| Literature DB >> 27141980 |
Rita Th E Harmsen1, Tsjitske M Haanstra2, Inger N Sierevelt3, Elise P Jansma4, Peter A Nolte5, Melianthe P J Nicolai6, Peter D H Wall7, Barend J Van Royen1.
Abstract
BACKGROUND: Total Hip Replacement (THR) is an effective treatment for end-stage hip osteoarthritis. Since the introduction of total joint replacement, the effect on the Sexual Quality of Life (SQoL) following THR has been addressed in scant studies. The aim of our study was to systematically review the literature, to summarise effects of THR on patients' SQoL.Entities:
Keywords: Hip (osteo)Arthritis; Sexual Quality of Life; Total Hip Replacement
Mesh:
Year: 2016 PMID: 27141980 PMCID: PMC4855489 DOI: 10.1186/s12891-016-1048-1
Source DB: PubMed Journal: BMC Musculoskelet Disord ISSN: 1471-2474 Impact factor: 2.362
Fig. 1Flowchart of the search and selection procedure of the studies
Characteristics of the included studies assessing the effects of THA on SQoL
| First author, country | Study design | Aim/Objective | N of patients (Response Rate) | Diagnosis n (%) | Main inclusion criteria | Mean Age (years) | n (%), Male | n (%), Female | Duration of follow up, after surgery |
|---|---|---|---|---|---|---|---|---|---|
| Todd 1972 UK | Retrospective, cohort studyd Interview (Int) and Survey | Incidence of SD and influence of THR on SQoL | Int: 123/292 (42 %) Surv: 79/134 (58 %) | HAa | Patients undergone THR with active sexual relationship at time of onset HA; | Interview NA M61 (30–79) F 60 (29–79) | Interview NA 49(40) 36 (46) | Interview NA 74(60) 43 (54) | Int: NA Surv: NA |
| Wiklund 1991 Sweden | Case-control study, Survey | To evaluation of QoL before and after THR in patients with HA | 56/57 (98 %)g | Prim. HA: 40 (71 %) Sec. HA: 16 (29 %) incl 1 RAb | Patients with HA < 80 year; awaiting THR | 65 (30–79) | 21 (38) | 35 (63) | 1 year |
| Stern 1991 USA | Retrospective, cohort study, Survey | To determine the effect of THR on SF incl. sexual positions and resumption SA after THA | 86/100 (86 %) | Prim. HA: 74 (86 %) Sec. HA: 12 (14 %) of which 4 dysplasia and 8 RAb | Patients with predominantly HA all undergone THR and <70 y, all satisfied about results THR | 57 (20–70) | 39 (45) | 47 (55) | At time postoperative routine visit |
| Laupacis 1993 Canada | Prospective, double-blind randomized trial, Survey | Effect of THR on health related QoL | 188/ 251 (75 %) | HAa | Patients with HA, < 75 years, no severe OA of other hip, no previous THR or THK (knee) < 5 years, nor infectious arthritis | 64 (40–75) | 97 (53) | 91 (47) | 3 months 6 monthsh 1 year 2 year |
| Gogia 1994 USA | Prospective cohort study, Survey | Developing evaluation system to assess clinical outcome of THR related to changes in functional status and pain | 22/24 (92 %) | HAa | Patients with HA, undergoing THR; alert oriented, ambulatory with or without assistive devices | 69,2 (57–86) | 4 (18) | 18 (82) | 3 and 6 monthsh |
| Gosens 2005, The Netherlands | Prospective, multicentre cohort study, Survey | Translating and validating Oxford Hip Score into Dutch | 146/150 (100 %) | Prim. HA: 117 (78 %) Sec. HA: 33 (22 %) | Age >35 year; patients awaiting THR; No systematic illness and physically and mentally suitable, understanding Dutch language | 65 (38–85) | 52 (35) | 98 (65) | 7 weeks, 3 months, 6 monthsh; 1 year; 2 year |
| First author, country | Study design | Aim/Objective | N of patients (Response Rate) | Diagnosis n (%) | Main inclusion criteria | Mean Age (years) | n (%), Male | n (%), Feale | Duration of follow up, after surgery |
| Laffosse 2007 France | Retrospective, cohort study, Survey | SD in patients before and after THR; receiving sufficient information | 135/346 (39 %) | Prim. HA: 56 (42 %) | <65 year, undergone THR min. 6 months previously; Revision and Femoral Neck Fracture excluded | 51,8 (22–65) | 77 (57) | 58 (43) | ≥6 months |
