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Revista Española de Cirugía Ortopédica y Traumatología Utility of postoperative drainage in total hip arthroplasty. A systematic revie...
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Vol. 69. Núm. 6.
Páginas T587-T596 (Noviembre - Diciembre 2025)
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829
Vol. 69. Núm. 6.
Páginas T587-T596 (Noviembre - Diciembre 2025)
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Utility of postoperative drainage in total hip arthroplasty. A systematic review
Utilidad del drenaje postoperatorio en la artroplastia total de cadera. Una revisión sistemática
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829
C. Moreno-Beneta, P. Castells-Ayusob, I. Mirandaa,c,
Autor para correspondencia
nachomigo@hotmail.com

Corresponding author.
, F.J. Mirandad
a Facultad de Ciencias de la Salud, Universidad Católica de Valencia, Valencia, Spain
b Hospital Vithas Valencia 9 de Octubre, Valencia, Spain
c Servicio de Cirugía Ortopédica y Traumatología, Hospital Arnau de Vilanova, Valencia, Spain
d Departamento de Fisiología, Universidad de Valencia, Valencia, Spain
Contenido relacionado
Rev Esp Cir Ortop Traumatol. 2025;69:587-9610.1016/j.recot.2025.02.019
C. Moreno-Benet, P. Castells-Ayuso, I. Miranda, F.J. Miranda
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Table 1. Joanna Briggs Institute Critical Checklist for Randomized Controlled Trials.
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Table 2. Studies included in the systematic review.
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Table 3. Tranexamic acid, anticoagulant, haemoglobin, and transfusion.
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Table 4. Complications.
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Table 5. Conclusions.
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Abstract
Aim and hypothesis

To investigate the advantages associated with the use of drainage in primary total hip arthroplasty (THA) versus not using drainage and to determine if drainage can be systematically discontinued. The starting hypothesis was that eliminating the use of drainage systematically in THA does not significantly increase the risk of postoperative complications.

Materials and methods

A systematic review was carried out following the PRISMA guidelines in the PubMed and Cochrane Library databases. The search was conducted on February 15, 2024, by entering the terms (“suction drainage”) AND (“total hip arthroplasty”). The Joanna Briggs Institute quality assessment tool was used to assess the quality of the included studies.

Results

Sixteen clinical trials comparing the use of drainage with no drainage in THA were included. No differences were observed in terms of infection rate or haematoma. Some authors find that the use of drainage increases the percentage of patients requiring transfusion and the length of hospitalisation. Of 16 studies, 13 recommend not to use drainage routinely in THA.

Conclusions

The use of drainage in THA has no advantage over no drainage. The results of the clinical trials reviewed suggest that drainage should not be used routinely in THA.

Keywords:
Drainage
Total hip arthroplasty
Transfusion
Resumen
Objetivo e hipótesis

Conocer las ventajas asociadas al uso de drenaje en la artroplastia total de cadera (ATC) primaria frente a su no utilización y determinar si se puede dejar de utilizar el drenaje de forma sistemática. La hipótesis de partida fue que la eliminación del uso de drenaje de forma sistemática en la ATC no aumenta significativamente el riesgo de complicaciones postoperatorias.

Materiales y métodos

Se realizó una revisión sistemática siguiendo la guía PRISMA en las bases de datos PubMed y Cochrane Library. Se realizó la búsqueda el 15 de febrero de 2024, introduciendo los términos («suction drainage») AND («total hip arthroplasty»). Se utilizó la herramienta de evaluación de calidad del Instituto Joanna Briggs para evaluar la calidad de los estudios incluidos.

Resultados

Se han incluido 16 ensayos clínicos que comparan la utilización de drenaje con su no utilización en la ATC. No se observan diferencias en cuanto a tasa de infección ni hematoma. Algunos autores encuentran que con el uso de drenaje aumenta el porcentaje de pacientes que precisaron transfusión y el tiempo de hospitalización. De 16 estudios, 13 recomiendan dejar de usar el drenaje en la ATC de forma rutinaria.

Conclusiones

El uso de drenaje en la ATC no presenta ventajas frente a su no utilización. Los resultados obtenidos en los ensayos clínicos revisados sugieren que el drenaje no debería utilizarse de forma rutinaria en la ATC.

