatment
plus specific stabilising exercises for 6 weeks.
Details of the interventions are given in a previous
paper (19).
Measurements before inclusion in the study
Each patient completed a previously used question-
naire (8) including a detailed history of back pain,
ascertained vocational factors, previous back pain,
level of physical exercise before pregnancy, and they
assessed their present pain on a 100-point visual
analogue scale (VAS) every morning and evening for
5�7 days before inclusion.
A detailed, standardised, physical examination was
performed by 1 of 3 independent specially trained
physiotherapists. The women were then randomised
individually. The full examination programme
and randomisation procedure have been extensively
described previously (19).
Measurements showing regression of pregnancy-related
pelvic girdle pain
The women’s reports of pain (VAS) and the results
from the physical examination 12 weeks after deliv-
ery were used as measures of regression of pelvic
girdle pain. Patients were instructed to estimate their
present pain related to motion every morning and
every evening. They were instructed not to continue
with their diaries if the pain disappeared and to
restart the registration if the pain returned. The
diaries were collected at follow-up.
Analysis/statistics
Calculating of sample size has been reported earlier
(19). The median VAS levels were defined in
the mornings and evenings for each patient by
calculating the median for the first 5�7 days after
delivery. The same calculations were carried out
for the following 11 weeks. We chose VAS B10 mm
as a definition of no pain according to the literature
(1,21). The main analyses were performed by
intention to treat. If values were missing or the
women had stopped registration due to disappear-
ance of pain, the last value was carried forward. An
analysis to investigate if the severity of pelvic girdle
pain during pregnancy affected the recovery after
delivery was carried out. The women were divided
into 5 subgroups (6).
Data were compared using the Mann�Whitney
U-test. Medians, 25�75th percentiles, means and
standard deviations were calculated when possible.
x2-tests were used as appropriate. Adjustments
(multiplication by three) of the p-values due to
multiple comparisons were performed by Bonferro-
ni’s method; an adjusted p-value B0.05 was con-
sidered significant. The SAS software package,
version V8 and SPSS, version 13.0, was used.
Table I. Pelvic girdle pain according to the criteria of Ostgaard.
All criteria have to be fulfilled for the diagnosis
. Time- and weight-bearing-related pain in the posterior pelvis,
deep in one or both gluteal areas
. Pain-drawing with markings in the gluteal area distal and
lateral to L5-S1 with or without radiating pain on the posterior
thigh but not down to the foot
. Pain-free intervals with sudden pain attacks
. Pain when turning in bed
. A free range of motion in the hips and spine
. No nerve root syndrome
. A positive posterior pelvic pain provocation test (the P4-test)
202 H. Elden et al.
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Results
Figure 1 shows the progress of patients through the
trial and withdrawals from the study. Of the 558
pregnant women assessed for eligibility, 172 women
were excluded because they did not fulfil the
inclusion criteria, 35 women were lost to follow-up
because they declined treatment, and 21 women
were lost to follow-up because they declined parti-
cipation after treatment.
Maternal age at inclusion was 30.8 (SD: 4.8) for
the standard group, 30.6 (SD: 4) for the acupunc-
ture group and 30.0 (SD: 4) for the stabilising
exercise group. Gestational week at inclusion was
24�3 (SD: 4.9) for the standard group, 24�3 (SD:
4.7) for the acupuncture group, and 24�3 (SD: 4.9)
for the stabilising exercise group, respectively. In
all, 33 women (25%) in the standard group, 34
(27%) in the acupuncture group, and 36 (28%) in
the stabilising group were primiparas (24). No
baseline differences between the women recruited
and the women who withdrew during the trial and
those who were followed up 12 weeks after delivery
were seen with respect to age, parity, and the results
of the physical examination, the questionnaire, and
the diaries (data not shown).
Regression of pregnancy-related pelvic girdle pain as
reported by the women
Figure 2 shows that about three-quarters of all the
women were free of pain 3 weeks after delivery, and
89% of the women reported no pain 12 weeks after
delivery. At 12 weeks follow-up, 33/99 women in the
standard group, 31/105 women in the acupuncture
group, and 25/107 women in the stabilising exercise
group stated that they experienced no pain after
delivery, and therefore they did not fill in a diary.
These women are included in Figure 2 from week 1.
Table II shows that no differences were found in pain
scores between the study groups among the women
that returned pain reports.