| Sec. HA: 76 (58 %) Incl. 3 RAb | |||||||||
| Wall 2011 UK | Prospective cohort study, Survey | To determine the effect of HA on SQoL and to assess wheter a SQoL is considered in surgical plan | 86/100 (86 %) | Prim. HA: 74 (86 %) | <75 Year, undergoing THR, living with a partner | 62 (48–74) | 39 (45) | 47 (55) | 6 months |
| Sec. HA: 12 (14 %) Incl. 3 RAb | |||||||||
| Yoon 2013 Korea | Retrospective, cohort study, face-to-face interview | To determine concerns related to SQoL; to determine changes in SA after THR | 64/512 (13 %) | Prim. HA: 11 (17 %) Sec. HA: 53 (83 %) Incl. 2 RAb, 5 ASd | Sexual active patients during previous last year, No dislocation, infection or stiffness. | 50e | 45 (NA) | 19 (NA) | ≥6 months, at routine follow up visit |
| Wang 2014 Japan | Prospective, multicentre cohort study, Survey | To evaluate the influence of ONFH and THR on SQoL | 247/300 (82 %) | Sec. HA: all males, ONFH patients (247) | SA married adults, only ONFH males, Age >25- < 60. Excluded severe comorbiditiesf | 46,8 (34.7–58.9) | 247 (100) | 1 year | |
| Nunley 2014 USA | Retrospective multicentre cohort study, Survey | To evaluate SQoL in young active patients following THR. | 791/806 (98 %)c | Prim. and non inflammentoire Sec. HAa | ≤60 year; THR and SRA patients, no history postoperative complications UCLA score >6i | 49,5 (42.3–56.7) | 531 (66) j | 275 (34) j | 2,3 years (±0,8) |
| Klit 2014 Denmark | Prospective multicentre cohort study, Survey | To explore any -positive or negative- effect THR have had on sexual function, sexual frequency and sexual practice, in younger THR patients | 136/153 (89 %) | Young HAa patients awaiting THR: n86) (Hip Resurfacing: n44) | <60 Year, undergoing primary THR/HR, not suffering from cognitive dysfunction or malignant disease, able to fill in questionnaire | 53 (48–57) | 68 (50) | 68 (50) | 3 months 6 months 1 year h |
aUnspecified numbers and HA type
bSome RA and AS patients were included because data could not slit up
cUsed modern bearing surfaces: SRA = Surface Replacement Arthroplasty; SRA treatment: n 122 (15 %) (181 control patients)
d started with interview, continued with survey
eMean age derived
fComorbidities e.g. affecting heart lung, liver, kidneys; patients under medications; psychiatric history; having mental retardation
gControl group not specified
hduration of follow up used in this review
iPre-symptomatic activity score of University of California Los Angeles (UCLA)
jN not corrected by gender (-15 respondents)
Methodological Quality Rating of the 12 included studies
| Study | Selection bias presenta | Information bias presenta | Statistical analysis bias presenta | Total bias Score | Level of Qualityb |
|---|---|---|---|---|---|
| Todd et al. | 1 | 1 | 1 | 3/3 | L |
| Wiklund and Romanus | 0 | 1 | 1 | 2/3 | L |
| Stern et al. | 1 | 1 | 1 | 3/3 | L |
| Laupacis et al. | 0 | 1 | 1 | 2/3 | L |
| Gogia et al. | 1 | 1 | 1 | 3/3 | L |
| Gosens et al. 2005 [ | 0 | 1 | 1 | 2/3 | L |
| Laffosse et al. | 1 | 1 | 1 | 3/3 | L |
| Wall et al. | 0 | 1 | 1 | 2/3 | L |
| Yoon et al. | 1 | 1 | 1 | 3/3 | L |
| Wang et al. | 0 | 0 | 1 | 1/3 | M |
| Nunley et al. | 0 | 1 | 0 | 1/3 | M |
| Klit et al. 2015 [ | 0 | 1 | 1 | 3/3 | L |
a1 = bias present or unclear; 0 = no bias present
bH = high quality: no evidence for selection bias, information bias or statistical analysis bias (not available); M = Moderate Quality: one or two aspects rated as bias present or unclear; L = Low quality: all three aspects rated as bias present or unclear. THR = Total Hip Replacement
Changes of SQoL after THR