Palabras clave:
Drenaje
Artroplastia total de cadera
Transfusión
Texto completo
Introduction

Total hip arthroplasty (THA) is a procedure that is currently widely performed for a variety of hip ailments. The use of closed suction drainage is routinely used to decrease the complications arising from this surgery, given that it removes the fluid that remains within the surgical wound (keeping haematomas from forming) and has been associated with lower rates of infection, pain, hospital stay, among others, although it has also been linked to an increased risk of infection as a result of having a port of entry; greater blood loss, and other problems with the wound.1–3

Recent studies that have probed the use of drainage in other joints (ankle, shoulder, knee) have also concluded that its use is not routinely indicated;4–6 indeed, some works do not recommend it for revision hip arthroplasty either.7,8

The following questions are posed: What are the advantages of using drainage versus not using it in THA and Should drainage be used routinely in all THA? The starting hypothesis was that it is possible that eliminating the routine use of drainage in THA does not significantly elevate the risk of postoperative complications, and could, in fact, contribute to shortening the duration of hospital stay and lowering the costs associated with the use of drainage.

The aim of this work was to ascertain the advantages associated with the use of drainage in THA relative to not using drainage, as well as to establish whether drainage can be discontinued as a routine practice in THA.

Material and methods

A systematic review was undertaken in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses -PRISMA-9 guidelines. The bibliographic search was carried out in the PubMed and Cochrane Library databases on 15 February 2024, by entering the terms (‘suction drainage’) AND (‘total hip arthroplasty’). A total of 237 articles resulted from this database search (fig. 1). The references of the selected articles were also cross-referenced (fig. 1). All abstracts and full texts were reviewed by two researchers; in the event of disagreement regarding the selection of the works, it was discussed, and, in case of doubt, they were assessed by another senior researcher in order to make a final decision

Figure 1.

Flow diagram depicting the bibliographic search undertaken.

Inclusion criteria: 1) studies involving the use of drainage in postoperative primary THA; 2) studies that compare the use of drainage with non-use of drainage in postoperative THA, and 3) full text available in English or Spanish.

Exclusion criteria: 1) bibliographic review, systematic review, and meta-analysis; 2) animal or cadaveric studies; 3) case reports or case series without a control group; 4) letters to the editor or editorial comments; 5) description of the study technique or protocol without clinical results; 6) oral communication at a conference/ poster at a conference; 7) article not available in English or Spanish, and 8) duplicate articles or results.

After having chosen the articles that were selected for full-text review, their methodological quality was determined and appraised on the basis of the Joanna Briggs Institute (JBI) checklist for randomised clinical trials10 (Table 1) (original in Annex I).

Table 1.

Joanna Briggs Institute Critical Checklist for Randomized Controlled Trials.

  Bartosz et al.11  Fagotti et al.12  Białecki et al.13  Suarez et al.14  Koyano et al.15  Kleinert et al.16  Cheung et al.17  Strahovnik et al.18  Dora et al.19  Matsuda et al.20  Walmsley et al.21  González della Valle et al.22  Niskanen et al.23  Crevoisier et al.24  Ovadia et al.25  Murphy and Scott26 
Was true randomization used for assignment of participants to treatment groups? 
Was allocation to treatment groups concealed? 
Were treatment groups similar at the baseline? 
Were participants blind to treatment assignment? 
Were those delivering the treatment blind to treatment assignment? 
Were outcome assessors blind to treatment assignment? 
Were treatment groups treated identically other than the intervention of interest? 
Was follow up complete and if not, were differences between groups in terms of their follow up adequately described and analysed? 
Were participants analysed in the groups to which they were randomized? 
Were outcomes measured in the same way for treatment groups? 
Were outcomes measured in a reliable way? 
Was appropriate statistical analysis used? 
Was the trial design appropriate and any deviations from the standard RCT design (individual randomization, parallel groups) accounted for in the conduct and analysis of the trial? 
Total score (%)  10 (77)  10 (77)  10 (77)  11 (85)  10 (77)  10 (77)  10 (77)  10 (77)  11 (85)  10 (77)  10 (77)  10 (77)  8 (62)  10 (77)  10 (77)  8 (62) 

D: doubtful; RCT: randomised clinical trial; N: no; Y: yes.

Results

This systematic review included 16 articles (fig. 1).11-26 All of them are randomised clinical trials that compare the use of drainage to non-use in primary THA; all are rated as level 1 evidence (Table 2). The tranexamic acid and antibiotic protocols used, pre- and postoperative haemoglobin (Hb) levels, and transfusion requirements (Table 3), complications (Table 4) and in all cases, the conclusions of the studies included are presented (Table 5).