Regression of pelvic girdle pain according to the
assessments 12 weeks after delivery
Table III shows that 12 weeks after delivery, pelvic
girdle pain had resolved in 99% of the women. The
Women assessed for eligibility (n=558)1-wk baseline registration before inclusion visit
Excluded at inclusion visit (n=172 ( Not meeting inclusioncriteria)
Low back pain (n=18)Pelvic girdle pain plus low back pain (n=17)Isolated symphysiolysis ( n=36)No provocation tests positive (n=64)Other pain conditions (n=10)Systemic disorders (n=4)High risk pregnancy ( n=6)No complaints (n=8)Declined participation (n=7)Gestation week>32 (n=1)Twin pregnancy (n=1)
Randomised (n=386)
Standard treatment (n=130)Declined treatment (n=15)
Acupuncture (n=125)Declined treatment (n=10) Stabilizing Exercises (n=131)
Declined treatment (n=9)Moved from the area (n=1)
Allocation
Missing diaries (n=49)Declined participation aftertreatment (n=10)Lost by patient (n=5)Did not fill in diary (n=1)No diary because of no pelvicgirdle pain (n=33)
Lost to follow-up (n =10)Declined participation aftertreatment (n=10)
Missing diaries (n=38)Declined participation aftertreatment (n=4)Lost by patient (n=3)Did not fill in diary (n=1)No diary because of no pelvicgirdle pain (n=30)
Lost to follow-up (n =4)Declined participation aftertreatment (n=4)
Diaries and assessments excludedfrom analysis (n=2)Nerve root syndrome (n=1)Low back pain (n=1)
Missing diaries (n=39)Declined participation aftertreatment (n=7)Lost by patient (n=7)No diary because of no pelvic girdlepain (n=25)
Lost to follow-up (n=7)Declined participation aftertreatment (n=7)
Analysed12 weeksafterdelivery
Pain reports (n=33)Diaries (n=66)Follow-up visits (n=105)
Pain reports (n=30)Diaries (n=75)Follow-up visits (n=109)
Pain reports (n=25)Diaries (n=82)Follow-up visits (n=114)
Follow-up12 weeksafterdelivery
Figure 1. Participants’ progress through trial and withdrawals.
Regression of pelvic girdle pain after delivery 203
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women randomised to the stabilising exercise had
fewer positive pain provocation tests 12 weeks after
delivery than controls (pB0.001). The results of the
examination confirmed excellent recovery among all
women including those who did not fill in diaries
postpartum. A majority of these women ((24/33;
73%) in the standard group, (27/30; 90%) in the
acupuncture group, and (22/25; 88%) in the stabi-
lising exercise group) did not fulfil any of the criteria
for pelvic girdle pain at the examination 12 weeks’
postpartum. The other women fulfilled 1 or 2 of the
criteria, but none of them fulfilled all the criteria for
pelvic girdle pain (data not shown). No difference in
numbers of women in the subgroups of pelvic girdle
pain or in numbers of women that fulfilled all criteria
for pelvic girdle pain was found in the study groups.
When combining the results of the pain ratings and
the pain drawings, 12/105 (11%) of the women in
the standard group, 12/109 (11%) of the women in
the acupuncture group, and 7/114 (6%) of the
women in the stabilising exercise group filled in
markings in the gluteal area on the pain drawings
and reported daily pain (VAS ]0 mm) in their
diaries (data not shown).
Discussion
The main finding of this study was that complete
regression of pelvic girdle pain occurred in 99% of
the patients 12 weeks after delivery.
Pelvic girdle pain was diagnosed according to the
criteria of Ostgaard (20). This definition is compar-
able to the definition of pelvic girdle pain in the
European guidelines (13), except for women with
isolated symphyseal pain where the criteria used
in this study did not allow inclusion (36 women
excluded). However, symphyseal pain combined
with sacroiliac pain was common in the studied
population. Thus, 159 women (41%) had symphy-
seal pain combined with sacroiliac pain at inclusion,
i.e. pelvic girdle syndrome or one-sided sacroiliac
pain plus symphyseal pain. In addition, our results
showing that only 3 women had isolated symphyseal
pain 12 weeks after delivery are in line with results
from Albert et al. (6), who showed that almost all
women with isolated symphyseal pain had recovered
within 4 months after delivery.