| Study | Quality level | Physical-Functional Outcomes of SQoL | Psychosocial Outcomes of SQoL | n in study | Pre-operative n | Post-operative n | Pre operative % (n) (score) | Post-operative % (n) (score) | Δ SQoL in % | Directionc of Change |
|
|---|---|---|---|---|---|---|---|---|---|---|---|
| Todd, et al. | L | SD in Females: | 123 | 74 | 74 | ᅟ | ᅟ | ᅟ | ᅟ | ||
| SD in Males: | 49 | 49 | ᅟ | ᅟ | ᅟ | ᅟ | |||||
| Wiklund and Romanus | L | SD | 57 | 57 | 56 | 34 | 9 | -25 | + | 0.001 | |
| Stern, et al. | L | SD | 86a | 86 | 83 | ᅟ | ᅟ | ᅟ | ᅟ | <0.001 | |
| SF: | 3,3 | 5,7 | 73d | +++ | <0.001 | ||||||
| Laupacis, et al. | L |
| 188 | 33b | 27b | 74(7,4) | 30(3,0) | −44 | ++ | ||
| Gogia, et al. | L |
| 22 | 7 | 7 | 47(2.36) | 100(5) | 53 | ++ | ||
| Gosens, et al. | L |
| 150 | 146 | 144 | ᅟ | ᅟ | ᅟ | ᅟ | ||
| Laffosse, et al. | L | SD: | 135 | 135 | 89 | ᅟ | ᅟ | ᅟ | ᅟ | ||
| SD: | 58 | 57 | 42 | ᅟ | ᅟ | ᅟ | ᅟ | 0.004 | |||
| SD: | 77 | 77 | 48 | ᅟ | ᅟ | ᅟ | ᅟ | 0.13 | |||
| Wall, et al. | L | Hip Interfering with | 86 | 71 | 54 | 77(55) | 0(0) | −77 | +++ | ||
| Like more information provided: | 55(39) | 83(45) | 28 | + | |||||||
| Wang, | M | Effect on: | |||||||||
|
| 247 | 247 | 247 | 29(2.3) | 23(1.8) | −6 | + | 0.14 | |||
|
| 65(6.5) | 9(0.9) | −56 | ++ | 0.009 | ||||||
|
| 28(1.4) | 82(4.1) | 54 | ++ | 0.012 | ||||||
| Effect on: | |||||||||||
|
| 66(5.3) | 29(2.3) | −37 | ++ | 0.026 | ||||||
| Overall | 54(2.7) | 94(4.7) | 40 | ++ | 0.018 | ||||||
| Overall | 76(3.8) | 86(4.3) | 10 | + | 0.4 | ||||||
| Klit, et al. | L |
| 136 | 68 | 68 | 67(4.0) | 83(5.0) | 16 | + | 0.008 | |
| SD due to hip Males (fOHS scale: 0–6; with 6 points being the best score) | 68 | 68 | 92(5.0) | 100(6.0) | 8 | + | 0.102 | ||||
| SF: SA before and at twelve month follow upe | 136 | 108 | 83 | 100(108) | 100(83) | 0 | +/- |
SD Sexual Difficulty or Sexual Dysfunction, SF Sexual Function, SA Sexually Active patients
aOnly satisfied patients (with results THR)
bPatients were asked to choose five most adversely affected activities (n33)
cRating the direction of change:
Positive effect: + (5–35 %); ++ (35–70 %); +++ (>70 %)
Negative effect: - (−5 to−35 %); -- (−35 to−70 %); --- (>−70 %)
Unchanged: +/- (between 0 and 5 %; between 0 and - 5 %)
dIncrease 2.4 times: 2.4/3.3 (.73)
eOnly SA patients were included
fOHS = Oxford Hip Score: scale 0–6 (score 0 means “due to other reason than hip”; this was not included in statistics)
Thus, 1 = no sex life able due to hip; 6 never disabled by the hip)
Postoperative outcomes of SQoL
| Study | Quality level |
|
| Postoperative n (%) |
|
|---|---|---|---|---|---|
| Todd, et al. | L | Relief | 4 (13 %) | - | |
| Relief | 6 (27 %) | - | |||
| (n 60) | Need for more advice | 34 (57 %) | |||
| Stern, et al. | L |
| ᅟ | ᅟ | |
| (n 64) | Need for more advice | 57 (89 %) | |||
| Argument to undergo THR: | 15 (20 %) | ||||
| Laffosse, et al. | L |
| 24 (18,5 %) | ||
| Increased, more women than men | 0.02 | ||||
| Not able to obtain information | 110 (83 %) | ||||
| Argument to undergo THR: | 21 (18,5 %) | ||||
|
| ᅟ | 66,5 days (4–365) | ᅟ | ||
| Wall, et al. 2011 [ | L |
| 44 (81 %) | ||
| Concerns partner: (Fear hurting spouse) | 7/54 (12 %) | ||||
| Yoon, et al. 2013 [ | L | Time to resume SA: (n 64/64) | 6,19 months (3weeks - 48months) | ||
| Difficulty with leg positioning (females more than males) | 25 (39 %) | 0.045 # | |||
| Changing Sexual Positions (more frequently for patients with diff. leg positioning) | 26 (40,6 %) | <0.01 | |||
| - Muscle weakness (Males n 6) | 11 (17,2 %) | ||||
| Not able to obtain information | 51/62 (80 %) | ||||
|
| 33 (51,6 %) | ||||
|
| ᅟ | ||||
|
| ᅟ | ||||
| Satisfaction correlated to stress | ≤stress = | 0.03 | |||
| Nunley, et al. | M | SA since surgery (n 791)c
| 708 (89,5 %) | # 0.0061 | |