Table 2.

Studies included in the systematic review.

Authors  Year  Comparison  Approach  Prosthesis  Drainage time 
Bartosz et al.11  2021  100  D/no D  PL  Uncemented 
Fagotti et al.12  2018  93  D/no D  Uncemented  24
Białecki et al.13  2017  90  D/no D  PL  Cemented/uncemented  48
Suarez et al.14  2016  120  D/no D 
Koyano et al.15  2015  54  BL, D/no D  AL/PL/A  Uncemented  48
Kleinert et al.16  2012  120  D/no D/AT  Uncemented  48
Cheung et al.17  2010  153  D/no D/AT  Cemented/uncemented/hybrid  24
Strahovnik et al.18  2010  139  No D/ D 24h/D 48Cemented/uncemented  24/48
Dora et al.19  2007  100  D/no D  Hybrid  48
Matsuda et al.20  2007  40  D/no D  Uncemented  48
Walmsley et al.21  2005  577  D/no D  AL  24
González della Valle et al.22  2004  104  D/no D  102 PL, 2 TransTr  Cemented/hybrid  24
Niskanen et al.23  2000  58  D/no D  Cemented  24
Crevoisier et al.24  1998  66  D/no D  Hybrid/uncemented  48
Ovadia et al.25  1997  30  D/no D  PL  Hybrid/cemented  48
Murphy and Scott26  1993  40  D/no D  Cemented  24

A: Anterior; AL: Anterolateral; AT: Autotransfusion; BL: Bilateral arthroplasty performed in a single surgical procedure, one with drainage and the other without drainage; D: Drainage; L: lateral; P: Posterior; PL: Posterolateral; TransTr: transtrochanteric.

Table 3.

Tranexamic acid, anticoagulant, haemoglobin, and transfusion.

Authors  Tranexamic acid  Protocol anticoagulant  Hb pre/Day 1 post (g/dL)Transfusionn (%)
      No D  No D 
Bartosz et al.11  2 doses (15mg/kg), 10min before  LMWH sc before and 35 days post-surgery  5 (10)  5 (10) 
Fagotti et al.12  Enoxaparin (40mg) sc 12h after and for 4 wk  10 (24)  7 (13) 
Białecki et al.13  One dose (15mg/kg) 10min before  LMWH sc adjusted for weight, 1st dose 12h before  -/11.4  -/11.4 
Suarez et al.14  2 doses (1g), 1st postoperative and 2nd 24ASA (325mg) po twice per day  13.7/10.8  13.8/10.9  1 (2) 
Koyano et al.15  Enoxaparin (4,000U/day) sc or edoxaban (30mg/ day) po 
Kleinert et al.16  Enoxaparin (40mg) sc day from before and 1 dose daily for 6 wk  14/10,2  13.6/9.9  4 (10)  4 (10) 
Cheung et al.17  ASA (150mg) po daily for 6 wk and a PPI. Compression tights and inflatable boots  13.7/10.5  14.0/10.4  19 (37)  6 (13)* 
Strahovnik et al.18  LMWH sc 12h before and 12h after surgery. Continue one dose per day for 35 days 
Dora et al.19  LMWH sc before and after surgery as per product recommendations 
Matsuda et al.20  Compression tights and inflatable boots. No medication was used  13.4/11.1  13.6/11.0 
Walmsley et al.21  UFH (15U/kg) sc and ASA (500mg) po for 3 wk. High-risk cases, enoxaparin (40mg) sc and ASA (500mg)  13.4/10.3  13.6/10.5  93 (33)  78 (26)* 
González della Valle et al.22  LMWH (5,000U) sc until discharge and compression tights  21 (40)  18 (36) 
Niskanen et al.23  LMWH (5,000U) sc until discharge and compression tights for 3 days 
Crevoisier et al.24  LMWH (0.3-0-4ml/24h) sc until discharge 
Ovadia et al.25  Heparin (5,000U) sc twice per day until discharge and compression tights  13.5/9.9  13.5/10.2  9 (50)  2 (17) 
Murphy and Scott26 

ASA: Acetylsalicylic acid (aspirin); D: Drainage; Hb: Haemoglobin; LMWH: Low molecular weight heparin; UFH: Unfractionated heparin; PPI: Proton pump inhibitor; sc: Subcutaneous; po: per os.