It is recommended that 2 pain provocation tests
should be positive for the diagnosis of pelvic girdle
pain (1,22) The physical examination in our study
included 7 tests, but only 1 positive pain provocation
test (the P4-test) was required for inclusion, which
might have led to inclusion of 30 women with ‘mild’
symptoms. On the other hand, 264 women (68%)
had ]3 positive pain provocation test suggesting
that most women were severely affected.
The women in the group with stabilising exercises
had less frequent positive pain provocation tests, this
may be explained by the recommended continuous
daily exercises, including exercises in short sessions
on several occasions during the day even after
delivery. This may have strengthened their pelvic
muscles and made the women less sensitive to the
pain provocation tests.
In several studies, the incidence and intensity of
pelvic girdle pain and/or lumbar pain changing
rapidly at the time of delivery has been described.
This is the first study to demonstrate by daily
recordings of VAS that there is progressive resolution
of pain. However, a drawback of the study is that
0
01
02
03
04
05
06
07
08
09
001
211101987654321
)99=n(puorgdradnatS )501=n(puorgerutcnupucA )701=n(puorgesicrexegnisilibatS
skeeWretfa
yreviled
Per
cent
ages
of
wom
en
Figure 2. Percentages of women reporting pelvic girdle pain (VAS]10 mm) both in the mornings and in the evenings during 12 weeks after
delivery. VAS�Visual analogue scale.
204 H. Elden et al.
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about 29% of the women did not fill in a complete
diary because of the instruction that they were not
obliged to continue their recording after disappear-
ance of the pain. Nevertheless, a majority of the
women did fill in diaries, and the number of women
who did not return diaries was similar in the different
treatment groups. In addition, the results of the
examinations showed that a majority (82%) of these
women did not fulfil any of the criteria for pelvic
girdle pain 12 weeks’ postpartum, which confirms
the assumption that these women did not complete
their diaries because of resolution of pain rather than
because of neglect or other reasons. Even if we do
not know the exact time of disappearance of pain in
these women, the physical examination showed that
most were fully recovered 12 weeks after delivery.
The women appeared to recover faster in our
study compared with previous observational studies
of women with pelvic girdle pain (1,6,9). An
explanation for this could be that all women in our
study were offered some treatment, which may not
have been the case for women in other studies.
However, the women also recovered faster compared
to earlier intervention studies (7,8,10,23). The
treatments offered in our study may have been
more effective because all women received individual
information, which is superior to group information
(20). In addition, 2/3 of the women were given
additional acupuncture or specific stabilising exer-
cises during pregnancy (19).
An explanation for our findings could be the
chosen definition of no pain (VAS B10 mm). If we
had chosen the definition no pain VAS B0 mm,
fewer women would have been considered pain-free.
Another reason for the discrepancy in recovery
between ours and other follow-up studies with
interventions could be that the women were clini-
cally examined in our study, which is important
when differing between pelvic girdle pain and
lumbar pain (13). In fact, quite a few women with
‘unspecific back pain’ would have been categorised
as having persistent pelvic girdle pain in our study if
we had restricted data collection to a questionnaire
and a pain drawing, and not applied the definition
Table II. Primary outcome measure: pain on the Visual Analogue Scale related to motion during 12 weeks after delivery.