| Sex Frequency: | n 694 | # ‘less’ | |||
| If ‘more’ caused by: | ᅟ | ||||
|
| (n 697) | # ‘Better’ <0.0001 Odds 10.596 | |||
| If ‘better’ caused by: | ᅟ | ||||
| -less apprehension | 310 (64,2 %) | ||||
|
| ᅟ | ||||
| Had | 81 (11,6 %) | # <0.0016 | |||
| Klit, et al. | L | Time to resume SA (n 136) | ᅟ | ||
| Sexual Frequency: females | 12 % increase 38 % better abilities sexual praxis | ||||
| 84 % of them experienced associated increased ROM, decreased pain and fear | |||||
| Sexual Frequency: males | No changes | ||||
| Erectile dysfunction: males | 3/68 (4 %) |
SD Sexual Dysfunction, SF Sexual Function, SA Sexual Activity
a adjusted for 5 = ‘No reply’
b adjusted for 1 = ‘No reply’
c within the past year #Comparison of SA, Quality and Frequency between THR and Control cohort with Odds ratios
Search strategy in PubMed February 9, 2015 (read from bottom-up)
| Set | Search terms | Result |
|---|---|---|
| #5 | #5 NOT (“addresses”[Publication Type] OR “biography”[Publication Type] OR “comment”[Publication Type] OR “directory”[Publication Type] OR “editorial”[Publication Type] OR “festschrift”[Publication Type] OR “interview”[Publication Type] OR “lectures”[Publication Type] OR “legal cases”[Publication Type] OR “legislation”[Publication Type] OR “letter”[Publication Type] OR “news”[Publication Type] OR “newspaper article”[Publication Type] OR “patient education handout”[Publication Type] OR “popular works”[Publication Type] OR “congresses”[Publication Type] OR “consensus development conference”[Publication Type] OR “consensus development conference, nih”[Publication Type] OR “practice guideline”[Publication Type]) NOT (animals[mh] NOT humans[mh]) | 88 |
| #5 | #3 AND #4 | 97 |
| #4 | “Sexuality”[Mesh] OR “Sexual Behavior”[Mesh] OR “Sexual Dysfunction, Physiological”[Mesh] OR “Sexual Partners”[Mesh] OR sexual*[tiab] OR “sex behavior”[tiab] OR “sex behaviour”[tiab] OR SQOL[tiab] | 221959 |
| #3 | #1 OR #2 | 60706 |
| #2 | “Arthroplasty, Replacement, Hip”[Mesh] OR “Hip Prosthesis”[Mesh] OR ((“Arthroplasty”[Mesh:NoExp] OR “Arthroplasty, Replacement”[Mesh:NoExp] OR “Arthrodesis”[Mesh] OR Arthroplasties[tiab] OR Arthroplasty[tiab] OR Arthrodes*[tiab] OR Prosthes*[tiab] OR Implant*[tiab] OR replacement*[tiab] OR revision[tiab] OR Arthrodes*[tiab]) AND (“Hip”[Mesh] OR “Hip Joint”[Mesh] OR Hip[tiab] OR hips[tiab])) | 43562 |
| #1 | “Osteoarthritis, Hip”[Mesh] OR “Hip Contracture”[Mesh] OR Coxarthrosis[tiab] OR Coxarthroses[tiab] OR “Femur Head Necrosis”[Mesh] OR Femur Head Necros*[tiab] OR Femur Head osteonecros*[tiab] OR ((“Joint Diseases”[Mesh:NoExp] OR “Arthritis”[Mesh:NoExp] OR “Osteoarthritis”[Mesh:NoExp] OR Osteoarthr*[tiab] OR Arthriti*[tiab] OR arthro*[tiab]) AND (“Hip”[Mesh] OR “Hip Joint”TMeshl OR hipftiab] OR hipsftiab])) | 41398 |
Checklist used for the assessment of the methodological quality of the included studies
| Theoretical background | Used for selection bias |
| 1. Is there a theoretical background for the hypothesis? | |
| Study participation | |
| 2. Is the study population clearly described in terms of age, gender, and important patients’ characteristics? | Used for selection bias |
| 3. Is the percentage of eligible subjects who participated in the study (response rate) adequate? (More than 30 % is considered inappropriate) | Used for selection bias |
| Sampling | |
| 4. Are patients who participated in the study similar to eligible non-participants (the population), in terms of age, gender, and important disease characteristics? | Used for selection bias |
| Study attrition | |
| 5. Is the percentage of subjects available for analysis adequate? (<30 % not too many missing values or loss to follow-up)? | Used for selection bias |