*

p<0.05.

Table 4.

Complications.

Authors  Infection profunda, n (%)Haematoma, n (%)Days of hospitalisation
  No D  No D  No D 
Bartosz et al.11  2 (4)  8 (16)  7 (14) 
Fagotti et al.12  1 (2)  3 (6) 
Białecki et al.13  2 (4)  3 (6)  6 (15) 
Suarez et al.14  1.6  1.5 
Koyano et al.15  3 (6) 
Kleinert et al.16  6.6  5.4* 
Cheung et al.17  6* 
Strahovnik et al.18 
Dora et al.19 
Matsuda et al.20  2 (10) 
Walmsley et al.21  2 (0.7)  2 (0.7)  1 (0.3)  10  10 
González della Valle et al.22  2 (4)  5.1  4.7* 
Niskanen et al.23 
Crevoisier et al.24  3 (9)  2 (6)  18  17 
Ovadia et al.25  10.1  8.3 
Murphy and Scott26  1 (5) 

D: Drainage.

*

p<0.05.

Table 5.

Conclusions.

Works  Conclusions 
Bartosz et al.11  Does not recommend the use of drainage in patients who undergo thromboprophylaxis 
Fagotti et al.12  Recommends stopping the use of drainage, inasmuch as it has revealed no changes with respect to complication rates 
Białecki et al.13  Recommends stopping the use of drainage, except for selected cases, given that it has failed to demonstrate any statistically significant changes 
Suarez et al.14  Does not recommend that drainage be used routinely, due to the fact that they find no benefits to its use in patients in whom they used drainage 
Koyano et al.15  Closed suction drainage improves aspects that have to do with inflammation of the surgical site; as a result, they recommend its use to decrease recovery time 
Kleinert et al.16  Recommends discontinuing the use of drainage in hip surgeries performed with the anterior approach and uncemented prostheses. 
Cheung et al.17  Demonstrates that there is no clear benefit associated with the use of suction drainage other than for autologous transfusions. 
Strahovnik et al.18  Asserts that the use of drainage is independent of associated complications and that it is safe, as well as improving the patient's well-being in the postoperative period. 
Dora et al.19  Does not advocate the routine use of drainage because it has been found that those in whom drainage was not used had faster wound care and recovered more quickly, in addition to having a shorter hospital stay. 
Matsuda et al.20  Evinces that not using drainage does not lower the incidence of postoperative anaemia. 
Walmsley et al.21  Claims that there is evidence that there is no benefit to the use of drainage as regards complications in total hip arthroplasty. 
González della Valle et al.22  Recommends discontinuing the routine use of drainage because there are no significant differences between the two groups; furthermore, its use increases costs and can expose the patient to adverse effects. 
Niskanen et al.23  Recommends abandoning the routine use of drainage, inasmuch as all the clinical parameters studied revealed comparable outcomes in those cases in which drainage was used and those in which it was not. 
Crevoisier et al.24  Indicates that drainage is not required when the surgery is uncomplicated, given that the use of drainage has not proven to yield significant differences among patients as regards haematomas, transfusion, rehabilitation, or length of hospitalisation. 
Ovadia et al.25  Claims that routine drainage use is no longer necessary. 
Murphy and Scott26  Asserts that drainage is associated with increased blood loss, does not reduce haematoma, and is unlikely to improve infection rates. 
Discussion

All of the clinical works included in this systematic review are clinical trials that carry an evidence level of 1.

In the studies analysed, a variety of surgical approaches were used: anterior,15,16 lateral,12,18,19,24 anterolateral,15,21 posterolateral,11,13,15,22,25 and posterior;17,20 the posterolateral approach was the most frequently used. Both cemented prostheses and uncemented prostheses or hybrids have been used in the works. In some studies, several types of prostheses have been used simultaneously.13,17,18,22,24,25 This variability of approaches and types of implants notwithstanding, it does not appear that any of them benefit especially from or are particularly disadvantaged by the use of drainage.