Standard group Acupuncture group Stabilising exercise group
Pain n
Median (25�75th
percentile) n
Median (25�75th
percentile) n
Median (25�75th
percentile)
Morning
1 week after delivery 64 9 (3�28) 73 14 (3�36) 77 9 (3�28)
2 weeks after delivery 66 4 (0�17) 72 6 (0�18) 77 4 (0�17)
3 weeks after delivery 66 3 (0�12) 73 3 (0�10) 81 3 (0�12)
4 weeks after delivery 66 2 (0�10) 73 1 (0�7) 81 2 (0�10)
5 weeks after delivery 66 1 (0�7) 74 0 (0�6) 81 1 (0�7)
6 weeks after delivery 66 0 (0�6) 74 0 (0�5) 81 0 (0�6)
7 weeks after delivery 66 0 (0�3) 74 0 (0�4) 81 0 (0�3)
8 weeks after delivery 66 0 (0�3) 74 0 (0�5) 81 0 (0�3)
9 weeks after delivery 66 0 (0�3) 75 0 (0�5) 81 0 (0�3)
10 weeks after delivery 66 0 (0�3) 75 0 (0�4) 81 0 (0�3)
11 weeks after delivery 66 0 (0�2) 75 0 (0�4) 82 0 (0�2)
12 weeks after delivery 66 0 (0�2) 75 0 (0�3) 80 0 (0�2)
Evening
1 week after delivery 64 25 (4�49) 73 17 (3�53) 77 12 (4�36)
2 weeks after delivery 66 11 (1�43) 72 9 (0�35) 77 5 (0�22)
3 weeks after delivery 66 4 (0�39) 73 3 (0�17) 81 3 (0�17)
4 weeks after delivery 66 3 (0�31) 73 0 (0�10) 81 2 (0�11)
5 weeks after delivery 66 0 (0�10) 74 0 (0�10) 81 2 (0�11)
6 weeks after delivery 66 0 (0�5) 74 0 (0�7) 81 0 (0�7)
7 weeks after delivery 66 0 (0�10) 74 0 (0�5) 81 0 (0�4)
8 weeks after delivery 66 0 (0�6) 74 0 (0�5) 81 0 (0�4)
9 weeks after delivery 66 0 (0�5) 75 0 (0�6) 81 0 (0�4)
10 weeks after delivery 66 0 (0�5) 75 0 (0�5) 81 0 (0�4)
11 weeks after delivery 66 0 (0�5) 75 0 (0�5) 82 0 (0�3)
12 weeks after delivery 66 0 (0�5) 75 0 (0�4) 80 0 (0�2)
*p Values: Mann�Whitney U-test. All original two-tailed p values were multiplied by three (Bonferroni’s correction), and there were no
statistically significant differences between the groups.
ACU, acupuncture; S, standard; SE, stabilising exercise.
Regression of pelvic girdle pain after delivery 205
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Table III. Secondary outcome measure: assessment of the severity of pelvic girdle pain by an independent examiner at inclusion during pregnancy and at follow-up 12 weeks after delivery.
Pooled data Standard group Acupuncture group Stabilising exercise group
Group comparisons
at follow-up
Inclusion
(n�386)
Follow-up
(n�328)
Inclusion
(n�130)
Follow-up
(n�109)
Inclusion
(n�125)
Follow-up
(n�105)
Inclusion
(n�131)
Follow-up
(n�114) Comparison p*
Tests for assessment of pelvic girdle pain
Positive pain drawing 386 [100] 55 [17] 130 [100] 22 [21] 125 [100] 19 [17] 131 [100] 14 [12] All groups NS
P4-test 386 [100] 73 [22] 130 [100] 28 [27] 125 [100] 27 [25] 131 [100] 18 [16] All groups NS
Pain when turning in bed 386 [100] 19 [6] 130 [100] 8 [8] 125 [100] 8 [8] 131 [100] 3 [3] All groups NS
Palpation of the pubic symphysis 160 [41] 21 [6] 47 [36] 8 [8] 51 [41] 7 [7] 62 [47] 5 [4] All groups NS
Patrick’s Fabere test 208 [54] 24 [7] 65 [50] 11 [10] 69 [55] 6 [6] 74 [56] 7 [6] All groups NS
Modified Trendelenburg test 148 [38] 15 [5] 51 [39] 8 [8] 52 [42] 3 [3] 45 [34] 4 [4] All groups NS
Number of positive pain provocation tests
0 positive pain provocation test 0 242 [74] 0 71 [65] 0 78 [74] 0 93 [82] S-ACU NS
S-SE 0.001
ACU-SE NS
1 positive pain provocation test 30 [8] 27 [8] 13 [10] 11 [10] 6 [5] 7 [6] 11 [8] 9 [8] All groups NS
2 positive pain provocation test 92 [24] 37 [11] 34 [26] 13 [12] 26 [21] 17 [16] 32 [24] 7 [6] All groups NS
]3 positive pain provocation test 264 [68] 22 [7] 83 [64] 10 [9] 93 [74] 7 [7] 88 [67] 5 [4] All groups NS
Fulfilling Ostgaards criteria for pelvic
girdle pain
386 [100] 4 [1] 130 [100] 2 [2] 125 [100] 1 [1] 131 [100] 1 [1] All groups NS
Subgroups of pelvic girdle pain
Pelvic girdle syndrome 124 [35] 2 34 [26] 1 42 [34] 0 48 [37] 1 All groups NS
Double sided sacroiliac pain 159 [41] 6 [2] 58 [45] 2 [2] 57 [46] 4 [4] 44 [34] 0 All groups NS
One-sided sacroiliac pain�symphyseal pain
35 [11] 0 13 [10] 0 8 [6] 0 14 [11] 0 All groups NS
One-sided sacroiliac pain 68 [18] 6 [2] 25 [19] 4 [4] 18 [14] 1 25 [19] 1 All groups NS
Barely pain in the symphysis pubis 0 3 0 1 0 2 [2] 0 0 All groups NS
P4 test, posterior pelvic pain provocation test; fulfilling Ostgaards criteria for pelvic girdle pain, women with positive pain drawing, a positive P4 test, pain when turning in bed and daily pain
(VAS ]10 mm); subgroups of pelvic girdle pain, pain in the pelvic joint after pain provocation test plus daily pain (VAS ]10 mm); pelvic girdle syndrome, double-sided sacroiliac pain plus
symphysis pubis pain. S, standard group; ACU, acupuncture group; SE, stabilising exercise group; NS, not significant.