| 6. Were reasons for loss to follow-up presented and assessed during the study for possible systematic attrition? (Subjects that did not finish the study) | Used for selection bias |
| Outcome measurement | |
| Definition of outcome variable(s) | Used for information bias |
| 7. Are clear definitions of each outcome variable provided? | |
| 8. Is clear operationalization of each outcome variable provided? How is it measured? | Used for information bias |
| Measurement of outcome variable(s) | Used for information bias |
| 9. Are the measurement instruments used for the measurement of the outcome variable(s) reliable and valid? | |
| Method and setting of the outcome variable(s) | Used for information bias |
| 10. Were the measurement approach, time and place of measurement of the outcome variable(s) standardized or conducted in a way that limits systematically different measurement? | |
| Study confounding | |
| Definition of potential confounders | Used for information bias |
| 11. Are clear definitions of each confounder provided? | |
| 12. Is clear operationalization of each confounder provided? | Used for information bias |
| Measurement of potential confounders | Used for information bias |
| 13.Are the measurement instruments used for the measurement of the confounder(s) reliable and valid? | |
| Method and setting of the confounder(s) | Used for information bias |
| 14. Were the measurement approach, time and place of measurement of the confounder(s) standardized or conducted in a way that limits systematically different measurement? | |
| Statistical analyses | |
| 15. Is the percentage of missing values adequate? Less < 30 % | Used for statistical analysis bias |
| 16. Were multivariable analyses performed? Yes is rated as “0” if yes | Used for statistical analysis bias |
| 17. Was it clearly described which variables were included in the (multivariable) model(s)? | Used for statistical analysis bias |
Based on Hayden and Shamliyan, and used by Tibury [18, 20]
Individual scores of the Quality Assessment per study, per item
| First author | 1 | 2 | 3 | 4 | 5 | 6 | SubTa | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | SubTb | 15 | 16 | 17 | SubTc | Total score |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Todd | 0 | 1 | 1 | 1 | 0 | 1 | 4/6 = 1 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 5/8 = 1 | NA | NA | NA | 3/3 = 1 | LOW 3/3 |
| Wiklund | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 4/8 = 1 | 0 | 1 | 1 | 2/3 = 1 | LOW 2/3 |
| Stern | 0 | 0 | 0 | 1 | 0 | 0 | 1/6 = 1 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 6/8 = 1 | 0 | 1 | 1 | 2/3 = 1 | LOW 3/3 |
| Laupacis | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 4/8 = 1 | 0 | 1 | 1 | 2/3 = 1 | LOW 2/3 |
| Gogia | 0 | 0 | 1 | 1 | 0 | 0 | 2/6 = 0 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 6/8 = 1 | 0 | 1 | 1 | 2/3 = 1 | LOW 3/3 |
| Gosens | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 4/8 = 1 | NA | NA | NA | 3/3 = 1 | LOW 2/3 |
| Laffosse | 0 | 0 | 1 | 1 | 1 | 1 | 4/6 = 1 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 5/8 = 1 | 1 | 1 | 1 | 3/3 = 1 | LOW 3/3 |
| Wall | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 4/8 = 1 | NA | NA | NA | 3/3 = 1 | LOW 3/3 |
| Yoon | 0 | 0 | 1 | 1 | 0 | 0 | 2/6 = 1 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 6/8 = 1 | 0 | 1 | 1 | 2/3 = 1 | LOW 3/3 |
| Wang | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/8 = 0 | 0 | 1 | 1 | 2/3 = 1 | MED 1/3 |
| Nunley | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 1 | 2/8 = 1 | 0 | 0 | 0 | 0/3 = 0 | MED 1/3 |
| Klit | 0 | 0 | 0 | 0 | 0 | 0 | 0/6 = 0 | 0 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 6/8 = 1 | 0 | 1 | 1 | 2/3 = 1 | LOW 3/3 |
SubTotal aSelection bias bInformation bias c Statistical analysis bias