Intravenous tranexamic acid has proven to significantly decrease the incidence of anaemia, transfusions, as well as to shorten hospital stay following THA,27–29 and is being used more and more in standard protocols. In keeping with this trend, tranexamic acid was used as an antifibrinolytic in three of the four most recently published studies included in this series.11,13,14 Tranexamic acid use has no bearing on the outcomes with respect to the use of drainage, and all three works recommend discontinuing the use of drainage as a matter of course.11,13,14

Most of the works analysed used different pharmacological measures for antithrombotic prophylaxis, with the exception of one26 that did not use any measure whatsoever,26 and another one20 that used only compression tights and inflatable boots.20 The remaining studies predominantly used LMWH;11,13,15,16,18,19,22–24 others administered heparin,25 and still others, aspirin14 in different doses; however, one study used a combination of prophylactic options, heparin and aspirin,21 while still another called for aspirin together with compression tights.17 Following these various protocols was not associated with any impact on the outcomes of the use of drainage.

Drainage was left in place for 24 or 48h in the studies analysed, and 24h drainage versus 48h drainage was only compared by Strahovnik et al.18 in as many groups, finding no significant differences. Removing drainage at 24 or 48h makes no difference to the majority conclusion to the effect that it is not required on a routine basis.

Haematomas are difficult to prevent as a complication post-THA. They can exert extra pressure on the surrounding tissues and decrease perfusion, thereby fostering bacterial growth.23 Consequently, while drainage has been proposed as a solution to the accumulation of blood and to promote wound healing,1 studies have concluded that drainage does not reduce the volume of haematomas after THA.24,26,30 Subjects with haematomas have been found in both treatment groups, and there is no statistically significant difference between the groups with and without drainage (table 4).

THA is a procedure that involves considerable bleeding, with statistically significant differences between pre- and postoperative Hb values, according to most works. The use of drainage has been associated with greater blood loss11,12 and significantly lower postoperative Hb and hematocrit levels.1 Some of the literature reviewed reports no significant differences in postoperative Hb or hematocrit levels, total blood loss, or transfusion12,16,19,20,24 (table 3). Nevertheless, other studies have documented a substantially greater need for transfusion in the group in which drainage was used.17,21 These two studies are the ones with the largest sample of all those included in this review, which suggests that, given that the actual transfusion rate in THA is relatively low, in studies involving a small study sample, albeit there is a trend toward more transfusions being administered in those cases in which drainage has been placed,12,22,25 it is not enough to detect statistically significant differences because it is a relatively rare event. However, in studies involving larger samples, those groups in whom drainage is used are found to have a higher rate of transfusions.17,21

Postoperative infection is another possible complication of THA and drainage use.1,31 Drainage has been linked to the development of infection, as it allows the soft tissues to communicate with the exterior, thereby enabling retrograde migration of micro-organisms.32,33 Despite the fact that drainage has been correlated with the presence of infection, in these clinical trials, the sample size is not large enough to detect differences in this complication at such a low incidence. In almost all studies a prophylactic antibiotic regimen was administered, with cefuroxime the drug most frequently used.

A hospital stay is a necessary part of the recovery process, which has been found to be prolonged when drainage is used. In three of the studies examined, significant differences with respect to the number of days spent in hospital following surgery were observed among, with a longer mean length of stay in the group in which drainage was used.16,17,22

Of the 16 studies included in this systematic review, 13 conclude that drainage should not be routinely used in Primary THA (Table 5), whereas on work concludes that it does not improve anaemia,20 and only two advocate its use as a matter of course.15,18

The present work has its limitations, inasmuch as a variety of surgical approaches, and cemented and uncemented prostheses were used; furthermore, different protocols for thromboprophylaxis and antibiotic therapy were applied, and, in the more recent studies, the use of tranexamic acid was introduced. All of these variables, while they have not been linked to changes in the outcomes from the use of drainage in, could be a potential risk for bias. The selection of the works selected might be too modest to pick up on statistically significant differences in uncommon complication rates, such as infection or the need for transfusion.

Conclusions

Using drainage in THA does not yield any advantages versus not using it.

The outcomes attained in the clinical trials reviewed point toward drainage not being recommended for routine use in THA.

Level of evidence

Level of evidence I.

Registration

The protocol for this systematic review has not been registered.

Ethical considerations

This study has not involved the use of humans or animals. No patient data has been extracted; a systematic review of the bibliography has been carried out and, therefore, does not require the approval of the ethics committee or informed consent to be given by the patients.

Funding

No funding has been received to conduct this work.

Conflict of interests

The authors have no conflict of interests to declare.

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