*p-Values from x2-test. All original p-values were multiplied by 3 (Bonferroni’s correction).
Results are presented for each intervention group and for pooled data. Values are numbers [percentages].
206
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of ‘no pain’ to VAS ]10 mm at follow-up. About
13% of the women in the standard and acupuncture
groups filled in markings in the gluteal area on
the pain drawings and reported daily pain (VAS
]0 mm) in their diaries. A similar prevalence (15%)
of low back pain was found in non-pregnant women
aged 35 years (24).
An important difference between our study and
other follow-up studies is that stricter criteria had to
be fulfilled than in other published studies. The
criteria used by Albert et al. (6) were pain in one or
more of the pelvic joints confirmed with unspecified
objective findings. The criteria used by Larsen et al.
(12) were pain in the lower back when performing at
least 2 of 5 daily activities and a positive Patrick’s
fabere test, which is used primarily for provocation
of pain originating from the hip joints and not from
the gluteal area. Some of the criteria in the study of
Gutke et al. (1) were similar to our criteria. Women
with isolated symphyseal pain in that study were
not classified as having pelvic girdle pain, but other
criteria differed. They required ]2 positive pain
provocation tests and the women did not have to
experience pain when turning in bed. They reported
that 17% of the women had pelvic girdle pain
3 months postpartum, which is a higher estimate
than in our study. One explanation for the difference
in recovery could be that only 46/262 of the women
received some sort of treatment (1), whereas all
women in our study received treatment during their
pregnancies.
We do not know if women in our study received
any additional interventions during the postpartum
period. However, all women knew that those with
persistent pelvic girdle pain at follow-up would be
referred to specially trained physiotherapists. There-
fore, we believe that additional post-delivery therapy
is an unlikely confounder.
The finding that only 4 women had persistent
pelvic girdle pain is promising, but prospective
randomised studies with follow-up as well as epide-
miological studies are needed to confirm our find-
ings and to further investigate the natural regression
of pelvic girdle pain after pregnancy.
References
1. Gutke A, Ostgaard HC, Oberg B. Pelvic girdle pain and
lumbar pain in pregnancy: a cohort study of the consequences
in terms of health and functioning. Spine. 2006;/31:/149�55.
2. Wu WH, Meijer OG, Uegaki K, Mens JM, Van Dieen JH,
Wuisman PI, et al. Pregnancy-related pelvic girdle pain
(PPP). I: Terminology, clinical presentation, and prevalence.
Eur Spine J. 2004;/13:/575�89.
3. Albert HB, Godskesen M, Korsholm L, Westergaard JG. Risk
factors in developing pregnancy-related pelvic girdle pain.
Acta Obstet Gynecol Scand. 2006;/85:/539�44.
4. Svensson HO, Andersson GB, Hagstad A, Jansson PO. The
relationship of low-back pain to pregnancy and gynecologic
factors. Spine. 1990;/15:/371�5.
5. Hansen A, Jensen DV, Larsen EC, Wilken-Jensen C, Kaae
BE, Frolich S, et al. Postpartum pelvic pain � the ‘pelvic joint
syndrome’: a follow-up study with special reference to
diagnostic methods. Acta Obstet Gynecol Scand. 2005;/84:/
170�6.
6. Albert H, Godskesen M, Westergaard J. Prognosis in four
syndromes of pregnancy-related pelvic pain. Acta Obstet
Gynecol Scand. 2001;/80:/505�10.
7. Rost CC, Jacqueline J, Kaiser A, Verhagen AP, Koes BW.
Prognosis of women with pelvic pain during pregnancy: a
long-term follow-up study. Acta Obstet Gynecol Scand. 2006;/
85:/771�7.
8. Ostgaard HC, Andersson GB. Previous back pain and risk of
developing back pain in a future pregnancy. Spine. 1991;/16:/
432�6.
9. Kristiansson P, Svardsudd K, von Schoultz B. Back pain
during pregnancy: a prospective study. Spine. 1996;/21:/702�9.
10. Nilsson-Wikmar L, Holm K, Oijerstedt R, Harms-Ringdahl
K. Effect of three different physical therapy treatments on
pain and activity in pregnant women with pelvic girdle pain: a
randomized clinical trial with 3, 6, and 12 months follow-up
postpartum. Spine. 2005;/30:/850�6.
11. Bastiaenen CH, de Bie RA, Wolters PM, Vlaeyen JW, Leffers
P, Stelma F, et al. Effectiveness of a tailor-made intervention
for pregnancy-related pelvic girdle and/or low back pain
after delivery: short-term results of a randomized clinical
trial [ISRCTN08477490]. BMC Musculoskelet Disord.
2006;/7:/19.
12. Larsen EC, Wilken-Jensen C, Hansen A, Jensen DV, Johan-
sen S, Minck H, et al. Symptom-giving pelvic girdle relaxa-
tion in pregnancy. I: Prevalence and risk factors. Acta Obstet
Gynecol Scand. 1999;/78:/105�10.
13. Vleeming A, Albert H, Ostgaard H, Stuge B, Sturesson B.
European guidelines on the diagnosis and treatment of pelvic
girdle pain. DOI; 2004. Available online at: http://www.back-
paineurope.org/web/html/wg4 results.html
14. Stuge B, Hilde G, Vollestad N. Physical therapy for preg-
nancy-related low back and pelvic pain: a systematic review.
Acta Obstet Gynecol Scand. 2003;/82:/983�90.
15. Kvorning N, Holmberg C, Grennert L, Aberg A, Akeson J.
Acupuncture relieves pelvic and low-back pain in late
pregnancy. Acta Obstet Gynecol Scand. 2004;/83:/246�50.
16. Lund I, Lundeberg T, Lonnberg L, Svensson E. Decrease of
pregnant women’s pelvic pain after acupuncture: a rando-
mized controlled single-blind study. Acta Obstet Gynecol
Scand. 2006;/85:/12�9.
17. Wedenberg K, Moen B, Norling A. A prospective randomized
study comparing acupuncture with physiotherapy for low-
back and pelvic pain in pregnancy. Acta Obstet Gynecol
Scand. 2000;/79:/331�5.
18. Guerreiro da Silva JB, Nakamura MU, Cordeiro JA, Kulay L
Jr. Acupuncture for low back pain in pregnancy � a
prospective, quasi-randomised, controlled study. Acupunct
Med. 2004;/22:/60�7.
19. Elden H, Ladfors L, Olsen MF, Ostgaard HC, Hagberg H.
Effects of acupuncture and stabilising exercises as adjunct to
standard treatment in pregnant women with pelvic girdle
pain: randomised single blind controlled trial. BMJ. 2005;/
330:/761.
Regression of pelvic girdle pain after delivery 207
Downloaded By: [Swedish Consortia Trial] At: 08:46 9 September 2008
20. Ostgaard HC, Andersson GB, Karlsson K. Prevalence of back
pain in pregnancy. Spine. 1991;/16:/549�52.
21. Enthoven P, Skargren E, Kjellman G, Oberg B. Course of
back pain in primary care: a prospective study of physical
measures. J Rehabil Med. 2003;/35:/168�73.
22. Laslett M, Aprill C, McDonald B, Young S. Diagnosis of
sacroiliac joint pain: validity of individual provocation tests
and composites of tests. Man Ther. 2005;10:207�18.
23. Ostgaard HC, Zetherstrom G, Roos-Hansson E, Svanberg B.
Reduction of back and posterior pelvic pain in pregnancy.
Spine. 1994;/19:/894�900.
24. Biering-Sorensen F. Low back trouble in a general population
of 30-, 40-, 50-, and 60-year-old men and women. Study
design, representativeness and basic results. Danish Med
Bull. 1982;/29:/289�99.
208 H. Elden et al.
Downloaded By: [Swedish Consortia Trial] At: 08:46 9 September 2008